Keller Funnel Efficacy in No Touch Breast Augmentation and Reconstruction: A Systematic Review

dc.contributor.authorMorkuzu, Suat
dc.contributor.authorOzdemir, Mehmet
dc.contributor.authorLeach, Garrison A. A.
dc.contributor.authorKanapathy, Muholan
dc.contributor.authorMosahebi, Afshin
dc.contributor.authorReid, Chris M. M.
dc.date.accessioned2024-04-24T17:08:16Z
dc.date.available2024-04-24T17:08:16Z
dc.date.issued2022
dc.departmentDicle Üniversitesien_US
dc.description.abstractBackground:Breast augmentation is one of the most common aesthetic surgical procedures. Tissue expansion followed by permanent implants is the most frequent postmastectomy breast reconstruction method. Implant contamination remains a critical problem with these procedures, resulting in acute infection as well as capsular contracture. To reduce the risk of implant contamination, the no-touch technique utilizing the Keller funnel has been adopted by many surgeons. This systematic review aims to investigate the advantages of the Keller funnel method for breast augmentation-reconstruction. Methods:A systematic review of PubMed, Embase, the Cochrane database, and Google Scholar was performed between 2005 and 2021. All clinical-based, retrospective and prospective studies utilizing the Keller funnel method for breast implant insertion were selected. Results:Six studies were identified for evaluation: five were retrospective cohorts and one was a prospective trial. No randomized controlled trials were found. Outcomes reported included lower rates of capsular contracture (RR, 0.42; P = 0.0006; 95% CI, 0.25-0.69), shorter incision lengths (35.5 +/- 2.1 mm), less insertion time (mean = 6 seconds), and decreased complications, and one paper reported ultimately greater patient satisfaction with outcomes (BREAST-Q Score: 92%). Conclusions:This review suggests that the Keller funnel is a useful method for no-touch breast augmentation and reconstruction surgery. The Keller funnel reduces subsequent capsular contracture rate, surgical time, and incision length and allows for easier insertion. However, our findings support recommendation of a prospective randomized controlled clinical trial with larger population size and follow-up intervals.en_US
dc.identifier.doi10.1097/GOX.0000000000004676
dc.identifier.issn2169-7574
dc.identifier.issue11en_US
dc.identifier.pmid36448016
dc.identifier.scopus2-s2.0-85149628178
dc.identifier.scopusqualityQ2
dc.identifier.urihttps://doi.org/10.1097/GOX.0000000000004676
dc.identifier.urihttps://hdl.handle.net/11468/17280
dc.identifier.volume10en_US
dc.identifier.wosWOS:000891161300003
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoenen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.relation.ispartofPlastic and Reconstructive Surgery-Global Open
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subject[No Keyword]en_US
dc.titleKeller Funnel Efficacy in No Touch Breast Augmentation and Reconstruction: A Systematic Reviewen_US
dc.titleKeller Funnel Efficacy in No Touch Breast Augmentation and Reconstruction: A Systematic Review
dc.typeReview Articleen_US

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