Comparative Analysis of Outcomes Among Patients Treated W... | NCT03964649 | Trialant
NCT03964649
Sponsor
Pfizer
Status
Completed
Last Update Posted
Jun 2, 2021Actual
Enrollment
7,308Actual
Phase
Not provided
Conditions
Arthritis, Rheumatoid
Interventions
Not provided
Countries
United States
Protocol Section
Identification Module
NCT ID
Results Section
Participant Flow Module
Pre-assignment Details
Annotation Section
No data available
No data is available for this block.
Document Section
Large Document Module
Document Has No Statistical Analysis Plan (SAP)
Derived Section
Miscellaneous Info Module
Version Holder
NCT03964649
Obsolete or Duplicate NCT IDs
Not provided
Organization Study
A3921305
Secondary IDs
Not provided
Brief Title
Comparative Analysis of Outcomes Among Patients Treated With Xeljanz vs Biologics
Official Title
Comparative Analysis of Outcomes Among Rheumatoid Arthritis Patients Treated With Xeljanz Versus Biologic DMARDs Using a United States Healthcare Claims Database
Acronym
Not provided
Organization
PfizerINDUSTRY
Status Module
Record Verification Date
May 2021
Overall Recruitment Status or Expanded Access Status
Completed
Last Known Status
Not provided
Delayed Posting
Not provided
Why Stopped
Not provided
Expanded Access Info
No
Start Date
Jan 1, 2019Actual
Primary Completion Date
Apr 6, 2020Actual
Completion Date
Apr 6, 2020Actual
First Submitted Date
May 20, 2019
First Submission Date that Met QC Criteria
May 24, 2019
First Posted Date
May 28, 2019Actual
Results Waived
Not provided
Results First Submitted Date
Apr 3, 2021
Results First Submitted that Met QC Criteria
Apr 3, 2021
Results First Posted Date
Apr 30, 2021Actual
Certification/Extension (aka Delayed Results) First Submitted Date
Not provided
Certification/Extension First Submitted that Passed QC Review
Not provided
Certification/Extension First Posted Date
Not provided
Last Update Submitted Date
May 12, 2021
Last Update Posted Date
Jun 2, 2021Actual
Sponsor/Collaborators Module
Responsible Party, by Official Title
Sponsor
Lead Sponsor
PfizerINDUSTRY
Collaborators
Not provided
Oversight Module
No data available
No data is available for this block.
Description Module
Brief Summary
To compare rheumatoid arthritis (RA) patient characteristics, adherence, and costs between patients treated with tofacitinib (IR, XR and combined groups) to patients treated with each of the bDMARDs.
Detailed Description
Not provided
Conditions Module
Conditions
Arthritis, Rheumatoid
Keywords
Not provided
Design Module
Study Type
Observational
Number of References to an Expanded Access Study
Not provided
Expanded Access Types
Not provided
Patient Registry
No
Target Follow-Up Duration
Not provided
Phases
Not provided
Interventional Study Design
Allocation
Not provided
Intervention Model
Biospecimen
No data available
No data is available for this block.
Enrollment
7,308Actual
Arms/Interventions Module
Arm Groups
Label
Type
Description
Intervention Names
Truven Health MarketScan Research Database
To compare RA-related costs among patients treated with tofacitinib (IR, XR and combined groups) to patients treated with each of the bDMARDs (individually, as well as to TNFi and to non-TNFi each combined as groups).
Interventions
Not provided
Outcomes Module
Primary Outcomes
Measure
Description
Time Frame
Number of Participants Who Were on Combination Therapy and Monotherapy During 90 Days After Index Date
In this outcome measure number of participants who were on combination therapy with index medication and who were on monotherapy during 12 months pre-index date were reported. Participants with a use of at least 1 of 4 specific csDMARDs (methotrexate, sulfasalazine, hydroxychloroquine, leflunomide) within 90 days on or after the index date were considered as being treated with combination therapy. Participants who did not take any csDMARDs along with index medication were considered being treated with monotherapy.
Within 90 days after index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Number of participants with most commonly used medications use during 12 months post index period are reported. The 25 most medications: 1) methotrexate sodium, 2) prednisone, 3) folic acid, 4) adalimumab, 5) etanercept, 6) acetaminophen/hydrocodone bitartrate, 7) hydroxychloroquine sulfate, 8) azithromycin, 9) levothyroxine sodium, 10) tramadol hydrochloride, 11) methylprednisolone, 12) gabapentin, 13) albuterol sulfate, 14) amoxicillin/clavulanate potassium, 15) omeprazole, 16) amoxicillin, 17) meloxicam, 18) tofacitinib citrate, 19) fluticasone propionate, 20) cyclobenzaprine hydrochloride, 21) diclofenac sodium, 22) duloxetine hydrochloride, 23) atorvastatin calcium, 24) leflunomide, 25) fluconazole. A participant could have received >=1 most common medication.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Number of Participants Who Used Opioids and Non-steroidal Anti-inflammatory Drug (NSAIDs) During 12 Months Post Index Period
Number of participants who used at least 1 opioid and NSAID during post-index period are reported.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Secondary Outcomes
Not provided
Other Outcomes
Not provided
Eligibility Module
Eligibility Criteria
Inclusion Criteria:
At least one claim for methotrexate during the variable-length pre-index period.
At least one claim for tofacitinib or bDMARDs between 01 February 2016 and 31 July 2019 (the identification period).
Exclusion Criteria:
Patients with claims for other conditions for which bDMARDs are used during the one-year pre-index period or on the index date: ankylosing spondylitis, Crohn's disease, psoriasis, psoriatic arthritis, or ulcerative colitis will be excluded from the study.
Patients with evidence of the index medication during the one-year pre-index period will be removed from the analysis. Patients will be allowed to have been treated with (other) bDMARDs during the one-year pre-index period.
Patients with more than 1 bDMARD or bDMARD with tofacitinib filled on the index date will be removed from the study.
Accepts Healthy Volunteers
No
Sex
All
Sex/Gender Based
Not provided
Sex/Gender Description
Not provided
Minimum Age
0 Years
Maximum Age
Not provided
Standard Ages
ChildAdultOlder Adult
Study Population
This study will utilize the de-identified claims data in the Truven Health MarketScan Research Database.
