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升压治疗脓毒性和血管扩张性休克时较高与较低血压目标值的汇总分析。

Pooled analysis of higher versus lower blood pressure targets for vasopressor therapy septic and vasodilatory shock.

机构信息

Department of Medicine, Université de Sherbrooke, 3001, 12th Avenue North, Sherbrooke, QC, J1H 5N4, Canada.

Centre de recherche du CHU de Sherbrooke, Sherbrooke, Canada.

出版信息

Intensive Care Med. 2018 Jan;44(1):12-21. doi: 10.1007/s00134-017-5016-5. Epub 2017 Dec 19.

Abstract

PURPOSE

Guidelines for shock recommend mean arterial pressure (MAP) targets for vasopressor therapy of at least 65 mmHg and, until recently, suggested that patients with underlying chronic hypertension and atherosclerosis may benefit from higher targets. We conducted an individual patient-data meta-analysis of recent trials to determine if patient variables modify the effect of different MAP targets.

METHODS

We searched the MEDLINE, EMBASE, and Cochrane Central Register of Controlled Trials for randomized controlled trials of higher versus lower blood pressure targets for vasopressor therapy in adult patients in shock (until November 2017). After obtaining individual patient data from both eligible trials, we used a modified version of the Cochrane Collaboration's instrument to assess the risk of bias of included trials. The primary outcome was 28-day mortality.

RESULTS

Included trials enrolled 894 patients. Controlling for trial and site, the OR for 28-day mortality for the higher versus lower MAP targets was 1.15 (95% CI 0.87-1.52). Treatment effect varied by duration of vasopressors before randomization (interaction p = 0.017), but not by chronic hypertension, congestive heart failure or age. Risk of death increased in higher MAP groups among patients on vasopressors > 6 h before randomization (OR 3.00, 95% CI 1.33-6.74).

CONCLUSIONS

Targeting higher blood pressure targets may increase mortality in patients who have been treated with vasopressors for more than 6 h. Lower blood pressure targets were not associated with patient-important adverse events in any subgroup, including chronically hypertensive patients.

摘要

目的

休克治疗指南建议使用血管加压剂时的平均动脉压(MAP)目标值至少为 65mmHg,直到最近,还建议患有慢性高血压和动脉粥样硬化的患者可能受益于更高的目标值。我们对最近的试验进行了个体患者数据荟萃分析,以确定患者变量是否会改变不同 MAP 目标值的效果。

方法

我们在 MEDLINE、EMBASE 和 Cochrane 对照试验中心注册库中搜索了成人休克患者接受更高与更低血压目标值的血管加压剂治疗的随机对照试验(截至 2017 年 11 月)。从合格试验中获得个体患者数据后,我们使用 Cochrane 协作组工具的修改版本来评估纳入试验的偏倚风险。主要结局是 28 天死亡率。

结果

纳入的试验共纳入 894 名患者。控制试验和地点因素后,较高与较低 MAP 目标值的 28 天死亡率的 OR 为 1.15(95%CI 0.87-1.52)。治疗效果因随机分组前血管加压剂的使用时间而有所不同(交互作用 p = 0.017),但与慢性高血压、充血性心力衰竭或年龄无关。在随机分组前血管加压剂使用>6 小时的患者中,较高 MAP 组的死亡风险增加(OR 3.00,95%CI 1.33-6.74)。

结论

对于已经接受血管加压剂治疗超过 6 小时的患者,目标较高的血压可能会增加死亡率。在任何亚组中,包括慢性高血压患者,较低的血压目标值与患者重要的不良事件无关。

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