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一项多中心、随机、对照试验,旨在评估优化老年人群药物处方在18个月随访期内对功能自主性演变的疗效:OPTIM研究方案。

A multi-center, randomized, controlled trial to assess the efficacy of optimization of drug prescribing in an elderly population, at 18 months of follow-up, in the evolution of functional autonomy: the OPTIM study protocol.

作者信息

Dauphinot Virginie, Jean-Bart Elodie, Krolak-Salmon Pierre, Mouchoux Christelle

机构信息

Memory Research Centre of Lyon (CMRR); Geriatrics Unit, Charpennes Hospital, University Hospital of Lyon, Villeurbanne, France.

Research Clinic Centre (CRC) - VCF (Aging - Brain - Frailty), Charpennes Hospital, University Hospital of Lyon, Villeurbanne, France.

出版信息

BMC Geriatr. 2017 Aug 30;17(1):195. doi: 10.1186/s12877-017-0600-7.

Abstract

BACKGROUND

Pharmacotherapy is necessary for the management of many diseases which number increased with aging. However, potentially inappropriate prescriptions and polymedication increases iatrogenic risks and can lead to adverse events. To limit the consequences of potentially harmful prescriptions, optimization of drug prescribing is a major stake of improving quality and safety of care in the elderly. The purpose of the OPTIM study is to study the impact of the optimization of drug prescribing on the evolution of functional autonomy at 18 months of follow-up.

METHODS

A multicenter, open-label, Randomized Controlled Trial was designed to assess the impact of an optimization program of drug prescribing consisting in a clinical medication review by a pharmacist, in collaboration with specialist physician of the geriatric/memory center and the referent physician, on the evolution of functional autonomy level, measured during 18 months of follow-up. The study will include 302 elderly outpatients visiting geriatric and memory centers, randomly distributed in one of the two parallel groups. One group will benefit of the intervention, while the other will be considered as control group. The effect of the intervention on evolution of the level of autonomy function, defined with repeated measures, will be estimated in a generalized linear mixed model. The intervention will be considered significant if the interaction between time and the study group is significant. Secondary analysis will be conducted to assess the impact of the intervention on secondary clinical outcomes.

DISCUSSION

The "OPTIM" program should enable optimization of drug prescribing in elderly patients and therefore slow or prevent progression to loss of functional autonomy. It should also help to strengthen collaboration between the hospital team of geriatric/neurologist, the pharmacist and the private practice who are all involved in caring for the patient's health. The benefits for the patient are thus optimizing its medical management by linking health professionals met during his care pathway. In addition, pharmaceutical recommendations sent to referent physicians should help raise awareness of the prescription of drugs in these patients.

TRIAL REGISTRATION NUMBER CLINICALTRIALS

NCT02740764.

摘要

背景

药物治疗对于许多随着年龄增长而增多的疾病的管理是必要的。然而,潜在不适当的处方和多重用药会增加医源性风险,并可能导致不良事件。为了限制潜在有害处方的后果,优化药物处方是提高老年人护理质量和安全性的一项重要工作。OPTIM研究的目的是研究药物处方优化对随访18个月时功能自主性演变的影响。

方法

设计了一项多中心、开放标签的随机对照试验,以评估药物处方优化计划的影响,该计划包括由药剂师与老年病/记忆中心的专科医生和转诊医生合作进行临床用药审查,对随访18个月期间测量的功能自主性水平的演变的影响。该研究将纳入302名到老年病和记忆中心就诊的老年门诊患者,随机分配到两个平行组中的一组。一组将接受干预,而另一组将被视为对照组。将在广义线性混合模型中估计干预对重复测量定义的自主功能水平演变的影响。如果时间与研究组之间的交互作用显著,则认为干预具有显著性。将进行二次分析以评估干预对次要临床结果的影响。

讨论

“OPTIM”计划应能优化老年患者的药物处方,从而减缓或防止功能自主性丧失的进展。它还应有助于加强老年病/神经科医生的医院团队、药剂师和参与患者健康护理的私人执业医生之间的合作。因此,对患者的好处是通过联系其护理过程中遇到的医疗专业人员来优化其医疗管理。此外,发送给转诊医生的药学建议应有助于提高对这些患者药物处方的认识。

试验注册号

临床试验:NCT02740764。

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