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Structured Abstract
Objectives:
Because mechanical ventilation incurs significant morbidity, mortality, and costs and because premature extubation as well as delayed extubation can cause harm, weaning that is both expeditious and safe is highly desirable. We sought to determine whether the current literature elucidates when and how weaning should begin, proceed, and end.
Search Strategy:
We used five computerized bibliographic databases, hand searching, bibliographic references, expert consultation, and a duplicate independent review process to identify relevant articles.
Selection Criteria:
Our eligibility criteria were broad. We selected studies evaluating any weaning modes, algorithms, or other interventions to facilitate weaning; studies of weaning predictors; and studies evaluating patient and nursing experiences during weaning.
Data Collection and Analysis:
We developed generic forms to abstract data from all studies, in addition to forms specific to randomized trials, nonrandomized controlled studies, and studies of weaning predictors. We developed an instruction manual and trained eight individuals to abstract data related to study characteristics and results using duplicate, independent review. Quantitative data were abstracted using several metrics. We pooled results across randomized trials and across studies of weaning predictors only when our assessment of the patients, interventions, and outcomes indicated that pooling was legitimate.
Main Results:
We reviewed 154 articles. For stepwise reductions in mechanical support, pressure support mode or multiple daily T-piece trials may be superior to synchronized intermittent mandatory ventilation. For trials of unassisted breathing, low levels of pressure support may be beneficial. There may be substantial benefits to early extubation and institution of noninvasive positive pressure ventilation before patients are ready to breathe without mechanical assistance. The value of differing modes as reflected in these studies depends on the thresholds for initiating, progressing through, and terminating weans in the specific study protocols. Unfortunately, these thresholds involve more than objective data and appear to be related to physician judgment.
The implementation of nurse-driven or respiratory therapist-driven weaning protocols, regardless of what modes are employed, significantly expedites weaning and is probably safe. Following cardiac surgery, early extubation is unequivocably achieved with a variety of anesthetic interventions and intensive care unit protocols; however, the corresponding reduction in intensive care unit stay is generally small and the impact on complications, though rare, remains unclear. The role of computerized protocols has not been established.
We did not uncover any consistently powerful weaning predictors. The most frequently studied and one of the most helpful tests is the rapid shallow breathing index; however, the pooled likelihood ratio for a positive test ranged from 1.3 to 2.8. Two other predictors, occlusion pressure/maximum inspiratory pressure and the compliance, rate, oxygenation, and pressure index, are more powerful, though less intensively studied. In general, the probable reason for the poor performance of weaning predictors is that physicians have already considered the results of these predictors when they select patients for study.
Conclusions:
Future research initiatives should include: determining the optimal tradeoff between prolonged time on a ventilator and reintubation in specific patient groups, further evaluation of weaning protocols (What types of patients are most likely to benefit? Which protocols are most effective? How large are the associated cost reductions? Is there a role for computers?), and clarification of the risk-benefit of early extubation with noninvasive positive pressure ventilation.
Contents
- Preface
- Acknowledgments
- Summary
- 1. Introduction
- 2. Methodology
- Eligibility Criteria
- Search for Relevant Studies
- Data Abstraction and Assessment of Methodologic Quality
- Statistical Synthesis
- Controlled Comparisons of Alternative Treatments
- Observational Studies Addressing Prediction of Successful Weaning and Duration of Ventilation
- Methodology For Pooling Study Results
- Other Types of Studies
- 3. Results
- Randomized and Nonrandomized Controlled Trials
- Controlled Trials of Discontinuation Assessment Strategies
- Controlled Trials of Progressive Reduction in Mechanical Support
- Controlled Trials Comparing Alternative Ventilation Modes for Weans Lasting Less Than 48 Hours
- Controlled Trials Comparing Weaning Protocols to Physician-Directed Weaning
- Controlled Trials of Early Versus Late Extubation Following Cardiac Surgery
