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在药物治疗管理项目(MTMP)中,评估处方医生对通过传真传达的药剂师建议的反应。

Evaluation of prescriber responses to pharmacist recommendations communicated by fax in a medication therapy management program (MTMP).

作者信息

Perera Prasadini N, Guy Mignonne C, Sweaney Ashley M, Boesen Kevin P

机构信息

Center for Health Outcomes and PharmacoEconomic Research, University of Arizona, 1295 N. Martin Ave., Tucson, AZ 85721-0202, USA.

出版信息

J Manag Care Pharm. 2011 Jun;17(5):345-54. doi: 10.18553/jmcp.2011.17.5.345.

DOI:10.18553/jmcp.2011.17.5.345
PMID:21657804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5013826/
Abstract

BACKGROUND

As defined by the Medicare Prescription Drug, Improvement, and Modernization Act of 2003, medication therapy management programs (MTMPs) must be designed to decrease adverse drug events and improve patient outcomes by promoting appropriate medication use. WellPoint Inc. contracted with the pharmacist-run University of Arizona College of Pharmacy Medication Management Center (UA MMC) to provide a pilot telephone-based MTMP to approximately 5,000 high-risk beneficiaries from among its nearly 2 million Medicare prescription drug plan (PDP) beneficiaries. Eligibility for the program was determined by a minimum of 2 of 6 chronic diseases (dyslipidemia, cardiovascular disease, depression, diabetes mellitus, congestive heart failure, and chronic obstructive pulmonary disease; at least 1 of the latter 2 diseases must be present), at least 3 Part-D covered medications, and greater than $4,000 per year in predicted drug spending. In addition to these criteria, WellPoint Inc. used the Johns Hopkins adjusted clinical groups (ACG) predictive model to identify the high-risk beneficiaries to be enrolled in the program. Medication therapy reviews were conducted for these patients. If any medication-related problems (MRPs) were identified, the patient's prescribers were contacted via a fax communication with recommendation(s) to resolve these MRPs. The UA MMC fax interventions were categorized as cost saving, guideline adherence, or safety concerns.

OBJECTIVES

To (a) determine prescriber responses to pharmacist-initiated recommendations in an MTMP for the 3 intervention categories, (b) compare prescriber responses between intervention categories, and (c) compare prescriber response by prescriber type (primary care physician [PCP] vs. specialist) within each intervention category.

METHODS

A retrospective analysis of pharmacist-initiated interventions from August through December 2008 was performed using data collected from the UA MMC database. Data were collected on intervention category (cost saving, guideline adherence, or safety concerns), and responses of prescribers were recorded as either approval or decline (no response was considered decline). Prescriber specialty was identified from searching records of state medical boards. Logistic regression analyses with the robust variance option to adjust for correlation within prescribers were conducted to compare prescriber approval rates between and within intervention categories. Significance was assessed at alpha 0.05.

RESULTS

Of 4,967 Medicare Part D beneficiaries determined to be MTMP-eligible, 4,277 beneficiaries (86.1%) were available for assessment (400 declined, 186 disenrolled, and 104 were deceased). Pharmacists initiated 1,548 valid medication recommendations (i.e., recommendations were excluded for deceased patients, incorrect prescribers, and where prescriber specialty was not identified). These recommendations for 1,174 beneficiaries (27.5% of those available) were faxed to prescribers requesting approval. Mean (SD) age for beneficiaries having recommendations was 72.9 (9.4) years, and the majority (57.6%) was female. By category of recommendation, 58.3% (n=902) were guideline adherence, 33.3% (n=515) were cost saving, and 8.5% (n=131) were safety concerns. Prescriber approval rates were 47.2% overall (n =731/1,548), 41.4% (n=373/902) for guideline adherence, 58.3% (n=300/515) for cost savings, and 44.3% (n=58/131) for safety concerns; 817 recommendations were not approved by prescribers (n= 255 [16.5%] denials and 562 no response [36.3%]). Prescriber approval was significantly higher for cost-saving interventions compared with guideline adherence interventions (odds ratio [OR]=1.98, 95% CI=1.56-2.51, P< 0.001) and compared with safety interventions (OR=1.76, 95% CI=1.19, 2.59, P=0.004); there was no significant difference in the prescriber approval rates for the interventions for safety versus guideline adherence. The overall approval rate was higher for PCPs (49.8%, n=525/1,054) versus specialists (41.7%, n=206/494; OR=1.39, 95% CI=1.08-1.78, P=0.011) and for the category for guideline adherence interventions (44.0% for PCPs vs. 35.9% for specialists; OR =1.40, 95% CI=1.01-1.95, P=0.044), but not for the other 2 intervention categories.