Sampling Method
Non-Probability Sample
Contacts/Locations Module
Central Contacts
Not provided
Overall Officials
Name
Affiliation
Role
Pfizer CT.gov Call Center
Pfizer
Study Director
Locations
Facility
Status
City
State
ZIP
Country
Contacts
Pfizer
New York
New York
10017
United States
References Module
Citations
Not provided
See Also Links
Label
URL
To obtain contact information for a study center near you, click here.
Pfizer will provide access to individual de-identified participant data and related study documents (e.g. protocol, Statistical Analysis Plan (SAP), Clinical Study Report (CSR)) upon request from qualified researchers, and subject to certain criteria, conditions, and exceptions. Further details on Pfizer's data sharing criteria and process for requesting access can be found at: https://www.pfizer.com/science/clinical\_trials/trial\_data\_and\_results/data\_requests.
Types
Not provided
Time Frame
Not provided
Access Criteria
Not provided
URL
Not provided
Baseline characteristics- age, sex, region of enrollment were evaluated at index date. Other study specific characteristics were observed over 12 months before index date (12 months pre-index baseline period) and/or over variable-length pre-index baseline period. Variable-length pre-index baseline period was minimum of 1 year and could have been maximum up to 5.68 years before index date.
Recruitment Details
Participants with rheumatoid arthritis (RA), who newly initiated tofacitinib or biologic disease-modifying antirheumatic drug (bDMARDs), between 01 February 2016 and 31 July 2019 (identification period), were identified using Truven Health MarketScan Research database. Data for eligible participants from database were evaluated in this retrospective observational study. Index date = date of first claim for index medication (bDMARDs or tofacitinib) during identification period of 3.5 years.
Type of Units Analyzed
Not provided
Arm/Group Information
ID
Title
Description
FG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
FG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
FG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
FG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
FG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
FG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
FG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
FG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
FG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
FG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Periods
Title
Milestones
Reasons Not Completed
Overall Study
Type
Comment
Milestone Data
STARTED
FG000349 subjects
FG001304 subjects
FG0022728 subjects
FG003192 subjects
FG0041948 subjects
FG005349 subjects
FG006376 subjects
FG007325 subjects
FG008204 subjects
FG009533 subjects
COMPLETED
FG000349 subjects
FG001304 subjects
FG0022728 subjects
FG003192 subjects
FG004
NOT COMPLETED
FG0000 subjects
FG0010 subjects
FG0020 subjects
FG0030 subjects
FG004
Baseline Characteristics Module
Baseline Analysis Population Description
Analysis was performed on all participants included in the study.
Type of Units Analyzed
Not provided
Arm/Group Information
ID
Title
Description
BG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
BG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
Denominators
Units
Counts
Participants
BG000
Baseline Measures
Title
Description
Population Description
Parameter Type
Dispersion Type
Unit of Measure
Calculate Percentage
Denominator Units Selected
Denominators
Classes
Age, Continuous
Mean
Outcome Measures Module
Outcome Measures
Type
Title
Description
Population Description
Reporting Status
Anticipated Posting Date
Parameter Type
Dispersion Type
Unit of Measure
Calculate Percentage
Time Frame
Units Analyzed
Denominator Units Selected
Arm/Group Information
Denominators
Classes
Analyses
Primary
Number of Participants Who Were on Combination Therapy and Monotherapy During 90 Days After Index Date
In this outcome measure number of participants who were on combination therapy with index medication and who were on monotherapy during 12 months pre-index date were reported. Participants with a use of at least 1 of 4 specific csDMARDs (methotrexate, sulfasalazine, hydroxychloroquine, leflunomide) within 90 days on or after the index date were considered as being treated with combination therapy. Participants who did not take any csDMARDs along with index medication were considered being treated with monotherapy.
Analysis was performed on all participants included in the study.
Posted
Count of Participants
Participants
Within 90 days after index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Adverse Events Module
Frequency Threshold
0
Time Frame
Not applicable as safety data was not planned to be collected and evaluated during the study
Description
Due to the nature of claims data base from which these data where queried, as planned no adverse events were collected in this study.
All-Cause Mortality Comment
Not provided
Arm/Groups
ID
Title
Description
Deaths (Affected)
Deaths (At Risk)
Serious Events (Affected)
Serious Events (At Risk)
Other Events (Affected)
Other Events (At Risk)
EG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
Mean Number of Pharmacy Claims for Opioids and NSAIDS During 12 Months Post Index Period
The mean number of pharmacy claims for opioids and NSAIDs during the post-index period are reported. A pharmacy claim was defined as a claim made by participants to their insurance provider in purchasing opioids and NSAIDs from the pharmacy.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Mean Number of Days From The Index Date to the First Opioid and NSAIDs Claim During 12 Months Post Index Period
Mean number of days from the index date to the first opioid and NSAIDs claim during post index period are reported.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Number of Participants Who Used Opioids and NSAIDs While Persistent and After Persistent With Index Medication During 12 Months Post Index Period
Number of participants who used opioids and NSAIDs during tofacitinib persistency and post-persistency are reported. Persistence with the index medication was defined as not having a gap in therapy of at least 60 days between fills/infusions.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Number of Participants Who Used Oral Corticosteroids During 12 Months Post-Index Period
The number of participants who used at least 1 oral corticosteroid during the 12 months post-index period are reported.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Number of Participants Who Were Non-persistent to Index Medication
Non-persistence was defined as the gap of at least 60 days in treatment with the index medication or switching to other biologic.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Number of Participants Who Switched Immediately From Index Medication
Participants were classified as switched immediately if they initiated a non-index bDMARD before a 60-day gap in index medication treatment.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Number of Participants Who Discontinued Then Restarted Index Medication
Participants were classified as discontinued and then restarted index medication if there was a gap in the index therapy of at least 60 days and the first medication observed after the gap was the index medication.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Number of Participants Who Discontinued Then Switched From Index Medication
Participants were classified as discontinued and then switched from index medication if there was a gap in the index therapy of at least 60 days and the first medication observed after the gap was a bDMARD (including tofacitinib) different from index medication.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Number of Participants Who Discontinued Without Switching or Restarting Index Medication
Participants were classified as discontinued without switching or restarting index medication if they had a gap in therapy of at least 60 days and there were no claims for either the index medication or a different bDMARD for the remainder of the follow-up period.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Number of Participants Who Switched Any Time From Index Medication
Number of participants who switched from index medication to a biologic at any time during post-index period are reported.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Number of Participants Who Re-started Index Medication at Any Time
Participants who had a claim for the index medication any time after they were considered non-persistent with the index treatment (i.e, including after switching) during the 12-month follow-up are reported. Non-persistence was defined as the gap of at least 60 days in treatment with the index medication or switching to other biologic.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Mean Medication Possession Ratio (MPR) for Methotrexate
MPR was calculated as the total days supply of methotrexate between the first and including the last prescription/administration divided by the time between the first through and including last biologic prescription/administration days supply.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Proportion of Days Covered (PDC)
