Suppr超能文献

患者对二尖瓣手术相关风险的接受意愿因心力衰竭症状严重程度而异。

Patients' Willingness to Accept Mitral Valve Procedure-Associated Risks Varies Across Severity of Heart Failure Symptoms.

机构信息

Department of Population Health Sciences (S.D.R., F.R.J., J.M.G.), Duke University School of Medicine, Durham, NC.

Duke Clinical Research Institute (S.D.R., A.O.F., F.R.J., J.M.G., R.J.M., M.W.K., S.V.), Duke University School of Medicine, Durham, NC.

出版信息

Circ Cardiovasc Interv. 2019 Dec;12(12):e008051. doi: 10.1161/CIRCINTERVENTIONS.119.008051. Epub 2019 Nov 22.

Abstract

BACKGROUND

The Food and Drug Administration's Center for Drugs and Radiological Health issued Guidance in 2016 on generating patient preference information to aid evaluation of medical devices. Consistent with this guidance, we aimed to provide quantitative patient preference evidence on benefit-risk tradeoffs relevant to transcatheter mitral valve repair versus medical therapy for patients with heart failure and symptomatic secondary mitral regurgitation.

METHODS

A discrete-choice experiment survey was designed to quantify patients' tolerance for 30-day mortality or serious bleeding risks to achieve improvements in physical functioning or reductions in heart failure hospitalizations. Two samples were recruited: an online US panel of individuals reporting a diagnosis of heart failure (n=244) and patients with heart failure treated at Duke University Health System (n=175). Random-effects logit regression was used to model treatment choices as a function of benefit and risk levels.

RESULTS

Across both samples, approximately one-quarter (23.5%) consistently chose device profiles offering the higher level of physical functioning despite mortality and bleeding risks as high as 10%. Among respondents who at least once chose a device profile offering a lower level of functioning, improvement in physical functioning equivalent to a change from New York Heart Association class IV to III was ≈6 times more preferred than a change from New York Heart Association class III to II. Estimated discrete-choice experiment utility gains and losses revealed that respondents would accept up to a 9.7 percentage-point (95% CI, 8.2%-13.3%) increase in risk of 30-day mortality with devices that could improve functioning from New York Heart Association class IV to III, or up to 2.0% (95% CI, 1.4%-2.7%) for an improvement from New York Heart Association class III to II.

CONCLUSIONS

Severity of heart failure symptoms influences patients' willingness to accept risks associated with mitral valve medical devices. These findings can inform shared decision-making discussions with patients who are being evaluated for transcatheter mitral valve repair.

摘要

背景

2016 年,美国食品和药物管理局药品和放射卫生中心发布了关于生成患者偏好信息以辅助医疗器械评估的指南。为了遵循这一指南,我们旨在为接受经导管二尖瓣修复术与药物治疗的心力衰竭伴症状性二尖瓣反流患者提供关于获益-风险权衡的定量患者偏好证据。

方法

设计了一项离散选择实验调查,以量化患者对 30 天死亡率或严重出血风险的容忍度,以实现体力功能的改善或心力衰竭住院次数的减少。招募了两个样本:一个是在线美国报告心力衰竭诊断的个体小组(n=244),另一个是杜克大学卫生系统治疗的心力衰竭患者小组(n=175)。使用随机效应对数回归模型将治疗选择作为获益和风险水平的函数进行建模。

结果

在两个样本中,大约四分之一(23.5%)的患者始终选择具有更高体力功能水平的设备方案,尽管死亡率和出血风险高达 10%。在至少一次选择提供较低功能水平的设备方案的受访者中,体力功能的改善相当于从纽约心脏协会(NYHA)心功能分级 IV 级变为 III 级,比从 NYHA 心功能分级 III 级变为 II 级更受青睐,其比值约为 6 倍。估计离散选择实验的效用增益和损失表明,患者愿意接受二尖瓣医疗设备的 30 天死亡率风险增加 9.7 个百分点(95%置信区间,8.2%-13.3%),从而使功能从 NYHA 心功能分级 IV 级变为 III 级,或者愿意接受 2.0%(95%置信区间,1.4%-2.7%)的风险,从而使功能从 NYHA 心功能分级 III 级变为 II 级。

结论

心力衰竭症状的严重程度影响患者对与二尖瓣医疗设备相关风险的承受能力。这些发现可以为接受经导管二尖瓣修复术评估的患者提供共享决策讨论的信息。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验