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脓毒症和脓毒性休克患者乳酸/白蛋白比值与序贯器官衰竭评估(SOFA)评分的相关性

The Correlation Between the Lactate/Albumin Ratio and Sequential Organ Failure Assessment (SOFA) Score in Patients With Sepsis and Septic Shock.

作者信息

Mahashabde Madhulika L, Bhimani Yash R, Bhavsar Harin M

机构信息

General Medicine, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Dr. D. Y. Patil Vidyapeeth, Pune, IND.

出版信息

Cureus. 2024 Jul 29;16(7):e65616. doi: 10.7759/cureus.65616. eCollection 2024 Jul.

DOI:10.7759/cureus.65616
PMID:39205773
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11357719/
Abstract

Background Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection, often resulting in severe outcomes such as septic shock and death. Globally, sepsis ranks among the most common causes of illness and death. The Sequential Organ Failure Assessment (SOFA) score is an established marker used to assess and predict the extent of organ failure in septic patients. The introduction of novel markers, such as the lactate/albumin (L/A) ratio, serves as a prognostic indicator in critical care settings, particularly for patients with sepsis. In this context, a higher L/A ratio upon admission aids in assessing disease severity and improving clinical decision-making to reduce mortality and adverse outcomes, which we aim to correlate through our study. Materials and methods This was an observational cross-sectional analysis conducted on 100 patients aged over 18 years who met the "Sepsis-3" guidelines and were admitted to the medical intensive care unit of Dr. D. Y. Patil Hospital, Pune, Maharashtra, India, between October 2022 and May 2024. Patients with chronic liver disease classified as Child-Pugh class C were excluded, as were those with chronic kidney disease (CKD). Written informed consent was obtained from each participant before the study. Data were collected through physical examination, routine laboratory investigations, and radiological assessments. Statistical analysis was performed using IBM SPSS version 20 (IBM Corp., Armonk, NY). Descriptive statistical analyses were conducted using the SPSS data editor. Statistical significance was considered at a p-value of less than 0.05 for all analyses. Results In the study population, 78 patients survived, while 22 patients died. The L/A ratio and SOFA score were significantly higher in non-survivors compared to survivors, both upon admission and thereafter, with statistical significance (p < 0.05). The correlation between the L/A ratio and the SOFA score was examined upon admission at 24 hours, 48 hours, day 7, and day 28. Pearson correlation analysis revealed statistically significant results (p < 0.05) throughout the entire study period. Conclusion A high L/A ratio, along with the SOFA score at ICU admission, was associated with a grave prognosis and poor outcomes, serving as independent risk factors for ICU admission. Therefore, patients with a high L/A ratio and SOFA score should be identified early and managed aggressively to avoid poor outcomes. Our study demonstrates that combining serum lactate and serum albumin levels into the L/A ratio significantly enhances prognostic accuracy compared to using serum lactate alone.

摘要

背景

脓毒症被定义为由宿主对感染的失调反应引起的危及生命的器官功能障碍,常常导致诸如感染性休克和死亡等严重后果。在全球范围内,脓毒症位列疾病和死亡的最常见原因之中。序贯器官衰竭评估(SOFA)评分是一种既定的标志物,用于评估和预测脓毒症患者的器官衰竭程度。引入诸如乳酸/白蛋白(L/A)比值等新型标志物,在重症监护环境中可作为一种预后指标,尤其是对于脓毒症患者。在此背景下,入院时较高的L/A比值有助于评估疾病严重程度并改善临床决策以降低死亡率和不良后果,我们旨在通过研究将二者关联起来。

材料与方法

这是一项对100名年龄超过18岁的患者进行的观察性横断面分析,这些患者符合“脓毒症-3”指南,并于2022年10月至2024年5月期间被收治入印度马哈拉施特拉邦浦那市D.Y.帕蒂尔医院的内科重症监护病房。排除了被归类为Child-Pugh C级的慢性肝病患者以及慢性肾脏病(CKD)患者。在研究前从每位参与者处获得了书面知情同意书。通过体格检查、常规实验室检查和影像学评估收集数据。使用IBM SPSS 20版(IBM公司,纽约州阿蒙克)进行统计分析。使用SPSS数据编辑器进行描述性统计分析。所有分析的统计学显著性以p值小于0.05来判定。

结果

在研究人群中,78名患者存活,22名患者死亡。非存活者的L/A比值和SOFA评分在入院时及之后均显著高于存活者,具有统计学显著性(p < 0.05)。在入院时、24小时、48小时、第7天和第28天对L/A比值与SOFA评分之间的相关性进行了检查。Pearson相关性分析在整个研究期间均显示出统计学显著性结果(p < 0.05)。

结论

较高的L/A比值以及ICU入院时的SOFA评分与严重的预后和不良后果相关,是ICU入院的独立危险因素。因此,应尽早识别L/A比值和SOFA评分较高的患者并积极进行管理以避免不良后果。我们的研究表明,与单独使用血清乳酸相比,将血清乳酸和血清白蛋白水平合并为L/A比值可显著提高预后准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/11357719/3e71026f70dd/cureus-0016-00000065616-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/11357719/c22141c74abc/cureus-0016-00000065616-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/11357719/c43e56f260cb/cureus-0016-00000065616-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/11357719/3e71026f70dd/cureus-0016-00000065616-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/11357719/c22141c74abc/cureus-0016-00000065616-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/11357719/c43e56f260cb/cureus-0016-00000065616-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/11357719/3e71026f70dd/cureus-0016-00000065616-i03.jpg

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