The PDC was calculated based on total days supply over the 12 months follow-up. The PDC was calculated by using the date of service and the day supply for each fill of the index medication.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Addition of Conventional Synthetic Disease-modifying Antirheumatic Drug (Cs-DMARDs) in Participants With Monotherapy
Participants with monotherapy who used additional csDMARD during post index period are reported.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Adherence to Cs-DMARDs in Participants With Combination Therapy
Adherence was calculated as the total day supply for csDMARDs divided by the number of days from the first claim during the follow-up until the end of the follow-up.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Number of Participants Who Met Different Medication Effectiveness Criteria
Adherence criteria: PDC >=0.8, proportion of days of supply during post-index period of 12 months.Dose escalation criteria: no increase in dose for index drug compared to starting dose during post-index period. Switch criteria: no switching from index drug to (different) biologic agent during post-index period. DMARD criteria: no addition of new csDMARD to index drug during post-index period. Oral glucocorticoid criteria: Participants with no claims for oral glucocorticoids in 6 months pre-index cannot receive oral glucocorticoids for greater than (>)30 days between (index date +91 days) to (index date + 365 days); or participants with claims for oral glucocorticoids in 6 months pre-index no increase in oral glucocorticoid dose during months 6-12 post-index.Injectable glucocorticoid criteria: at most 1 parenteral or intra-articular glucocorticoid joint injection on unique days after participant had been on bDMARD treatment for >3 months between (index date + 91) to (index date + 365).
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
All Cause Inpatient Visits Costs, Outpatient Visits Costs and Emergency Room (ER) Visits Costs During 12 Months Post Index Period
All cause inpatient visits costs, outpatient visits costs and emergency room visits costs during 12 months post index period are reported. Inpatient visit costs consisted of expenses during hospital visit for formal admission. Outpatient visit costs consisted of expenses when participants visited hospital but not for formal admission. Emergency room visit costs consisted of expenses during visit to hospital emergency room.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Rheumatoid Arthritis (RA) Related Inpatient Visits Costs, Outpatient Visits Costs and Emergency Room (ER) Visits Costs During 12 Months Post Index Period
RA related inpatient visit costs consisted of expenses during hospital visits for formal admission for RA. Outpatient visit costs consisted of expenses when participants visited hospital but not for formal admission for RA. ER visit costs consisted of expenses during visit to ER of hospital for RA.
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
All Cause Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Post-Index Period
All cause total health care costs, medical costs, pharmacy costs during 12 months post-index period are reported. All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs).
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
RA Related Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Post-Index Period
RA related total health care costs, medical costs, pharmacy costs during 12 months post-index period are reported. RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs).
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total All Cause Monthly Health Care Cost at Month 1 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 1 post-index date.
Month 1 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total All Cause Monthly Health Care Cost at Month 2 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 2 post-index date.
Month 2 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total All Cause Monthly Health Care Cost at Month 3 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 3 post-index date.
Month 3 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total All Cause Monthly Health Care Cost at Month 4 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 4 of post-index date.
Month 4 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total All Cause Monthly Health Care Cost at Month 5 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 5 post-index date.
Month 5 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total All Cause Monthly Health Care Cost at Month 6 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 6 post-index date.
Month 6 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total All Cause Monthly Health Care Cost at Month 7 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 7 post-index date.
Month 7 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total All Cause Monthly Health Care Cost at Month 8 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 8 post-index date.
Month 8 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total All Cause Monthly Health Care Cost at Month 9 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 9 post-index date.
Month 9 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total All Cause Monthly Health Care Cost at Month 10 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 10 post-index date.
Month 10 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total All Cause Monthly Health Care Cost at Month 11 Post-index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 11 post-index date.
Month 11 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total All Cause Monthly Health Care Cost at Month 12 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 12 post-index date.
Month 12 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total RA Related Monthly Health Care Cost at Month 1 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 1 post-index date.
Month 1 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total RA Related Monthly Health Care Cost at Month 2 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measurec RA related total all cause health care cost in dollars is reported for Month 2 post-index date.
Month 2 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total RA Related Monthly Health Care Cost at Month 3 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 3 post-index date.
Month 3 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total RA Related Monthly Health Care Cost at Month 4 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 4 post-index date.
Month 4 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total RA Related Monthly Health Care Cost at Month 5 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 5 post-index date.
Month 5 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total RA Related Monthly Health Care Cost at Month 6 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 6 post-index date.
Month 6 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total RA Related Monthly Health Care Cost at Month 7 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 7 post-index date.
Month 7 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total RA Related Monthly Health Care Cost at Month 8 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 8 post-index date.
Month 8 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total RA Related Monthly Health Care Cost at Month 9 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 9 post-index date.
Month 9 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total RA Related Monthly Health Care Cost at Month 10 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 10 post-index date.
Month 10 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total RA Related Monthly Health Care Cost at Month 11 Post-index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 11 post-index date.
Month 11 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
Total RA Related Monthly Health Care Cost at Month 12 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 12 post-index date.
Month 12 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
1948 subjects
FG005349 subjects
FG006376 subjects
FG007325 subjects
FG008204 subjects
FG009533 subjects
0 subjects
FG0050 subjects
FG0060 subjects
FG0070 subjects
FG0080 subjects
FG0090 subjects
BG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
BG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
BG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
BG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
BG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
BG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
BG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
BG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
BG010
Total
Total of all reporting groups
349
BG001304
BG0022728
BG003192
BG0041948
BG005349
BG006376
BG007325
BG008204
BG009533
BG0107308
Standard Deviation
years
Title
Denominators
Categories
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG00055.48± 11.04
BG00155.93± 11.26
BG00251.42± 10.35
BG003
Sex: Female, Male
Count of Participants
Participants
Title
Denominators
Categories
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
Female
BG000282
BG001250
BG0022124
BG003
Race and Ethnicity Not Collected
Race and Ethnicity were not collected from any participant.
