Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA; Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Lancet Glob Health. 2024 Apr;12(4):e652-e661. doi: 10.1016/S2214-109X(23)00592-2. Epub 2024 Feb 23.
Although evidence-based treatments for depression in low-resource settings are established, implementation strategies to scale up these treatments remain poorly defined. We aimed to compare two implementation strategies in achieving high-quality integration of depression care into chronic medical care and improving mental health outcomes in patients with hypertension and diabetes.
We conducted a parallel, cluster-randomised, controlled, implementation trial in ten health facilities across Malawi. Facilities were randomised (1:1) by covariate-constrained randomisation to either an internal champion alone (ie, basic strategy group) or an internal champion plus external supervision with audit and feedback (ie, enhanced strategy group). Champions integrated a three-element, evidence-based intervention into clinical care: universal depression screening; peer-delivered psychosocial counselling; and algorithm-guided, non-specialist antidepressant management. External supervision involved structured facility visits by Ministry officials and clinical experts to assess quality of care and provide supportive feedback approximately every 4 months. Eligible participants were adults (aged 18-65 years) seeking hypertension and diabetes care with signs of depression (Patient Health Questionnaire-9 score ≥5). Primary implementation outcomes were depression screening fidelity, treatment initiation fidelity, and follow-up treatment fidelity over the first 3 months of treatment, analysed by intention to treat. This trial is registered with ClinicalTrials.gov, NCT03711786, and is complete.
Five (50%) facilities were randomised to the basic strategy and five (50%) to the enhanced strategy. Between Oct 1, 2019, and Nov 30, 2021, in the basic group, 587 patients were assessed for eligibility, of whom 301 were enrolled; in the enhanced group, 539 patients were assessed, of whom 288 were enrolled. All clinics integrated the evidence-based intervention and were included in the analyses. Of 60 774 screening-eligible visits, screening fidelity was moderate (58% in the enhanced group vs 53% in the basic group; probability difference 5% [95% CI -38% to 47%]; p=0·84) and treatment initiation fidelity was high (99% vs 98%; 0% [-3% to 3%]; p=0·89) in both groups. However, treatment follow-up fidelity was substantially higher in the enhanced group than in the basic group (82% vs 20%; 62% [36% to 89%]; p=0·0020). Depression remission was higher in the enhanced group than in the basic group (55% vs 36%; 19% [3% to 34%]; p=0·045). Serious adverse events were nine deaths (five in the basic group and four in the enhanced group) and 26 hospitalisations (20 in the basic group and six in the enhanced group); none were treatment-related.
The enhanced implementation strategy led to an increase in fidelity in providers' follow-up treatment actions and in rates of depression remission, consistent with the literature that follow-up decisions are crucial to improving depression outcomes in integrated care models. These findings suggest that external supervision combined with an internal champion could offer an important advance in integrating depression treatment into general medical care in low-resource settings.
The National Institute of Mental Health.
尽管在资源匮乏的环境中已经有了针对抑郁症的循证治疗方法,但扩大这些治疗方法的实施策略仍未得到明确界定。我们旨在比较两种实施策略,以实现将抑郁症护理高质量整合到慢性医疗护理中,并改善高血压和糖尿病患者的心理健康结果。
我们在马拉维的 10 个卫生机构进行了一项平行、集群随机、对照、实施试验。根据协变量约束随机化,将设施(1:1)随机分配到内部冠军组(即基本策略组)或内部冠军加外部监督与审计和反馈(即增强策略组)。冠军们将一个三要素的、基于证据的干预措施整合到临床护理中:普遍的抑郁症筛查;同行提供的心理社会咨询;以及算法指导的、非专科抗抑郁药物管理。外部监督涉及卫生部官员和临床专家对设施进行结构化访问,以评估护理质量并提供大约每 4 个月一次的支持性反馈。符合条件的参与者是寻求高血压和糖尿病护理且有抑郁迹象(患者健康问卷-9 评分≥5)的成年人(18-65 岁)。主要实施结果是在治疗的头 3 个月内的抑郁症筛查保真度、治疗启动保真度和随访治疗保真度,通过意向治疗进行分析。这项试验在 ClinicalTrials.gov 上注册,编号为 NCT03711786,现已完成。
在基本策略组中,有 5(50%)个设施被随机分配,5(50%)个设施被随机分配到增强策略组。2019 年 10 月 1 日至 2021 年 11 月 30 日期间,在基本组中,有 587 名患者接受了资格评估,其中 301 名患者被纳入;在增强组中,有 539 名患者接受了评估,其中 288 名患者被纳入。所有诊所都整合了基于证据的干预措施,并纳入了分析。在 60774 次筛查合格的就诊中,筛查保真度适中(增强组为 58%,基本组为 53%;概率差异为 5%[95%CI -38%至 47%];p=0.84),治疗启动保真度较高(99%对 98%;0%[-3%至 3%];p=0.89),两组均较高。然而,增强组的治疗随访保真度明显高于基本组(82%对 20%;62%[36%至 89%];p=0.0020)。增强组的抑郁症缓解率高于基本组(55%对 36%;19%[3%至 34%];p=0.045)。严重不良事件有 9 例死亡(基本组 5 例,增强组 4 例)和 26 例住院治疗(基本组 20 例,增强组 6 例);均与治疗无关。
增强的实施策略导致提供者后续治疗行动的保真度和抑郁症缓解率的提高,这与文献一致,即后续决策对改善综合护理模式中的抑郁症结果至关重要。这些发现表明,外部监督与内部冠军相结合,可能为在资源匮乏的环境中整合抑郁症治疗提供重要进展。
美国国立精神卫生研究所。