<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Negeri ZF</submitter><funding>Swiss National Science Foundation</funding><funding>Wellcome Trust</funding><pagination>28</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10832258</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Selective reporting of results from only well-performing cut-offs leads to biased estimates of accuracy in primary studies of questionnaire-based screening tools and in meta-analyses that synthesize results. Individual participant data meta-analysis (IPDMA) of sensitivity and specificity at each cut-off via bivariate random-effects models (BREMs) can overcome this problem. However, IPDMA is laborious and depends on the ability to successfully obtain primary datasets, and BREMs ignore the correlation between cut-offs within primary studies.&lt;h4>Methods&lt;/h4>We compared the performance of three recent multiple cut-off models developed by Steinhauser et al., Jones et al., and Hoyer and Kuss, that account for missing cut-offs when meta-analyzing diagnostic accuracy studies wit</pubmed_abstract><journal>BMC medical research methodology</journal><pubmed_title>An empirical comparison of statistical methods for multiple cut-off diagnostic test accuracy meta-analysis of the Edinburgh postnatal depression scale (EPDS) depression screening tool using published results vs individual participant data.</pubmed_title><pmcid>PMC10832258</pmcid><funding_grant_id>071571</funding_grant_id><funding_grant_id>082384/Z/07/Z</funding_grant_id><funding_grant_id>125493</funding_grant_id><funding_grant_id>211374/Z/18/Z</funding_grant_id><pubmed_authors>Gilbody S</pubmed_authors><pubmed_authors>Su KP</pubmed_authors><pubmed_authors>Rice DB</pubmed_authors><pubmed_authors>Khalifa DS</pubmed_authors><pubmed_authors>Bunevicius A</pubmed_authors><pubmed_authors>Garcia-Esteve L</pubmed_authors><pubmed_authors>Cuijpers P</pubmed_authors><pubmed_authors>Toreki A</pubmed_authors><pubmed_authors>Kozinszky Z</pubmed_authors><pubmed_authors>Markham S</pubmed_authors><pubmed_authors>Sharp DJ</pubmed_authors><pubmed_authors>Neupane D</pubmed_authors><pubmed_authors>Kloda LA</pubmed_authors><pubmed_authors>Wu Y</pubmed_authors><pubmed_authors>He C</pubmed_authors><pubmed_authors>Ioannidis JPA</pubmed_authors><pubmed_authors>Tandon SD</pubmed_authors><pubmed_authors>Levis B</pubmed_authors><pubmed_authors>Torres-Gimenez A</pubmed_authors><pubmed_authors>Sun Y</pubmed_authors><pubmed_authors>Vigod SN</pubmed_authors><pubmed_authors>Kusminskas L</pubmed_authors><pubmed_authors>Tadinac M</pubmed_authors><pubmed_authors>Favez N</pubmed_authors><pubmed_authors>Azar M</pubmed_authors><pubmed_authors>Krishnan A</pubmed_authors><pubmed_authors>Vega-Dienstmaier JM</pubmed_authors><pubmed_authors>Benedetti A</pubmed_authors><pubmed_authors>van Heyningen T</pubmed_authors><pubmed_authors>Negeri ZF</pubmed_authors><pubmed_authors>Patten SB</pubmed_authors><pubmed_authors>Chorwe-Sungani G</pubmed_authors><pubmed_authors>Bhandari PM</pubmed_authors><pubmed_authors>Imran M</pubmed_authors><pubmed_authors>Couto TCE</pubmed_authors><pubmed_authors>Rochat TJ</pubmed_authors><pubmed_authors>Smith-Nielsen J</pubmed_authors><pubmed_authors>Chiovitti MJ</pubmed_authors><pubmed_authors>Thombs BD</pubmed_authors><pubmed_authors>Honikman S</pubmed_authors><pubmed_authors>Mitchell ND</pubmed_authors><pubmed_authors>Field S</pubmed_authors><pubmed_authors>DEPRESsion Screening Data (DEPRESSD) EPDS Group</pubmed_authors><pubmed_authors>Riehm KE</pubmed_authors><pubmed_authors>Ziegelstein RC</pubmed_authors><pubmed_authors>Bakare MO</pubmed_authors><pubmed_authors>Kohlhoff J</pubmed_authors><pubmed_authors>Nakic Rados S</pubmed_authors><pubmed_authors>Thiagayson P</pubmed_authors><pubmed_authors>Pawlby SJ</pubmed_authors><pubmed_authors>Boruff JT</pubmed_authors><pubmed_authors>Comeau L</pubmed_authors><pubmed_authors>Beck CT</pubmed_authors></additional><is_claimable>false</is_claimable><name>An empirical comparison of statistical methods for multiple cut-off diagnostic test accuracy meta-analysis of the Edinburgh postnatal depression scale (EPDS) depression screening tool using published results vs individual participant data.</name><description>&lt;h4>Background&lt;/h4>Selective reporting of results from only well-performing cut-offs leads to biased estimates of accuracy in primary studies of questionnaire-based screening tools and in meta-analyses that synthesize results. Individual participant data meta-analysis (IPDMA) of sensitivity and specificity at each cut-off via bivariate random-effects models (BREMs) can overcome this problem. However, IPDMA is laborious and depends on the ability to successfully obtain primary datasets, and BREMs ignore the correlation between cut-offs within primary studies.&lt;h4>Methods&lt;/h4>We compared the performance of three recent multiple cut-off models developed by Steinhauser et al., Jones et al., and Hoyer and Kuss, that account for missing cut-offs when meta-analyzing diagnostic accuracy studies wit</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2026-07-15T01:22:09.831Z</modification><creation>2025-04-05T21:27:16.724Z</creation></dates><accession>S-EPMC10832258</accession><cross_references><pubmed>38302928</pubmed><doi>10.1186/s12874-023-02134-w</doi></cross_references></HashMap>