Count of Participants
Participants
Title
Denominators
Categories
ParticipantsBG0000
ParticipantsBG0010
ParticipantsBG0020
ParticipantsBG0030
ParticipantsBG0040
ParticipantsBG0050
ParticipantsBG0060
ParticipantsBG0070
ParticipantsBG0080
ParticipantsBG0090
ParticipantsBG0100
Title
Measurements
BG0100
Region of Enrollment
Count of Participants
Participants
Title
Denominators
Categories
United States
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
Northeast Region
BG00096
BG00169
BG002422
BG003
Mean Number of bDMARDs Received During 12 Months Pre-Index Baseline Period
bDMARDs included: Tumor-necrosis factor-alpha inhibitors (TNFi) [adalimumab, etanercept, certolizumab pegol, golimumab, infliximab] and non-TNFi's [abatacept, rituximab and tocilizumab].
Mean
Standard Deviation
number of bDMARDs
Title
Denominators
Categories
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG0001.11± 0.32
BG0011.40± 0.59
BG0021.11± 0.31
BG003
Mean Number of bDMARDs Received During Variable Length Pre-Index Baseline Period
Biologic DMARDs included: Tumor-necrosis factor-alpha inhibitors (TNFi) [adalimumab, etanercept, certolizumab pegol, golimumab, infliximab] and non-TNFi's [abatacept, rituximab and tocilizumab].
Mean
Standard Deviation
number of bDMARDs
Title
Denominators
Categories
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG0001.46± 0.73
BG0011.61± 0.81
BG0021.24± 0.55
BG003
Mean Number of csDMARDs Received During 12 Months Pre-Index Baseline Period
In this baseline measure mean of number of conventional synthetic disease-modifying antirheumatic drugs (csDMARDs) used during 12 months pre-index period is reported.
Mean
Standard Deviation
csDMARDs
Title
Denominators
Categories
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG0001.58± 0.66
BG0011.48± 0.66
BG0021.56± 0.69
BG003
Mean Number of csDMARDs Received During Variable Length Pre-Index Baseline Period
In this baseline measure mean of number of conventional synthetic disease-modifying antirheumatic drugs (csDMARDs) used during the variable length pre-index period is reported.
Mean
Standard Deviation
csDMARDs
Title
Denominators
Categories
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG0001.91± 0.89
BG0011.88± 0.87
BG0021.76± 0.82
BG003
Quan-Charlson Comorbidity Score During 12 Months Pre-Index Baseline Period
The mean Quan-Charlson Comorbidity score during pre-index baseline period is reported. Quan-Charlson Comorbidity score predicts probability of death within one year in participants and was based on presence of any diagnosis codes on medical claims at any time during the 12-months pre-index baseline period, based on the international classification of diseases (ICD) diagnosis codes. Total score ranges from 0 to 9.0. A score of 0 indicated that no comorbidities were found. The higher the score, the more likely predicted outcome could result in mortality or higher healthcare resource utilization.
Mean
Standard Deviation
units on a scale
Title
Denominators
Categories
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG0001.77± 1.14
BG0011.89± 1.32
BG0021.63± 1.04
BG003
Number of Participants With Most Commonly Used Medications During 12 Month Pre-index Baseline Period
Number of participants for each of the most commonly used medications during the 12 months pre-index baseline period are reported.
Count of Participants
Participants
Title
Denominators
Categories
Methotrexate Sodium
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG000279
BG001220
BG0022440
BG003
Folic Acid
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Prednisone
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Hydroxychloroquine Sulfate
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Acetaminophen/Hydrocodone Bitartrate
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Methylprednisolone
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Tramadol Hydrochloride
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Azithromycin
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Meloxicam
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Levothyroxine Sodium
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Gabapentin
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Omeprazole
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Albuterol Sulfate
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Diclofenac Sodium
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Leflunomide
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Amoxicillin
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Cyclobenzaprine Hydrochloride
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Fluticasone Propionate
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Amoxicillin/Clavulanate Potassium
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Acetaminophen/Oxycodone Hydrochloride
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Ibuprofen
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Ergocalciferol
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Duloxetine Hydrochloride
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Ciprofloxacin Hydrochloride
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Atorvastatin Calcium
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Number of Participants Who Used Opioids or NSAIDs During 12 Months Pre-Index Baseline Period
Number of participants who used at least one opioid or NSAID during pre-index period are reported.
Count of Participants
Participants
Title
Denominators
Categories
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG000214
BG001236
BG0021,867
BG003
Mean Number of Pharmacy Claims for Opioids and NSAIDS During 12 Months Pre-Index Baseline Period
The mean number of pharmacy claims for opioids and NSAIDs during the pre-index period are reported. A pharmacy claim was defined as a claim made by participants to their insurance provider in purchasing opioids and NSAIDs from the pharmacy.
Here, "overall number of participants analyzed" signifies participants evaluable for this baseline measure.
Mean
Standard Deviation
pharmacy claims
Title
Denominators
Categories
ParticipantsBG000214
ParticipantsBG001236
ParticipantsBG0021867
ParticipantsBG003134
ParticipantsBG0041360
ParticipantsBG005265
ParticipantsBG006277
ParticipantsBG007229
ParticipantsBG008157
ParticipantsBG009380
ParticipantsBG0105119
Title
Measurements
BG0004.04± 6.39
BG0015.31± 6.85
BG0024.08± 5.84
BG003
Number of Participants Who Used Oral Corticosteroids During 12 Months Pre-Index Baseline Period
Count of Participants
Participants
Title
Denominators
Categories
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG000254
BG001222
BG0022,138
BG003
Mean Number of Visits to Rheumatologist During 12 Months Pre-Index Baseline Period
In this baseline measure mean of number of visits made by participants to rheumatologist during 12 months pre-index period is reported.
