Salam Abdul, Dhurjati Rupasvi, Vidyasagar Kota, Kaistha Prachi, Esam Hariprasad, Haghdoost Faraidoon, Pant Rashmi, Kumar Amit, Kanukula Raju, Thode Rakesh, Baddam Ravali, Chaudhri Kanika, Wang Nelson, Bhaumik Soumyadeep, Gnanenthiran Sonali R, Tiruttani Sasi Kumar, Rodgers Anthony
The George Institute for Global Health, Hyderabad, Telangana, India.
The George Institute for Global Health, University of New South Wales, Sydney, Australia.
JMIR Res Protoc. 2025 Aug 21;14:e65205. doi: 10.2196/65205.
A comprehensive evaluation of short-term effects of antihypertensive medicines is important for informing guidelines and clinical practice.
We aimed to develop the Double-blind Randomized trials of Effects of Antihypertensive Medicines (DREAM) database to facilitate a series of meta-analyses evaluating the short-term effects of antihypertensive medicines.
We searched the Cochrane Central Register of Controlled Trials, MEDLINE, and Epistemonikos from inception until December 2022 to identify relevant randomized clinical trials (RCTs). We included RCTs in the DREAM database if they were double-blind, enrolled adult participants, evaluated the 5 major classes of antihypertensive medicines over a duration of 2 to 26 weeks, and were published in the English language. Screening of records for inclusion and data collection were both conducted in duplicate. The planned meta-analyses using the DREAM database will follow standard methods as recommended by the Cochrane Handbook for Systematic Reviews. The general methods for these meta-analyses are outlined.
The DREAM database includes 1623 RCTs (4359 comparisons), of which 44% (707/1623) were placebo-controlled, 70% (1141/1623) had parallel-group allocation, and 37% (607/1623) had 3 or more randomized groups. A total of 304,253 participants (mean age 54 years; 509/1623, 46% female) were included, 86% (1391/1623) of RCTs had participants with hypertension, and 11% (175/1623) of RCTs had participants with cardiovascular disease at baseline. RCTs with at least 1 group randomized to combination therapy accounted for 23%(371/1623). The median duration of treatment was 8 weeks. Most (93%, 1509/1623) RCTs reported data on effects on blood pressure.
The first series of meta-analyses using the DREAM database will assess the effects of antihypertensive medicines on blood pressure and safety outcomes, including effects on headache, and cardiovascular events. The findings of these meta-analyses will inform clinical practice guidelines and help identify priorities for future research.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/65205.
对抗高血压药物的短期效果进行全面评估对于指导指南制定和临床实践至关重要。
我们旨在建立抗高血压药物效果双盲随机试验(DREAM)数据库,以促进一系列评估抗高血压药物短期效果的荟萃分析。
我们检索了Cochrane对照试验中央注册库、MEDLINE和Epistemonikos,检索时间从建库至2022年12月,以识别相关的随机临床试验(RCT)。如果RCT为双盲试验、纳入成年参与者、在2至26周的时间内评估了5大类抗高血压药物且以英文发表,我们将其纳入DREAM数据库。纳入记录的筛选和数据收集均进行了两次。使用DREAM数据库进行的计划荟萃分析将遵循Cochrane系统评价手册推荐的标准方法。概述了这些荟萃分析的一般方法。
DREAM数据库包括1623项RCT(4359项比较),其中44%(707/1623)为安慰剂对照试验,70%(1141/1623)采用平行组分配,37%(607/1623)有3个或更多随机组。共纳入304,253名参与者(平均年龄54岁;509/1623,46%为女性),86%(1391/1623)的RCT纳入了高血压患者,11%(175/1623)的RCT在基线时纳入了心血管疾病患者。至少有1组随机接受联合治疗的RCT占23%(371/1623)。治疗的中位持续时间为8周。大多数(93%,1509/1623)RCT报告了对血压影响的数据。
使用DREAM数据库进行的首批荟萃分析将评估抗高血压药物对血压和安全性结局的影响,包括对头痛和心血管事件的影响。这些荟萃分析的结果将为临床实践指南提供参考,并有助于确定未来研究的重点。
国际注册报告识别号(IRRID):DERR1-10.2196/65205。