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在退伍军人医院建立集中专科生物制剂药物管理诊所的可行性。

Feasibility of a centralized specialty biologic medication management clinic at a VA hospital.

出版信息

J Am Pharm Assoc (2003). 2022 Sep-Oct;62(5):1694-1699. doi: 10.1016/j.japh.2022.05.004. Epub 2022 May 7.

Abstract

BACKGROUND

Given the cost and complexity of home subcutaneous biologic use, a centralized specialty medication management (CSMM) service was developed utilizing clinical pharmacist practitioners (CPPs).

OBJECTIVE

To determine the implementation feasibility of the CSMM service.

PRACTICE DESCRIPTION

The CSMM service was implemented in a Veterans Health Administration (VHA) hospital. The VHA does not use dedicated specialty pharmacies.

PRACTICE INNOVATION

The CSMM service was developed utilizing CPPs who operated as an advance practice provider under a national VHA scope of practice. The CPP staffing the CSMM service performed patient education, screened for medication appropriateness, and monitored for safety and efficacy via videoconference or telephone. All patients newly starting a home subcutaneous biologic were offered the service from allergy, cardiology, dermatology, gastroenterology, and rheumatology clinics, as appropriate.

EVALUATION METHODS

A retrospective chart review was completed through the first year the service was offered, which included the recruitment and retention of patients, number of follow-up appointments, and interventions made.

RESULTS

Of the 68 patients offered clinic enrollment, 54 were enrolled in the service (79.4%). Of the 44 who had completed an initial appointment with the CPP, 42 had either received an initial follow-up or were scheduled for a follow-up (95.5%). A total of 161 clinical outcomes have been performed by the CSMM CPP including administrative assistance (33.5%), initial patient education (17.4%), technique correction (7.5%), and medication changes or discontinuations (6.8%).

CONCLUSION

Given the high rate of enrollment and retention, the implementation of the CSMM service at a VA hospital was feasible. The service contributed to safe and effective medication use for enrolled patients and continues to grow in both patient enrollment and services offered.

摘要

背景

鉴于家庭皮下使用生物制剂的成本和复杂性,开发了一种集中的专科药物管理(CSMM)服务,利用临床药师从业者(CPP)。

目的

确定 CSMM 服务的实施可行性。

实践描述

CSMM 服务在退伍军人健康管理局(VA)医院实施。VA 不使用专用专科药房。

实践创新

CSMM 服务是利用 CPP 开发的,他们在国家 VA 实践范围内作为高级实践提供者运作。负责 CSMM 服务的 CPP 进行患者教育、筛选药物适宜性,并通过视频会议或电话监测安全性和疗效。所有新开始家庭皮下生物制剂治疗的患者都可以从过敏、心脏病学、皮肤病学、胃肠病学和风湿病学诊所获得该服务。

评估方法

在提供服务的第一年完成了回顾性图表审查,其中包括患者的招募和保留、随访预约次数以及干预措施。

结果

在提供诊所注册的 68 名患者中,有 54 名(79.4%)注册了该服务。在完成与 CPP 首次预约的 44 名患者中,有 42 名(95.5%)接受了初始随访或安排了随访。CSMM CPP 共进行了 161 项临床结果,包括行政协助(33.5%)、初始患者教育(17.4%)、技术纠正(7.5%)和药物更改或停药(6.8%)。

结论

鉴于高招募率和保留率,VA 医院实施 CSMM 服务是可行的。该服务有助于为注册患者安全有效地使用药物,并继续在患者注册和提供的服务方面不断增长。

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