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dc.contributor.authorBurnell, Men_US
dc.contributor.authorIyer, Ren_US
dc.contributor.authorGentry-Maharaj, Aen_US
dc.contributor.authorNordin, Aen_US
dc.contributor.authorListon, Ren_US
dc.contributor.authorManchanda, Ren_US
dc.contributor.authorDas, Nen_US
dc.contributor.authorGornall, Ren_US
dc.contributor.authorBeardmore-Gray, Aen_US
dc.contributor.authorHillaby, Ken_US
dc.contributor.authorLeeson, Sen_US
dc.contributor.authorLinder, Aen_US
dc.contributor.authorLopes, Aen_US
dc.contributor.authorMeechan, Den_US
dc.contributor.authorMould, Ten_US
dc.contributor.authorNevin, Jen_US
dc.contributor.authorOlaitan, Aen_US
dc.contributor.authorRufford, Ben_US
dc.contributor.authorShanbhag, Sen_US
dc.contributor.authorThackeray, Aen_US
dc.contributor.authorWood, Nen_US
dc.contributor.authorReynolds, Ken_US
dc.contributor.authorRyan, Aen_US
dc.contributor.authorMenon, Uen_US
dc.date.accessioned2016-06-03T11:03:56Z
dc.date.available2015-12-27en_US
dc.date.issued2016-12en_US
dc.date.submitted2016-05-20T22:56:13.069Z
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/12657
dc.description.abstractOBJECTIVE: To explore the impact of risk-adjustment on surgical complication rates (CRs) for benchmarking gynaecological oncology centres. DESIGN: Prospective cohort study. SETTING: Ten UK accredited gynaecological oncology centres. POPULATION: Women undergoing major surgery on a gynaecological oncology operating list. METHODS: Patient co-morbidity, surgical procedures and intra-operative (IntraOp) complications were recorded contemporaneously by surgeons for 2948 major surgical procedures. Postoperative (PostOp) complications were collected from hospitals and patients. Risk-prediction models for IntraOp and PostOp complications were created using penalised (lasso) logistic regression using over 30 potential patient/surgical risk factors. MAIN OUTCOME MEASURES: Observed and risk-adjusted IntraOp and PostOp CRs for individual hospitals were calculated. Benchmarking using colour-coded funnel plots and observed-to-expected ratios was undertaken. RESULTS: Overall, IntraOp CR was 4.7% (95% CI 4.0-5.6) and PostOp CR was 25.7% (95% CI 23.7-28.2). The observed CRs for all hospitals were under the upper 95% control limit for both IntraOp and PostOp funnel plots. Risk-adjustment and use of observed-to-expected ratio resulted in one hospital moving to the >95-98% CI (red) band for IntraOp CRs. Use of only hospital-reported data for PostOp CRs would have resulted in one hospital being unfairly allocated to the red band. There was little concordance between IntraOp and PostOp CRs. CONCLUSION: The funnel plots and overall IntraOp (≈5%) and PostOp (≈26%) CRs could be used for benchmarking gynaecological oncology centres. Hospital benchmarking using risk-adjusted CRs allows fairer institutional comparison. IntraOp and PostOp CRs are best assessed separately. As hospital under-reporting is common for postoperative complications, use of patient-reported outcomes is important. TWEETABLE ABSTRACT: Risk-adjusted benchmarking of surgical complications for ten UK gynaecological oncology centres allows fairer comparison.en_US
dc.format.extent2171 - 2180en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofBJOGen_US
dc.subjectUKGOSOCen_US
dc.subjectBenchmarkingen_US
dc.subjectcentresen_US
dc.subjectcomparisonen_US
dc.subjectcomplicationsen_US
dc.subjectgynaecological oncologyen_US
dc.subjectrisk adjustmenten_US
dc.subjectsurgeryen_US
dc.subjectAdulten_US
dc.subjectAgeden_US
dc.subjectBenchmarkingen_US
dc.subjectCohort Studiesen_US
dc.subjectComorbidityen_US
dc.subjectFemaleen_US
dc.subjectGenital Neoplasms, Femaleen_US
dc.subjectGynecologic Surgical Proceduresen_US
dc.subjectHumansen_US
dc.subjectMiddle Ageden_US
dc.subjectOutcome Assessment (Health Care)en_US
dc.subjectPostoperative Complicationsen_US
dc.subjectPrevalenceen_US
dc.subjectProspective Studiesen_US
dc.subjectRisk Adjustmenten_US
dc.subjectRisk Assessmenten_US
dc.subjectRisk Factorsen_US
dc.subjectUnited Kingdomen_US
dc.titleBenchmarking of surgical complications in gynaecological oncology: prospective multicentre study.en_US
dc.typeArticle
dc.rights.holder© 2016 Royal College of Obstetricians and Gynaecologists
dc.identifier.doi10.1111/1471-0528.13994en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/27006076en_US
pubs.issue13en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume123en_US
dcterms.dateAccepted2015-12-27en_US


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