The role of chronic alcohol abuse in the development of acute respiratory distress syndrome in adults

被引:316
作者
Moss, M
Bucher, B
Moore, FA
Moore, EE
Parsons, PE
机构
[1] DENVER GEN HOSP,DEPT MED,DENVER,CO 80204
[2] DENVER GEN HOSP,DEPT SURG,DENVER,CO 80204
[3] NATL JEWISH CTR IMMUNOL & RESP MED,DEPT MED,DENVER,CO 80206
[4] NATL JEWISH CTR IMMUNOL & RESP MED,DEPT BIOSTAT,DENVER,CO 80206
[5] UNIV COLORADO,HLTH SCI CTR,DEPT MED,DENVER,CO 80262
[6] UNIV COLORADO,HLTH SCI CTR,DEPT SURG,DENVER,CO 80262
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 1996年 / 275卷 / 01期
关键词
D O I
10.1001/jama.275.1.50
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective.-To determine the effect of a history of chronic alcohol abuse on the incidence of acute respiratory distress syndrome (ARDS) and in-hospital mortality. Design.-Prospective cohort study. Patients.-A total of 351 medical and surgical intensive care unit patients with one of seven at-risk diagnoses for the development of ARDS. Main Outcome Measures.-The development of ARDS and in-hospital mortality. Results.-Of the 351 patients enrolled in the study, the incidence of ARDS in patients with a history of alcohol abuse was significantly higher than in patients without a history of alcohol abuse (43% vs 22%) (P<.001; relative risk [RR], 1.98; 95% confidence interval [Cl], 1.32 to 2.85), in patients with sepsis, ARDS developed in 52% of the patients with a prior history of alcohol abuse compared with only 20% in patients without a history of alcohol abuse (P<.001; RR, 2.59; 95% Cl, 1.29 to 5.12). Fifty-one percent (52/102) of the patients who developed ARDS died compared with only 14% (36/249) of patients who did not develop ARDS (P<.001). In the subset of patients who developed ARDS, the in-hospital mortality rate was 65% in patients with a prior history of alcohol abuse. This mortality rate was significantly higher (P=.003) than the mortality rate in patients without a history of alcohol abuse (36%). Conclusions.-A prior history of chronic alcohol abuse significantly increases the risk of developing ARDS in critically ill patients with an identified at-risk diagnosis. Our results may be useful in the earlier and more accurate identification of patients at high risk for developing ARDS.
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页码:50 / 54
页数:5
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