通过研究问卷和数据链接评估随机试验 50 年随访结果的比较:CONCUR 研究。

IF 2.2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Clinical Trials Pub Date : 2024-06-22 DOI:10.1177/17407745241259088
Mohammad Shahbaz, Jane E Harding, Barry Milne, Anthony Walters, Lisa Underwood, Martin von Randow, Lois Xu, Greg D Gamble
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引用次数: 0

摘要

背景/目的:随机试验后对健康状况的自我报告问卷调查耗时长、成本高,而且可能不可靠。行政数据集可以提供成本效益高、偏差较小的信息,但目前还不确定行政数据和自我报告数据在新西兰队列中识别慢性病方面的比较情况。本研究旨在确定记录链接是否能取代自我报告问卷,以确定试验随访结果所关注的慢性疾病:方法:一项随机试验的 50 年随访参与者被要求填写一份调查问卷,并同意访问管理数据。利用每个数据源计算了患有糖尿病、糖尿病前期、高脂血症、高血压、精神疾病和哮喘的参与者比例,并评估了数据源之间的一致性:参与者年龄为 49 岁(SD = 1,n = 424,50% 为男性)。对于糖尿病前期,调查问卷与行政数据的吻合度较低(kappa = 0.10);对于高脂血症,吻合度一般(kappa = 0.27);对于糖尿病,吻合度较高(kappa = 0.65);对于其他疾病,吻合度中等(所有吻合度均大于 0.42)。在所有结果中,行政数据单独发现的病例数是问卷调查的 2 到 3 倍,但高血压和精神疾病除外,在这两种疾病中,问卷调查单独发现的病例数是行政数据的 1 到 2 倍。在所有结果中,综合所有来源的数据可提高病例发现率:结论:在一项临床试验的后续研究中,需要将问卷、药物和实验室数据与专家小组审查相结合,才能识别出患有慢性疾病的参与者。
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Comparison of outcomes of the 50-year follow-up of a randomized trial assessed by study questionnaire and by data linkage: The CONCUR study.

Background/aims: Self-reported questionnaires on health status after randomized trials can be time-consuming, costly, and potentially unreliable. Administrative data sets may provide cost-effective, less biased information, but it is uncertain how administrative and self-reported data compare to identify chronic conditions in a New Zealand cohort. This study aimed to determine whether record linkage could replace self-reported questionnaires to identify chronic conditions that were the outcomes of interest for trial follow-up.

Methods: Participants in 50-year follow-up of a randomized trial were asked to complete a questionnaire and to consent to accessing administrative data. The proportion of participants with diabetes, pre-diabetes, hyperlipidaemia, hypertension, mental health disorders, and asthma was calculated using each data source and agreement between data sources assessed.

Results: Participants were aged 49 years (SD = 1, n = 424, 50% male). Agreement between questionnaire and administrative data was slight for pre-diabetes (kappa = 0.10), fair for hyperlipidaemia (kappa = 0.27), substantial for diabetes (kappa = 0.65), and moderate for other conditions (all kappa >0.42). Administrative data alone identified two to three times more cases than the questionnaire for all outcomes except hypertension and mental health disorders, where the questionnaire alone identified one to two times more cases than administrative data. Combining all sources increased case detection for all outcomes.

Conclusions: A combination of questionnaire, pharmaceutical, and laboratory data with expert panel review were required to identify participants with chronic conditions of interest in this follow-up of a clinical trial.

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来源期刊
Clinical Trials
Clinical Trials 医学-医学:研究与实验
CiteScore
4.10
自引率
3.70%
发文量
82
审稿时长
6-12 weeks
期刊介绍: Clinical Trials is dedicated to advancing knowledge on the design and conduct of clinical trials related research methodologies. Covering the design, conduct, analysis, synthesis and evaluation of key methodologies, the journal remains on the cusp of the latest topics, including ethics, regulation and policy impact.
期刊最新文献
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