Unité d'hémodynamique et Cardio-Vasculaire Interventionnel, Institut du Thorax, Centre Hospitalier Universitaire (CHU) Nantes, Nantes, France
Centre d'Investigations Cliniques, Service d'explorations Fonctionnelles Cardiovasculaires, Hôpital Cardiologique Louis Pradel, Bron, France.
J Am Heart Assoc. 2018 Feb 10;7(4):e006833. doi: 10.1161/JAHA.117.006833.
Morphine is commonly used to treat chest pain during myocardial infarction, but its effect on cardiovascular outcome has never been directly evaluated. The aim of this study was to examine the effect and safety of morphine in patients with acute anterior ST-segment elevation myocardial infarction followed up for 1 year.
We used the database of the CIRCUS (Does Cyclosporine Improve Outcome in ST Elevation Myocardial Infarction Patients) trial, which included 969 patients with anterior ST-segment elevation myocardial infarction, admitted for primary percutaneous coronary intervention. Two groups were defined according to use of morphine preceding coronary angiography. The composite primary outcome was the combined incidence of major adverse cardiovascular events, including cardiovascular death, heart failure, cardiogenic shock, myocardial infarction, unstable angina, and stroke during 1 year. A total of 554 (57.1%) patients received morphine at first medical contact. Both groups, with and without morphine treatment, were comparable with respect to demographic and periprocedural characteristics. There was no significant difference in major adverse cardiovascular events between patients who received morphine compared with those who did not (26.2% versus 22.0%, respectively; =0.15). The all-cause mortality was 5.3% in the morphine group versus 5.8% in the no-morphine group (=0.89). There was no difference between groups in infarct size as assessed by the creatine kinase peak after primary percutaneous coronary intervention (4023±118 versus 3903±149 IU/L; =0.52).
In anterior ST-segment elevation myocardial infarction patients treated by primary percutaneous coronary intervention, morphine was used in half of patients during initial management and was not associated with a significant increase in major adverse cardiovascular events at 1 year.
吗啡常用于治疗心肌梗死时的胸痛,但从未直接评估其对心血管结局的影响。本研究旨在探讨急性前壁 ST 段抬高型心肌梗死患者接受 1 年随访时使用吗啡的效果和安全性。
我们使用 CIRCUS(环孢素是否改善 ST 段抬高型心肌梗死患者的预后)试验的数据库,该数据库纳入了 969 例接受直接经皮冠状动脉介入治疗的前壁 ST 段抬高型心肌梗死患者。根据冠状动脉造影前使用吗啡的情况将患者分为两组。复合主要终点为 1 年内主要不良心血管事件(包括心血管死亡、心力衰竭、心源性休克、心肌梗死、不稳定型心绞痛和卒中)的发生率。共有 554 例(57.1%)患者在首次就诊时接受了吗啡治疗。接受和未接受吗啡治疗的两组患者在人口统计学和围术期特征方面无显著差异。与未接受吗啡治疗的患者相比,接受吗啡治疗的患者主要不良心血管事件发生率无显著差异(分别为 26.2%和 22.0%;=0.15)。吗啡组的全因死亡率为 5.3%,无吗啡组为 5.8%(=0.89)。两组患者经皮冠状动脉介入治疗后肌酸激酶峰值评估的梗死面积无差异(分别为 4023±118 和 3903±149 IU/L;=0.52)。
在接受直接经皮冠状动脉介入治疗的前壁 ST 段抬高型心肌梗死患者中,吗啡在初始治疗期间用于半数患者,与 1 年时主要不良心血管事件发生率无显著增加相关。