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Designing and Implementing an Electronic Patient Registry to Improve Warfarin Monitoring in the Ambulatory Setting

机译:设计和实施电子患者注册表,以改善门诊环境中的华法林监测

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Background: Warfarin requires individualized dosing and monitoring in the ambulatory setting for protection against thromboembolic disease. Yet in multiple settings, patients spend upwards of 30% of time outside the therapeutic range, subjecting them to an increased risk of adverse events. At an urban, publicly funded clinic, the electronic health record (EHR) would nor support integration with extant warfarin management software, which led to the creation and implementation of an electronic patient registry and a complementary team-based work flow to provide real-time health-system-level data for warfarin patients. Methods: Creation of the registry, which began in August 2014, entailed use of an existing platform, which could interface with the outpatient EHR. The registry was designed to help ensure regular testing and monitoring of patients while enabling identification of patients and subpopulations with suboptimal management. The work flow used for the clinic's warfarin patients was also redesigned. An assessment indicated that the registry identified 341 (96%) of 357 patients actively seen in the clinic. Results: For the cohort of the 357 patients in the registry, the no-show rate decreased from 31% (preimplementation, August 2014-December 2014) to 21% (postimplementation, January 2015-November 2015). The ratio of visits to no-shows increased from 2.3 to 4.0 visits. Conclusion: Design and implementation of an electronic registry in conjunction with a complementary work flow established an active tracking system that improved treatment monitoring for patients on anticoagulation therapy. Registry creation also facilitated assessment of the quality of care and laid the groundwork for ongoing evaluation and quality improvement efforts.
机译:背景:华法令需要在非卧床环境中进行个性化给药和监测,以预防血栓栓塞性疾病。然而,在多种情况下,患者会花费超过治疗范围30%的时间,使他们增加发生不良事件的风险。在城市的公共资助诊所中,电子健康记录(EHR)既不支持与现有的华法林管理软件的集成,后者导致了电子病历的创建和实施以及基于团队的互补工作流程的实时提供华法林患者的健康系统级数据。方法:2014年8月开始创建注册表,需要使用现有平台,该平台可以与门诊EHR交互。该注册表旨在帮助确保定期测试和监视患者,同时通过欠佳的管理来识别患者和亚人群。还重新设计了用于诊所华法林患者的工作流程。评估表明,注册中心确定了在诊所积极看诊的357位患者中的341位(96%)。结果:对于注册表中的357例患者,未出现率从31%(实施前,2014年8月至2014年12月)降低到21%(实施后,2015年1月至2015年11月)。访问量与未出现量的比例从2.3增加到4.0。结论:电子注册系统的设计和实施,结合补充的工作流程,建立了一个主动跟踪系统,可以改善对抗凝治疗患者的治疗监测。注册机构的建立还促进了对护理质量的评估,并为正在进行的评估和质量改进工作奠定了基础。

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