英国医疗保健系统数据识别脑内出血导致中风后心血管后果的准确性。

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Trials Pub Date : 2024-11-16 DOI:10.1186/s13063-024-08631-7
Alice Hosking, Jacqueline Stephen, Jonathan Drever, William N Whiteley, Cathie L M Sudlow, Rustam Al-Shahi Salman
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引用次数: 0

摘要

背景:医疗保健系统数据(HCSD)可提高临床试验的效率,但其准确性和有效性尚不确定。我们的目的是评估在 REstart 或 STop 抗血栓形成随机试验(RESTART;ISRCTN71907627)中,作为唯一结果检测方法的 HCSD 与裁定问卷随访相比的准确性,并比较治疗效果的估计值:RESTART是英国一项关于脑内出血(ICH)后抗血小板治疗的前瞻性、开放式、评估者盲法、平行组随机对照试验(RCT)。我们纳入了 537 名 RESTART 参与者中的 496 人(92%),他们在随机化时居住在英格兰或苏格兰。计算机随机化结合最小化,将参与者(1:1)分配到开始或避免抗血小板治疗。RESTART 采用年度问卷调查的方式来检测中位 2.0 年的主要结果(复发性 ICH)和次要结果(出血性或缺血性主要不良心血管事件 [MACE] 的复合结果);独立评审委员会通过医疗记录和脑成像来核实结果。我们获得了英格兰和苏格兰入院和死亡的 ICD10 编码 HCSD,以确定主要和次要结果。我们将 HCSD 与判定结果的参考标准进行了比较。我们在一个根据最小化变量调整的考克斯比例危险模型中使用HCSD单独估算了抗血小板治疗的效果:在最初的 RESTART 试验中,31 人发生了主要结局事件。HCSD对复发性ICH的敏感性为84%(95% CI为66%至95%),阳性预测值为68%(51%至82%)。HCSD 估算的抗血小板治疗效果(调整后危险比 [aHR] 0.51,95% CI 0.27 至 0.98;p = 0.044)与判定结果(aHR 0.51,95% CI 0.25 至 1.03;p = 0.060)几乎相同。HCSD对MACE的敏感性为84%(76%至91%),阳性预测值为78%(69%至85%),HCSD估计抗血小板治疗对MACE的影响(aHR 0.81,95% CI 0.56至1.16;p = 0.247)与判定结果相似(aHR 0.65,95% CI 0.44至0.95;p = 0.025):结论:在一项针对 ICH 患者的抗血小板治疗的 RCT 中,HCSD 的准确性相当高,对治疗效果的估计与判定结果相似:试验注册:ISRCTN71907627 .注册日期:2013 年 4 月 25 日。
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Accuracy of healthcare systems data for identifying cardiovascular outcomes after stroke due to intracerebral haemorrhage in the United Kingdom.

Background: Healthcare systems data (HCSD) could improve the efficiency of clinical trials, but their accuracy and validity are uncertain. Our objective was to assess the accuracy of HCSD as the sole method of outcome detection in the REstart or STop Antithrombotics Randomised Trial (RESTART; ISRCTN71907627) compared with adjudicated questionnaire follow-up and compare estimates of treatment effect.

Methods: RESTART was a prospective, open, assessor-blind, parallel-group randomised controlled trial (RCT) of antiplatelet therapy after intracerebral haemorrhage (ICH) in the UK. We included 496 (92%) of 537 RESTART participants, who were resident in England or Scotland at randomisation. Computerised randomisation incorporating minimisation allocated participants (1:1) to start or avoid antiplatelet therapy. RESTART used annual questionnaires to detect its primary outcome (recurrent ICH) and secondary outcome (a composite of haemorrhagic or ischemic major adverse cardiovascular events [MACE]) over a median of 2.0 years; an independent adjudication committee verified outcomes using medical records and brain imaging. We obtained ICD10-coded HCSD on hospital admissions and deaths in England and Scotland to identify primary and secondary outcomes. We compared HCSD with a reference standard of adjudicated outcomes. We estimated the effects of antiplatelet therapy using HCSD alone in a Cox proportional hazards model adjusted for minimisation variables.

Results: In the original RESTART trial, 31 people experienced a primary outcome event. HCSD had sensitivity of 84% (95% CI 66 to 95%) and positive predictive value of 68% (51 to 82%) for recurrent ICH. HCSD estimated an effect of antiplatelet therapy (adjusted hazard ratio [aHR] 0.51, 95% CI 0.27 to 0.98; p = 0.044) that was almost identical to adjudicated outcomes (aHR 0.51, 95% CI 0.25 to 1.03; p = 0.060). HCSD had sensitivity of 84% (76 to 91%) and positive predictive value of 78% (69 to 85%) for MACE, on which HCSD estimated an effect of antiplatelet therapy (aHR 0.81, 95% CI 0.56 to 1.16; p = 0.247) that was similar to adjudicated outcomes (aHR 0.65, 95% CI 0.44 to 0.95; p = 0.025).

Conclusions: In a RCT of antiplatelet therapy for people with ICH, HCSD was reasonably accurate and provided similar estimates of treatment effect compared with adjudicated outcomes.

Trial registration: ISRCTN71907627 . Registered on 25 April 2013.

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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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