对孤立性或偶发性肺栓塞停止抗凝治疗:STOPAPE RCT 方案。

IF 3.5 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Health technology assessment Pub Date : 2024-06-26 DOI:10.3310/HRCW7937
Daniel Lasserson, Pooja Gaddu, Samir Mehta, Agnieszka Ignatowicz, Sheila Greenfield, Clare Prince, Carole Cummins, Graham Robinson, Jonathan Rodrigues, Simon Noble, Sue Jowett, Mark Toshner, Michael Newnham, Alice Turner
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引用次数: 0

摘要

研究问题:与完全抗凝 3 个月相比,对孤立性或偶发性亚段肺栓塞患者暂停抗凝是否具有临床和成本效益?自从使用计算机断层扫描肺动脉造影检查疑似肺栓塞患者以来,肺动脉亚段栓塞的诊断率有所上升。老式的核医学诊断成像通常无法检测到通气/灌注不匹配的亚段肺栓塞。随着计算机断层扫描肺动脉造影诊断肺动脉栓塞亚段的增加,肺动脉栓塞的病死率也在降低。鉴于完全抗凝会有很大的出血风险,而且亚段肺动脉栓塞以前并不经常通过通气/灌注扫描诊断出来,因此在引入计算机断层扫描肺动脉造影扫描之前,亚段肺动脉栓塞很可能主要得不到治疗,因此关于亚段肺动脉栓塞患者的最佳治疗方法越来越不一致:确定在3个月、6个月和12个月时,与3个月的完全抗凝相比,暂停抗凝治疗孤立性或偶发性亚节段肺栓塞(即没有合并深静脉血栓形成的亚节段肺栓塞)是否会减少复发性血栓栓塞和大出血的危害。确定孤立性肺段下栓塞患者抗凝治疗并发症(主要是出血)的发生率。确定临床医生和患者是否可以接受不治疗孤立性亚段肺栓塞。确定普通放射科医生对肺动脉亚段栓塞诊断的重新分类率,并制定一套规则以改进普通放射科医生对肺动脉亚段栓塞的诊断。从医疗服务的角度评估不对孤立的亚段肺栓塞患者进行抗凝治疗的成本效益:方法:前瞻性个体随机开放对照试验,由终点委员会对结果进行盲法评估,对复发性静脉血栓栓塞进行非劣效性分析,对出血事件进行优效性分析。试验还包括一个内部试点阶段,以了解不进行抗凝治疗的可行性和可接受性。我们计划从至少 50 家急症医院招募 1466 名患者。如果考虑到 15% 的退出率,这将使我们有 90% 的能力检测到大出血和临床相关的非大出血从抗凝治疗组的 7.3% 减少到干预治疗组的 3%。我们的能力是确定不抗凝策略不劣于抗凝策略,其上限为接受完全抗凝治疗者的复发性静脉血栓栓塞率从预期的 2% 增加 2.3%。我们还计划开展一项研究,比较急诊报告放射科医生与呼吸科放射科专科医生对所有计算机断层扫描肺血管造影中肺段下栓塞的诊断结果。这将使我们能够确定试点研究的安全性(即发现肺栓塞实际上大于亚段的患者),并为普通放射科医生制定亚段肺栓塞诊断指南。有血栓形成亲身经历的患者参与了试验设计的各个方面,并加入了试验管理小组:STOPAPE 试验因 COVID 大流行后招募率低以及国家健康与护理研究所研究组合优先恢复而提前结束。目前还没有该试验的结果数据。国家健康与护理研究所图书馆的其他出版物将详细介绍相关的定性研究,该研究探讨了患者和临床医生对孤立的亚节段肺栓塞患者暂停抗凝治疗的看法,并介绍了收集到的所有入组患者数据:本文是由美国国家健康与护理研究所(NIHR)健康技术评估项目资助的独立研究,获奖编号为NIHR128073。该研究文章的通俗易懂的摘要可在 NIHR 期刊图书馆网站 https://doi.org/10.3310/HRCW7937 上查阅。
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Stopping anticoagulation for isolated or incidental pulmonary embolism: the STOPAPE RCT protocol.

