Antidepressant Advisor (ADeSS): a decision support system for antidepressant treatment for depression in UK primary care - a feasibility study

被引:4
|
作者
Harrison, Phillippa [1 ]
Carr, Ewan [2 ]
Goldsmith, Kimberley [2 ]
Young, Allan [1 ,3 ]
Ashworth, Mark [4 ]
Fennema, Diede [1 ]
Duan, Suqian [1 ]
Barrett, Barbara M. [5 ]
Zahn, Roland [1 ,3 ]
机构
[1] Kings Coll London, Inst Psychiat Psychol & Neurosci, Ctr Affect Disorders, Dept Psychol Med, London, England
[2] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Biostat & Hlth Informat, London, England
[3] South London & Maudsley Mental Hlth NHS Trust, Natl Serv Affect Disorders, London, England
[4] Kings Coll London, Dept Populat Hlth Sci, London, England
[5] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Hlth Serv & Populat Res, London, England
来源
BMJ OPEN | 2023年 / 13卷 / 03期
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
PRIMARY CARE; Depression & mood disorders; CLINICAL PHARMACOLOGY; STAR-ASTERISK-D; SUBGENUAL CORTICES; DISORDERS; UTILITY;
D O I
10.1136/bmjopen-2021-060516
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives To develop and probe the first computerised decision-support tool to provide antidepressant treatment guidance to general practitioners (GPs) in UK primary care.Design A parallel group, cluster-randomised controlled feasibility trial, where individual participants were blind to treatment allocation.Setting South London NHS GP practices.Participants Ten practices and eighteen patients with treatment-resistant current major depressive disorder.Interventions Practices were randomised to two treatment arms: (a) treatment-as-usual, (b) computerised decision support tool.Results Ten GP practices participated in the trial, which was within our target range (8-20). However, practice and patient recruitment were slower than anticipated and only 18 of 86 intended patients were recruited. This was due to fewer than expected patients being eligible for the study, as well as disruption resulting from the COVID-19 pandemic. Only one patient was lost to follow-up. There were no serious or medically important adverse events during the trial. GPs in the decision tool arm indicated moderate support for the tool. A minority of patients fully engaged with the mobile app-based tracking of symptoms, medication adherence and side effects.Conclusions Overall, feasibility was not shown in the current study and the following modifications would be needed to attempt to overcome the limitations found: (a) inclusion of patients who have only tried one Selective Serotonin Reuptake Inhibitor, rather than two, to improve recruitment and pragmatic relevance of the study; (b) approaching community pharmacists to implement tool recommendations rather than GPs; (c) further funding to directly interface between the decision support tool and self-reported symptom app; (d) increasing the geographic reach by not requiring detailed diagnostic assessments and replacing this with supported remote self-report.
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页数:11
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