Evaluation of a Ventilation Strategy to Prevent Barotrauma in Patients at High Risk for Acute Respiratory Distress Syndrome
Thomas E. Stewart, M.D., Maureen O. Meade, M.D., Deborah J. Cook, M.D., John T. Granton, M.D., Richard V. Hodder, M.D., Stephen E. Lapinsky, M.D., C. David Mazer, M.D., Richard F. McLean, M.D., Ted S. Rogovein, M.D., B. Diana Schouten, R.N., Thomas R.J. Todd, M.D., Arthur S. Slutsky, M.D., for The Pressure- and Volume-Limited Ventilation Strategy Group
Background A strategy of mechanical ventilation that limitsairway pressure and tidal volume while permitting hypercapniahas been recommended for patients with the acute respiratorydistress syndrome. The goal is to reduce lung injury due tooverdistention. However, the efficacy of this approach has notbeen established.
Methods Within 24 hours of intubation, patients at high riskfor the acute respiratory distress syndrome were randomly assignedto either pressure- and volume-limited ventilation (limited-ventilationgroup), with the peak inspiratory pressure maintained at 30cm of water or less and the tidal volume at 8 ml per kilogramof body weight or less, or to conventional ventilation (controlgroup), with the peak inspiratory pressure allowed to rise ashigh as 50 cm of water and the tidal volume at 10 to 15 ml perkilogram. All other ventilatory variables were similar in thetwo groups.
Results A total of 120 patients with similar clinical featuresunderwent randomization (60 in each group). The patients inthe limited-ventilation and control groups were exposed to differentmean (±SD) tidal volumes (7.2±0.8 vs. 10.8±1.0ml per kilogram, respectively; P<0.001) and peak inspiratorypressures (23.6±5.8 vs. 34.0±11.0 cm of water,P<0.001). Mortality was 50 percent in the limited-ventilationgroup and 47 percent in the control group (relative risk, 1.07;95 percent confidence interval, 0.72 to 1.57; P = 0.72). Inthe limited-ventilation group, permissive hypercapnia (arterialcarbon dioxide tension, >50 mm Hg) was more common (52 percentvs. 28 percent, P = 0.009), more marked (54.4±18.8 vs.45.7±9.8 mm Hg, P = 0.002), and more prolonged (146±265vs. 25±22 hours, P = 0.017) than in the control group.The incidence of barotrauma, the highest multiple-organ-dysfunctionscore, and the number of episodes of organ failure were similarin the two groups; however, the numbers of patients who requiredparalytic agents (23 vs. 13, P = 0.05) and dialysis for renalfailure (13 vs. 5, P = 0.04) were greater in the limited-ventilationgroup than in the control group.
Conclusions In patients at high risk for the acute respiratorydistress syndrome, a strategy of mechanical ventilation thatlimits peak inspiratory pressure and tidal volume does not appearto reduce mortality and may increase morbidity.
Source Information
From the Departments of Medicine (T.E.S., J.T.G., S.E.L., A.S.S.), Surgery (T.R.J.T.), and Anaesthesia (T.E.S., C.D.M., R.F.M.) and the Critical Care Medicine Programme (T.E.S., M.O.M., J.T.G., S.E.L., C.D.M., R.F.M., A.S.S.), University of Toronto; Wellesley Central Hospital (T.E.S., B.D.S.); Toronto Hospital (J.T.G., T.R.J.T.); St. Michael's Hospital (C.D.M.); Sunnybrook Health Sciences Centre (R.F.M.); Mount Sinai Hospital (S.E.L., A.S.S.); and St. Joseph's Health Centre (T.S.R.) all in Toronto; the Department of Medicine and the Critical Care Medicine Programme, McMaster University, Hamilton, Ont. (D.J.C.); and the Department of Medicine, University of Ottawa, Ottawa, Ont. (R.V.H.).
Address reprint requests to Dr. Stewart at Wellesley Central Hospital, Rm. 245, Jones Bldg., 160 Wellesley St. E., Toronto, ON M4Y 1J3, Canada.
Protective Ventilation for the Acute Respiratory Distress Syndrome
Chiche J.-D., Brunet F., Lamy M., Kacmarek R., Parsons P. E., Matthay M., Manning H. L., Shapira M. Y., Sviri S., Linton D. M., Weg J. G., Anzueto A., Amato M. B.P., Barbas C. S.V., Carvalho C. R.R., Stewart T. E., Meade M. O., Slutsky A. S.
Extract |
Full Text
N Engl J Med 1998;
339:196-199, Jul 16, 1998.
Correspondence
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