Department of Cardiology, Hospital Universitario de Canarias, Universidad Europea de Canarias, Tenerife, Spain.
CIBER de Enfermedades Cardiovasculares (CIBERCV), Madrid, Spain.
Eur J Heart Fail. 2022 Oct;24(10):1953-1962. doi: 10.1002/ejhf.2602. Epub 2022 Jul 16.
Benzodiazepines have been used as safe anxiolytic drugs for decades and some authors have suggested they could be an alternative for morphine for treating acute cardiogenic pulmonary oedema (ACPE). We compared the efficacy and safety of midazolam and morphine in patients with ACPE.
A randomized, multicentre, open-label, blinded endpoint clinical trial was performed in seven Spanish emergency departments (EDs). Patients >18 years old clinically diagnosed with ACPE and with dyspnoea and anxiety were randomized (1:1) at ED arrival to receive either intravenous midazolam or morphine. Efficacy was assessed by in-hospital all-cause mortality (primary endpoint). Safety was assessed through serious adverse event (SAE) reporting, and the composite endpoint included 30-day mortality and SAE. Analyses were made on an intention-to-treat basis. The trial was stopped early after a planned interim analysis by the safety monitoring committee. At that time, 111 patients had been randomized: 55 to midazolam and 56 to morphine. There were no significant differences in the primary endpoint (in-hospital mortality for midazolam vs. morphine 12.7% vs. 17.9%; risk ratio[RR] 0.71, 95% confidence interval [CI] 0.29-1.74; p = 0.60). SAE were less common with midazolam versus morphine (18.2% vs. 42.9%; RR 0.42, 95% CI 0.22-0.80; p = 0.007), as were the composite endpoint (23.6% vs. 44.6%; RR 0.53, 95% CI 0.30-0.92; p = 0.03).
Although the number of patients was too small to draw final conclusions and there were no significant differences in mortality between midazolam and morphine, a significantly higher rate of SAEs was found in the morphine group.
苯二氮䓬类药物已被用作安全的抗焦虑药物数十年,一些作者认为它们可能是治疗急性心源性肺水肿(ACPE)的吗啡替代药物。我们比较了咪达唑仑和吗啡在 ACPE 患者中的疗效和安全性。
在西班牙的七个急诊科进行了一项随机、多中心、开放标签、盲终点临床试验。在急诊科到达时,将 >18 岁的临床诊断为 ACPE 且呼吸困难和焦虑的患者随机(1:1)分为咪达唑仑或吗啡静脉注射组。以院内全因死亡率(主要终点)评估疗效。通过严重不良事件(SAE)报告评估安全性,并将包括 30 天死亡率和 SAE 的复合终点。分析采用意向治疗。在安全监测委员会进行计划的中期分析后,试验提前停止。当时,已随机分配了 111 名患者:咪达唑仑 55 例,吗啡 56 例。咪达唑仑与吗啡在主要终点(院内死亡率:咪达唑仑为 12.7%,吗啡为 17.9%;风险比[RR]0.71,95%置信区间[CI]0.29-1.74;p=0.60)方面无显著差异。咪达唑仑组 SAE 较吗啡组少(18.2% vs. 42.9%;RR 0.42,95% CI 0.22-0.80;p=0.007),复合终点也如此(23.6% vs. 44.6%;RR 0.53,95% CI 0.30-0.92;p=0.03)。
尽管患者数量太少,无法得出最终结论,且咪达唑仑和吗啡之间的死亡率无显著差异,但吗啡组的 SAE 发生率明显更高。