3.8 Article

Non-steroidal anti-inflammatory drug use in acute myopericarditis: 12-month clinical follow-up

期刊

OPEN HEART
卷 6, 期 1, 页码 -

出版社

BMJ PUBLISHING GROUP
DOI: 10.1136/openhrt-2018-000990

关键词

-

资金

  1. Swiss National Science Foundation
  2. Forschungskredit of the University of Zurich [FK-17-047]
  3. Holcim Foundation
  4. Walter and Gertrud Siegenthaler Stiftung at the University of Zurich

向作者/读者索取更多资源

Objective Clinical data on the effect of non-steroidal anti-inflammatory drugs (NSAIDs) in myopericarditis are limited. Since NSAIDs are standard therapy in pericarditis, we retrospectively investigated their safety in myopericarditis. Methods In a retrospective case-control study, we identified 60 patients with myopericarditis from September 2010 to August 2017. Diagnosis was based on clinical criteria, elevated high-sensitivity troponin T and cardiac magnetic resonance imaging (CMR). All patients received standard heart failure therapy if indicated. Twenty-nine patients (62%) received NSAIDs (acetylsalicylic acid: n=7, average daily dose =1300 mg or ibuprofen: n=22, average daily dose =1500 mg) for an average duration of 4 weeks. To create two cohorts with similar baseline conditions, 15 patients were excluded. Three months after diagnosis, 29 patients were re-evaluated by CMR to measure late gadolinium enhancement (LGE). Results Baseline characteristics of those treated with or without NSAIDs were similar. Mean age was 34 (+/- 13) years, 6 (13%) were women. Mean left ventricular ejection fraction (LVEF) was 56% (+/- 5). 82 % of the patients (14 of 17) treated with NSAIDs experienced a decrease in LGE at 3 months, while it was only 58 % (7 of 12) of those without NSAIDs (p=0.15). At 12-month follow-up, one of the patients treated without NSAIDs experienced polymorphic ventricular tachycardia (VT) with cardiac arrest, while one of the patients with NSAIDs experienced non-sustained VT. Conclusions This is the first case-control study demonstrating that NSAIDs are safe in patients with myopericarditis and preserved LVEF. Our data suggest that this drug class should be tested prospectively in a large randomised clinical trial.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

3.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据