早期干预无症状重度主动脉瓣狭窄和心肌纤维化患者:EVOLVED 随机临床试验。

IF 63.1 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Krithika Loganath, Neil J Craig, Russell J Everett, Rong Bing, Vasiliki Tsampasian, Patrycja Molek, Simona Botezatu, Saadia Aslam, Steff Lewis, Catriona Graham, Audrey C White, Tom MacGillivray, Christopher E Tuck, Phillip Rayson, Denise Cranley, Sian Irvine, Ruth Armstrong, Lynsey Milne, Calvin W L Chin, Graham S Hillis, Timothy Fairbairn, John P Greenwood, Richard Steeds, Stephen J Leslie, Chim C Lang, Chiara Bucciarelli-Ducci, Nikhil V Joshi, Vijay Kunadian, Vassilios S Vassiliou, Jason N Dungu, Sandeep S Hothi, Nicholas Boon, Sanjay K Prasad, Niall G Keenan, Dana Dawson, Thomas A Treibel, Mani Motwani, Christopher A Miller, Nicholas L Mills, Ronak Rajani, David P Ripley, Gerry P McCann, Bernard Prendergast, Anvesha Singh, David E Newby, Marc R Dweck
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引用次数: 0

摘要

重要性:主动脉瓣狭窄患者的心肌纤维化发生在左心室失代偿之前,与不良的长期预后有关:目的:研究早期瓣膜介入是否能降低无症状的重度主动脉瓣狭窄和心肌纤维化患者的全因死亡或主动脉瓣狭窄相关的非计划住院的发生率:这项前瞻性、随机、开放标签、掩盖终点的试验于2017年8月至2022年10月期间在英国和澳大利亚的24个心脏中心进行。试验纳入了严重主动脉瓣狭窄和心肌纤维化的无症状患者。最终随访日期为2024年7月26日:干预措施:经导管主动脉瓣置换术或外科主动脉瓣置换术的早期瓣膜干预,或指南指导下的保守治疗:主要结果是全因死亡或与主动脉瓣狭窄相关的计划外住院的复合结果。共有 9 项次要结果,包括主要结果的组成部分和 12 个月时的症状状况:试验招募了 224 名符合条件的患者(平均 [SD] 年龄 73 [9] 岁;63 名女性 [28%];平均 [SD] 主动脉瓣峰值速度 4.3 [0.5] m/s),原计划样本量为 356 名患者。在早期干预组的 113 名患者中,有 20 人(18%)出现了主要终点;在指南指导的保守治疗组的 111 名患者中,有 25 人(23%)出现了主要终点(危险比为 0.79 [95% CI,0.44-1.43];P = .44;组间差异为-4.82% [95% CI,-15.31% 至 5.66%])。在 9 个预先指定的次要终点中,有 7 个无显著差异。早期干预组 113 例患者中有 16 例(14%)发生全因死亡,指南指导组 111 例患者中有 14 例(13%)发生全因死亡(危险比为 1.22 [95% CI, 0.59-2.51]),113 例患者中有 7 例(6%)发生计划外主动脉瓣狭窄住院,111 例患者中有 19 例(17%)发生计划外主动脉瓣狭窄住院(危险比为 0.37 [95% CI, 0.16-0.88])。与指南指导下的保守治疗(21 [19.7%] vs 39 [37.9%];几率比,0.37 [95% CI,0.20-0.70])相比,早期干预与较低的 12 个月纽约心脏病协会 II-IV 级症状发生率相关:对于无症状的重度主动脉瓣狭窄和心肌纤维化患者,早期主动脉瓣介入治疗对全因死亡或主动脉瓣狭窄相关的意外住院没有明显影响。该试验的主要终点的95% CI较宽,需要进一步研究来证实这些结果:试验注册:ClinicalTrials.gov Identifier:试验注册:ClinicalTrials.gov Identifier:NCT03094143。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Early Intervention in Patients With Asymptomatic Severe Aortic Stenosis and Myocardial Fibrosis: The EVOLVED Randomized Clinical Trial.

Importance: Development of myocardial fibrosis in patients with aortic stenosis precedes left ventricular decompensation and is associated with an adverse long-term prognosis.

Objective: To investigate whether early valve intervention reduced the incidence of all-cause death or unplanned aortic stenosis-related hospitalization in asymptomatic patients with severe aortic stenosis and myocardial fibrosis.

Design, setting, and participants: This prospective, randomized, open-label, masked end point trial was conducted between August 2017 and October 2022 at 24 cardiac centers across the UK and Australia. Asymptomatic patients with severe aortic stenosis and myocardial fibrosis were included. The final date of follow-up was July 26, 2024.

Intervention: Early valve intervention with transcatheter or surgical aortic valve replacement or guideline-directed conservative management.

Main outcomes and measures: The primary outcome was a composite of all-cause death or unplanned aortic stenosis-related hospitalization in a time-to-first-event intention-to-treat analysis. There were 9 secondary outcomes, including the components of the primary outcome and symptom status at 12 months.

Results: The trial enrolled 224 eligible patients (mean [SD] age, 73 [9] years; 63 women [28%]; mean [SD] aortic valve peak velocity of 4.3 [0.5] m/s) of the originally planned sample size of 356 patients. The primary end point occurred in 20 of 113 patients (18%) in the early intervention group and 25 of 111 patients (23%) in the guideline-directed conservative management group (hazard ratio, 0.79 [95% CI, 0.44-1.43]; P = .44; between-group difference, -4.82% [95% CI, -15.31% to 5.66%]). Of 9 prespecified secondary end points, 7 showed no significant difference. All-cause death occurred in 16 of 113 patients (14%) in the early intervention group and 14 of 111 (13%) in the guideline-directed group (hazard ratio, 1.22 [95% CI, 0.59-2.51]) and unplanned aortic stenosis hospitalization occurred in 7 of 113 patients (6%) and 19 of 111 patients (17%), respectively (hazard ratio, 0.37 [95% CI, 0.16-0.88]). Early intervention was associated with a lower 12-month rate of New York Heart Association class II-IV symptoms than guideline-directed conservative management (21 [19.7%] vs 39 [37.9%]; odds ratio, 0.37 [95% CI, 0.20-0.70]).

Conclusions and relevance: In asymptomatic patients with severe aortic stenosis and myocardial fibrosis, early aortic valve intervention had no demonstrable effect on all-cause death or unplanned aortic stenosis-related hospitalization. The trial had a wide 95% CI around the primary end point, with further research needed to confirm these findings.

Trial registration: ClinicalTrials.gov Identifier: NCT03094143.

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来源期刊
CiteScore
48.20
自引率
0.90%
发文量
1569
审稿时长
2 months
期刊介绍: JAMA (Journal of the American Medical Association) is an international peer-reviewed general medical journal. It has been published continuously since 1883. JAMA is a member of the JAMA Network, which is a consortium of peer-reviewed general medical and specialty publications.
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