Comparative efficacy of Chinese tonic medicines for treating sepsis or septic shock: A systematic review and Bayesian network meta-analysis of randomized controlled trials

IF 8.3 1区 医学 Q1 CHEMISTRY, MEDICINAL Phytomedicine Pub Date : 2025-01-01 Epub Date: 2024-11-30 DOI:10.1016/j.phymed.2024.156295
Rui Yang , Cheng Hu , Yuxin Zhuo , Qingyuan Tan , Yuxin Shen , Kun Jiang , Qing Xia , Lihui Deng
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Abstract

Background

Sepsis or septic shock is a life-threatening medical emergency with a poor prognosis and a high economic burden for both individuals and healthcare resources. Evidence suggests that Chinese tonic medicines (CTMs), as adjuvant treatments, are effective in treating this disease. Nevertheless, the ongoing discourse regarding the optimal CTMs persists. This study was conducted to further explore the comparative effectiveness of CTMs for patients with sepsis or septic shock.

Methods

We systematically searched Pubmed, Embase, Cochrane Central Register of Controlled Trials, Chinese Biomedical Literature (CBM), Chinese National Knowledge Infrastructure (CNKI), Wanfang database, VIP database from inception to November 15, 2023. Primary outcomes encompassed the delta Sequential Organ Failure Assessment (ΔSOFA) score at day 7 after interventions and 28-day mortality. Secondary outcomes included delta serum lactate (ΔLac) and delta mean arterial pressure (ΔMAP) levels at day 7 after interventions, as well as the duration of vasoactive drug administration. The safety outcome was adverse drug reactions or adverse drug events (ADRs/ADEs). The risk ratio (RR) and mean difference (MD) with a 95 % confidence interval (95 %CI) were selected as effect measures. The Bayesian network meta-analysis was conducted by R version 4.2.2 software. The surface under the cumulative ranking curve (SUCRA) values were used to rank each treatment. The Cochrane Risk of Bias V.2.0 tool was employed to assess the within-study risk of bias. The CINeMA (Confidence in Network Meta-Analysis) web application was utilized to assess the quality of evidence. This protocol was prospectively registered in PROSPERO (CRD4202348572).

Results

A total of 45 randomized controlled trials (RCTs) involving 3433 patients were identified in this study. Seven CTMs including Shenfu injection (SF), Shenmai injection (SM), Sini decoction (SN), Shenfu and Shengmai granules (SF+SGM), Shengmai injection (SGM), Yiqifumai injection (YQFM), and Shenqifuzheng injection (SQFZ) were involved. Regarding the ΔSOFA score, interventions combining SM with Western medicine (WM) (MD, −2.77; 95 %CI, −3.28 to −2.27), YQFM+WM (MD, −1.76; 95 %CI, −2.73 to −0.79), SGM+WM (MD, −1.11; 95 %CI, −1.88 to −0.34), and SF+WM (MD, −0.98; 95 %CI, −1.17 to −0.78) demonstrated superiority over WM alone. According to the SUCRA values, SM+WM (99.28 %) achieved the highest ranking for the ΔSOFA score. Concerning 28-day mortality, SM+WM (RR, 0.51; 95 %CI, 0.35 to 0.72) and SF+WM (RR, 0.73; 95 %CI, 0.65 to 0.83) exhibited a superior effect in reducing 28-day mortality. Based on the SUCRA values, SM+WM (82.49 %) secured the top ranking for 28-day mortality. Among the secondary outcomes, SM+WM (MD, −2.50; 95 %CI, −4.15 to −0.83; SUCRA, 94.27 %) emerged as the most favorable in reducing serum lactate levels. SF+WM (MD, 10.78; 95 %CI, 3.11 to 18.71; SCURA, 78.3 %) exhibited superior effectiveness compared to other treatments in improving mean arterial pressure (MAP). The certainty of evidence for these outcomes was assessed as low.

