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Knee osteoarthritis is one of the most prevalent orthopedic conditions worldwide. With the aging population, a 40% patient increase is expected to present at clinics with complaints of primary osteoarthritis by 2025. Multiple studies have attempted to establish non-surgical criteria for knee arthritis and usage of resources to avoid major surgery. It has long been accepted as a treatment option for patients who have failed to respond to NSAIDs and other non-surgical therapies to receive intra-articular injections of steroid and anesthesia mixtures to hold off disease progression.
Various studies have compared different sites of injection and the accuracy rate of the injection being within the joint. Recent studies report a 66% accuracy on palpation-guided injection on the anterolateral knee, 93% accuracy on palpation-guided injection on the superolateral portal of the knee, and new studies show an improvement of up to 98% with use of ultrasound guiding software. However, in a health care system with limited resources, providing patients with US-guided injections represented an increased cost of $178.35 per patient as per 2010 Medicare reports.
Therefore, assuming these accuracy rates, we will compare the anterolateral and superolateral portals for knee injection and their clinical effect to monitor if in fact there is a difference in patient reported outcomes. As a secondary analysis, if no difference is found, a strong case for palpation-guided injections versus ultrasound-guided injections can be made.
In this study we will prospectively enroll 60 patients to be divided into two 30 patient groups with primary knee osteoarthritis. Patients that qualify as subjects will be treated with an intraarticular knee injection through an anterolateral portal or a suprapatellar portal as per group in which they are placed. Scores will be given for pain of the injection and of the baseline illness and compared on a subsequent visit to assess self-reported functional outcomes.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Suprapatellar Knee Injection Site | Active Comparator | Patients will be injected specified dose of lidocaine and depomedrol through suprapatellar-lateral knee entry site. |
|
| Anterolateral knee injection | Active Comparator | Patients will be injected specified dose of lidocaine and depomedrol through anterolateral knee entry site. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Depomedrol | Drug | Depomedrol 40 mg/ml, 1 ml injected to knee on day one of intervention. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Short Term Pain improvement | 1 week | |
| Medium Term Pain Improvement | 1 month | |
| Self Reported Patient Scores Improvement | WOMAC and Visual Analog Scale will be used to monitor improvement | 1 month |
| Measure | Description | Time Frame |
|---|---|---|
| Pain on injection site | Will compare pain on site of injection on study arms. | baseline |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Ariel D Davila-Parrilla, MD | University of Puerto Rico Orthopedics Department | Principal Investigator |
| Antonio Otero-Lopez, MD | University of Puerto Rico Orthopedics Department | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Puerto Rico School Of Medicine Outpatient Clinics | San Juan | 00918 | Puerto Rico |
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|
| Lidocaine | Drug | Lidocaine 2% soln, 4 ml injected to knee on day 1 of intervention |
|
|
| ID | Term |
|---|---|
| D020370 | Osteoarthritis, Knee |
| D001168 | Arthritis |
| ID | Term |
|---|---|
| D010003 | Osteoarthritis |
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
| D012216 | Rheumatic Diseases |
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| ID | Term |
|---|---|
| D008012 | Lidocaine |
| ID | Term |
|---|---|
| D000083 | Acetanilides |
| D000813 | Anilides |
| D000577 | Amides |
| D009930 | Organic Chemicals |
| D000814 | Aniline Compounds |
| D000588 | Amines |
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