The University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Drive, San Antonio, TX 78229 USA.
J Invasive Cardiol. 2020 Apr;32(4):E86-E96. doi: 10.25270/jic/19.00405.
Despite a range of devices, medical interventions, and revascularization techniques utilized in cardiogenic shock (CS), there is a lack of evidence guiding management. We sought to characterize the contemporary trials through utilization of the ClinicalTrials.gov database.
We investigated all phase II-IV interventional trials in the ClinicalTrials.gov database through June 29, 2019 that enrolled patients with CS. Published trials investigating medical interventions were evaluated for methodological quality using the Jadad scoring system.
The initial query yielded 28 registered studies, of which 28 directly studied CS through whole or subgroup analyses. Of these, five were withdrawn or terminated, while 13 were recruiting, not yet recruiting, or were of unknown recruitment status. The remaining 10 were published and had a median patient size of 69 patients and a median site size of 6. Of the published studies, all-cause mortality was the most common primary endpoint (60%), including composite endpoints that included mortality. The remaining endpoints examined surrogate hemodynamic parameters of cardiac function through echocardiography. The mean Jadad score of the published trials investigating pharmacological therapies was 2.42. Of the trials investigating device therapies or revascularization methods, all were randomized, parallel-arm studies that were open label.
Modern trials vary from single center to multicenter and are small in size. The primary endpoints were clinical, focusing on mortality and restoration of cardiac output or cardiac index. Methodological quality varies in the trials focused on pharmacologic therapy. Trials with devices or revascularization do not employ blinding, but do employ randomization.
尽管在心源性休克 (CS) 中使用了多种设备、医学干预措施和血运重建技术,但缺乏指导管理的证据。我们试图通过利用 ClinicalTrials.gov 数据库来描述当代试验。
我们通过 2019 年 6 月 29 日在 ClinicalTrials.gov 数据库中调查了所有 II-IV 期介入性试验,这些试验招募了 CS 患者。使用 Jadad 评分系统评估了调查医学干预措施的已发表试验的方法学质量。
最初的查询产生了 28 项已注册的研究,其中 28 项直接通过全或亚组分析研究 CS。其中,有 5 项被撤回或终止,有 13 项正在招募、尚未招募或招募情况不明。其余 10 项已发表,患者中位数为 69 例,中位数为 6 个。在已发表的研究中,全因死亡率是最常见的主要终点(60%),包括死亡率在内的复合终点。其余终点通过超声心动图检查心脏功能的替代血流动力学参数。研究药物治疗的已发表试验的平均 Jadad 评分为 2.42。研究器械治疗或血运重建方法的试验均为随机、平行臂、开放标签试验。
现代试验从单中心到多中心不等,规模较小。主要终点是临床终点,重点是死亡率和心输出量或心指数的恢复。专注于药物治疗的试验的方法学质量存在差异。器械或血运重建试验不采用盲法,但采用随机化。