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沟通工具在改善扩张型心肌病家庭成员筛查中的效果:一项随机试验的结果。

Effectiveness of the Communication Tool in Improving Family Member Screening for Dilated Cardiomyopathy: Results of a Randomized Trial.

机构信息

Department of Internal Medicine, Division of Human Genetics (D.D.K., E.J., J.O.M., H.N., R.E.H.), The Ohio State University, Columbus.

the Davis Heart and Lung Research Institute (D.D.K., E.J., G.J.H., J.O.M., H.N., R.E.H.), The Ohio State University, Columbus.

出版信息

Circulation. 2023 Apr 25;147(17):1281-1290. doi: 10.1161/CIRCULATIONAHA.122.062507. Epub 2023 Mar 20.

Abstract

BACKGROUND

Managing disease risk among first-degree relatives of probands diagnosed with a heritable disease is central to precision medicine. A critical component is often clinical screening, which is particularly important for conditions like dilated cardiomyopathy (DCM) that remain asymptomatic until severe disease develops. Nonetheless, probands are frequently ill-equipped to disseminate genetic risk information that motivates at-risk relatives to complete recommended clinical screening. An easily implemented remedy for this key issue has been elusive.

METHODS

The DCM Precision Medicine Study developed , a booklet designed to help probands with DCM communicate genetic risk and the need for cardiovascular screening to their relatives. The effectiveness of the booklet in increasing cardiovascular clinical screening uptake among first-degree relatives was assessed in a multicenter, open-label, cluster-randomized, controlled trial. The primary outcome measured in eligible first-degree relatives was completion of screening initiated within 12 months after proband enrollment. Because probands randomized to the intervention received the booklet at the enrollment visit, eligible first-degree relatives were limited to those who were alive the day after proband enrollment and not enrolled on the same day as the proband.

RESULTS

Between June 2016 and March 2020, 1241 probands were randomized (1:1) to receive (n=621) or not (n=620) within strata defined by site and self-identified race/ethnicity (non-Hispanic Black, non-Hispanic White, or Hispanic). Final analyses included 550 families (n=2230 eligible first-degree relatives) in the arm and 561 (n=2416) in the control arm. A higher percentage of eligible first-degree relatives completed screening in the arm (19.5% versus 16.0%), and the odds of screening completion among these first-degree relatives were higher in the arm after adjustment for proband randomization stratum, sex, and age quartile (odds ratio, 1.30 [1-sided 95% CI, 1.08-∞]). A prespecified subgroup analysis did not find evidence of heterogeneity in the adjusted intervention odds ratio across race/ethnicity strata (=0.90).

CONCLUSIONS

, a booklet that can be provided to patients with DCM by clinicians with minimal additional time investment, was effective in increasing cardiovascular clinical screening among first-degree relatives of these patients.

REGISTRATION

URL: https://www.

CLINICALTRIALS

gov; Unique identifier: NCT03037632.

摘要

背景

管理遗传性疾病先证者一级亲属的疾病风险是精准医学的核心。一个关键组成部分通常是临床筛查,这对于扩张型心肌病(DCM)等疾病尤为重要,因为这些疾病在严重疾病发生之前一直没有症状。尽管如此,先证者通常无法传播促使高危亲属完成推荐的临床筛查的遗传风险信息。对于这个关键问题,一个简单易行的解决方案一直难以实现。

方法

DCM 精准医学研究开发了一种小册子,旨在帮助 DCM 先证者向其亲属传达遗传风险和心血管筛查的必要性。在一项多中心、开放标签、聚类随机、对照试验中,评估了该小册子在增加一级亲属心血管临床筛查参与度方面的有效性。在符合条件的一级亲属中,主要测量指标是在先证者入组后 12 个月内开始的筛查完成情况。由于随机分配到干预组的先证者在入组就诊时收到了小册子,因此符合条件的一级亲属仅限于在入组后第二天仍存活且不在同一天入组的亲属。

结果

2016 年 6 月至 2020 年 3 月,1241 名先证者按 1:1 的比例随机分配(n=621)接受或不接受(n=620)在按地点和自我认定的种族/民族(非西班牙裔黑人、非西班牙裔白人或西班牙裔)定义的分层中。最终分析包括干预组的 550 个家庭(n=2230 名符合条件的一级亲属)和对照组的 561 个家庭(n=2416 名)。在干预组中,完成筛查的符合条件的一级亲属比例较高(19.5%比 16.0%),并且在调整先证者随机分层、性别和年龄四分位后,这些一级亲属的筛查完成率在干预组更高(比值比,1.30[单侧 95%CI,1.08-∞])。一项预设的亚组分析没有发现调整后的干预比值比在种族/民族分层之间存在异质性的证据(=0.90)。

结论

一种小册子,临床医生只需投入很少的额外时间即可提供给 DCM 患者,可有效增加这些患者一级亲属的心血管临床筛查参与度。

登记

网址:https://www.clinicaltrials.gov;唯一标识符:NCT03037632。

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