Prognostic Value of Inflammatory Markers in Septic Critically Ill Patients with Chronic Liver Disease: A Retrospective Analysis.

IF 1.4 4区 医学 Q4 GASTROENTEROLOGY & HEPATOLOGY
Nazlıhan Boyacı Dündar, Kamil İnci, Gülbin Aygencel, Melda Türkoğlu, Onur Gökçe, Mehmet Cindoruk
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引用次数: 0

Abstract

Background/aims: Septic patients with chronic liver disease (CLD) experience high morbidity and mortality rates, particularly in the intensive care unit (ICU) setting, due to immune dysfunction. Despite their vulnerability, data on prognostic markers remain scarce, particularly when assessed in conjunction with disease severity scores. This study aimed to evaluate the prognostic value of various inflammatory markers, including white blood cell count (WBC), neutrophil-to-lymphocyte ratio (NLR), lactate, and lactate-to-albumin ratio (LAR), in septic critically ill CLD patients.

Materials and methods: A retrospective cohort study was conducted on 126 septic CLD patients admitted to ICU. Data on demographics, clinical scores, inflammatory markers, and clinical outcomes were collected. Logistic regression and ROC analyses were used to identify independent predictors of ICU mortality.

Results: Intensive care unit mortality was 66%. In addition to higher Acute Physiology and Chronic Health Evaluation II (APACHE II) (39.3 ± 7.2 vs. 21 ± 5.1, P < .001), Sequential Organ Failure Assessment (12.4 ± 3.5 vs. 8.5 ± 3.1, P < .001), CLIF-C ACLF [63 (54-69) vs. 50 (41- 53)] scores, ICU non-survivors had higher WBC (median: 14 400/µL vs. 7300/µL, P < .001), lactate (median: 4.6mmol/L vs. 2.4mmol/L, P < .001), NLR (median: 12.5 vs. 9, P = .015), and LAR (median: 2.15 vs. 0.93, P < .001) compared to survivors. Multivariate analysis identified APACHE II (OR 1.183, 95% CI: 1.003-1.396, P = .046), CLIF-C ACLF (OR 1.104, 95% CI: 1.002-1.216, P = .046), and LAR (OR 2.992, 95% CI: 1.277-7.009, P = .012) as independent predictors of ICU mortality. The LAR was the most significant inflammatory marker (area under the curve: 0.783, cut-off: 1.17), even in the subgroup of patients with low acute decompensation scores based on the CLIF-C ACLF score.

Conclusion: The LAR was a valuable prognostic marker for ICU mortality in septic CLD patients, even in the absence of advanced organ failure. This marker potentially outperforms other traditional inflammatory markers and could aid in early risk stratification for critically ill septic CLD patients.

感染性重症慢性肝病患者炎症标志物的预后价值:回顾性分析
背景/目的:感染性慢性肝病(CLD)患者由于免疫功能障碍,具有很高的发病率和死亡率,特别是在重症监护病房(ICU)。尽管它们很脆弱,但关于预后标志物的数据仍然很少,特别是当与疾病严重程度评分一起评估时。本研究旨在评估各种炎症标志物,包括白细胞计数(WBC)、中性粒细胞与淋巴细胞比值(NLR)、乳酸和乳酸与白蛋白比值(LAR)在脓毒性危重症CLD患者中的预后价值。材料与方法:对ICU收治的126例脓毒性CLD患者进行回顾性队列研究。收集了人口统计学、临床评分、炎症标志物和临床结果的数据。采用Logistic回归和ROC分析确定ICU死亡率的独立预测因素。结果:重症监护病房死亡率为66%。除了更高的急性生理和慢性健康评估II (APACHE II)(39.3±7.2 vs . 21±5.1 P <措施),顺序器官衰竭评估(12.4±3.5和8.5±3.1,P <措施),CLIF-C ACLF[63(54 - 69)和50(41 - 53)]分数,ICU non-survivors有更高的白细胞(中值:14 400 /µL与7300 /µL P <措施),乳酸(中值:4.6更易与L和2.4更易与L P <措施),NLR(中值:12.5和9 P = .015),和政治(中值:2.15和0.93,幸存者相比P <措施)。多因素分析发现APACHE II (OR 1.183, 95% CI: 1.003-1.396, P = 0.046)、CLIF-C ACLF (OR 1.104, 95% CI: 1.002-1.216, P = 0.046)和LAR (OR 2.992, 95% CI: 1.277-7.009, P = 0.012)是ICU死亡率的独立预测因子。LAR是最显著的炎症标志物(曲线下面积:0.783,临界值:1.17),即使在基于CLIF-C ACLF评分的急性失代偿评分较低的患者亚组中也是如此。结论:即使在没有晚期器官衰竭的情况下,LAR也是脓毒性CLD患者ICU死亡率的一个有价值的预后指标。该标志物可能优于其他传统炎症标志物,并有助于危重感染性CLD患者的早期风险分层。
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来源期刊
Turkish Journal of Gastroenterology
Turkish Journal of Gastroenterology 医学-胃肠肝病学
CiteScore
1.90
自引率
0.00%
发文量
127
审稿时长
6 months
期刊介绍: The Turkish Journal of Gastroenterology (Turk J Gastroenterol) is the double-blind peer-reviewed, open access, international publication organ of the Turkish Society of Gastroenterology. The journal is a bimonthly publication, published on January, March, May, July, September, November and its publication language is English. The Turkish Journal of Gastroenterology aims to publish international at the highest clinical and scientific level on original issues of gastroenterology and hepatology. The journal publishes original papers, review articles, case reports and letters to the editor on clinical and experimental gastroenterology and hepatology.
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