Conclusion

CTMs combined with WM led to a significant improvement in ΔSOFA score and MAP, as well as a reduction in 28-day mortality and serum lactate levels. SM+WM emerged as the optimal treatment regimen for enhancing ΔSOFA, reducing 28-day mortality, and lowering serum lactate levels. Additionally, SF+WM exhibited superiority in improving MAP. Nevertheless, there is a need for large-scale, multicenter, and direct comparative RCTs to generate higher-quality evidence.
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中药治疗脓毒症或脓毒性休克的疗效比较:随机对照试验的系统综述和贝叶斯网络荟萃分析。
背景:脓毒症或脓毒性休克是一种危及生命的医疗紧急情况,预后差,对个人和医疗资源都是很高的经济负担。有证据表明,中药补益作为辅助治疗,对治疗本病是有效的。然而,关于最佳CTMs的讨论仍在继续。本研究旨在进一步探讨中西医结合治疗脓毒症或感染性休克的比较疗效。方法:系统检索Pubmed、Embase、Cochrane中央对照试验注册库、中国生物医学文献(CBM)、中国知网(CNKI)、万方数据库、VIP数据库,检索时间为2023年11月15日。主要结局包括干预后第7天delta序贯器官衰竭评估(ΔSOFA)评分和28天死亡率。次要结局包括干预后第7天的δ血清乳酸(ΔLac)和δ平均动脉压(ΔMAP)水平,以及血管活性药物给药的持续时间。安全性指标为药物不良反应或药物不良事件(adr /ADEs)。采用95%置信区间(95% CI)的风险比(RR)和平均差(MD)作为效果度量。贝叶斯网络meta分析采用R 4.2.2版软件进行。利用累积排序曲线下的曲面(SUCRA)值对各处理进行排序。采用Cochrane Risk of Bias V.2.0工具评估研究内偏倚风险。使用CINeMA (Confidence in Network Meta-Analysis)网络应用程序来评估证据的质量。该方案在PROSPERO (CRD4202348572)前瞻性注册。结果:本研究共纳入45项随机对照试验(RCTs),涉及3433例患者。涉及参附注射液(SF)、参脉注射液(SM)、四逆汤(SN)、参附生脉颗粒(SF+SGM)、生脉注射液(SGM)、益七补脉注射液(YQFM)、参芪扶正注射液(SQFZ)等7种中药。在ΔSOFA得分方面,SM与西医结合干预(WM) (MD, -2.77;95% CI, -3.28 ~ -2.27), YQFM+WM (MD, -1.76;95% CI, -2.73 ~ -0.79), SGM+WM (MD, -1.11;95% CI, -1.88 ~ -0.34), SF+WM (MD, -0.98;95% CI(-1.17 - -0.78)显示优于单纯WM。根据SUCRA值,SM+WM(99.28%)在ΔSOFA得分中排名最高。关于28天死亡率,SM+WM (RR, 0.51;95% CI, 0.35 ~ 0.72)和SF+WM (RR, 0.73;95% CI(0.65 ~ 0.83)在降低28天死亡率方面表现出优越的效果。根据SUCRA值,SM+WM(82.49%)在28天死亡率中排名第一。次要结局中,SM+WM (MD, -2.50;95% CI, -4.15 ~ -0.83;SUCRA(94.27%)在降低血清乳酸水平方面最有利。Sf + wm (md, 10.78;95% CI, 3.11 ~ 18.71;与其他治疗相比,SCURA(78.3%)在改善平均动脉压(MAP)方面表现出优越的效果。这些结果的证据的确定性被评估为低。结论:中西医结合治疗可显著改善ΔSOFA评分和MAP,降低28天死亡率和血清乳酸水平。SM+WM是提高ΔSOFA、降低28天死亡率和降低血清乳酸水平的最佳治疗方案。此外,SF+WM在改善MAP方面表现出优势。然而,需要大规模、多中心和直接比较的随机对照试验来产生更高质量的证据。
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来源期刊
Phytomedicine
Phytomedicine 医学-药学
CiteScore
10.30
自引率
5.10%
发文量
670
审稿时长
91 days
期刊介绍: Phytomedicine is a therapy-oriented journal that publishes innovative studies on the efficacy, safety, quality, and mechanisms of action of specified plant extracts, phytopharmaceuticals, and their isolated constituents. This includes clinical, pharmacological, pharmacokinetic, and toxicological studies of herbal medicinal products, preparations, and purified compounds with defined and consistent quality, ensuring reproducible pharmacological activity. Founded in 1994, Phytomedicine aims to focus and stimulate research in this field and establish internationally accepted scientific standards for pharmacological studies, proof of clinical efficacy, and safety of phytomedicines.
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