Mean
Standard Deviation
visits
Title
Denominators
Categories
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG0004.53± 2.38
BG0014.92± 2.90
BG0024.65± 2.47
BG003
Mean Number of Visits to Rheumatologist During Variable-Length Pre-Index Baseline Period
In this baseline measure mean of number of visits made by participants to rheumatologist during variable length pre-index period is reported.
Mean
Standard Deviation
visits
Title
Denominators
Categories
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG00011.28± 8.45
BG00112.12± 8.56
BG0028.21± 5.98
BG003
Disease Duration During Variable-Length Pre-Index Baseline Period
Disease duration was defined as the number of days from the first recorded date of diagnosis of rheumatoid arthritis to the date of the index day.
Mean
Standard Deviation
days
Title
Denominators
Categories
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG000882.61± 558.81
BG001919.71± 437.63
BG002570.38± 481.35
BG003
Out of Pocket Health Care Costs for Healthcare Services During 12 Months Pre-Index Baseline Period
In this baseline measure out of pocket medical care expenses not reimbursed by insurance during 12 months pre-index period is reported.
Mean
Standard Deviation
dollars
Title
Denominators
Categories
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG0001803.44± 1789.99
BG0012154.86± 1828.01
BG0022152.95± 1741.99
BG003
Out of Pocket Health Care Costs for Healthcare Services During Variable Length Pre-Index Period
In this baseline measure out of pocket medical care expenses not reimbursed by insurance during variable length pre-index period is reported.
Mean
Standard Deviation
dollars
Title
Denominators
Categories
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG0006626.03± 5819.96
BG0016549.23± 4717.18
BG0026270.02± 5087.71
BG003
Number of Participants With Comorbidities of Interest During 12 Months Pre-Index Baseline Period
The comorbidities of interest included cardiovascular diseases, chronic obstructive pulmonary disorder (COPD), asthma, kidney disease, diabetes, depression, anxiety, liver disease, sleep disorders, hypertension, hyperlipidemia. A participant could have greater than (>) 1 comorbidity of interest. Pre-index baseline period was the 12 month duration before the index date. The index date was the date of the first claim for bDMARDs or tofacitinib during the identification period.
Count of Participants
Participants
Title
Denominators
Categories
Cardiovascular disease
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG000198
BG001189
BG0021315
BG003
COPD
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Asthma
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Kidney disease
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Diabetes
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Depression
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Anxiety
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Liver disease
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Sleep disorders
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Hypertension
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Hyperlipidemia
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
All cause Inpatient, Outpatient and Emergency Room Visits Costs During 12 Months Pre-Index Period
All cause inpatient visit costs consisted of expenses during hospital visit for formal admission. Outpatient visit costs consisted of expenses when participants visited hospital but not for formal admission. Emergency room (ER) visit costs consisted of expenses during visit to hospital emergency room.
Mean
Standard Deviation
dollars
Title
Denominators
Categories
Inpatient visits costs
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG0006,439.48± 24,897.59
BG0015,918.18± 31,820.77
BG0022796.16± 13970.41
BG003
Outpatient visits costs
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Emergency Room visits costs
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
RA Related Inpatient, Outpatient and ER Visits Costs During 12 Months Pre-Index Baseline Period
RA related inpatient visit costs consisted of expenses during hospital visits for formal admission for RA. Outpatient visit costs consisted of expenses when participants visited hospital but not for formal admission for RA. ER visit costs consisted of expenses during visit to ER of hospital for RA.
Mean
Standard Deviation
dollars
Title
Denominators
Categories
Inpatient visits cost
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG0003,089.94± 14,786.15
BG0012,831.70± 14,317.53
BG0021151.57± 7901.71
BG003
Outpatient visits costs
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ER visits costs
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
All Cause Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Pre-Index Period
All cause total health care costs, medical costs, pharmacy costs during 12 months pre-index period are reported. All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs).
Mean
Standard Deviation
dollars
Title
Denominators
Categories
Health care costs
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG00024,420.92± 47,406.99
BG00130,416.53± 43,264.63
BG00216168.53± 25602.71
BG003
Medical costs
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Pharmacy costs
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
RA Related Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Pre-Index Period
RA related total health care costs, medical costs, pharmacy costs during 12 months pre-index period are reported. RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs).
Mean
Standard Deviation
dollars
Title
Denominators
Categories
Health care costs
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG0008,833.52± 25,667.44
BG00114,943.61± 24,196.06
BG0024546.86± 10379.97
BG003
Medical costs
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Pharmacy costs
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Total All Cause Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this baseline characteristic total all cause health care cost in dollars is reported for each month of pre-index baseline period.
Mean
Standard Deviation
dollars
Title
Denominators
Categories
Month 1
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG0001,472.00± 3,964.00
BG0011,585.23± 4,511.40
BG0021,195.47± 2,995.66
BG003
Month 2
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 3
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 4
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 5
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 6
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 7
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 8
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 9
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 10
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 11
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 12
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Total RA Related Monthly Health Care Cost During 12 Months Pre-Index Baseline Period
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this baseline characteristic RA related total all cause health care cost in dollars is reported for each month of pre-index baseline period.
Mean
Standard Deviation
dollars
Title
Denominators
Categories
Month 1
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
ParticipantsBG0041948
ParticipantsBG005349
ParticipantsBG006376
ParticipantsBG007325
ParticipantsBG008204
ParticipantsBG009533
ParticipantsBG0107308
Title
Measurements
BG000406.83± 1,619.24
BG001703.28± 3,907.43
BG002439.11± 1,589.58
BG003
Month 2
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 3
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 4
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 5
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 6
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 7
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 8
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 9
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 10
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 11
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Month 12
ParticipantsBG000349
ParticipantsBG001304
ParticipantsBG0022728
ParticipantsBG003192
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003192
OG0041948
OG005349
OG006376
OG007325
OG008204
OG009533
Title
Denominators
Categories
Combination therapy
Title
Measurements
OG000183
OG001168
OG0022001
OG003119
OG0041373
OG005266
OG006279
OG007194
OG008101
OG009350
Monotherapy
Title
Measurements
OG000166
OG001136
OG002727
OG003
Primary
Number of Participants for Each of the Most Commonly Used Medications During the 12 Months Post-index Date
Number of participants with most commonly used medications use during 12 months post index period are reported. The 25 most medications: 1) methotrexate sodium, 2) prednisone, 3) folic acid, 4) adalimumab, 5) etanercept, 6) acetaminophen/hydrocodone bitartrate, 7) hydroxychloroquine sulfate, 8) azithromycin, 9) levothyroxine sodium, 10) tramadol hydrochloride, 11) methylprednisolone, 12) gabapentin, 13) albuterol sulfate, 14) amoxicillin/clavulanate potassium, 15) omeprazole, 16) amoxicillin, 17) meloxicam, 18) tofacitinib citrate, 19) fluticasone propionate, 20) cyclobenzaprine hydrochloride, 21) diclofenac sodium, 22) duloxetine hydrochloride, 23) atorvastatin calcium, 24) leflunomide, 25) fluconazole. A participant could have received >=1 most common medication.
