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《中华肺部疾病杂志》[ISSN:1006-6977/CN:61-1281/TN]

卷:

期数:

2024年01期

页码:

73-77

栏目:

论著

出版日期:

2024-02-20

文章信息/Info

Title:

Effect analysis of different doses of imipenem/cilastatin sodium in the treatment of severe pneumonia

作者:

周 璐¹; 钱桂亮²; 黄 建¹; 辛永利³

214000 江苏,无锡市康复医院老年康复科¹214000 江苏,无锡市第二老年病医院呼吸内科²226003 江苏,南通市第一人民医院胸心外科³

Author(s):

Zhou Lu¹;  Qian Guiliang²;  Huang Jian¹;  Xin Yongli³.

¹Department of Elderly Rehabilitation, Wuxi Rehabilitation Hospital, Wuxi 214000, China; ²Department of Respiratory, Wuxi No.2 Geriatric Hospital, Wuxi 214000, China; ³Depatment of cardiothoracic surgery, the First People's Hospital of Nantong,Nantong 226003, China

关键词:

不同剂量;  亚胺培南西司他丁钠;  重症肺炎;  疗效;  不良反应

Keywords:

Different dose;  Imipenem cilastatin sodium;  Severe pneumonia;  Curative effect;  Adverse reaction

分类号:

R563

DOI:

10.3877/cma.j.issn.1674-6902.2024.01.014

摘要:

目的 分析不同剂量亚胺培南西司他丁钠治疗重症肺炎的疗效。方法 选择2021年7月至2023年8月我院收治的58例重症肺炎患者为对象,根据治疗方法不同分为对照组27例与观察组31例。两组接受基础治疗。对照组接受低剂量1.0 g亚胺培南西司他丁钠治疗,观察组接受高剂量2.0 g亚胺培南西司他丁钠治疗,疗程10 d。比较两组肺功能、血气参数、临床疗效、血清学指标、病原菌清除率及不良反应。结果 血清学指标,IL-8观察组和对照组治疗前/后[(0.47±0.06)vs.(0.46±0.05)比(0.21±0.03)vs.(0.28±0.04)ng/ml(P<0.05)]; CDL[(0.55±0.58)vs.(0.37±0.052)比(1.65±0.31)vs.(2.24±0.43)ng/L,(P<0.05)]; sICAM-1[(33.57±4.96)vs.(32.48±4.32)比(8.25±2.08)vs.(14.19±3.27)ng/L,(P<0.05)]。动脉血气参数,PaCO₂观察组和对照组治疗前(83.57±7.22)vs.(82.43±7.68)mmHg,治疗后(56.38±5.07)vs.(67.23±6.15)mmHg(P<0.05); PaO₂两组治疗前(54.83±6.79)vs.(53.40±6.51)mmHg,治疗后(91.35±9.81)vs.(77.36±8.42)mmHg(P<0.05),SaO₂两组治疗前(85.26±6.64)vs.(86.77±6.24)%,治疗后(95.63±8.97)vs.(90.82±7.39)%(P<0.05)。两组最大呼气中段流量(maximum midexpiratory flow, MMF)、第1秒内用力呼气容积(forced expiratory volume within 1 second, FEV₁)及用力肺活量(forced vital capacity, FVC)水平升高(P<0.05),观察组FVC(2.99±0.48)L, FEV₁(2.18±0.35)%, MMF(1.59±0.31)L/s高于对照组(P<0.05)。结论 低剂量亚胺培南西司他丁钠相比,高剂量亚胺培南西司他丁钠治疗重症肺炎疗效确切,可改善患者肺功能与血气参数,减轻炎症反应,调节血清sICAM-1、CD40L水平,提高病原菌清除率。

Abstract:

Objective To analyze the efficacy of different doses of imipenem/cilastatin sodium in the treatment of severe pneumonia. Methods A total of 58 patients with severe pneumonia admitted to the hospital from July 2021 to August 2023 were selected and divided into a control group(27 cases)and an observation group(31 cases)according to different treatment methods. Both groups received basic treatment. The control group received low dose(1.0 g)of imipenem and cilastatin sodium, while the observation group received high dose(2.0 g)of imipenem and cilastatin sodium. Both groups were treated for 7 days. Lung function, blood gas indexes, clinical efficacy, serological indexes, pathogenic bacteria clearance and adverse reactions were compared in two groups. Results Serum indicators, IL-8 of observation and control groups before treatment(0.47±0.06)vs.(0.46±0.05), after treatment(0.21±0.03)vs.(0.28±0.04)ng/ml(P<0.05); sICAM-1 before treatment(33.57±4.96)vs.(32.48±4.32), after treatment(8.25±2.08)vs.(14.19±3.27)ng/L(P<0.05). Arterial blood gas parameters, PaCO₂ of observation and control groups, before treatment(83.57±7.22)vs.(82.43±7.68)mmHg, after treatment(56.38±5.07)vs.(67.23±6.15)mmHg(P<0.05); PaO₂ before treatment(54.83±6.79)vs.(53.40±6.51)mmHg, after treatment(91.35±9.81)vs.(77.36±8.42)mmHg(P<0.05); SaO₂ before treatment(85.26±6.64)vs.(86.77±6.24)%, after treatment(95.63±8.97)vs.(90.82±7.39)%(P<0.05). After treatment, maximum mid-expiratory flow(MMF), forced expiratory volume in the first second(FEV₁)and forced vital capacity(FVC)levels in 2 groups were increased(P<0.05), and those in observation group were higher [FVC(2.99±0.48)L, FEV₁(2.18±0.35)%, MMF(1.59±0.31)L/s(P<0.05)]. Conclusion Compared with low dose imipenem cilastatin sodium, high dose imipenem cilastatin sodium is effective in the treatment of severe pneumonia, can improve lung function and blood gas indexes, reduce inflammatory response, regulate serum sICAM-1 and CD40L levels, and increase the clearance rate of pathogenic bacteria, and is safe and reliable.

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备注/Memo

备注/Memo:

基金项目: 江苏省自然科学基金面上项目(BK20201491)
通信作者:钱桂亮, Email: kilip520@gmail.com

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更新日期/Last Update: 2024-02-20