Oncoplastic Breast-Conserving Surgery in Iceland: A Population-Based Study

dc.contributorHáskóli Íslands (HÍ)en_US
dc.contributorUniversity of Iceland (UI)en_US
dc.contributor.authorPálsdóttir, Edda
dc.contributor.authorLund, Sigrún Helga
dc.contributor.authorÁsgeirsson, Kristján Skúli
dc.contributor.departmentFaculty of Medicine (UI)en_US
dc.contributor.departmentLæknadeild (HÍ)en_US
dc.contributor.schoolHeilbrigðisvísindasvið (HÍ)en_US
dc.contributor.schoolSchool of Health Sciences (UI)en_US
dc.date.accessioned2020-01-24T13:54:31Z
dc.date.available2020-01-24T13:54:31Z
dc.date.issued2018-05-14
dc.descriptionPublisher's version (útgefin grein).en_US
dc.description.abstractBackground and Aims: In Iceland, oncoplastic breast-conservation surgery has been performed since 2008. The aim of this population-based study was to assess and compare the efficacy and patient satisfaction of standard breast-conservation surgery with oncoplastic breast-conservation surgery. Materials and methods: This is a population-based, retrospective, observational cohort study on all women undergoing breast-conservation surgery in Iceland from the 1 January 2008 to 31 December 2014. A multivariate logistic regression and linear regression were performed to assess differences in outcomes and a patient satisfaction questionnaire was used to assess certain patient-related outcome measures. Results and conclusion: A total of 750 women underwent breast-conserving surgery, 665 had standard breast-conservation surgery and 85 oncoplastic breast-conservation surgery. Oncoplastic breast-conservation surgery was associated with a significantly larger mean size (2.4 cm vs 1.7 cm, p < 0.001) and weight (181.8 g vs 63.4 g, p < 0.001) of breast specimen excised when compared to standard breast-conservation surgery. After correcting for confounding factors, there was no significant difference in surgical margin involvement (odds ratio = 0.97, confidence interval = 0.44–1.97), frequency of complications (odds ratio = 1.06, confidence interval = 0.46–2.18), frequency of reoperations (odds ratio = 0.98; confidence interval = 0.50–1.81), or time to first adjuvant therapy (–0.23 days for oncoplastic breast-conservation surgery, p = 0.95). Patient satisfaction was high in both groups, although not statistically different (96% in oncoplastic breast-conservation surgery group vs 89% in the standard breast-conservation surgery group, p = 0.84). Our results show that oncoplastic breast-conservation surgery is at least as safe as standard breast-conservation surgery in selected cases and may be preferable in ductal carcinoma in situ.en_US
dc.description.sponsorshipThe author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: The study was funded by Vísindasjóður Landspítalans (Landspítali University Hospital research fund).en_US
dc.description.versionPeer Revieweden_US
dc.format.extent224-229en_US
dc.identifier.citationPalsdottir, E. P., Lund, S. H. L., & Asgeirsson, K. S. A. (2018). Oncoplastic Breast-Conserving Surgery in Iceland: A Population-Based Study. Scandinavian Journal of Surgery, 107(3), 224–229. https://doi.org/10.1177/1457496918766686en_US
dc.identifier.doi10.1177/1457496918766686
dc.identifier.issn1457-4969
dc.identifier.issn1799-7267 (eISSN)
dc.identifier.journalScandinavian Journal of Surgeryen_US
dc.identifier.urihttps://hdl.handle.net/20.500.11815/1466
dc.language.isoenen_US
dc.publisherSAGE Publicationsen_US
dc.relation.ispartofseriesScandinavian Journal of Surgery;107(3)
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBreasten_US
dc.subjectCanceren_US
dc.subjectSurgeryen_US
dc.subjectOncoplasticen_US
dc.subjectBreast conservationen_US
dc.subjectDuctal carcinoma in situen_US
dc.subjectPopulationen_US
dc.subjectBrjóstaaðgerðiren_US
dc.subjectKrabbameinen_US
dc.titleOncoplastic Breast-Conserving Surgery in Iceland: A Population-Based Studyen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dcterms.license© The Finnish Surgical Society 2018 Creative Commons Attribution Non-Commercial Licenseen_US

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