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医疗保险和医疗补助服务中心严重脓毒症和脓毒性休克管理捆绑包(SEP-1)的证据基础:系统评价。

Evidence Underpinning the Centers for Medicare & Medicaid Services' Severe Sepsis and Septic Shock Management Bundle (SEP-1): A Systematic Review.

机构信息

National Institutes of Health, Bethesda, Maryland (D.J.P., D.J., J.S., J.W., C.N., P.Q.E.).

出版信息

Ann Intern Med. 2018 Apr 17;168(8):558-568. doi: 10.7326/M17-2947. Epub 2018 Feb 20.

Abstract

UNLABELLED

This article has been corrected. To see what has changed, please read the Letter to the Editor and the authors' response. The original version (PDF) is appended to this article as a Supplement.

BACKGROUND

The Severe Sepsis and Septic Shock Early Management Bundle (SEP-1), the sepsis performance measure introduced in 2015 by the Centers for Medicare & Medicaid Services (CMS), requires the reporting of up to 5 hemodynamic interventions, as many as 141 tasks, and 3 hours to document for a single patient.

PURPOSE

To evaluate whether moderate- or high-level evidence shows that use of the 2015 SEP-1 or its hemodynamic interventions improves survival in adults with sepsis.

DATA SOURCES

PubMed, Embase, Scopus, Web of Science, and ClinicalTrials.gov from inception to 28 November 2017 with no language restrictions.

STUDY SELECTION

Randomized and observational studies of death among adults with sepsis who received versus those who did not receive either the entire SEP-1 bundle or 1 or more SEP-1 hemodynamic interventions, including serial lactate measurements; a fluid infusion of 30 mL/kg of body weight; and assessment of volume status and tissue perfusion with a focused examination, bedside cardiovascular ultrasonography, or fluid responsiveness testing.

DATA EXTRACTION

Two investigators independently extracted study data and assessed each study's risk of bias; 4 authors rated level of evidence by consensus using CMS criteria published in 2013. High- or moderate-level evidence required studies to have no confounders and low risk of bias.

DATA SYNTHESIS

Of 56 563 references, 20 studies (18 reports) met inclusion criteria. One single-center observational study reported lower in-hospital mortality after implementation of the SEP-1 bundle. Sixteen studies (2 randomized and 14 observational) reported increased survival with serial lactate measurements or 30-mL/kg fluid infusions. None of the 17 studies were free of confounders or at low risk of bias. In 3 randomized trials, fluid responsiveness testing did not alter survival.

LIMITATIONS

Few trials, poor-quality and confounded studies, and no studies (with survival outcomes) of the focused examination or bedside cardiovascular ultrasonography. Use of the 2015 version of SEP-1 and 2013 version of CMS evidence criteria, both of which were updated in 2017.

CONCLUSION

No high- or moderate-level evidence shows that SEP-1 or its hemodynamic interventions improve survival in adults with sepsis.

PRIMARY FUNDING SOURCE

National Institutes of Health. (PROSPERO: CRD42016052716).

摘要

未标注

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背景

医疗保险和医疗补助服务中心(CMS)于 2015 年推出的严重脓毒症和脓毒性休克早期管理捆绑包(SEP-1)要求报告多达 5 种血流动力学干预措施、多达 141 项任务,并为单个患者记录 3 小时。

目的

评估 2015 年 SEP-1 或其血流动力学干预措施是否有中度或高度证据表明可提高脓毒症成人的生存率。

数据来源

PubMed、Embase、Scopus、Web of Science 和 ClinicalTrials.gov,从建立到 2017 年 11 月 28 日,无语言限制。

研究选择

接受或未接受 SEP-1 捆绑包或 1 项或多项 SEP-1 血流动力学干预措施(包括连续乳酸测量)、30ml/kg 体重的液体输注以及使用焦点检查、床边心血管超声或液体反应性测试评估容量状态和组织灌注的成人脓毒症死亡的随机和观察性研究。

数据提取

两名调查员独立提取研究数据并评估每项研究的偏倚风险;4 名作者根据 CMS 于 2013 年发布的标准通过共识对证据水平进行分级。高或中等级别的证据要求研究没有混杂因素和低偏倚风险。

数据综合

在 56563 条参考文献中,有 20 项研究(18 项报告)符合纳入标准。一项单中心观察性研究报告称,实施 SEP-1 捆绑包后住院死亡率降低。16 项研究(2 项随机和 14 项观察性)报告称,连续乳酸测量或 30ml/kg 液体输注可提高生存率。没有一项研究没有混杂因素或低偏倚风险。在 3 项随机试验中,液体反应性测试并未改变生存率。

局限性

试验数量少,研究质量差且混杂,没有关于焦点检查或床边心血管超声的研究(有生存结果)。使用 2015 年版 SEP-1 和 2013 年版 CMS 证据标准,两者均在 2017 年进行了更新。

结论

没有高或中等级别的证据表明 SEP-1 或其血流动力学干预措施可提高脓毒症成人的生存率。

主要资金来源

美国国立卫生研究院。(PROSPERO:CRD42016052716)。

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