危重感染性休克患者血浆肾素活性和醛固酮浓度的意义

K. Chung, J. H. Song, W. Jung, Y. S. Kim, S. K. Kim, Joon Chang, M. Park
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Results Patients were divided into two groups according to 28-day mortality: survivors (n = 59) and non-survivors (n = 46). The survivor group showed lower PRA, PAC, Acute Physiologic and Chronic Health Evaluation (APACHE) II score, and Sequential Organ Failure Assessment (SOFA) score than did the non-survivor group (all P < 0.05). The SOFA score was positively correlated with PRA (r = 0.373, P < 0.001) and PAC (r = 0.316, P = 0.001). According to receiver operating characteristic analysis, the areas under the curve of PRA and PAC to predict 28-day mortality were 0.69 (95% confidence interval [CI], 0.58 to 0.79; P = 0.001) and 0.67 (95% CI, 0.56 to 0.77; P = 0.003), respectively, similar to the APACHE II scores and SOFA scores. In particular, the group with PRA value ≥3.5 ng ml-1 h-1 on day 1 showed significantly greater mortality than did the group with PRA value <3.5 ng ml-1 h-1 (log-rank test, P < 0.001). 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引用次数: 12

摘要

背景肾素-血管紧张素-醛固酮系统与感染性休克的容量状态和血管张力密切相关。本研究旨在评估与传统严重程度指标相比,血浆肾素活性(PRA)和血浆醛固酮浓度(PAC)测量值是否与感染性休克患者的死亡率相关。方法对105例因感染性休克入院的患者进行评估。连续测量第1、3和7天的生物标志物PRA和PAC的血浆水平、PAC/PRA比率、C反应蛋白(CRP)水平和皮质醇水平。在重症监护室期间,记录了相关的临床信息和实验室结果。结果根据28天死亡率将患者分为两组:存活组(n=59)和非存活组(n=46)。幸存者组的PRA、PAC、急性生理和慢性健康评估(APACHE)II评分和顺序器官衰竭评估(SOFA)评分均低于非幸存者组(均P<0.05)。SOFA评分与PRA(r=0.373,P<0.001)和PAC(r=0.316,P=0.001)呈正相关。根据受试者操作特征分析,PRA和PAC预测28天死亡率的曲线下面积分别为0.69(95%置信区间[CI],0.58至0.79;P=0.001)和0.67(95%可信区间,0.56至0.77;P=0.003),与APACHE II评分和SOFA评分相似。特别是,第1天PRA值≥3.5 ng/ml-1 h-1的组的死亡率明显高于PRA值<3.5 ng/ml--1 h-1的对照组(log-rank检验,P<0.001)。根据多变量分析,SOFA评分(危险比,1.11;95%CI,1.01至1.22),PRA值≥3.5ng ml-1 h-1(危险比:3.25;95%CI:1.60至6.60),既往有癌症病史(危险比,3.44;95%置信区间,1.72至6.90)和冠状动脉闭塞性疾病(危险比:2.99;95%可信区间,1.26至7.08)是28天死亡率的预测因素。结论PRA升高是对感染性休克危重患者风险进行分层的有用生物标志物,也是28天死亡率的预后预测指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Implications of Plasma Renin Activity and Plasma Aldosterone Concentration in Critically Ill Patients with Septic Shock
Background The renin-angiotensin-aldosterone system is closely associated with volume status and vascular tone in septic shock. The present study aimed to assess whether plasma renin activity (PRA) and plasma aldosterone concentration (PAC) measurements compared with conventional severity indicators are associated with mortality in patients with septic shock. Methods We evaluated 105 patients who were admitted for septic shock. Plasma levels of the biomarkers PRA and PAC, the PAC/PRA ratio, C-reactive protein (CRP) level, and cortisol level on days 1, 3, and 7 were serially measured. During the intensive care unit stay, relevant clinical information and laboratory results were recorded. Results Patients were divided into two groups according to 28-day mortality: survivors (n = 59) and non-survivors (n = 46). The survivor group showed lower PRA, PAC, Acute Physiologic and Chronic Health Evaluation (APACHE) II score, and Sequential Organ Failure Assessment (SOFA) score than did the non-survivor group (all P < 0.05). The SOFA score was positively correlated with PRA (r = 0.373, P < 0.001) and PAC (r = 0.316, P = 0.001). According to receiver operating characteristic analysis, the areas under the curve of PRA and PAC to predict 28-day mortality were 0.69 (95% confidence interval [CI], 0.58 to 0.79; P = 0.001) and 0.67 (95% CI, 0.56 to 0.77; P = 0.003), respectively, similar to the APACHE II scores and SOFA scores. In particular, the group with PRA value ≥3.5 ng ml-1 h-1 on day 1 showed significantly greater mortality than did the group with PRA value <3.5 ng ml-1 h-1 (log-rank test, P < 0.001). According to multivariate analysis, SOFA score (hazard ratio, 1.11; 95% CI, 1.01 to 1.22), PRA value ≥3.5 ng ml-1 h-1 (hazard ratio, 3.25; 95% CI, 1.60 to 6.60), previous history of cancer (hazard ratio, 3.44; 95% CI, 1.72 to 6.90), and coronary arterial occlusive disease (hazard ratio, 2.99; 95% CI, 1.26 to 7.08) were predictors of 28-day mortality. Conclusions Elevated PRA is a useful biomarker to stratify the risk of critically ill patients with septic shock and is a prognostic predictor of 28-day mortality.
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