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西维来司他对伴有全身炎症反应综合征的急性重症胰腺炎的疗效及安全性:一项回顾性研究。

Effect and safety of sivelestat on acute severe pancreatitis with systemic inflammatory response syndrome: a retrospective study.

作者信息

Xie Jiafeng, Lei Ruyi, Pei Hui, Gu Yulei, Zhang Luanluan, Liu Jingrong, Huang Yahui, Zhang Yepeng, Zi Yanan, Zhu Changju, Zhu Zhiqiang

机构信息

Department of emergency ICU, the first affiliated hospital of Zhengzhou University, Henan, 450052, China.

Henan Medical Key Laboratory of Emergency and Trauma Research, Henan, 450052, China.

出版信息

Sci Rep. 2025 Jan 2;15(1):150. doi: 10.1038/s41598-024-84600-z.

DOI:10.1038/s41598-024-84600-z
PMID:39747371
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11695592/
Abstract

The study was to explore the efficacy and safety of sivelestat (SV) in the treatment of severe acute pancreatitis (SAP) with systemic inflammatory response syndrome (SIRS). A total of 102 SAP patients diagnosed and treated in the Emergency Intensive Care Unit of the First Affiliated Hospital of Zhengzhou University from January 2021 to August 2024 were selected. The changes of disease outcome, hospital stays and mortality were compared between the two groups. A total of 102 patients were recruited to control group (n = 56) or SV group (n = 46) according to whether SV was applied or not. There was no significant difference in baseline data at admission between the two groups. After 1 week of treatment, all the indexes in both groups improved. The duration of ventilator use (p = 0.0400) and ICU stays (p  = 0.0495) in SV group was shorter than that in control group, but there was no significant difference in mortality between the two groups. Although SV did not reduce the mortality of patients with SAP, it reduced the length of ventilator use and ICU stay.

摘要

本研究旨在探讨西维来司他(SV)治疗伴有全身炎症反应综合征(SIRS)的重症急性胰腺炎(SAP)的疗效和安全性。选取2021年1月至2024年8月在郑州大学第一附属医院急诊重症监护病房诊断并治疗的102例SAP患者。比较两组患者的疾病转归、住院时间和死亡率。根据是否应用SV,将102例患者分为对照组(n = 56)和SV组(n = 46)。两组患者入院时的基线数据无显著差异。治疗1周后,两组各项指标均有所改善。SV组的呼吸机使用时间(p = 0.0400)和ICU住院时间(p = 0.0495)均短于对照组,但两组患者的死亡率无显著差异。虽然SV未降低SAP患者的死亡率,但缩短了呼吸机使用时间和ICU住院时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d967/11695592/b587e6b8d2cb/41598_2024_84600_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d967/11695592/ad0511a11fc4/41598_2024_84600_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d967/11695592/b587e6b8d2cb/41598_2024_84600_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d967/11695592/ad0511a11fc4/41598_2024_84600_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d967/11695592/b587e6b8d2cb/41598_2024_84600_Fig2_HTML.jpg

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本文引用的文献

1
Comparison of Interleukin-6, C-Reactive Protein, Procalcitonin, and the Computed Tomography Severity Index for Early Prediction of Severity of Acute Pancreatitis.比较白细胞介素-6、C 反应蛋白、降钙素原和计算机断层扫描严重程度指数对急性胰腺炎严重程度的早期预测。
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New guidelines for the treatment of severe acute pancreatitis.重症急性胰腺炎治疗新指南。
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Improving the management of severe acute pancreatitis: The new guidelines from the French Society of Anaesthesia and Intensive Care Medicine.
改善重症急性胰腺炎的管理:法国麻醉与重症医学学会的新指南
Anaesth Crit Care Pain Med. 2022 Jun;41(3):101103. doi: 10.1016/j.accpm.2022.101103.
4
Preclinical efficacy investigation of human neutrophil elastase inhibitor sivelestat in animal model of psoriasis.人中性粒细胞弹性蛋白酶抑制剂西维来司他在银屑病动物模型中的临床前疗效研究。
Skin Health Dis. 2021 Dec 30;2(2):e90. doi: 10.1002/ski2.90. eCollection 2022 Jun.
5
Sivelestat Alleviates Atherosclerosis by Improving Intestinal Barrier Function and Reducing Endotoxemia.西维来司他通过改善肠道屏障功能和降低内毒素血症来减轻动脉粥样硬化。
Front Pharmacol. 2022 Apr 4;13:838688. doi: 10.3389/fphar.2022.838688. eCollection 2022.
6
Positive Effects of Neutrophil Elastase Inhibitor (Sivelestat) on Gut Microbiome and Metabolite Profiles of Septic Rats.中性粒细胞弹性蛋白酶抑制剂(西维来司他)对脓毒症大鼠肠道微生物组和代谢物谱的积极影响。
Front Cell Infect Microbiol. 2022 Mar 15;12:818391. doi: 10.3389/fcimb.2022.818391. eCollection 2022.
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Efficacy, safety, and pharmacoeconomics of sivelestat sodium in the treatment of septic acute respiratory distress syndrome: a retrospective cohort study.西维来司他钠治疗脓毒症急性呼吸窘迫综合征的疗效、安全性和药物经济学:一项回顾性队列研究。
Ann Palliat Med. 2021 Nov;10(11):11910-11917. doi: 10.21037/apm-21-3164.
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