Implementation of a nonstatin prior authorization checklist for patients with hypercholesterolemia: In 2 community health care systems.

IF 2.9 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Dana McCormick, Pam R Taub, Jeffrey Carter, Kathleen Moreo, Cherilyn L Heggen
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引用次数: 0

Abstract

Background: Health plans have acknowledged there is a significant unmet need to improve prior authorization (PA) processes to increase patient access to life saving nonstatin therapies. Outcomes from a series of regional working groups in the United States provided recommendations for developing standardized patient eligibility criteria and a checklist for streamlining the PA process.

Objective: To (1) develop a standardized PA checklist to streamline collection of adequate PA documentation by prescribers, regardless of health insurance plan type, and (2) measure the impact of the PA checklist in clinical practice in a controlled observational study.

Methods: A working group of thought leaders representing payers and providers was assembled by PRIME Education, in collaboration with the Academy of Managed Care Pharmacy, the American Society for Preventive Cardiology, and the Preventive Cardiovascular Nurses Association. The working group developed and finalized a PA checklist for PCSK9 inhibitors that was integrated into the electronic medical record for 2 large community health care systems with geographic representation of patients with cardiovascular disease: Random chart audits were conducted prior to (historical controls) and 6 months after (post-intervention) implementation of the checklist (n = 100 each set). Primary study endpoints were rates of approvals and time to approval/receipt of prescribed drug. Statistical analyses measured changes in PA documentation outcomes, including treatment history and authorization approvals/denials. Survey questions provided to health care provider teams before and after integration of the PA checklist measured changes in prescriber attitudes on effectiveness and efficiency of the PA checklist.

Results: Following implementation of the PA checklist, a 19% absolute increase in initial PA approvals and a 2-day overall reduction in time-to-treatment with prescribed PCSK9 inhibitor therapy were observed. Documentation of side effects (54%; P < 0.0001), statin contraindications (31%; P < 0.0001), and prior lipid therapies failed (20%; P < 0.0001) also increased postimplementation. In surveys, prescribers reported greater efficiency and effectiveness of the PA process when using the standardized PA checklist.

Conclusions: Time-to-treatment for nonstatin therapies for eligible patients with hypercholesterolemia was decreased in 2 community health systems following integration of a standardized PA checklist developed through a collaboration between patients and providers.

高胆固醇血症患者非他汀类药物预先授权清单的实施:在2个社区卫生保健系统
背景:健康计划已经认识到,改善事先授权(PA)流程以增加患者获得挽救生命的非他汀类药物治疗的机会,存在显著的未满足需求。美国一系列区域工作组的结果为制定标准化的患者资格标准和简化PA流程的清单提供了建议。目的:在一项对照观察性研究中,(1)制定一份标准化的PA清单,以简化处方者收集足够的PA文件,而不管健康保险计划类型如何;(2)衡量PA清单在临床实践中的影响。方法:PRIME教育与管理护理药房学会、美国预防心脏病学会和预防心血管护士协会合作,召集了一个代表支付方和提供者的思想领袖工作组。工作组制定并最终确定了PCSK9抑制剂的PA清单,并将其整合到2个具有心血管疾病患者地理代表性的大型社区卫生保健系统的电子病历中:在实施清单之前(历史对照)和6个月后(干预后)进行随机图表审计(每组n = 100)。主要研究终点是批准率和批准/接收处方药的时间。统计分析测量了PA文件结果的变化,包括治疗历史和授权批准/拒绝。在整合PA核对表前后向卫生保健提供者团队提供的调查问题测量了处方医师对PA核对表的有效性和效率的态度的变化。结果:在实施PA检查表后,观察到初始PA批准绝对增加了19%,并且处方PCSK9抑制剂治疗的总治疗时间减少了2天。不良反应记录(54%;结论:在2个社区卫生系统中,通过患者和提供者之间的合作,整合了标准化的PA检查表,减少了符合条件的高胆固醇血症患者接受非他汀类药物治疗的时间。
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来源期刊
Journal of managed care & specialty pharmacy
Journal of managed care & specialty pharmacy Health Professions-Pharmacy
CiteScore
3.50
自引率
4.80%
发文量
131
期刊介绍: JMCP welcomes research studies conducted outside of the United States that are relevant to our readership. Our audience is primarily concerned with designing policies of formulary coverage, health benefit design, and pharmaceutical programs that are based on evidence from large populations of people. Studies of pharmacist interventions conducted outside the United States that have already been extensively studied within the United States and studies of small sample sizes in non-managed care environments outside of the United States (e.g., hospitals or community pharmacies) are generally of low interest to our readership. However, studies of health outcomes and costs assessed in large populations that provide evidence for formulary coverage, health benefit design, and pharmaceutical programs are of high interest to JMCP’s readership.
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