Study of Knowledge Translation of Clinical Practice Guidelines for Ventilator Associated Pneumonia (ABATEVAP)
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Purpose
The purpose of this prospective, multicentre, time-series study is to develop, implement, refine, and evaluate a sustainable behaviour change strategy in the intensive care unit (ICU).
| Condition | Intervention |
|---|---|
|
Ventilator Associated Pneumonia |
Behavioral: Education |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Active Observational Study of the Adoption and Transfer of Clinical Practice Guidelines Through Education, for Ventilator Associated Pneumonia (ABATE VAP Study) |
| Enrollment: | 1320 |
| Study Start Date: | April 2007 |
| Study Completion Date: | July 2010 |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
1
Patients receiving invasive mechanical ventilation > 48 hours.
|
Behavioral: Education
Implementation of clinical practice guideline for ventilator associated pneumonia through education.
|
Detailed Description:
Background:
In order to improve the care of our patients, it is necessary for research evidence to be translated into clinical practice. There are gaps in our understanding of knowledge translation (KT) and this is evident in the Intensive Care Unit (ICU), specifically as it applies to the prevention, diagnosis and treatment of ventilator-associated pneumonia (VAP). VAP is associated with a high burden of illness in the critically ill and there is an extensive amount of research evidence on this disease. It has been demonstrated that best practice as defined by research evidence is not uniformly applied to VAP. In addition, recent advances in VAP knowledge need be disseminated and implemented in order to improve patient safety and outcomes from VAP. A systematic process of knowledge transfer is crucial to translate this research into evidence-based bedside practice and the development and implementation of evidence based Clinical Practice Guidelines (CPGs) may facilitate VAP knowledge uptake. In addition, there is a need to study knowledge translation (KT) in the ICU since there is little information about optimal KT and CPG implementation strategies in this environment and efforts that are effective in other clinical areas may not result in meaningful change in the ICU.
Research Question:
What is the effect of VAP CPGs implemented by a multidisciplinary behaviour change strategy (consisting of multifaceted educational strategies led by local opinion leaders and augmented with reminders) on VAP guideline concordance and on clinical VAP outcomes in the ICU?
Research Plan:
Data will only be collected on consecutive patients mechanically ventilated for at least 48 hours. The following health care professionals will be studied to assess the behaviour change strategy for the VAP CPGs: physicians (intensivists, ICU fellows, ICU rotating residents), nurses, respiratory therapists, dieticians, physiotherapists and ICU administrators.
The study will be conducted in 3 phases:
Development of a behaviour change strategy consisting of three components:
- Local opinion leader team
- Educational strategy
- Reminder system
- Prospective implementation of the behaviour change strategy over a 24 month period
Prospective evaluation of the behaviour change strategy over a 24 month period
- Concordance with VAP guidelines over time
- Factors associated with VAP guideline concordance
- Clinical VAP outcomes pre- and post-guideline implementation
Eligibility| Ages Eligible for Study: | 17 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Patients invasively mechanically ventilated > 48 hours in the critical care setting.
Inclusion Criteria:
- Age >= 17 years old
- Mechanically ventilated > 48 hours < 96 hours
Exclusion Criteria:
- Previous enrollment in the study
Contacts and Locations| United States, Pennsylvania | |
| Geisinger Health Centre, Temple University | |
| Danville, Pennsylvania, United States, 17821-4400 | |
| Canada, British Columbia | |
| Royal Columbian Hospital, University of British Columbia | |
| New Westminister, British Columbia, Canada, V3L 3W4 | |
| St. Paul Hospital, University of British Columbia | |
| Vancouver, British Columbia, Canada, V6Z 1Y6 | |
| Vancouver Island Health Research Centre | |
| Victoria, British Columbia, Canada, V8R 1J8 | |
| Canada, Ontario | |
| St. Joseph's Healthcare, McMaster University | |
| Hamilton, Ontario, Canada, L8N 4A6 | |
| Kingston General Hospital, Queen's University | |
| Kingston, Ontario, Canada, K7L 2V7 | |
| The Ottawa Hospital, University of Ottawa | |
| Ottawa, Ontario, Canada, K1H 8L7 | |
| Thunder Bay Regional Health Sciences Centre | |
| Thunder Bay, Ontario, Canada, P7B 6V4 | |
| William Osler Health Centre | |
| Toronto, Ontario, Canada | |
| Sunnybrook Health Sciences Centre, University of Toronto | |
| Toronto, Ontario, Canada, M4N 3M5 | |
| Hotel Dieu Grace Hospital | |
| Windsor, Ontario, Canada, N4A 1E1 | |
| Study Chair: | John Muscedere, MD | Kingston General Hospital, Queen's University |
| Study Chair: | Tasmin Sinuff, MD, PhD | Sunnybrook Health Sciences Centre, University of Toronto |
| Principal Investigator: | Daren Heyland, MD | Kingston General Hospital, Queen's University |
| Principal Investigator: | Deborah Cook, MD | St. Joseph's Healthcare, McMaster University |
| Principal Investigator: | Peter Dodek, MD | St. Paul's University, University of British Columbia |
| Principal Investigator: | Redouane Bouali, MD | The Ottawa Hospital, University of Ottawa |
| Principal Investigator: | Sean Keenan, MD | Royal Columbian Hospital, University of British Columbia |
| Principal Investigator: | Kevin Eva, PhD | McMaster University |
| Principal Investigator: | Brenda Morgan, RN | London Health Sciences Centre, University of Western Ontario |
| Principal Investigator: | Lori Hand, RRT | Hamilton Health Sciences Centre, McMaster University |
More Information
Additional Information:
No publications provided by Canadian Critical Care Trials Group
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Dr. John Muscedere, Kingston General Hospital, Queen's University |
| ClinicalTrials.gov Identifier: | NCT00434460 History of Changes |
| Other Study ID Numbers: | ABATE VAP |
| Study First Received: | February 12, 2007 |
| Last Updated: | August 31, 2010 |
| Health Authority: | Canada: Canadian Institutes of Health Research |
Keywords provided by Canadian Critical Care Trials Group:
|
Ventilator Associated Pneumonia Knowledge Translation Clinical Practice Guidelines Education Behaviour Change |
Additional relevant MeSH terms:
|
Pneumonia Pneumonia, Ventilator-Associated Lung Diseases Respiratory Tract Diseases Respiratory Tract Infections |
Cross Infection Infection Ventilator-Induced Lung Injury Lung Injury |
ClinicalTrials.gov processed this record on May 19, 2013