Use of Bromocriptine for the Treatment of Peripartum Cardiomyopathy: A Meta-Analysis of Randomized Controlled Trials

E. VillanuevaDanielleLouis, Evangelista Lauren Kay, Espanillo-Villanueva Ma Cristina, C. AnonuevoJohn
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引用次数: 2

Abstract

Background Peripartum cardiomyopathy is a rare, pregnancy associated cause of left ventricular heart failure in previously healthy women. It remains an important cause of cardiac-related maternal morbidity and mortality worldwide. Half of the patients will recover left ventricular function after 6 months. However, in the remainder of patients who do not recover cardiac function, they will require advanced heart failure therapies. Bromocriptine, a dopamine agonist which inhibits prolactin release, has demonstrated improvement in left ventricular recovery and clinical outcome. We sought to determine the effect of adding Bromocriptine to standard heart failure therapy on the improvement and recovery of left ventricular function and cardiovascular mortality of these patients. Inclusion Criteria. Studies were included if they satisfied the following criteria:1) Randomized Controlled Trials; 2) Pregnant patients who fulfilled the criteria for diagnosis of peripartum cardiomyopathy and 3) Reported data on improvement in left ventricular ejection fraction and clinical outcomes. Methods. Using PUBMED, Clinical Key, Science Direct, Scopus, and Cochrane databases, a search for eligible studies was conducted from June to December 31, 2018. The quality of each study was evaluated using the Cochrane Risk of Bias Tool. The primary outcome of interest is on the effect of Bromocriptine on the improvement of left ventricular function and clinical outcomes among these patients. Review Manager 5.3 was utilized to perform analysis of random effects for continuous outcomes. Results. We identified 2 randomized controlled trials of 116 pregnant patients diagnosed with peripartum cardiomyopathy, showing that among those who received Bromocriptine on top of standard heart failure therapy, there is a significant improvement in the left ventricular ejection fraction at 6 months [mean difference 15.14 (95% CI, 6.53 to 23.75) p <0.05] compared to standard heart failure therapy alone. It was also observed that those who received Bromocriptine had better clinical outcomes. Conclusion. The addition of Bromocriptine on top of standard heart failure therapy significantly improved the left ventricular ejection fraction of patients with peripartum cardiomyopathy at 6-months post-partum. This novel therapy may be considered to improve the management of these patients.
溴隐亭治疗围产期心肌病:随机对照试验的荟萃分析
背景围产期心肌病是一种罕见的,妊娠相关的左心室心力衰竭的原因,以前的健康妇女。它仍然是全世界与心脏有关的产妇发病率和死亡率的一个重要原因。半数患者6个月后左心室功能恢复。然而,在其余不能恢复心脏功能的患者中,他们将需要先进的心力衰竭治疗。溴隐亭是一种抑制催乳素释放的多巴胺激动剂,已被证明可改善左心室恢复和临床结果。我们试图确定在标准心力衰竭治疗中加入溴隐亭对这些患者左心室功能的改善和恢复以及心血管死亡率的影响。入选标准。符合以下标准的研究被纳入:1)随机对照试验;2)符合围产期心肌病诊断标准的孕妇;3)报告左室射血分数改善及临床转归的资料。方法。使用PUBMED、Clinical Key、Science Direct、Scopus和Cochrane数据库,检索2018年6月至12月31日符合条件的研究。使用Cochrane偏倚风险工具评估每项研究的质量。研究的主要结果是溴隐亭对这些患者左心室功能改善和临床结果的影响。使用Review Manager 5.3对连续结果进行随机效应分析。结果。我们对116例诊断为围产期心肌病的孕妇进行了2项随机对照试验,结果显示,在标准心力衰竭治疗的基础上接受溴隐亭治疗的患者,与单独接受标准心力衰竭治疗的患者相比,6个月时左心室射血分数有显著改善[平均差值15.14 (95% CI, 6.53 ~ 23.75) p <0.05]。还观察到,接受溴隐亭治疗的患者有更好的临床结果。结论。在标准心力衰竭治疗基础上加用溴隐亭可显著提高围产期心肌病患者产后6个月左心室射血分数。这种新疗法可能被认为可以改善这些患者的管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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