Research question: Is withholding anticoagulation for patients with isolated or incidental subsegmental pulmonary embolism clinically and cost-effective compared with full anticoagulation for 3 months?

Background: There has been an increase in the diagnosis of subsegmental pulmonary embolism since the advent of computed tomography pulmonary angiogram to investigate patients with suspected pulmonary embolism. Subsegmental pulmonary embolism is not often detectable with older nuclear medicine-based diagnostic imaging for ventilation/perfusion mismatch. The case fatality of pulmonary embolism has reduced as subsegmental pulmonary embolism diagnoses from computed tomography pulmonary angiogram have increased. There is growing equipoise about the optimal treatment for patients with subsegmental pulmonary embolism, given that full anticoagulation has significant risks of bleeding and subsegmental pulmonary embolism was not often diagnosed previously with ventilation/perfusion scanning and therefore most likely left predominantly untreated prior to the introduction of computed tomography pulmonary angiogram scanning.

Objectives: Determine whether withholding anticoagulation for isolated or incidental subsegmental pulmonary embolism (i.e. subsegmental pulmonary embolism with no coexisting deep-vein thrombosis) reduces the harms of recurrent thromboembolism and major bleeding compared with 3 months of full anticoagulation at 3, 6 and 12 months. Determine the rate of complications of anticoagulation therapy (predominantly bleeding) in patients with isolated subsegmental pulmonary embolism. Determine whether not treating isolated subsegmental pulmonary embolism is acceptable to clinicians and patients. Determine the reclassification rate of subsegmental pulmonary embolism diagnoses made by general reporting radiologists when reviewed by specialist respiratory radiologists and develop a set of rules to improve general radiologists' diagnoses of subsegmental pulmonary embolism. Assess cost-effectiveness of not treating patients with isolated subsegmental pulmonary embolism with anticoagulation, taking a health service perspective.

Methods: Prospective individually randomised open controlled trial with blinded end-point committee assessment for outcomes, powered for non-inferiority for recurrent venous thromboembolism and for superiority for bleeding events. An internal pilot phase is included for feasibility and acceptability of no anticoagulation. We planned to recruit 1466 patients from at least 50 acute hospital sites. Allowing for a dropout rate of 15%, this would have given us 90% power to detect a reduction in major and clinically relevant non-major bleeding from 7.3% in the anticoagulation arm to 3% in the intervention arm. We were powered to determine that a strategy of no anticoagulation was non-inferior to anticoagulation with an upper margin of a 2.3% increase in recurrent venous thromboembolism from an expected rate of 2% in those who receive full anticoagulation. We also planned to undertake a study comparing acute reporting radiologists' diagnoses of subsegmental pulmonary embolism from all computed tomography pulmonary angiograms with specialist respiratory radiologists. This would have allowed us to determine safety in the pilot study (i.e. patients with pulmonary embolism that was in fact larger than subsegmental would have been identified) and develop guidance for subsegmental pulmonary embolism diagnosis for general radiologists. Patients with lived experience of thrombosis contributed to all aspects of the trial design and were part of the Trial Management Group.

Progress of study: The STOPAPE trial was stopped prematurely due to a low recruitment rate in the wake of the COVID pandemic and prioritisation of recovery of the National Institute for Health and Care Research research portfolio. There are no outcome data available for this trial. Separate NIHR Library publications will detail the linked qualitative study examining the views of patients and clinicians around withholding anticoagulation for isolated subsegmental pulmonary embolism as well as presenting all collected data of recruited patients.

Funding: This article presents independent research funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment programme as award number NIHR128073. A plain language summary of this research article is available on the NIHR Journals Library Website https://doi.org/10.3310/HRCW7937.

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来源期刊
Health technology assessment
Health technology assessment 医学-卫生保健
CiteScore
6.90
自引率
0.00%
发文量
94
审稿时长
>12 weeks
期刊介绍: Health Technology Assessment (HTA) publishes research information on the effectiveness, costs and broader impact of health technologies for those who use, manage and provide care in the NHS.
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