High values of the pulmonary artery wedge pressure in patients with acute lung injury and acute respiratory distress syndrome

被引:84
作者
Ferguson, ND
Meade, MO
Hallett, DC
Stewart, TE
机构
[1] Univ Toronto, Mt Sinai Hosp, Dept Med, Div Respirol,Crit Care Med Program, Toronto, ON M5G 1X5, Canada
[2] McMaster Univ, Dept Med, Hamilton, ON, Canada
[3] McMaster Univ, Dept Clin Epidemiol & Biostat, Hamilton, ON, Canada
关键词
acute lung injury; acute respiratory distress syndrome; congestive heart failure; pulmonary artery catheters; pulmonary artery wedge pressure;
D O I
10.1007/s00134-002-1354-y
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: To determine the incidence and severity of pulmonary artery wedge pressure (PAWP) elevation in patients with ALI/ARDS. In addition, to examine the effects of clinical variables on the presence of a high PAWP (>18 mmHg) and the effect of an elevated PAWP on mortality. Design and patients: Post hoc analysis of 120 patients with or at high risk of ARDS, enrolled in a randomized controlled trial of pressure-and volume-limited ventilation. Patients with or at high risk of congestive heart failure were excluded from the original study. Setting: Eight tertiary intensive care units. Measurements and results: Pulmonary artery catheters were inserted at the discretion of the attending physician, and PAWP was collected every 8 h when present. Of 120 subjects 71 (59%) had a pulmonary artery catheter (44 at randomization, 27 later). The mean maximum PAWP reading among patients was 22.5 mmHg (95% CI 21.2-23.8) and mean median was 16.6 mmHg (95% CI 15.6-17.5). Patients who met standard criteria for ARDS were more likely to develop a high PAWP. In a multivariate stepwise logistic regression model a persistently elevated PAWP (median > 18 mmHg) was a strong predictor of mortality after correction for baseline differences (OR estimate 6.82; 95% CI 1.66-37.81). Conclusions: We conclude that in this group of patients a PAWP higher than 18 mmHg is common. Mandating a PAWP of 18 mmHg or less may negatively impact clinical trials in which ARDS is an inclusion/exclusion criteria or an endpoint.
引用
收藏
页码:1073 / 1077
页数:5
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