CONCLUSIONS

Prescriber approval rates for pharmacist recommendations for drug therapy changes for MTMP beneficiaries were approximately 47% overall and higher for recommendations that involved cost savings compared with recommendations for safety concerns or guideline adherence. Compared with specialists, PCPs had higher approval rates for pharmacist recommendations overall and for the intervention category guideline adherence.

摘要

背景

根据2003年《医疗保险处方药、改进与现代化法案》的定义,药物治疗管理项目(MTMPs)必须旨在通过促进合理用药来减少药物不良事件并改善患者预后。WellPoint公司与由药剂师运营的亚利桑那大学药学院药物管理中心(UA MMC)签约,为其近200万医疗保险处方药计划(PDP)受益人中的约5000名高风险受益人提供一项基于电话的试点MTMP。该项目的资格由以下条件确定:患有6种慢性病中的至少2种(血脂异常、心血管疾病、抑郁症、糖尿病、充血性心力衰竭和慢性阻塞性肺疾病;后2种疾病中至少1种必须存在),至少使用3种D部分涵盖的药物,且每年预计药物花费超过4000美元。除了这些标准外,WellPoint公司还使用约翰霍普金斯调整临床组(ACG)预测模型来识别将被纳入该项目的高风险受益人。对这些患者进行了药物治疗评估。如果发现任何与药物相关的问题(MRPs),则通过传真与患者的开处方者联系,并提出解决这些MRPs的建议。UA MMC的传真干预措施分为节省成本、遵循指南或安全问题三类。

目的

(a)确定开处方者对MTMP中针对三类干预措施由药剂师发起的建议的反应,(b)比较不同干预措施类别之间开处方者的反应,以及(c)在每个干预措施类别中比较不同开处方者类型(初级保健医生[PCP]与专科医生)的开处方者反应。

方法

利用从UA MMC数据库收集的数据,对2008年8月至12月由药剂师发起的干预措施进行回顾性分析。收集了干预措施类别(节省成本、遵循指南或安全问题)的数据,开处方者的反应记录为批准或拒绝(无反应视为拒绝)。通过搜索州医学委员会的记录确定开处方者的专业。进行了逻辑回归分析,并使用稳健方差选项来调整开处方者内部的相关性,以比较不同干预措施类别之间以及同一类别内开处方者的批准率。显著性评估的α值为0.05。

结果

在确定符合MTMP资格的4967名医疗保险D部分受益人中,有4277名受益人(86.1%)可供评估(400人拒绝,186人退出项目,104人死亡)。药剂师发起了1548项有效的药物建议(即因患者死亡、开处方者信息错误以及未确定开处方者专业而排除的建议)。这些针对1174名受益人的建议(占可评估受益人的27.5%)被传真给开处方者以请求批准。有建议的受益人的平均(标准差)年龄为72.9(9.4)岁,大多数(57.6%)为女性。按建议类别划分,58.3%(n = 902)为遵循指南,33.3%(n = 515)为节省成本,8.5%(n = 131)为安全问题。开处方者的总体批准率为47.2%(n = 731/1548),遵循指南的批准率为41.4%(n = 373/902),节省成本的批准率为58.3%(n = 300/515),安全问题的批准率为44.3%(n = 58/131);817项建议未得到开处方者的批准(n = 255[16.5%]被拒绝,562项无反应[36.3%])。与遵循指南的干预措施相比,节省成本的干预措施的开处方者批准率显著更高(优势比[OR]=1.98,95%置信区间[CI]=1.56 - 2.51,P < 0.001),与安全干预措施相比也显著更高(OR = 1.76,95% CI = 1.19,2.59,P = 0.004);安全干预措施与遵循指南的干预措施的开处方者批准率没有显著差异。初级保健医生的总体批准率(49.8%,n = 525/1054)高于专科医生(41.7%,n = 206/494;OR = 1.39,95% CI = 1.08 - 1.78,P = 0.011),遵循指南干预措施类别的批准率也是如此(初级保健医生为44.0%,专科医生为35.9%;OR = 1.40,95% CI = 1.01 - 1.95,P = 0.044),但其他2个干预措施类别并非如此。

结论

MTMP受益人的药物治疗变更由药剂师发起的建议,开处方者的总体批准率约为47%,与安全问题或遵循指南的建议相比,涉及节省成本的建议的批准率更高。与专科医生相比,初级保健医生对药剂师建议的总体批准率以及遵循指南干预措施类别的批准率更高。

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