Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| GlaxoSmithKline | INDUSTRY |
| Institut National en Santé Publique du Québec | OTHER |
| Laval University | OTHER |
| CHU de Quebec-Universite Laval |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Influenza vaccines are continuously modified to adjust to the virus antigenic shifts or drifts, and its safety profile may vary. While generally considered safe, influenza vaccines have been associated in the past with increases in cases of Guillain-Barré syndrome (1976) or with oculorespiratory syndrome (2001). The emergence of a novel strain of H1N1 influenza virus (pH1N1) has prompted health departments worldwide to prepare for mass vaccination campaigns with a new H1N1 pandemic vaccine. Following recommendations of the World Health Organization (WHO), Canada immunized its population with a dose-sparing adjuvanted vaccine. While the adjuvant developed by GlaxoSmithKline (GSK) has been administered to over 39 000 people, only a few hundred will have been vaccinated with the H1N1 formulation in clinical trials before the mass campaign was launched. With this small number, adverse events occurring at a rate < 1% will not be detected by these clinical trials.
Considering that most cases of pH1N1 to date have been relatively mild, it will be imperative to rapidly detect adverse events serious enough to reconsider the use of the vaccine. Passive surveillance is collecting notifications of adverse events but the sensitivity of this system is not high and its timeliness is not necessarily optimal.
In Canada, healthcare workers (HCW) are among those who were offered the new pandemic vaccine in priority. Because they were offered the vaccine early in the campaign and because they constitute a well-defined group in good general health, this group of people may be well suited for monitoring the safety of the pH1N1 vaccine.
The main objective of this project was to estimate in HCW vaccinated against pH1N1 the frequency of adverse events of sufficient severity to cause work absenteeism or medical consultation.
The active surveillance was done in HCW from 3 sites (Canadian hospitals) participating in the Pandemic Influenza Research Network (PCIRN): (1) Halifax (Nova Scotia), (2) Quebec City (Quebec): 3 hospitals, (3) Toronto
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Health care workers in Québec | Health care workers from CHUQ hospitals | ||
| Health care workers in Toronto | Health care workers from the Mount Sinai Hospital | ||
| Health care workers in Halifax | Health care workers from the Queen Elizabeth Hospital |
Not provided
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants Who Had Experienced a New Health Problem or the Worsening of an Existing Health Condition That Resulted in a Medical Consultation. | at day 8, 15 and 29 | |
| Number of Participants Who Had Experienced a New Health Problem or the Worsening of an Existing Health Condition That Resulted in Work Absenteeism. | day 8, 15 and 29 | |
| the Occurrence of Serious Adverse Events (SAE) | 6 months |
Not provided
Not provided
Inclusion Criteria:
Exclusion Criteria:
-
Not provided
Not provided
Not provided
The active surveillance was conducted in three Canadian hospitals participating in the Public Health Agency of Canada/Canadian Institutes for Health Research- Influenza Research Network (PCIRN): Quebec City, Toronto, and Halifax. Healthcare workers immunized in these institutions were offered to participate in a web-based active surveillance of vaccine safety.
