Department of Surgery, University of Minnesota, 420 Delaware St SE, MMC 195, Minneapolis, MN, 55455, USA.
Institute for Health Informatics, University of Minnesota, Minneapolis, MN, USA.
Implement Sci. 2024 Aug 5;19(1):57. doi: 10.1186/s13012-024-01386-4.
Venous thromboembolism (VTE) is a preventable medical condition which has substantial impact on patient morbidity, mortality, and disability. Unfortunately, adherence to the published best practices for VTE prevention, based on patient centered outcomes research (PCOR), is highly variable across U.S. hospitals, which represents a gap between current evidence and clinical practice leading to adverse patient outcomes. This gap is especially large in the case of traumatic brain injury (TBI), where reluctance to initiate VTE prevention due to concerns for potentially increasing the rates of intracranial bleeding drives poor rates of VTE prophylaxis. This is despite research which has shown early initiation of VTE prophylaxis to be safe in TBI without increased risk of delayed neurosurgical intervention or death. Clinical decision support (CDS) is an indispensable solution to close this practice gap; however, design and implementation barriers hinder CDS adoption and successful scaling across health systems. Clinical practice guidelines (CPGs) informed by PCOR evidence can be deployed using CDS systems to improve the evidence to practice gap. In the Scaling AcceptabLE cDs (SCALED) study, we will implement a VTE prevention CPG within an interoperable CDS system and evaluate both CPG effectiveness (improved clinical outcomes) and CDS implementation.
The SCALED trial is a hybrid type 2 randomized stepped wedge effectiveness-implementation trial to scale the CDS across 4 heterogeneous healthcare systems. Trial outcomes will be assessed using the RE-AIM planning and evaluation framework. Efforts will be made to ensure implementation consistency. Nonetheless, it is expected that CDS adoption will vary across each site. To assess these differences, we will evaluate implementation processes across trial sites using the Exploration, Preparation, Implementation, and Sustainment (EPIS) implementation framework (a determinant framework) using mixed-methods. Finally, it is critical that PCOR CPGs are maintained as evidence evolves. To date, an accepted process for evidence maintenance does not exist. We will pilot a "Living Guideline" process model for the VTE prevention CDS system.
The stepped wedge hybrid type 2 trial will provide evidence regarding the effectiveness of CDS based on the Berne-Norwood criteria for VTE prevention in patients with TBI. Additionally, it will provide evidence regarding a successful strategy to scale interoperable CDS systems across U.S. healthcare systems, advancing both the fields of implementation science and health informatics.
Clinicaltrials.gov - NCT05628207. Prospectively registered 11/28/2022, https://classic.
gov/ct2/show/NCT05628207 .
静脉血栓栓塞症(VTE)是一种可预防的医疗状况,对患者的发病率、死亡率和残疾率有重大影响。不幸的是,根据以患者为中心的结果研究(PCOR)制定的 VTE 预防最佳实践,美国各家医院的执行情况差异很大,这代表了当前证据与临床实践之间存在差距,导致患者预后不良。在创伤性脑损伤(TBI)的情况下,这种差距尤其大,由于担心颅内出血风险增加,而不愿意开始 VTE 预防,导致 VTE 预防的比例很低。尽管有研究表明,在 TBI 中早期开始 VTE 预防是安全的,不会增加延迟神经外科干预或死亡的风险。临床决策支持(CDS)是缩小这一实践差距的不可或缺的解决方案;然而,设计和实施障碍阻碍了 CDS 在整个医疗系统中的采用和成功扩展。基于 PCOR 证据制定的临床实践指南(CPG)可以通过 CDS 系统来实施,以缩小证据与实践之间的差距。在可扩展的可接受的 CDS(SCALED)研究中,我们将在一个互操作的 CDS 系统中实施 VTE 预防 CPG,并评估 CPG 的有效性(改善临床结果)和 CDS 的实施情况。
SCALED 试验是一项混合 2 型随机阶跃楔形有效性实施试验,旨在跨 4 个异构医疗系统扩展 CDS。将使用 RE-AIM 规划和评估框架评估试验结果。将努力确保实施的一致性。尽管如此,预计 CDS 的采用情况在每个站点都会有所不同。为了评估这些差异,我们将使用混合方法,通过探索、准备、实施和维持(EPIS)实施框架(一个决定因素框架),在试验现场评估实施过程。最后,至关重要的是,随着证据的发展,PCOR CPG 应保持更新。迄今为止,还没有一个被接受的证据维护流程。我们将对 VTE 预防 CDS 系统进行试点“活指南”流程模型。
基于 Berne-Norwood 标准,本阶跃楔形混合 2 型试验将为 TBI 患者的 VTE 预防提供基于 CDS 的有效性证据。此外,它还将为跨美国医疗系统成功扩展互操作 CDS 系统提供证据,推进实施科学和健康信息学领域的发展。
Clinicaltrials.gov-NCT05628207。前瞻性注册于 2022 年 11 月 28 日,https://classic.clinicaltrials.gov/ct2/show/NCT05628207。
ClinicalTrials.gov/NCT05628207。前瞻性注册于 2022 年 11 月 28 日,https://classic.clinicaltrials.gov/ct2/show/NCT05628207。