- Controlled Trials of Corticosteroids to Prevent Post-Extubation Airway Complications
- Controlled Trials of Enteral Nutrition
- Randomized Trials of Miscellaneous Studies
- Observational Studies Addressing Prediction of Successful Weaning and Duration of Ventilation
- Qualitative Studies of Weaning From Mechanical Ventilation
- Observational Studies Describing Patient Experience During Weaning
- 4. Conclusions and Future Research
- Controlled Trials of Unassisted Ventilation
- Controlled Trials of Progressive Reduction in Mechanical Support
- Controlled Trials Comparing Alternative Ventilation Modes for Weans Lasting Less Than 48 Hours
- Controlled Trials Comparing Weaning Protocols to Physician-Directed Weaning
- Controlled Trials of Early Versus Late Extubation Following Cardiac Surgery
- Controlled Trials of Corticosteroids to Prevent Postextubation Airway Complications
- Controlled Trials of Enteral Nutrition
- Controlled Trials: Miscellaneous Studies
- Observational Studies Addressing Prediction of Successful Weaning and Duration of Ventilation
- Observational Studies Describing Patient Experience During Weaning
- Strengths and Limitations of This Review
- Summary of Inferences From This Review
- Summary of Recommendations for Future Research
- Evidence Tables
- Appendixes
- Appendix A. Search Strategy: MEDLINE and HealthSTAR for Intervention Studies
- Appendix B. Search Strategy: MEDLINE AND HealthSTAR for Observational Studies
- Appendix C. Search Strategy: CINAHL for Intervention Studies
- Appendix D. Search Strategy: CINAHL for Observational Studies
- Appendix E. Search Strategy: EMBASE for Intervention Studies
- Appendix F. Search Strategy: EMBASE for Observational Studies
- Appendix G. Relevance Form: Weaning from Mechanical Ventilation
- Appendix H. Selection Criteria for Articles About Weaning
- Appendix I. Extraction Form for General Characteristics fo All Studies
- Appendix J. Extraction Form for Randomized Clinical Trials
- Appendix K. Extraction Form for Nonrandomized Controlled Clinical Trials
- Appendix L. Extraction Form for Observational Studies
- Appendix M. Acronyms and Abbreviations
- References
- Bibliography
Prepared for: Agency for Healthcare Research and Quality, U.S. Department of Health and Human Services.1 Contract No. 290-97-0017. Prepared by: Department of Medicine and Clinical Epidemiology & Biostatistics, McMaster University, Hamilton, Ontario, Canada.
Suggested citation:
Cook D, Meade M, Guyatt G, et al. Criteria for Weaning From Mechanical Ventilation. Evidence Report/Technology Assessment No. 23 (Prepared by McMaster University under Contract No. 290-97-0017). AHRQ Publication No. 01-E010. Rockville MD: Agency for Healthcare Research and Quality. November 2000.
On December 6, 1999, under Public Law 106-129, the Agency for Health Care Policy and Research (AHCPR) was reauthorized and renamed the Agency for Healthcare Research and Quality (AHRQ). The law authorizes AHRQ to continue its research on the cost, quality, and outcomes of health care, and expands its role to improve patient safety and address medical errors.
This report may be used, in whole or in part, as the basis for development of clinical practice guidelines and other quality enhancement tools, or a basis for reimbursement and coverage policies. AHRQ or U.S. Department of Health and Human Services endorsement of such derivative products may not be stated or implied.
The authors of this report are responsible for its content. Statements in the report should not be construed as endorsement by the Agency for Healthcare Research and Quality or the U.S. Department of Health and Human Services of a particular drug, test, treatment, or other clinical service.
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2101 East Jefferson Street, Rockville, MD 20852. www
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- Review Weaning from mechanical ventilation.[J Matern Fetal Neonatal Med. 2...]Review Weaning from mechanical ventilation.Gizzi C, Moretti C, Agostino R. J Matern Fetal Neonatal Med. 2011 Oct; 24 Suppl 1:61-3.
- Review Do clinical parameters predict first planned extubation outcome in the pediatric intensive care unit?[J Intensive Care Med. 2015]Review Do clinical parameters predict first planned extubation outcome in the pediatric intensive care unit?Laham JL, Breheny PJ, Rush A. J Intensive Care Med. 2015 Feb; 30(2):89-96. Epub 2013 Jun 27.
- Review [Role of noninvasiveness ventilation in the weaning phase of mechanical ventilation].[Schweiz Med Wochenschr. 2000]Review [Role of noninvasiveness ventilation in the weaning phase of mechanical ventilation].Jolliet P. Schweiz Med Wochenschr. 2000 Dec 16; 130(50):1948-53.
- Criteria for Weaning from Mechanical VentilationCriteria for Weaning from Mechanical Ventilation
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