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通过减少多重用药来治疗多重用药:疗效与安全性

Poly-de-prescribing to treat polypharmacy: efficacy and safety.

作者信息

Garfinkel Doron

机构信息

Geriatric Palliative service, E. Wolfson Medical Center, Holon 58100 & Homecare hospice, Israel Cancer Association, Israel.

出版信息

Ther Adv Drug Saf. 2018 Jan;9(1):25-43. doi: 10.1177/2042098617736192. Epub 2017 Oct 27.

Abstract

BACKGROUND

The aim of this study was to evaluate efficacy and safety of poly-de-prescribing (PDP) based on the Garfinkel method in older people with polypharmacy.

METHODS

A longitudinal, prospective, nonrandomized study in Israel was carried out between 2009 and 2016. Comprehensive geriatric assessments were performed at home in people age ⩾66 years consuming ⩾6 prescription drugs. Exclusion criteria were life expectancy <6 months and a seeming unwillingness to cooperate (poor compliance). PDP of ⩾3 prescription drugs was recommended. Follow up was at ⩾3 years. Between April 2015 and April 2016 Likert scale questionnaires were filled by all participants/families to evaluate overall satisfaction and clinical outcomes. The outcome measures were change in functional, mental and cognitive status, sleep quality, appetite, continence; major complication, hospitalizations, mortality, and family doctor's cooperation.

RESULTS

Poly-de-prescribing of ⩾3 drugs was eventually achieved by 122 participants (PDP group); ⩽2 drugs stopped by 55 'nonresponders' (NR group). The average age was 83.4 ± 5.3 in the PDP group, and 80.8 ± 6.3 in the NR group ( = 0.0045). Follow up was 43.6 ± 14 months (PDP) and 39.5 ± 16.6 months (NR) ( = 0.09). The prevalence of most diseases/symptoms was comparable except for a higher prevalence for dementia, incontinence and functional decline in the PDP group. The main barrier to de-prescribing was the family doctor's unwillingness to adopt PDP recommendations ( < 0.0001). The baseline median number of medications taken by both groups was 10 (IQR 8 to 12) ( = 0.55). On the last follow up, the drug count was 11 (IQR 8 to 12) in the NR group and 4 (IQR 2 to 5) in the PDP group ( =0.0001). The PDP group showed significantly less deterioration (sometimes improvement) in general satisfaction, functional, mental and cognitive status, sleep quality, appetite, sphincter control, and the number of major complications was significantly reduced ( < 0.002 in all). The rate of hospitalizations and mortality was comparable. Health improvement occurred within 3 months after de-prescribing in 83%, and persisted for ⩾2 years in 68%.

CONCLUSIONS

This self-selected sample longitudinal research strongly suggests that the negative, usually invisible effects of polypharmacy are reversible. PDP is well tolerated and associated with improved clinical outcomes, in comparison with outcomes of older people who adhere to all clinical guidelines and take all medications conventionally. Future double-blind studies will probably prove beneficial economic outcomes as well.

摘要

背景

本研究旨在评估基于加芬克尔方法的多药减量处方(PDP)在老年多重用药患者中的疗效和安全性。

方法

2009年至2016年在以色列进行了一项纵向、前瞻性、非随机研究。对年龄≥66岁且服用≥6种处方药的患者进行了居家综合老年评估。排除标准为预期寿命<6个月以及明显不愿合作(依从性差)。建议进行≥3种处方药的PDP。随访时间≥3年。2015年4月至2016年4月期间,所有参与者/家属填写了李克特量表问卷,以评估总体满意度和临床结局。结局指标包括功能、心理和认知状态、睡眠质量、食欲、大小便失禁情况的变化;主要并发症、住院次数、死亡率以及家庭医生的合作情况。

结果

最终122名参与者实现了≥3种药物的多药减量处方(PDP组);55名“无反应者”(NR组)停用了≤2种药物。PDP组的平均年龄为83.4±5.3岁,NR组为80.8±6.3岁(P = 0.0045)。随访时间PDP组为43.6±14个月,NR组为39.5±16.6个月(P = 0.09)。除PDP组痴呆、大小便失禁和功能下降的患病率较高外,大多数疾病/症状的患病率相当。减药的主要障碍是家庭医生不愿采纳PDP建议(P<0.0001)。两组基线时服用药物的中位数均为10种(四分位间距8至12种)(P = 0.55)。在最后一次随访时,NR组的药物数量为11种(四分位间距8至12种),PDP组为4种(四分位间距2至5种)(P = 0.0001)。PDP组在总体满意度、功能、心理和认知状态、睡眠质量、食欲、括约肌控制方面的恶化程度明显较低(有时有所改善),主要并发症的数量显著减少(所有P<0.002)。住院率和死亡率相当。83%的患者在减药后3个月内健康状况得到改善,68%的患者持续改善≥2年。

结论

这个自我选择样本的纵向研究有力地表明,多重用药的负面、通常不可见的影响是可逆的。与遵循所有临床指南并按常规服用所有药物的老年人相比,PDP耐受性良好且与改善的临床结局相关。未来的双盲研究可能也会证明其具有有益的经济结局。

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