Primary Care-PsychiatryScreening and case finding for major depressive disorder using the Patient Health Questionnaire (PHQ-9): a meta-analysis
Introduction
Major depressive disorder (MDD) has a high prevalence in the general population and is associated with considerable morbidity, as well as a high financial cost to society [1]. The Patient Health Questionnaire (PHQ-9) is a self-report tool for screening and case finding for MDD and is based on the Primary Care Evaluation of Mental Disorders, a diagnostic tool developed in the mid-1990s. It is widely used in both clinical and research settings. An indication of its importance comes from its recommendation as a measurement tool for depressive symptoms by the most recent iteration of the Diagnostic and Statistical Manual of Mental Disorders (DSM, Fifth Edition).
Four systematic reviews and meta-analyses previously evaluated the diagnostic properties of the PHQ-9. One of these [2] evaluated how the instrument performs in primary care settings and compared the algorithm scoring method with the summed score ≥ 10. A meta-analysis published in 2015 by Manea et al. examined the psychometric properties of the PHQ-9 using the algorithm scoring method and compared this scoring method in different settings with the summed score method at cutoff point of 10 [3]. Another review conducted by Gilbody et al. (published in 2007) summarized the diagnostic properties of the PHQ-9 in different settings [4]. The authors of this review also attempted to summarize the psychometric properties of the PHQ-9 at alternative cutoff points; however, not enough validation studies were found at the time. This analysis was subsequently carried out by Manea et al. in 2012 [5]. This diagnostic meta-analysis has suggested that the performance of the instrument at cutoff point 10 may be lower than that observed in the original validation study. The authors also suggested that different cutoff points may be required for different settings. It is therefore important to examine the performance of other cutoff points which is one of the aims of this review. The review by Manea et al. also highlighted the possibility that there may be selective reporting of cutoff points and that this may artificially inflate the observed diagnostic performance of the measure, at least for cutoff points other than the standard one, which tends to be reported by all studies.
On the basis of this, the current review has three aims: firstly, to establish the diagnostic performance of the PHQ-9 at the standard cutoff point (given the popularity of the PHQ-9, the number of studies available to assess this has grown rapidly since the previous review); secondly, to compare the diagnostic performance of the PHQ-9 at the standard cutoff point in different clinical settings; thirdly, to assess whether there is selective reporting of cutoff points for cutoffs other than 10.
Section snippets
Search strategy
We searched Embase, MEDLine and PSYCHInfo from 1999 (when the PHQ-9 was issued) to September 2013 using the terms “PHQ-9,” “PHQ,” “PHQ$” and “patient health questionnaire.” We manually searched the reference lists of studies fitting the inclusion criteria and performed a reverse citation search in Web of Science. We contacted authors of unpublished studies and conference abstracts in an attempt to minimize publication bias. The search was performed by two independent reviewers (A.M. and L.M.),
Results
After removing the duplicates, we screened 4513 records for eligibility. Full text was reviewed for 65 papers that met initial inclusion criteria. Thirty-six of 65 met final-stage inclusion criteria. Study selection is summarized in the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) flowchart in Fig. 1, and further details about the reasons for exclusion are given in Appendix 1.
Main findings
Since the first diagnostic meta-analysis of the diagnostic accuracy of the PHQ-9 at different cutoff points was conducted, the number of validation studies that fulfilled the inclusion criteria has doubled. The PHQ-9 has been translated and validated in many languages, countries and settings, and significantly more data were available for this review. However, given that most studies reported a small range of cutoff points, the results for other cutoff points than 10 are more difficult to
Conclusions
The aims of the review were to establish the diagnostic performance of the PHQ-9 at the standard cutoff point (10), to compare the diagnostic performance of the PHQ-9 at the standard cutoff point in different clinical settings and to assess whether there is selective reporting of cutoff points other than 10.
Our results further support the conclusions of the previous meta-analysis that the sensitivity of the PHQ-9 at cutoff point 10 is lower than that reported in the original validation study,
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