Evaluating patient-reported adherence and outcomes in specialty disease states: A dual-site initiative.

IF 2.3 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
E Danielle Bryan, Chelsea P Renfro, Rebekah H Anguiano, Lisa Kumor, Josh DeClercq, Leena Choi, Autumn D Zuckerman
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引用次数: 0

Abstract

Background: Patient-reported outcomes (PROs) are often used by clinicians to evaluate patient response to specialty medications used to treat multiple sclerosis (MS) and rheumatologic conditions. Identifying associations among PROs and patient characteristics could inform patient-centered treatment monitoring.

Objective: To examine the association among patient characteristics and PROs, including patient-reported adherence (defined as no missed doses), medication tolerance, patient perceived effectiveness, and health care resource utilization (HCRU; defined as emergency department visits or hospitalizations), for patients prescribed specialty medications in 2 health system specialty pharmacies.

Methods: A dual-center, retrospective review of monthly medication assessments completed by Vanderbilt Specialty Pharmacy and University of Illinois Hospital and Health Sciences System specialty pharmacy was conducted. Patients were included if they received at least 3 fills of a specialty medication from rheumatology or MS clinics from October 2019 to March 2022, excluding patients with more than a 30-day supply. Primary outcomes were the PROs of patient-reported adherence, medication tolerability, perceived effectiveness, and HCRU. For each of the 2 primary outcomes (adherence and tolerability), a mixed-effects logistic regression model was used to test for associations with age, sex, race, clinic, site, and the other PROs.

Results: A total of 61,926 assessments were completed from 3,677 patients (Site 1 = 3,346; 91.0% and Site 2 = 331; 9.0%). Patients were predominantly White (75.6%) and female (71.7%) with a median age of 50 years (IQR = 37-61). Assessments most frequently originated from rheumatology (76.0%). Nonadherence was reported 4.0% of the time, with the most common explanations being forgetfulness (33.1%) and medication being held because of a procedure or illness (29.5%). Most responses indicated perceived effectiveness as good/excellent (93.9%), with 98.5% of responses indicating no issues with tolerability. Patients who reported tolerability issues were 2.5 times more likely to report a missed dose (95% CI = 1.87-3.23, P < 0.001). An effectiveness rating of fair was associated with a 61% increase in the odds of a missed dose compared with a rating of good/excellent (95% CI = 1.33-1.94).

Conclusions: Patients filling rheumatology or MS specialty medications within health system specialty pharmacies reported high rates of medication effectiveness and adherence and low rates of issues with tolerability and HCRU. Patients who report tolerability issues or lower perceived effectiveness may benefit from additional monitoring to prevent nonadherence.

评估特殊疾病状态下患者报告的依从性和结果:双站点倡议。
背景:临床医生经常使用患者报告结果(PROs)来评估患者对治疗多发性硬化症(MS)和风湿病的特效药物的反应。确定PROs与患者特征之间的关联可为以患者为中心的治疗监测提供依据:目的:研究在两家医疗系统专科药房开具专科药物处方的患者的患者特征与PROs之间的关联,包括患者报告的依从性(定义为无漏服)、药物耐受性、患者感知的有效性以及医疗资源利用率(HCRU;定义为急诊就诊或住院):对范德比尔特专科药房和伊利诺伊大学医院与健康科学系统专科药房每月完成的用药评估进行了双中心回顾性审查。如果患者在 2019 年 10 月至 2022 年 3 月期间从风湿病学或多发性硬化症诊所接受了至少 3 次专科药物治疗,则将其纳入研究范围,但不包括供应量超过 30 天的患者。主要结果为患者报告的依从性、药物耐受性、疗效感知和HCRU等PROs。对于 2 个主要结果(依从性和耐受性)中的每一个结果,均采用混合效应逻辑回归模型来检验与年龄、性别、种族、诊所、地点和其他 PROs 之间的关联:共有 3,677 名患者完成了 61,926 项评估(第一治疗点 = 3,346; 91.0%,第二治疗点 = 331; 9.0%)。患者主要为白人(75.6%)和女性(71.7%),中位年龄为 50 岁(IQR = 37-61)。大多数评估来自风湿免疫科(76.0%)。不坚持用药的报告占 4.0%,最常见的解释是健忘(33.1%)和因手术或疾病而暂停用药(29.5%)。大多数回复表示疗效良好/出色(93.9%),98.5%的回复表示没有耐受性问题。报告有耐受性问题的患者漏服药物的可能性是未服药患者的 2.5 倍(95% CI = 1.87-3.23,P < 0.001)。与良好/优秀相比,疗效评级为一般的患者漏服的几率增加了61%(95% CI = 1.33-1.94):在医疗系统专科药房购买风湿病或多发性硬化症专科药物的患者对药物疗效和依从性的评价较高,对耐受性和 HCRU 问题的评价较低。报告耐受性问题或疗效感知较低的患者可能会受益于额外的监测以防止不依从性。
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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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