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测量血流感染后以患者为中心的长期结局:一项试点研究。

Measuring patient-centred long-term outcome following a bloodstream infection: a pilot study.

机构信息

The University of Queensland, Centre for Clinical Research, Herston, Brisbane, Australia; The Prince Charles Hospital, Brisbane, Australia.

The University of Queensland, Centre for Clinical Research, Herston, Brisbane, Australia; Pathology Queensland, Central Laboratory, Royal Brisbane and Women's Hospital, Herston, Australia.

出版信息

Clin Microbiol Infect. 2020 Feb;26(2):257.e1-257.e4. doi: 10.1016/j.cmi.2019.10.011. Epub 2019 Oct 23.

DOI:10.1016/j.cmi.2019.10.011
PMID:31654791
Abstract

OBJECTIVES

To evaluate the sequential organ failure assessment (SOFA) and modified SOFA (mSOFA) scoring and a novel performance score based on the Karnofsky score for measuring outcome following a bloodstream infection (BSI).

METHOD

This prospective observational cohort study assessed patients with BSI for mortality and functional outcomes with a novel performance score: the functional bloodstream infection score (FBIS). We also tested the SOFA and, given the difficulties with measuring SOFA on ward-based patients, the mSOFA over the first 7 days following a BSI for their association with outcomes.

RESULTS

One hundred participants were prospectively recruited. Mortality at 52 weeks following BSI was 21% (21/100). Only 57% of survivors (39/69) were at their baseline functional status at 52 weeks. Stable or improved SOFA/mSOFA over the first 7 days was associated with survival and return to premorbid performance score (risk ratio 3.2, 95%CI 1.3-9.4, p < 0.01).

CONCLUSIONS

The acute change in SOFA/mSOFA was associated with 52-week survival and return to premorbid functional performance. The FBIS measurement represents a simple and easy-to-apply measure of functional performance for patients with BSI and was associated with a high response rate (89%) from participants.

摘要

目的

评估序贯器官衰竭评估(SOFA)和改良 SOFA(mSOFA)评分以及基于卡诺夫斯基评分的新型评分,以衡量血流感染(BSI)后的结局。

方法

本前瞻性观察性队列研究评估了 BSI 患者的死亡率和功能结局,并采用新型功能血流感染评分(FBIS)进行评估。我们还测试了 SOFA,鉴于在基于病房的患者中测量 SOFA 存在困难,还测试了 mSOFA 在 BSI 后第 7 天内与结局的相关性。

结果

前瞻性招募了 100 名参与者。BSI 后 52 周的死亡率为 21%(21/100)。只有 57%的幸存者(39/69)在 52 周时恢复到基线功能状态。第 1 天到第 7 天内 SOFA/mSOFA 稳定或改善与生存和恢复到发病前的功能评分相关(风险比 3.2,95%CI 1.3-9.4,p<0.01)。

结论

SOFA/mSOFA 的急性变化与 52 周生存率和恢复到发病前的功能表现相关。FBIS 测量代表了一种简单易用的 BSI 患者功能表现的衡量方法,参与者的响应率高达 89%。

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