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急性呼吸窘迫综合征患者的呼气末正压与心指数之间的关系。

The relationship between positive end-expiratory pressure and cardiac index in patients with acute respiratory distress syndrome.

机构信息

Yale University, School of Medicine, Department of Internal Medicine, Section of Pulmonary, Critical Care & Sleep Medicine, New Haven, CT 06510.

出版信息

J Crit Care. 2013 Dec;28(6):992-7. doi: 10.1016/j.jcrc.2013.06.021. Epub 2013 Aug 28.

Abstract

PURPOSE

The purpose of the study is to evaluate the association between positive end-expiratory pressure (PEEP) and cardiac index in patients with acute respiratory distress syndrome (ARDS).

METHODS

This is a secondary cross-sectional analysis of the multicenter randomized controlled Fluid and Catheter Treatment Trial enrolling adult patients within 48 hours of ARDS onset. Patients randomized to the pulmonary artery catheter arm, who had PEEP and cardiac index measurements performed within a short period of each other during the first 3 days of the FACTT study enrollment, were included in this study. Because FACTT had a 2 × 2 factorial design, half of the patients were in a "liberal fluids" study arm, and the other half were in a "conservative fluids" study arm.

RESULTS

The final study population (833 measurements or observations, in 367 patients) was comparable with the original overall FACTT study population. The mean PEEP level used was 8.2 ± 3.4 cm H2O, and the mean cardiac index was 4.2 ± 1.2 L/min per square meter. There was no association between PEEP and cardiac index in patients with ARDS, even when adjusted for Acute Physiology and Chronic Health Evaluation score, age, fluid study arm in FACTT, and sepsis.

CONCLUSION

In patients with ARDS who are managed with liberal or conservative fluid management protocols, PEEP is not associated with lower cardiac index.

摘要

目的

本研究旨在评估急性呼吸窘迫综合征(ARDS)患者的呼气末正压(PEEP)与心指数之间的关系。

方法

这是一项多中心随机对照的液体和导管治疗试验(Fluid and Catheter Treatment Trial,FACTT)的二次横断面分析,纳入 ARDS 发病后 48 小时内的成年患者。在 FACTT 研究入组的前 3 天内,随机分配到肺动脉导管组的患者在短时间内进行 PEEP 和心指数测量,被纳入本研究。由于 FACTT 采用了 2×2 析因设计,一半患者处于“自由液体”研究臂,另一半患者处于“保守液体”研究臂。

结果

最终的研究人群(367 例患者的 833 次测量或观察)与原始的 FACTT 总体研究人群具有可比性。使用的平均 PEEP 水平为 8.2±3.4cmH2O,平均心指数为 4.2±1.2L/min/平方米。ARDS 患者的 PEEP 与心指数之间没有关联,即使在调整急性生理学和慢性健康评估评分、年龄、FACTT 中的液体研究臂以及脓毒症后也是如此。

结论

在接受自由或保守液体管理方案治疗的 ARDS 患者中,PEEP 与较低的心指数无关。

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