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斯堪的纳维亚复杂性主动脉夹层治疗试验:一项随机对照试验的研究方案。

Scandinavian trial of uncomplicated aortic dissection therapy: study protocol for a randomized controlled trial.

机构信息

Division of Vascular Surgery, Department of Cardiovascular Surgery, Aarhus University Hospital, Aarhus, Denmark.

Department of Cardiothoracic Surgery, Oslo University Hospital, Rikshospitalet, Oslo, Norway.

出版信息

Trials. 2023 Mar 23;24(1):217. doi: 10.1186/s13063-023-07255-7.

Abstract

BACKGROUND

Contemporary management of uncomplicated type B aortic dissections (uTBAD) is based on the acuity and various morphological features. Medical therapy is mandatory, while the risks of early thoracic endovascular aortic repair (TEVAR) are balanced against the potential for rupture, complex surgery, and death. Improved aortic morphology following TEVAR is documented, but evidence for improved overall survival is lacking. The costs and impact on quality of life are also needed.

METHODS

The trial is a randomized, open-label, superiority clinical trial with parallel assignment of subjects at 23 clinical sites in Denmark, Norway, Sweden, Finland, and Iceland. Eligibility includes patients aged ≥ 18 with uTBAD of < 4 weeks duration. Recruited subjects will be randomized to either standard medical therapy (SMT) or SMT + TEVAR, where TEVAR must be performed between 2-12 weeks from the onset of symptoms.

DISCUSSION

This trial will evaluate the primary question of whether early TEVAR improves survival at 5 years among uTBAD patients. Moreover, the costs and the impact on quality of life should provide sorely needed data on other factors that play a role in treatment strategy decisions. The common Nordic healthcare model, with inclusion of all aortic centers, provides a favorable setting for carrying out this trial, while the robust healthcare registries ensure data validity.

TRIAL REGISTRATION

ClinicalTrials.gov NCT05215587. Registered on January 31, 2022.

摘要

背景

目前,复杂型 B 型主动脉夹层(uTBAD)的治疗主要基于发病的急缓程度和各种形态特征。药物治疗是必须的,而早期胸主动脉腔内修复术(TEVAR)的风险需要与破裂、复杂手术和死亡的潜在风险相平衡。TEVAR 后主动脉形态得到改善已有相关文献记载,但改善整体生存率的证据尚缺乏。此外,还需要考虑成本和对生活质量的影响。

方法

该试验是一项在丹麦、挪威、瑞典、芬兰和冰岛的 23 个临床中心进行的随机、开放标签、优效性临床试验,采用平行分组方法对受试者进行分组。纳入标准为年龄≥18 岁、病程<4 周的 uTBAD 患者。入选患者将被随机分为标准药物治疗(SMT)组或 SMT+TEVAR 组,其中 TEVAR 必须在症状出现后 2-12 周内进行。

讨论

该试验将评估早期 TEVAR 是否能提高 uTBAD 患者 5 年生存率这一主要问题。此外,成本和对生活质量的影响应该为治疗策略决策中起作用的其他因素提供急需的数据。常见的北欧医疗保健模式,包括所有的主动脉中心,为开展这项试验提供了有利的环境,而强大的医疗保健登记系统确保了数据的有效性。

试验注册

ClinicalTrials.gov NCT05215587。于 2022 年 1 月 31 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9173/10035204/dc4af3bd2867/13063_2023_7255_Fig1_HTML.jpg

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