Abstract

BackgroundClinical guidelines for depression in adults recommend the use of outcome measures and stepped care models in routine care. Such measures are based on symptom severity, but response to treatment is likely to also be influenced by personal and contextual factors. This observational study of a routine clinical sample sought to examine the extent to which “symptom severity measures” and “complexity measures” assess different aspects of patient experience, and how they might relate to clinical outcomes, including disengagement from treatment.MethodsSubjects with symptoms of depression (with or without comorbid anxiety) were recruited from people referred to an established Primary Care Mental Health Team using a stepped care model. Each participant completed three baseline symptom measures (the Personal Health Questionnaire (PHQ), Generalised Anxiety Disorder questionnaire (GAD) and Clinical Outcomes in Routine Evaluation (CORE-10)), and two assessments of “case complexity” (the Minnesota-Edinburgh Complexity Assessment Measure (MECAM) and a local complexity assessment). Clinician perception of likely completion of treatment and patient recovery was also assessed. Outcome measures were drop out and clinical improvement on the PHQ.Results298 subjects were recruited to the study, of whom 258 had a sufficient dataset available for analysis. Data showed that the three measures of symptom severity used in this study (PHQ, GAD and CORE-10) seemed to be measuring distinct characteristics from those associated with the measures of case complexity (MECAM, previous and current problem count). Higher symptom severity scores were correlated with improved outcomes at the end of treatment, but there was no association between outcome and complexity measures. Clinicians could predict participant drop-out from care with some accuracy, but had no ability to predict outcome from treatment.ConclusionsThese results highlight the extent to which drop-out complicates recovery from depression with or without anxiety in real-world settings, and the need to consider other factors beyond symptom severity in planning care. The findings are discussed in relation to a growing body of literature investigating prognostic indicators in the context of models of collaborative care for depression.

Highlights

  • Clinical guidelines for depression in adults recommend the use of outcome measures and stepped care models in routine care

  • Clinical guidelines for the management of depression recommend the use of clinical outcome measures and stepped care models in routine care [1], but it can be difficult for health services to match individual patients to the most appropriate intervention, and outcomes are often poor

  • This study aimed to investigate the feasibility of measuring a broader range of contextual factors when planning care for people with depression, and to assess the association of those factors with clinical outcomes, including drop out from treatment

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Summary

Introduction

Clinical guidelines for depression in adults recommend the use of outcome measures and stepped care models in routine care Such measures are based on symptom severity, but response to treatment is likely to be influenced by personal and contextual factors. “Collaborative care” is an approach to the delivery of evidence-based mental health care for primary care patients which seeks to address these problems [5] It includes three core elements: team-based multidisciplinary care delivery, implementation of a stepped care model (in which the intensity of care is stepped up or down depending on response to treatment), and the systematic collection of clinical outcome data to inform decisions about treatment [6,7,8]. Guidance on depression care issued by the UK National Centre for Health and Care Excellence (NICE) recognises that “a wide range of biological, psychological and social factors, which are not captured well by current diagnostic systems, have a significant impact on the course of depression and the response to treatment” [10]

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