{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,2,21]],"date-time":"2025-02-21T11:01:53Z","timestamp":1740135713306,"version":"3.37.3"},"reference-count":15,"publisher":"Cambridge University Press (CUP)","issue":"6","license":[{"start":{"date-parts":[[2018,3,21]],"date-time":"2018-03-21T00:00:00Z","timestamp":1521590400000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/www.cambridge.org\/core\/terms"}],"content-domain":{"domain":["www.cambridge.org"],"crossmark-restriction":true},"short-container-title":["Epidemiol. Infect."],"published-print":{"date-parts":[[2018,4]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Commercial point-of-care (POC) diagnostic tests for Group A <jats:italic>Streptococcus<\/jats:italic>, <jats:italic>Streptococcus pneumoniae<\/jats:italic>, and influenza virus have large potential diagnostic and financial impact. Many published reports on test performance, often funded by diagnostics companies, are prone to bias. The Standards for Reporting of Diagnostic Accuracy (STARD 2015) are a protocol to encourage accurate, transparent reporting. The Quality Assessment of Diagnostic Accuracy Studies (QUADAS-2) tool evaluates risk of bias and transportability of results. We used these tools to evaluate diagnostic test accuracy studies of POC studies for three respiratory pathogens. For the 96 studies analysed, compliance was &lt;25% for 14\/34 STARD 2015 standards, and 3\/7 QUADAS-2 domains showed a high risk of bias. All reports lacked reporting of at least one criterion. These biases should be considered in the interpretation of study results.<\/jats:p>","DOI":"10.1017\/s0950268818000596","type":"journal-article","created":{"date-parts":[[2018,3,21]],"date-time":"2018-03-21T05:19:57Z","timestamp":1521609597000},"page":"747-756","update-policy":"https:\/\/doi.org\/10.1017\/policypage","source":"Crossref","is-referenced-by-count":2,"title":["Risk of bias and limits of reporting in diagnostic accuracy studies for commercial point-of-care tests for respiratory pathogens"],"prefix":"10.1017","volume":"146","author":[{"given":"J.M.","family":"Hughes","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Penney","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.","family":"Boyd","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7068-8056","authenticated-orcid":false,"given":"P.","family":"Daley","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"56","published-online":{"date-parts":[[2018,3,21]]},"reference":[{"key":"S0950268818000596_ref15","doi-asserted-by":"publisher","DOI":"10.1148\/radiol.2483072067"},{"key":"S0950268818000596_ref14","first-page":"e54695","article-title":"Are Treponema pallidum specific rapid and point-of-care tests for syphilis accurate enough for screening in resource limited settings? 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