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Gaston De Serres, MD, PhD | Institut National en Santé Publique du Québec | Principal Investigator |
Not provided
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 22802929 | Derived | De Serres G, Gariepy MC, Coleman B, Rouleau I, McNeil S, Benoit M, McGeer A, Ambrose A, Needham J, Bergeron C, Grenier C, Sleigh K, Kallos A, Ouakki M, Ouhoummane N, Stiver G, Valiquette L, McCarthy A, Bettinger J; PHAC-CIHR influenza Research Network (PCIRN). Short and long-term safety of the 2009 AS03-adjuvanted pandemic vaccine. PLoS One. 2012;7(7):e38563. doi: 10.1371/journal.pone.0038563. Epub 2012 Jul 3. |
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Title | Description |
|---|---|---|
| FG000 | Health Care Workers | Health care workers from all hospitals |
| Title | Milestones | Reasons Not Completed | |||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Day 8 Survey |
|
| |||||||||||||||||||||
| Day 29 Survey |
|
Not provided
Not provided
| ID | Title | Description |
|---|---|---|
| BG000 | Health Care Workers in Quebec | Health care workers from Quebec |
| BG001 | Health Care Workers in Toronto | Health Care Workers from Toronto |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age Categorical | Demographic data was collected in only one site (n=3159). Some participants did not complete all the questions. That's why we don't have the age and the gender for all the participants. |
| 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 Had Experienced a New Health Problem or the Worsening of an Existing Health Condition That Resulted in a Medical Consultation. | Posted | Number | participants | at day 8, 15 and 29 |
|
|
6 months
Not provided
Not provided
| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Health Care Workers From CHUQ Hospitals |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Breast cancer | Reproductive system and breast disorders |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Local reaction | Skin and subcutaneous tissue disorders |
Only 52% answered the 3 surveys. We don't know why 48% didn't complete the 3 surveys (were they too sick or not motivated).We didn't have a group of comparable unvaccinated individuals (to estimate the risks attributable to the vaccine).
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Gaston De Serres | Laval University | 418-666-7000 | 274 | gaston.deserres@ssss.gouv.qc.ca |
Not provided
| OTHER |
| Queen Elizabeth II Health Sciences Centre | OTHER |
| Mount Sinai Hospital, New York | OTHER |
| The Ottawa Hospital | OTHER |
| Hamilton Health Sciences Corporation | OTHER |
| Alberta Children's Hospital | OTHER |
| Vancouver General Hospital | OTHER |
Not provided
Not provided
Not provided
|
| BG002 | Health Care Workers in Halifax | Health Care Workers from Halifax |
| BG003 | Total | Total of all reporting groups |
| Number |
| participants |
|
| Age Continuous | Mean | Standard Deviation | years |
|
| Gender | Demographic data was collected in only one site (n=3159). Some participants did not complete all the questions. That's why we don't have the age and the gender for all the participants. | Number | participants |
|
| Region of Enrollment | Number | participants |
|
|
| Primary | Number of Participants Who Had Experienced a New Health Problem or the Worsening of an Existing Health Condition That Resulted in Work Absenteeism. | Posted | Number | participants | day 8, 15 and 29 |
|
|
|
| Primary | the Occurrence of Serious Adverse Events (SAE) | Posted | Number | participants | 6 months |
|
|
|
| 35 |
| 3,064 |
| 383 |
| 4,984 |
| lung cancer | Respiratory, thoracic and mediastinal disorders |
|
| pancreas cancer | Endocrine disorders |
|
| cervix precancerous cells | Reproductive system and breast disorders |
|
| gynecologic problems/obstetrical | Pregnancy, puerperium and perinatal conditions |
|
| gynecologic problems | Reproductive system and breast disorders |
|
| Respiratory infection | Infections and infestations |
|
| Gastroenteritis | Gastrointestinal disorders |
|
| cutaneous infection | Infections and infestations |
|
| toxic shock syndrome | Infections and infestations |
|
| abdominal problems | Gastrointestinal disorders |
|
| Musculoskeletal problems | Musculoskeletal and connective tissue disorders |
|
| depression | Psychiatric disorders |
|
| Anaphylactic shock | Immune system disorders |
|
| Chronic pericarditis | Cardiac disorders |
|
| Eye problem | Eye disorders |
|
| ear surgery | Surgical and medical procedures |
|
| severe headaches | General disorders |
|
| Asthma | Respiratory, thoracic and mediastinal disorders |
|
| Vaso-vasectomy | Surgical and medical procedures |
|
| no diagnosis | Injury, poisoning and procedural complications | intermittent pain in the arm. |
|
| myalgia | General disorders |
|
| respiratory problems | Respiratory, thoracic and mediastinal disorders |
|
| gastroenteritis | Gastrointestinal disorders |
|
Not provided
Not provided