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跨二级和初级保健的跨学科协作,以提高老年人的药物安全(IMMENSE 研究)-一项随机对照试验。

Interdisciplinary collaboration across secondary and primary care to improve medication safety in the elderly (The IMMENSE study) - a randomized controlled trial.

机构信息

Department of Pharmacy, Faculty of Health Sciences, UiT the Arctic University of Norway, Tromsø, Norway.

Surgery, Cancer and Women's Health Clinic, The University Hospital of North Norway, Tromsø, Norway.

出版信息

BMC Health Serv Res. 2022 Oct 26;22(1):1290. doi: 10.1186/s12913-022-08648-1.

Abstract

BACKGROUND

Suboptimal medication use contributes to a substantial proportion of hospitalizations and emergency department visits in older adults. We designed a clinical pharmacist intervention to optimize medication therapy in older hospitalized patients. Based on the integrated medicine management (IMM) model, the 5-step IMMENSE intervention comprise medication reconciliation, medication review, reconciled medication list upon discharge, patient counselling, and post discharge communication with primary care. The objective of this study was to evaluate the effects of the intervention on healthcare use and mortality.

METHODS

A non-blinded parallel group randomized controlled trial was conducted in two internal medicine wards at the University Hospital of North Norway. Acutely admitted patients ≥ 70 years were randomized 1:1 to intervention or standard care (control). The primary outcome was the rate of emergency medical visits (readmissions and emergency department visits) 12 months after discharge.

RESULTS

Of the 1510 patients assessed for eligibility, 662 patients were asked to participate, and 516 were enrolled. After withdrawal of consent and deaths in hospital, the modified intention-to-treat population comprised 480 patients with a mean age of 83.1 years (SD: 6.3); 244 intervention patients and 236 control patients. The number of emergency medical visits in the intervention and control group was 497 and 499, respectively, and no statistically significant difference was observed in rate of the primary outcome between the groups [adjusted incidence rate ratio of 1.02 (95% CI: 0.82-1.27)]. No statistically significant differences between groups were observed for any of the secondary outcomes, neither in subgroups, nor for the per-protocol population.

CONCLUSIONS

We did not observe any statistical significant effects of the IMMENSE intervention on the rate of emergency medical visits or any other secondary outcomes after 12 months in hospitalized older adults included in this study.

TRIAL REGISTRATION

The trial was registered in clinicaltrials.gov on 28/06/2016, before enrolment started (NCT02816086).

摘要

背景

药物使用不当是导致老年人住院和急诊就诊的主要原因之一。我们设计了一种临床药师干预措施,以优化老年住院患者的药物治疗。该干预措施基于综合医学管理(IMM)模型,由 5 个步骤组成,包括药物重整、药物审查、出院时的药物清单、患者咨询以及与初级保健的出院后沟通。本研究的目的是评估该干预措施对医疗保健使用和死亡率的影响。

方法

在挪威北大学医院的两个内科病房进行了一项非盲平行组随机对照试验。≥70 岁的急性入院患者以 1:1 的比例随机分为干预组或标准护理(对照组)。主要结局是出院后 12 个月内急诊就诊(再入院和急诊就诊)的发生率。

结果

在评估合格性的 1510 名患者中,有 662 名患者被要求参与,其中 516 名患者被纳入。在撤回同意和院内死亡后,修改后的意向治疗人群包括 480 名平均年龄为 83.1 岁(SD:6.3)的患者;244 名干预组患者和 236 名对照组患者。干预组和对照组的急诊就诊次数分别为 497 次和 499 次,两组主要结局发生率无统计学差异[调整后的发生率比为 1.02(95%CI:0.82-1.27)]。在亚组和方案人群中,两组在任何次要结局上均无统计学差异。

结论

在这项研究中,我们没有观察到 IMMENSE 干预措施对住院老年患者在 12 个月内急诊就诊率或任何其他次要结局的任何统计学显著影响。

试验注册

该试验于 2016 年 6 月 28 日在 clinicaltrials.gov 注册,在开始入组前(NCT02816086)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a646/9597977/ebe3e7cbcd06/12913_2022_8648_Fig1_HTML.jpg

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