Affiliations 

  • 1 Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montréal, Québec H3A 1A2, Canada
  • 2 Department of Clinical, Neuro and Developmental Psychology, Vrije Universiteit (VU) Amsterdam, Amsterdam 1018 HV, The Netherlands
  • 3 Department of Medicine, Department of Health Research and Policy, Department of Statistics, Stanford University, Stanford, CA 94305, USA
  • 4 Departments of Community Health Sciences and Psychiatry, University of Calgary, Calgary, Alberta T2N 1N4, Canada
  • 5 Department of Rehabilitation Medicine, University of Washington, Seattle, WA 98195, USA
  • 6 Department of Neuroscience and Behavior, Faculty of Medicine of Ribeirão Preto, University of São Paulo, Ribeirão, Preto 14049, Brazil
  • 7 Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA 98195, USA
  • 8 Department of Family Medicine and Community Health, University of Minnesota, Minneapolis, MN 55455, USA
  • 9 Department of Psychiatry, EMGO Institute, VU University Medical Center, Amsterdam 1081 HL, The Netherlands
  • 10 Department of Psychiatry, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand
  • 11 Department of Psychosomatic Medicine and Psychotherapy, University Medical Center Hamburg-Eppendorf and Schön Klinik Hamburg Eilbek, Hamburg 20246, Germany
  • 12 Department of Family Medicine, School of Medical Sciences, Universiti Sains Malaysia, Kelantan 16150, Malaysia
  • 13 Centre for Women's Mental Health, Royal Women's Hospital, Parkville, Victoria 3052, Australia
  • 14 Department of General Practice, Academic Medical Center, University of Amsterdam, Amsterdam 1081 HV, The Netherlands
  • 15 Department of Veterans Affairs Medical Center, San Francisco, CA 94121, USA
  • 16 Depression Clinical and Research Program, Massachussets General Hospital, Boston, MA 02114, USA
Biom J, 2017 Nov;59(6):1317-1338.
PMID: 28692782 DOI: 10.1002/bimj.201600184

Abstract

Individual patient data (IPD) meta-analyses are increasingly common in the literature. In the context of estimating the diagnostic accuracy of ordinal or semi-continuous scale tests, sensitivity and specificity are often reported for a given threshold or a small set of thresholds, and a meta-analysis is conducted via a bivariate approach to account for their correlation. When IPD are available, sensitivity and specificity can be pooled for every possible threshold. Our objective was to compare the bivariate approach, which can be applied separately at every threshold, to two multivariate methods: the ordinal multivariate random-effects model and the Poisson correlated gamma-frailty model. Our comparison was empirical, using IPD from 13 studies that evaluated the diagnostic accuracy of the 9-item Patient Health Questionnaire depression screening tool, and included simulations. The empirical comparison showed that the implementation of the two multivariate methods is more laborious in terms of computational time and sensitivity to user-supplied values compared to the bivariate approach. Simulations showed that ignoring the within-study correlation of sensitivity and specificity across thresholds did not worsen inferences with the bivariate approach compared to the Poisson model. The ordinal approach was not suitable for simulations because the model was highly sensitive to user-supplied starting values. We tentatively recommend the bivariate approach rather than more complex multivariate methods for IPD diagnostic accuracy meta-analyses of ordinal scale tests, although the limited type of diagnostic data considered in the simulation study restricts the generalization of our findings.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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