Perioperative Parenteral Nutrition: A Meta-Analysis
- ALLAN S. DETSKY, M.D., Ph.D.;
- JEFFREY P. BAKER, M.D.;
- KEITH O'ROURKE, M.B.A.; and
- VIVEK GOEL, M.D.
Abstract
We used a meta-analysis protocol to evaluate the results of 18 controlled trials that measured the effectiveness of perioperative total parenteral nutrition. The pooled results of 11 trials that were randomized or quasi-randomized showed trends suggesting that total parenteral nutrition reduced the risk for complications from major surgery (p = 0.21) and fatalities (p = 0.21). Consideration of these pooled estimates of the effectiveness of this intervention must be offset by the poor quality of the trials' methodologies and the iatrogenic complications (pneumothorax, septicemia) that occurred at a pooled rate of 0.067. Alternately, other design flaws, such as the failure to exclude patients who were not malnourished from the trials, may have limited the ability of these trials to show the effectiveness of total parenteral nutrition. The evidence available up to August 1986 shows that the routine use of perioperative total parenteral nutrition in unselected patients having major surgery is not justified; however, this intervention may be helpful in subgroups of these patients who are at high risk.
- cost-benefit analysis
- esophageal neoplasms
- gastrointestinal neoplasms
- intraoperative period
- nutrition disorders
- parenteral hyperalimentation
- peritonitis
- postoperative care
- preoperative care
- random allocation
- small intestine
- surgery
- digestive system
- surgery
- operative
- stomach neoplasms
- meta-analysis
- cost-benefit analysis
- esophageal neoplasms
- gastrointestinal neoplasms
- intraoperative period
- nutrition disorders
- parenteral hyperalimentation
- peritonitis
- postoperative care
- preoperative care
- random allocation
- small intestine
- surgery
- digestive system
- surgery
- operative
- stomach neoplasms
- meta-analysis
Article and Author Information
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▸From the Departments of Health Administration and Medicine, University of Toronto; the Divisions of General Internal Medicine and Clinical Epidemiology, Toronto General Hospital; and the Division of Gastroenterology, St. Michael's Hospital; Toronto, Ontario, Canada.
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Grant support: in part by grant 1 R01 HS0 5374 from the National Center for Health Services Research and Health Care Technology Assessment, grant 6606-2362-42 from the National Health Research and Development Program (Canada), and a National Health Research Scholar Award to Dr. Detsky.
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▸Requests for reprints should be addressed to Linda Johnson White; Clinical Efficacy Assessment Project, Department of Scientific Policy, American College of Physicians, 4200 Pine Street; Philadelphia, PA 19104.
- ©1987 American College of Physicians
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