Early use of the pulmonary artery catheter and outcomes in patients with shock and acute respiratory distress syndrome - A randomized controlled trial

被引:397
作者
Richard, C
Warszawski, J
Anguel, N
Deye, N
Combes, A
Barnoud, D
Boulain, T
Lefort, Y
Fartoukh, M
Baud, F
Boyer, A
Brochard, L
Teboul, JL
机构
[1] Univ Paris 11, Assistance Publ Hop Paris, Hop Bicetre, Serv Reanimat Med, F-94275 Le Kremlin Bicetre, France
[2] Univ Paris 11, Assistance Publ Hop Paris, Hop Bicetre, Serv Sante Publ & Epidemiol, F-94275 Le Kremlin Bicetre, France
[3] Univ Paris 06, Assistance Publ Hop Paris, Hop Europeen Georges Pompidou, Serv Reanimat Med, Paris, France
[4] Univ Paris 06, Assistance Publ Hop Paris, Grp Hosp Pitie Salpetriere, Serv Reanimat Med, Paris, France
[5] Univ Paris 06, Assistance Publ Hop Paris, Grp Hosp Pitie Salpetriere, Serv Pneumol & Reanimat, Paris, France
[6] CHU A Michallon, Serv Reanimat Med, Grenoble, France
[7] CHR Orleans La Source, Serv Reanimat, Orleans, France
[8] Univ Paris 12, Hop Henri Mondor, Assistance Publ Hop Paris, Serv Reanimat Med, F-94010 Creteil, France
[9] Univ Paris 07, Assistance Publ Hop Paris, Hop Lariboisiere, Serv Reanimat Med, Paris, France
[10] Univ Paris 07, Assistance Publ Hop Paris, Hop Louis Mourier, Serv Reanimat Med, Colombes, France
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2003年 / 290卷 / 20期
关键词
D O I
10.1001/jama.290.20.2713
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Many physicians believe that the pulmonary artery catheter (PAC) is useful for the diagnosis and treatment of cardiopulmonary disturbances; however, observational studies suggest that its use may be harmful. Objective To determine the effects on outcome of the early use of a PAC in patients with shock mainly of septic origin, acute respiratory distress syndrome (ARDS), or both. Design, Setting, and Patients A multicenter randomized controlled study of 676 patients aged 18 years or older who fulfilled the standard criteria for shock, ARDS, or both conducted in 36 intensive care units in France from January 30, 1999, to June 29, 2001. Intervention Patients, were randomly assigned to either receive a PAC (n=335) or not (n=341). The treatment was left to the discretion of each individual physician. Main Outcome Measures The primary end point was mortality at 28 days. The principal secondary end points were day 14 and 90 mortality; day 14 organ system, renal support, and vasoactive agents-free days; hospital, intensive care unit, and mechanical ventilation-free days at day 28. Results The 2 groups were similar at baseline. There were no significant differences in mortality with or without the PAC at day 14: 49.9% vs 51.3% (mortality relative risk [RR], 0.97; 95% confidence interval [CI], 0.84-1.13; P=.70); day 28: 59.4% vs 61.0% (RR, 0.97; 95% CI, 0.86-1.10; P=.67); or day 90:70.7% vs 72.0% (RR, 0.98; 95% CI, 0.89-1.08; P-.71). At day 14, the mean (SD) number of days free of organ system failures with or without the PAC (2.3 [3.6] vs 2.4 [3.5]), renal support (7.4 [6.0] vs 7.5 [5.9]), and vasoactive agents (3.8 [4.8] vs 3.9 [4.9]) did not differ. At day 28, mean (SD) days in hospital with or without the PAC (0.9 [3.6] vs 0.9 [3.3]), in the intensive care unit (3.4 [6.8] vs 3.3 [6.9]), or mechanical ventilation use (5.2 [8.5] vs 5.0 [8.5]) did not differ. Conclusion Clinical management involving the early use of a PAC in patients with shock, ARDS, or both did not significantly affect mortality and morbidity.
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收藏
页码:2713 / 2720
页数:8
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