Analysis was performed on all participants included in the study.
Posted
Count of Participants
Participants
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Methotrexate Sodium
Title
Measurements
OG000163
OG001136
OG0021,789
OG003
Primary
Number of Participants Who Used Opioids and Non-steroidal Anti-inflammatory Drug (NSAIDs) During 12 Months Post Index Period
Number of participants who used at least 1 opioid and NSAID during post-index period are reported.
Analysis was performed on all participants included in the study.
Posted
Count of Participants
Participants
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG000210
OG001205
OG0021,623
OG003
Primary
Mean Number of Pharmacy Claims for Opioids and NSAIDS During 12 Months Post Index Period
The mean number of pharmacy claims for opioids and NSAIDs during the post-index period are reported. A pharmacy claim was defined as a claim made by participants to their insurance provider in purchasing opioids and NSAIDs from the pharmacy.
Analysis was performed on all participants included in the study. Here, "overall number of participants analyzed" signifies participants evaluable for this outcome measure.
Posted
Mean
Standard Deviation
pharmacy claims
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000210
OG001205
OG0021623
OG003
Title
Denominators
Categories
Title
Measurements
OG0003.68± 6.04
OG0014.99± 6.87
OG0023.78± 5.98
OG003
Primary
Mean Number of Days From The Index Date to the First Opioid and NSAIDs Claim During 12 Months Post Index Period
Mean number of days from the index date to the first opioid and NSAIDs claim during post index period are reported.
Analysis was performed on all participants included in the study. Here, "overall number of participants analyzed" signifies participants evaluable for this outcome measure.
Posted
Mean
Standard Deviation
days
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000210
OG001205
OG0021623
OG003
Title
Denominators
Categories
Days to First Opioid
Title
Measurements
OG00085.35± 94.49
OG00183.31± 95.78
OG00295.67± 98.71
OG003
Primary
Number of Participants Who Used Opioids and NSAIDs While Persistent and After Persistent With Index Medication During 12 Months Post Index Period
Number of participants who used opioids and NSAIDs during tofacitinib persistency and post-persistency are reported. Persistence with the index medication was defined as not having a gap in therapy of at least 60 days between fills/infusions.
Analysis was performed on all participants included in the study.
Posted
Count of Participants
Participants
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Used Opioids While Persistent
Title
Measurements
OG000138
OG001128
OG0021,035
OG003
Primary
Number of Participants Who Used Oral Corticosteroids During 12 Months Post-Index Period
The number of participants who used at least 1 oral corticosteroid during the 12 months post-index period are reported.
Analysis was performed on all participants included in the study.
Posted
Count of Participants
Participants
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG000198
OG001216
OG0021,713
OG003
Primary
Number of Participants Who Were Non-persistent to Index Medication
Non-persistence was defined as the gap of at least 60 days in treatment with the index medication or switching to other biologic.
Analysis was performed on all participants included in the study.
Posted
Count of Participants
Participants
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG000166
OG001189
OG0021381
OG003
Primary
Number of Participants Who Switched Immediately From Index Medication
Participants were classified as switched immediately if they initiated a non-index bDMARD before a 60-day gap in index medication treatment.
Analysis was performed on all participants included in the study.
Posted
Count of Participants
Participants
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG00041
OG00170
OG002575
OG003
Primary
Number of Participants Who Discontinued Then Restarted Index Medication
Participants were classified as discontinued and then restarted index medication if there was a gap in the index therapy of at least 60 days and the first medication observed after the gap was the index medication.
Analysis was performed on all participants included in the study.
Posted
Count of Participants
Participants
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG00043
OG00133
OG002201
OG003
Primary
Number of Participants Who Discontinued Then Switched From Index Medication
Participants were classified as discontinued and then switched from index medication if there was a gap in the index therapy of at least 60 days and the first medication observed after the gap was a bDMARD (including tofacitinib) different from index medication.
Analysis was performed on all participants included in the study.
Posted
Count of Participants
Participants
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG00012
OG00124
OG002127
OG003
Primary
Number of Participants Who Discontinued Without Switching or Restarting Index Medication
Participants were classified as discontinued without switching or restarting index medication if they had a gap in therapy of at least 60 days and there were no claims for either the index medication or a different bDMARD for the remainder of the follow-up period.
Analysis was performed on all participants included in the study.
Posted
Count of Participants
Participants
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG00070
OG00162
OG002478
OG003
Primary
Number of Participants Who Switched Any Time From Index Medication
Number of participants who switched from index medication to a biologic at any time during post-index period are reported.
Analysis was performed on all participants included in the study.
Posted
Count of Participants
Participants
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG00055
OG00196
OG002727
OG003
Primary
Number of Participants Who Re-started Index Medication at Any Time
Participants who had a claim for the index medication any time after they were considered non-persistent with the index treatment (i.e, including after switching) during the 12-month follow-up are reported. Non-persistence was defined as the gap of at least 60 days in treatment with the index medication or switching to other biologic.
Analysis was performed on all participants included in the study.
Posted
Count of Participants
Participants
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG00025
OG00125
OG002132
OG003
Primary
Mean Medication Possession Ratio (MPR) for Methotrexate
MPR was calculated as the total days supply of methotrexate between the first and including the last prescription/administration divided by the time between the first through and including last biologic prescription/administration days supply.
Analysis was performed on all participants included in the study. As per planned analysis MPR was not evaluated for Rituximab arm.
