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C 反应蛋白、降钙素原和白细胞值在预测患有脓毒症性肺炎和感染性休克患者预后中的作用。

The Utility of C-Reactive Protein, Procalcitonin, and Leukocyte Values in Predicting the Prognosis of Patients with Pneumosepsis and Septic Shock.

机构信息

Department of Anesthesiology and Reanimation, Ankara Ataturk Sanatorium Training and Research Hospital, University of Health Sciences, 06290 Ankara, Turkey.

出版信息

Medicina (Kaunas). 2024 Sep 24;60(10):1560. doi: 10.3390/medicina60101560.

Abstract

The predictive value of changes in C-reactive protein (CRP), procalcitonin, and leukocyte levels, which are commonly used in the diagnosis of infection in sepsis and septic shock, remains a topic of debate. The aim of this study was to evaluate the effectiveness of changes in CRP, procalcitonin, and leukocyte counts on the prognosis of 230 patients admitted to the intensive care unit (ICU) with the diagnosis of sepsis and pneumonia-related septic shock between 1 April 2022 and 31 December 2023, and to investigate whether any of these markers have a superior predictive value over the others in forecasting prognosis. This single-center, retrospective, cross-sectional observational study included patients who developed sepsis and septic shock due to community-acquired pneumonia and were admitted to the ICU. Demographic data, 1-month and 90-day mortality rates, length of stay in the ICU, discharge to the ward or an outside facility, need for dialysis after sepsis, need for invasive or noninvasive mechanical ventilation during the ICU stay and the duration of this support, whether patients admitted with sepsis or septic shock required inotropic agent support during their stay in the ICU and whether they received monotherapy or combination therapy with antibiotics during their admission to the ICU, the Comorbidity Index score (CCIS), CURB-65 score (confusion, uremia, respiratory rate, BP, age ≥ 65), and Acute Physiology and Chronic Health Evaluation II (APACHE-II) score were analyzed. Additionally, CRP, procalcitonin, and leukocyte levels were recorded, and univariate and multivariate logistic regression analyses were performed to evaluate their effects on 1- and 3-month mortality outcomes. In all statistical analyses, a -value of <0.05 was accepted as a significant level. According to multivariate logistic regression analysis, low BMI, male gender, and high CCIS, CURB-65, and APACHE-II scores were found to be significantly associated with both 1-month and 3-month mortality ( < 0.05). Although there was no significant relationship between the first-day levels of leukocytes, CRP, and PCT and mortality, their levels on the third day were observed to be at their highest in both the 1-month and 3-month mortality cases ( < 0.05). Additionally, a concurrent increase in any two or all three of CRP, PCT, and leukocyte values was found to be higher in patients with 3-month mortality compared with those who survived ( = 0.004). In patients with pneumoseptic or pneumonia-related septic shock, the persistent elevation and concurrent increase in PCT, CRP, and leukocyte values, along with male gender, advanced age, low BMI, and high CCIS, CURB-65, and APACHE-II scores, were found to be significantly associated with 3-month mortality.

摘要

C 反应蛋白(CRP)、降钙素原和白细胞水平的变化在脓毒症和感染性休克中的诊断中被广泛应用,但它们的预测价值仍存在争议。本研究旨在评估 CRP、降钙素原和白细胞计数变化对 230 例因社区获得性肺炎导致脓毒症和肺炎相关性感染性休克而入住重症监护病房(ICU)患者预后的影响,并探讨这些标志物中是否有任何一种具有优于其他标志物的预测价值。

这项单中心、回顾性、横断面观察性研究纳入了因社区获得性肺炎导致脓毒症和感染性休克而入住 ICU 的患者。收集患者的人口统计学数据、1 个月和 90 天的死亡率、入住 ICU 的时间、出院至病房或其他医疗机构、脓毒症后需要透析、入住 ICU 期间需要有创或无创机械通气以及支持的持续时间、入住 ICU 期间是否需要脓毒症或感染性休克的正性肌力药物支持以及是否接受抗生素单药或联合治疗、合并症指数评分(CCIS)、CURB-65 评分(意识障碍、尿素氮、呼吸频率、血压、年龄≥65 岁)和急性生理学和慢性健康评估 II 评分(APACHE-II)。此外,还记录了 CRP、降钙素原和白细胞水平,并进行了单变量和多变量逻辑回归分析,以评估它们对 1 个月和 3 个月死亡率的影响。在所有的统计分析中,-值<0.05 被认为具有统计学意义。

多变量逻辑回归分析显示,低 BMI、男性、高 CCIS、CURB-65 和 APACHE-II 评分与 1 个月和 3 个月的死亡率显著相关(<0.05)。虽然白细胞、CRP 和 PCT 的第 1 天水平与死亡率无显著关系,但第 3 天的水平在 1 个月和 3 个月死亡率病例中均最高(<0.05)。此外,与存活患者相比,3 个月死亡率患者的 CRP、PCT 和白细胞值同时升高或任意两种或三种值同时升高的比例更高(=0.004)。

在患有肺炎相关性脓毒症或肺炎相关性感染性休克的患者中,PCT、CRP 和白细胞值的持续升高和同时升高,以及男性、高龄、低 BMI 和高 CCIS、CURB-65 和 APACHE-II 评分与 3 个月死亡率显著相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65a0/11509754/1d80120c57b5/medicina-60-01560-g001.jpg

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