脓毒症患者代谢功能障碍的回顾性单中心队列评估。

IF 1.8 Q3 CRITICAL CARE MEDICINE Critical Care Research and Practice Pub Date : 2021-12-20 eCollection Date: 2021-01-01 DOI:10.1155/2021/3045454
Julien Goutay, Juliette Perche, Aurelia Toussaint, Elodie Drumez, Michael Howsam, Claire Bourel, Benoit Brassart, Alexandre Pierre, Morgan Caplan, Arthur Durand, Marion Houard, Saad Nseir, Raphael Favory, Sébastien Preau
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引用次数: 0

摘要

目的:我们的主要目的是评估选定的代谢功能障碍参数,无论是独立的还是作为SOFA评分的补充,作为重症监护病房(ICU)感染患者短期死亡率的预测因子。方法:回顾性纳入2015年1月至2016年9月在里尔大学医院8个icu连续收治的所有疑似或确诊感染的成年患者。除了年龄和Charlson合并症评分外,我们还选择了7个常规测量的代谢功能障碍的生物学和临床参数(最大动脉乳酸血症、最低和最高体温、最低和最高血糖、胆固醇血症和甘油三酯血症)。入院24 h内记录所有参数及SOFA评分。结果:纳入956例感染患者,其中295例(30.9%)在90天内死亡。在调查的7个代谢参数中,在sofa校正分析中,只有最大乳酸血症与90天住院死亡率的高风险相关(sofa校正OR, 1.17;95%CI, 1.10 ~ 1.25;P < 0.001)。在sofa校正分析中,年龄和Charlson合并症评分也与预后不良相关。因此,我们能够基于乳酸血症、年龄和Charlson评分制定代谢衰竭、年龄和合并症评估(MACA)评分,拟与SOFA评分结合使用。结论:在7项代谢功能障碍指标中,入院24 h内最大乳酸水平是预测短期死亡率的最佳指标。我们的联合“SOFA + MACA”评分有助于早期发现可能发生严重感染的患者。其准确性有待进一步评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Assessment of Metabolic Dysfunction in Sepsis in a Retrospective Single-Centre Cohort.

Objective: Our primary aim was to assess selected metabolic dysfunction parameters, both independently and as a complement to the SOFA score, as predictors of short-term mortality in patients with infection admitted to the intensive care unit (ICU).

Methods: We retrospectively enrolled all consecutive adult patients admitted to the eight ICUs of Lille University Hospital, between January 2015 and September 2016, with suspected or confirmed infection. We selected seven routinely measured biological and clinical parameters of metabolic dysfunction (maximal arterial lactatemia, minimal and maximal temperature, minimal and maximal glycaemia, cholesterolemia, and triglyceridemia), in addition to age and the Charlson's comorbidity score. All parameters and SOFA scores were recorded within 24 h of admission.

Results: We included 956 patients with infection, among which 295 (30.9%) died within 90 days. Among the seven metabolic parameters investigated, only maximal lactatemia was associated with higher risk of 90-day hospital mortality in SOFA-adjusted analyses (SOFA-adjusted OR, 1.17; 95%CI, 1.10 to 1.25; p < 0.001). Age and the Charlson's comorbidity score were also statistically associated with a poor prognosis in SOFA-adjusted analyses. We were thus able to develop a metabolic failure, age, and comorbidity assessment (MACA) score based on scales of lactatemia, age, and the Charlson's score, intended for use in combination with the SOFA score.

Conclusions: The maximal lactatemia level within 24 h of ICU admission is the best predictor of short-term mortality among seven measures of metabolic dysfunction. Our combined "SOFA + MACA" score could facilitate early detection of patients likely to develop severe infections. Its accuracy requires further evaluation.

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来源期刊
Critical Care Research and Practice
Critical Care Research and Practice CRITICAL CARE MEDICINE-
CiteScore
3.60
自引率
0.00%
发文量
34
审稿时长
14 weeks
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