Posted
Mean
Standard Deviation
ratio
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0000.89± 0.16
OG0010.87± 0.18
OG0020.91± 0.14
OG003
Primary
Proportion of Days Covered (PDC)
The PDC was calculated based on total days supply over the 12 months follow-up. The PDC was calculated by using the date of service and the day supply for each fill of the index medication.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
proportion of days
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0000.65± 0.32
OG0010.55± 0.32
OG0020.66± 0.31
OG003
Primary
Addition of Conventional Synthetic Disease-modifying Antirheumatic Drug (Cs-DMARDs) in Participants With Monotherapy
Participants with monotherapy who used additional csDMARD during post index period are reported.
Analysis was performed on all participants included in the study. Here, "overall number of participants analyzed" signifies the participants who initiated treatment as monotherapy with index medication only.
Posted
Count of Participants
Participants
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000166
OG001136
OG002727
OG003
Title
Denominators
Categories
Title
Measurements
OG00048
OG00137
OG002247
OG003
Primary
Adherence to Cs-DMARDs in Participants With Combination Therapy
Adherence was calculated as the total day supply for csDMARDs divided by the number of days from the first claim during the follow-up until the end of the follow-up.
Analysis was performed on all participants included in the study. Here, "overall number of participants analyzed" signifies the participants who initiated treatment as combination therapy with index medication and cs-DMARDs.
Posted
Mean
Standard Deviation
ratio
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000183
OG001168
OG0022001
OG003
Title
Denominators
Categories
Title
Measurements
OG0000.72± 0.30
OG0010.79± 0.26
OG0020.77± 0.27
OG003
Primary
Number of Participants Who Met Different Medication Effectiveness Criteria
Adherence criteria: PDC >=0.8, proportion of days of supply during post-index period of 12 months.Dose escalation criteria: no increase in dose for index drug compared to starting dose during post-index period. Switch criteria: no switching from index drug to (different) biologic agent during post-index period. DMARD criteria: no addition of new csDMARD to index drug during post-index period. Oral glucocorticoid criteria: Participants with no claims for oral glucocorticoids in 6 months pre-index cannot receive oral glucocorticoids for greater than (>)30 days between (index date +91 days) to (index date + 365 days); or participants with claims for oral glucocorticoids in 6 months pre-index no increase in oral glucocorticoid dose during months 6-12 post-index.Injectable glucocorticoid criteria: at most 1 parenteral or intra-articular glucocorticoid joint injection on unique days after participant had been on bDMARD treatment for >3 months between (index date + 91) to (index date + 365).
Analysis was performed on all participants included in the study.
Posted
Count of Participants
Participants
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Met adherence criteria
Title
Measurements
OG000168
OG00198
OG0021249
OG003
Primary
All Cause Inpatient Visits Costs, Outpatient Visits Costs and Emergency Room (ER) Visits Costs During 12 Months Post Index Period
All cause inpatient visits costs, outpatient visits costs and emergency room visits costs during 12 months post index period are reported. Inpatient visit costs consisted of expenses during hospital visit for formal admission. Outpatient visit costs consisted of expenses when participants visited hospital but not for formal admission. Emergency room visit costs consisted of expenses during visit to hospital emergency room.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Inpatient visits costs
Title
Measurements
OG0005,301.85± 20,548.39
OG0014,326.53± 18,879.99
OG0023,863.95± 20,664.73
OG003
Primary
Rheumatoid Arthritis (RA) Related Inpatient Visits Costs, Outpatient Visits Costs and Emergency Room (ER) Visits Costs During 12 Months Post Index Period
RA related inpatient visit costs consisted of expenses during hospital visits for formal admission for RA. Outpatient visit costs consisted of expenses when participants visited hospital but not for formal admission for RA. ER visit costs consisted of expenses during visit to ER of hospital for RA.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Inpatient visits costs
Title
Measurements
OG0002,465.50± 13,108.37
OG0012,470.87± 13,911.22
OG0022,215.74± 15,372.12
OG003
Primary
All Cause Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Post-Index Period
All cause total health care costs, medical costs, pharmacy costs during 12 months post-index period are reported. All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs).
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Total health care costs
Title
Measurements
OG00061,431.53± 50,673.36
OG00153,150.92± 35,767.69
OG00266,645.17± 38,833.73
OG003
Primary
RA Related Total Health Care Costs, Medical Costs, Pharmacy Costs During 12 Months Post-Index Period
RA related total health care costs, medical costs, pharmacy costs during 12 months post-index period are reported. RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs).
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
During 12 months post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Total health care costs
Title
Measurements
OG00044,134.19± 24,089.13
OG00138,462.40± 22,381.48
OG00254,892.62± 27,900.44
OG003
Primary
Total All Cause Monthly Health Care Cost at Month 1 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 1 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 1 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0007,985.18± 5,870.38
OG0016,989.92± 3,627.60
OG0029,290.98± 4,894.97
OG003
Primary
Total All Cause Monthly Health Care Cost at Month 2 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 2 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 2 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0004,805.26± 8,465.89
OG0013,207.83± 2,974.52
OG0024,661.95± 5,512.59
OG003
Primary
Total All Cause Monthly Health Care Cost at Month 3 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 3 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 3 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0005,093.95± 7,838.08
OG0014,551.06± 5,175.57
OG0025,975.14± 6,404.19
OG003
Primary
Total All Cause Monthly Health Care Cost at Month 4 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 4 of post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 4 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0005,079.28± 10,071.92
OG0013,969.48± 5,061.60
OG0025,301.22± 6,550.05
OG003
Primary
Total All Cause Monthly Health Care Cost at Month 5 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 5 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 5 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0004,122.15± 6,848.85
OG0014,874.41± 9,227.40
OG0024,828.27± 5,749.33
OG003
Primary
Total All Cause Monthly Health Care Cost at Month 6 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 6 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 6 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0004,867.20± 11,052.21
OG0013,826.79± 6,801.85
OG0025,997.83± 13,221.77
OG003
Primary
Total All Cause Monthly Health Care Cost at Month 7 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 7 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 7 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0004,950.36± 8,724.15
OG0014,939.24± 11,793.47
OG0025,004.78± 6,780.50
OG003
Primary
Total All Cause Monthly Health Care Cost at Month 8 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 8 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 8 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0003,815.56± 5,915.52
OG0014,139.87± 6,027.39
OG0025,021.37± 6,364.92
OG003
Primary
