Acceptability of patient-centered, multi-disciplinary medication therapy management recommendations: results from the INCREASE randomized study.

Acceptability of patient-centered, multi-disciplinary medication therapy management recommendations: results from the INCREASE randomized study.
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DOI:
10.1186/s12877-023-03876-4
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发表时间:
2023-03-10
期刊:
影响因子:
4.1
通讯作者:
Moga, Daniela C. C.
Moga, Daniela C. C.
中科院分区:
医学2区
文献类型:
--
作者:
Smith, Noah I. I.;Martinez, Ashley I. I.;Huffmyer, Mark;Eckmann, Lynne;George, Rosmy;Abner, Erin L. L.;Jicha, Gregory A. A.;Moga, Daniela C. C.

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服用多种药物和不适当的药物可能是阿尔茨海默病和相关痴呆(ADRD)的一个可改变的危险因素。药物治疗管理(MTM)干预可以减轻药物引起的认知功能障碍,延迟症状性功能障碍的发生。本研究的目的是描述一项旨在延缓ADRD症状发作的随机对照试验(RCT)中以患者为中心的团队干预(药剂师和非药剂师临床医生)的MTM方案。65 + 岁的非痴呆、使用 ≥ 1潜在不适当药物(PIM)的社区居住成年人参加了一项随机对照试验,以评估MTM干预在改善药物适当性和认知方面的效果(NCT02849639)。MTM干预包括三个步骤:(1)药剂师识别潜在的药物相关问题(MRP),并为处方药和非处方药、维生素和补充剂提出初步建议;(2)研究小组与参与者一起审查所有初步建议,允许在最终建议之前进行修改;(3)记录参与者对最终建议的反应。在这里,我们描述最初的建议、团队参与过程中的变化以及参与者对最终建议的反应。在90名参与者中,每个参与者报告的平均 ± 为6.7MRP±3.6MRP。在为治疗组参与者(N = 46)提出的259项初步MTM建议中,40%在第二步中进行了修订。参与者报告愿意采纳46%的最终建议,并表示需要针对38%的最终建议提供额外的初级保健投入。当提供治疗切换和/或使用抗胆碱能药物时,采用最终建议的意愿最高。对MTM建议修改的评估表明,药剂师最初的MTM建议经常在参与纳入患者偏好的多学科决策过程后发生变化。该团队受到鼓舞,看到了患者参与度与参与者接受最终MTM建议的总体积极反应之间的相关性。研究注册号:Clinicaltrial.gov NCT02849639,注册日期:2016年7月29日。网上版载有补充材料,可在10.1186/s12877-023-03876-4查阅。
Polypharmacy and inappropriate medications may be a modifiable risk factor for Alzheimer’s Disease and Related Dementias (ADRD). Medication therapy management (MTM) interventions may mitigate medication-induced cognitive dysfunction and delay onset of symptomatic impairment. The objective of the current study is to describe an MTM protocol for a patient-centered team intervention (pharmacist and non-pharmacist clinician) in a randomized controlled trial (RCT) directed at delaying the symptomatic onset of ADRD. Community dwelling adults 65 + years, non-demented, using ≥ 1 potentially inappropriate medications (PIM) were enrolled in an RCT to evaluate the effect of an MTM intervention on improving medication appropriateness and cognition (NCT02849639). The MTM intervention involved a three-step process: (1) pharmacist identified potential medication-related problems (MRPs) and made initial recommendations for prescribed and over-the-counter medications, vitamins, and supplements; (2) study team reviewed all initial recommendations together with the participants, allowing for revisions prior to the finalized recommendations; (3) participant responses to final recommendations were recorded. Here, we describe initial recommendations, changes during team engagement, and participant responses to final recommendations. Among the 90 participants, a mean 6.7 ± 3.6 MRPs per participant were reported. Of the 259 initial MTM recommendations made for the treatment group participants (N = 46), 40% percent underwent revisions in the second step. Participants reported willingness to adopt 46% of final recommendations and expressed need for additional primary care input in response to 38% of final recommendations. Willingness to adopt final recommendations was highest when therapeutic switches were offered and/or with anticholinergic medications. The evaluation of modifications to MTM recommendations demonstrated that pharmacists’ initial MTM recommendations often changed following the participation in the multidisciplinary decision-making process that incorporated patient preferences. The team was encouraged to see a correlation between engaging patients and a positive overall response towards participant acceptance of final MTM recommendations. Study registration number: clinicaltrial.gov NCT02849639 registered on 29/07/2016. The online version contains supplementary material available at 10.1186/s12877-023-03876-4.
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