神麻注射液对蒽环类药物引起的心脏毒性的影响:系统回顾和荟萃分析。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Lili Yang , Xiaorui Liu , Wen Yang , Siqi Wang , Zimu Li , Yiming Lei , Dongling Liu
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引用次数: 0

摘要

目的:神麦注射液是一种经典的中药处方,常被推荐用于治疗蒽环类药物引起的心脏毒性。然而,神麦注射液治疗蒽环类药物所致心脏毒性的有效性和安全性尚未见报道:我们对8个文献数据库和2个临床试验登记处进行了全面检索,检索了自数据库建立至2023年7月1日期间所有与神麻注射液治疗蒽环类药物诱导的心脏毒性相关的随机对照试验(RCT)。数据分析使用 RStudio 中的 Meta 软件包和 RevMan 5.4 进行。使用 GRADE pro3.6.1 软件评估证据质量:本研究共纳入了 16 项 RCT,包括 2140 名患者。Meta分析显示,神麻注射液在改善ST-T段变化(RR = 0.28; 95% CI, 0.20 to 0.39; P < 0.0001)(P < 0.01)、肌酸激酶同工酶(SMD = -3.49; 95% CI, -5.24 to -1.74; P < 0.0001)、QT 间期延长(RR = 0.46;95% CI,0.28 至 0.75;P = 0.0018)、QRS 低电压(RR = 0.44;95% CI,0.27 至 0.71;P = 0.0007)、窦性心动过速(RR = 0.41;95% CI,0.28 至 0.60;P < 0.0001)、房性早搏(RR = 0.55; 95% CI, 0.35 to 0.87; P = 0.01)、室性早搏(RR = 0.39; 95% CI, 0.26 to 0.59; P < 0.0001)和肌酸激酶(SMD = -1.43; 95% CI, -2.57 to -0.29;P < 0.0001)。敏感性分析证实了这一优势,但在改善左室射血分数(MD = 16.01;95% CI,-3.10 至 35.12;P = 0.10)和房室传导阻滞(RR = 0.49;95% CI,0.24 至 1.03;P = 0.06)方面没有优势。本研究收录的文献未提及有关神麦注射液安全性方面的数据,因此我们尚不清楚神麦注射液的安全性。亚组分析结果表明,异质性与给药剂量和化疗方案无关。发表偏倚检验显示无发表偏倚。研究结果的证据质量从 "非常低 "到 "中等 "不等:本研究表明,参麦注射液能有效治疗蒽环类药物诱导的心脏毒性,是治疗蒽环类药物诱导的心脏毒性的一种潜在方法。然而,由于纳入的研究性临床试验的方法学质量不高,我们建议进行严格的、高质量的大样本试验来证实我们的研究结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of shenmai injection on anthracycline-induced cardiotoxicity: A systematic review and meta-analysis

Objective

Shenmai injection is a classic herbal prescription, and is often recommended for the treatment of anthracycline-induced cardiotoxicity. However, the efficacy and safety of Shenmai injection for the treatment of anthracycline-induced cardiotoxicity have not been reported.

Materials and methods

We conducted a comprehensive search of eight literature databases and two clinical trial registries, retrieving all randomized controlled trials (RCTs) related to the treatment of anthracycline-induced cardiotoxicity with Shenmai injection from the establishment of the databases to July 1, 2023. Data analysis was performed using the Meta package in RStudio and RevMan 5.4. The GRADE pro3.6.1 software was utilized for assessing the quality of evidence.

Results

A total of 16 RCTs including 2140 patients were included in this study. Meta-analysis showed that Shenmai injection had an advantage in improving ST-T segment changes (RR = 0.28; 95 % CI, 0.20 to 0.39; P < 0.0001) (P < 0.01), creatine kinase isoenzyme (SMD = −3.49; 95 % CI, −5.24 to −1.74; P < 0.0001), Prolonged QT interval (RR = 0.46; 95 % CI, 0.28 to 0.75; P = 0.0018), Low QRS Voltage (RR = 0.44; 95 % CI, 0.27 to 0.71; P = 0.0007), sinus tachycardia (RR = 0.41; 95 % CI, 0.28 to 0.60; P < 0.0001), atrial premature beats (RR = 0.55; 95 % CI, 0.35 to 0.87; P = 0.01), Premature Ventricular Contractions (RR = 0.39; 95 % CI, 0.26 to 0.59; P < 0.0001) and creatine kinase (SMD = −1.43; 95 % CI, −2.57 to −0.29; P < 0.0001) in patients with anthracycline-induced cardiotoxicity. advantage, which was supported by sensitivity analyses, but not in improving left ventricular ejection fraction (MD = 16.01; 95 % CI, −3.10 to 35.12; P = 0.10) and atrioventricular block (RR = 0.49; 95 % CI, 0.24 to 1.03; P = 0.06). The literature included in the study did not refer to data regarding the safety aspects of Shenmai injection, so we do not yet know the safety of Shenmai injection. The results of subgroup analyses suggested that heterogeneity was not related to the administered dose and chemotherapy regimen. The publication bias test showed no publication bias. The quality of evidence for the results ranged from “very low” to “moderate.”

Conclusion

This study suggests that Shenmai injection is effective in treating anthracycline-induced cardiotoxicity and is a potential treatment for anthracycline-induced cardiotoxicity. However, due to the poor methodological quality of the included RCTs, we recommend rigorous, high-quality, large-sample trials to confirm our findings.

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来源期刊
CiteScore
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