Total All Cause Monthly Health Care Cost at Month 9 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 9 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 9 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0004,300.84± 5,689.33
OG0014,399.74± 7,749.58
OG0025,335.04± 7,227.68
OG003
Primary
Total All Cause Monthly Health Care Cost at Month 10 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 10 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 10 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0005,670.69± 21,678.99
OG0013,939.86± 4,973.50
OG0025,186.08± 11,341.01
OG003
Primary
Total All Cause Monthly Health Care Cost at Month 11 Post-index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 11 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 11 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0004,244.03± 6,261.71
OG0014,083.34± 7,378.37
OG0025,032.88± 6,919.38
OG003
Primary
Total All Cause Monthly Health Care Cost at Month 12 Post Index Date
All cause refers to cost spent due to all comorbidities including RA. Total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure total all cause health care cost in dollars is reported for Month 12 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 12 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0006,497.03± 16,191.59
OG0014,229.36± 4,796.31
OG0025,009.64± 6,414.68
OG003
Primary
Total RA Related Monthly Health Care Cost at Month 1 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 1 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 1 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0006,743.68± 3,290.35
OG0016,021.42± 3,153.69
OG0028,562.89± 4,383.18
OG003
Primary
Total RA Related Monthly Health Care Cost at Month 2 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measurec RA related total all cause health care cost in dollars is reported for Month 2 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 2 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0002,998.35± 3,709.88
OG0012,450.14± 2,559.50
OG0023,876.12± 4,442.59
OG003
Primary
Total RA Related Monthly Health Care Cost at Month 3 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 3 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 3 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0003,747.82± 4,128.35
OG0013,494.46± 3,952.15
OG0025,049.33± 5,212.08
OG003
Primary
Total RA Related Monthly Health Care Cost at Month 4 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 4 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 4 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0003,935.88± 8,393.52
OG0012,932.92± 4,452.72
OG0024,279.35± 4,913.29
OG003
Primary
Total RA Related Monthly Health Care Cost at Month 5 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 5 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 5 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0002,872.41± 4,212.74
OG0013,192.69± 5,189.22
OG0023,951.04± 4,643.52
OG003
Primary
Total RA Related Monthly Health Care Cost at Month 6 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 6 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 6 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0003,914.17± 8,567.41
OG0012,567.31± 3,448.98
OG0024,657.35± 8,370.54
OG003
Primary
Total RA Related Monthly Health Care Cost at Month 7 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 7 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 7 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0003,493.19± 3,937.61
OG0013,724.00± 10,798.76
OG0023,937.19± 4,482.39
OG003
Primary
Total RA Related Monthly Health Care Cost at Month 8 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 8 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 8 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0002,724.51± 3,993.58
OG0012,945.03± 5,092.32
OG0024,118.25± 5,281.28
OG003
Primary
Total RA Related Monthly Health Care Cost at Month 9 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 9 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 9 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0003,304.66± 4,833.81
OG0012,938.67± 5,812.01
OG0024,368.93± 6,456.66
OG003
Primary
Total RA Related Monthly Health Care Cost at Month 10 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 10 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 10 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0003,416.78± 5,512.87
OG0012,848.24± 4,237.09
OG0024,146.86± 10,401.39
OG003
Primary
Total RA Related Monthly Health Care Cost at Month 11 Post-index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 11 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 11 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0003,010.75± 4,511.85
OG0012,418.53± 3,287.81
OG0023,926.41± 4,868.49
OG003
Primary
Total RA Related Monthly Health Care Cost at Month 12 Post Index Date
RA related total health care cost was calculated as the total of pharmacy cost (home healthcare cost, urgent care cost and other medical services costs) and medical cost (ambulatory cost, emergency department visits cost, inpatient admission cost and other costs). In this outcome measure RA related total all cause health care cost in dollars is reported for Month 12 post-index date.
Analysis was performed on all participants included in the study.
Posted
Mean
Standard Deviation
dollars
Month 12 post-index date (index date =date of first claim for index medication [bDMARDs or tofacitinib] during identification period of 3.5 years)
ID
Title
Description
OG000
Tofacitinib XR
Participants who started treatment with modified-release (XR) tofacitinib during identification period were included in this arm.
OG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
OG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
OG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
OG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
OG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
OG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
OG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
OG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
OG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
Units
Counts
Participants
OG000349
OG001304
OG0022728
OG003
Title
Denominators
Categories
Title
Measurements
OG0003,971.99± 7,435.02
OG0012,929.00± 3,457.82
OG0024,018.90± 5,462.12
OG003
0
0
0
0
0
0
EG001
Tofacitinib IR
Participants who started treatment with immediate-release (IR) tofacitinib during identification period were included in this arm.
0
0
0
0
0
0
EG002
Adalimumab
Participants who started treatment with adalimumab (tumor-necrosis factor-alpha inhibitor [TNFI]) during identification period were included in this arm.
0
0
0
0
0
0
EG003
Certolizumab Pegol
Participants who started treatment with certolizumab pegol (TNFI) during identification period were included in this arm.
0
0
0
0
0
0
EG004
Etanercept
Participants who started treatment with etanercept (TNFI) during identification period were included in this arm.
0
0
0
0
0
0
EG005
Infliximab
Participants who started treatment with infliximab (TNFI) during identification period were included in this arm.
0
0
0
0
0
0
EG006
Golimumab
Participants who started treatment with golimumab (TNFI) during identification period were included in this arm.
0
0
0
0
0
0
EG007
Rituximab
Participants who started treatment with rituximab (non-TNFI) during identification period were included in this arm.
0
0
0
0
0
0
EG008
Tocilizumab
Participants who started treatment with tocilizumab (non-TNFI) during identification period were included in this arm.
0
0
0
0
0
0
EG009
Abatacept
Participants who started treatment with abatacept (non-TNFI) during identification period were included in this arm.
0
0
0
0
0
0
OTHER
Results Disclosure Restriction on PI(s)?
Yes
Other Details
Pfizer has the right to review disclosures, requesting a delay of less than 60 days. Investigator will postpone single center publications until after disclosure of pooled data (all sites), less than 12 months from study completion/termination at all participating sites. Investigator may not disclose previously undisclosed confidential information other than study results.