International Journal of Clinical Research
International Journal of Clinical Research. 2025; 9: (10) ; 10.12208/j.ijcr.20250471 .
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1 阳西总医院人民医院药剂科 广东阳江
2 阳西总医院人民医院重症医学科 广东阳江
*通讯作者: 梁显湛,单位: 阳西总医院人民医院重症医学科 广东阳江;
目的 观察西维来司他钠治疗急性肺挫伤的临床疗效及相关风险因素。方法 选取 2023年5月-2025年7月符合筛选条件的的急性肺挫伤患者60例,回顾性收集患者临床资料,根据不同治疗方案将患者分为对照组(常规治疗方案)和试验组(常规治疗方案+西维来司他钠),各30例。分析比较两组患者一般基线资料、治疗前和治疗后血清炎症因子指标水平、动脉血气指标水平、生活自理能力评分、住院时长以及病死率等指标,采用χ2检验、线性回归分析西维来司他钠治疗急性肺挫伤影响患者预后相关风险因素。结果 本研究共纳入60例患者,治疗前PCT 试验组>对照组,差异有统计学意义(P<0.05)试验组;PCT治疗后<治疗前,差异有统计学意义(P<0.05);两组BADL评分均为治疗后>治疗前,差异有统计学意义(P<0.05);治疗前SaO2对照组>试验组,差异有统计学意义(P<0.05);对照组PaO2治疗前<治疗后,差异有统计学意义(P<0.05);单因素分析结果:创伤性休克、肝功能异常是试验组影响患者预后的相关风险因素,差异有统计学意义(P<0.05),线性回归分析结果:肝功能异常是试验组影响患者预后的独立风险因素,差异有统计学意义(P<0.05)。结论 西维来司他钠能减轻急性肺挫伤患者的炎症反应,改善患者生活自理能力,治疗期间需提高对患者肝功能指标的关注,以辅助优化治疗方案。
Objective To observe the clinical efficacy of sivelestat sodium in the treatment of acute pulmonary contusion and the related risk factors. Methods Sixty patients with acute pulmonary contusion who met the screening criteria from May 2023 to July 2025 were selected. The clinical data of the patients were retrospectively collected. According to different treatment regimens, the patients were divided into the control group (conventional treatment regimen) and the experimental group (conventional treatment regimen + siverestat sodium), with 30 cases in each group. The general baseline data, serum inflammatory factor index levels before and after treatment, arterial blood gas index levels, self-care ability scores, length of hospital stay and mortality rate of the two groups of patients were analyzed and compared. The χ2 test and linear regression were used to analyze the risk factors related to the prognosis of patients with acute pulmonary contusion treated with siverestat sodium. Results A total of 60 patients were included in this study. Before treatment, the PCT in the experimental group was greater than that in the control group, and the difference was statistically significant (P < 0.05). After PCT treatment, the value was less than that before treatment, and the difference was statistically significant (P < 0.05). The BADL scores of both groups were higher after treatment than before treatment, and the difference was statistically significant (P < 0.05). Before treatment, the SaO2 in the control group was greater than that in the experimental group, and the difference was statistically significant (P < 0.05). In the control group, PaO2 was less before treatment than after treatment, and the difference was statistically significant (P < 0.05). Univariate analysis results: Traumatic shock and abnormal liver function were the related risk factors affecting the prognosis of patients in the experimental group, and the difference was statistically significant (P < 0.05). Linear regression analysis results: Abnormal liver function was an independent risk factor affecting the prognosis of patients in the experimental group, and the difference was statistically significant (P < 0.05). Conclusion Sivelestat sodium can alleviate the inflammatory response in patients with acute pulmonary contusion and improve their self-care ability. During the treatment period, more attention should be paid to the liver function indicators of patients to assist in optimizing the treatment plan.
[1] Choudhary S, Pasrija D, Mendez M D. Pulmonary Contusion[J]. 2025.
[2] Bassi E, Merighi C T, Tomizuka C I, et al. Association of antimicrobial use and incidence of hospital-acquired pneumonia in critically ill trauma patients with pulmonary contusion: an observational study[J]. Braz J Anesthesiol, 2024,74(3):744454.
[3] 邵炜慧, 刘宏. 西维来司他钠治疗ARDS患者的效果及其应用价值[J]. 河南医学研究, 2025,34(2):329-332.
[4] 中国研究型医院学会危重医学专业委员会, 中国医药教育协会重症医学专业委员会. 西维来司他钠临床应用专家共识[J]. 中国研究型医院, 2022,9(1):9-13.
[5] Zhang X, Hu H, Li Z, et al. Population pharmacokinetics of sivelestat in Chinese patients with severe pneumonia[J]. Fundam Clin Pharmacol, 2025,39(2):e70001.
[6] Liu M, Zhang J, Dong L, et al. Detection of sivelestat and its metabolite in small volumes of plasma from Chinese ALI/ARDS patients with SIRS via high-throughput UPLC-MS/MS: A pharmacokinetic study[J]. J Pharm Biomed Anal, 2021,195:113876.
[7] Geng H, Zhang H, Cheng L, et al. Sivelestat ameliorates sepsis-induced myocardial dysfunction by activating the PI3K/AKT/mTOR signaling pathway[J]. Int Immuno-pharmacol, 2024,128:111466.
[8] Ren J, Deng G, Li R, et al. Possible pharmacological targets and mechanisms of sivelestat in protecting acute lung injury[J]. Comput Biol Med, 2024,170:108080.