分组随机 II 型混合实施效果试验的方法,用于前瞻性评估为高危出院内科病人提供的延长血栓预防措施,以预防医院相关静脉血栓栓塞症

IF 3.4 3区 医学 Q2 HEMATOLOGY
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引用次数: 0

摘要

背景静脉血栓栓塞症(VTE)是可预防的医院相关(HA)死亡的第三大原因。大多数医源性血栓栓塞(包括致命的肺栓塞)发生在内科病人中。在出院后的头 21 天内,有症状的 VTE 发生率增加了一倍多。试验证明,出院后采取血栓预防措施可以减轻 HA-VTE 的负担;然而,接受这种治疗的患者却寥寥无几。我们以前曾验证过 eVTE(eVTE 是一种风险评估工具的缩写,由两种计算方法组成:一种预测 90 天内的 VTE,另一种预测 30 天内的大出血,仅从全血细胞计数和基础代谢全套指标以及年龄中得出)识别 VTE 风险较高而出血风险较低的出院内科患者的能力。目标在一家 23 家医院的非营利性医疗保健系统中实施一项群集随机、阶梯楔形、II 型混合实施/效果试验,在选定的高危患者出院时发出警报,以实施血栓化学预防。结果目标 1(实施)的主要结果是在高危患者中开具利伐沙班 10 毫克,每天 30 天,作为出院后血栓预防药物。eVTE试验将提供高质量、真实的证据,证明利用嵌入电子病历的决策支持实施有针对性的出院后血栓预防的实用干预措施的有效性和安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Methods of a cluster-randomized, type II hybrid implementation effectiveness trial to prospectively assess extended-duration thromboprophylaxis for at-risk medical patients being discharged to prevent hospital-associated venous thromboembolism

Background

Venous thromboembolism (VTE) is the third leading cause of preventable hospital-associated (HA) death. Most HA-VTE, including fatal pulmonary emboli, occur among medically ill patients. The rate of symptomatic VTE more than doubles over the first 21 days after hospital discharge. Trials have demonstrated that the burden of HA-VTE may be reduced with postdischarge thromboprophylaxis; however, few patients receive this therapy. We formerly validated the ability of eVTE (eVTE is the abbreviation for a risk assessment tool constituted by 2 calculations: one predicts 90-day VTE and the other predicts 30-day major bleeding derived from only elements of the complete blood count and basic metabolic panel and age) to identify medical patients being discharged with both an elevated risk of VTE and a low risk of bleeding.

Objectives

Implement a cluster-randomized, stepped wedge, type II hybrid implementation/effectiveness trial generating an alert among select at-risk patients upon discharge for implementation of thrombosis chemoprophylaxis in a 23-hospital not-for-profit healthcare system.

Methods

We use the Reach, Effectiveness, Adoption, Implementation, and Maintenance framework to guide implementation and outcomes reporting.

Results

The primary outcome for aim 1 (implementation) is the prescription of rivaroxaban 10 mg daily for 30 days as postdischarge thromboprophylaxis among at-risk patients. The primary efficacy and safety outcomes (effectiveness) are the 90-day composite of symptomatic VTE, myocardial infartcion, nonhemorrhagic stroke, all-cause mortality, and 30-day major bleeding.

Conclusion

The eVTE trial will provide high-quality, real-world evidence on the effectiveness and safety of a pragmatic intervention to implement targeted postdischarge thromboprophylaxis using decision support embedded in the electronic health record.
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来源期刊
CiteScore
5.60
自引率
13.00%
发文量
212
审稿时长
7 weeks
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