Show simple item record

dc.contributor.authorEkinci, Mürsel
dc.contributor.authorÇiftçi, Bahadır
dc.contributor.authorÇelik, Erkan Cem
dc.contributor.authorKarakaya, Muhammet Ahmet
dc.contributor.authorDemiraran, Yavuz
dc.date.accessioned10.07.201910:49:13
dc.date.accessioned2019-07-10T19:49:38Z
dc.date.available10.07.201910:49:13
dc.date.available2019-07-10T19:49:38Z
dc.date.issued2019
dc.identifier.citationEkinci, M., Çiftçi, B., Çelik, E. C., Karakaya, M. A. ve Demiraran, Y. (2019). The efficacy of different volumes on ultrasound-guided type-I pectoral nerve block for postoperative analgesia after subpectoral breast augmentation: a prospective, randomized, controlled study. Aesthetic Plastic Surgery, 43(2), 297-304. https://dx.doi.org/10.1007/s00266-019-01322-8en_US
dc.identifier.issn0364-216X
dc.identifier.issn1432-5241
dc.identifier.urihttps://dx.doi.org/10.1007/s00266-019-01322-8
dc.identifier.urihttps://hdl.handle.net/20.500.12511/1691
dc.descriptionWOS: 000461390200002en_US
dc.descriptionPubMed ID: 30756142en_US
dc.description.abstractBackgroundPECS type-1 block, a US-guided superficial interfacial block, provides effective analgesia after breast surgery. Aesthetic breast augmentation is one of the most common surgical procedures in plastic surgery. Subpectoral prostheses cause severe pain. The aim of this study was to investigate the effect of different volumes of the solution on the efficacy of PECS type-I block for postoperative analgesia after breast augmentation surgery. MethodsNinety ASA status I-II female patients aged between 18 and 65years who scheduled breast augmentation surgery under general anesthesia were included in this study. The patients were randomly divided into three groups of 30 patients each (Group 20=20ml of anaesthetic solution, Group 30=30ml anaesthetic solution, and Group K=Control group). Postoperative assessment was performed using the VAS score. The VAS scores were recorded postoperatively at 1, 2, 4, 8, 16 and 24h.ResultsFentanyl consumption was statistically significantly lower in Group 20 and Group 30 compared to the Control group (p<0.05). There was no statistically significant difference in fentanyl consumption between Group 20 and Group 30. The right and left VAS scores were statistically significantly lower in Groups 20 and 30 than in the Control group (p<0.05). There was no statistical difference in terms of VAS scores between Group 20 and Group 30. The use of rescue analgesia was statistically lower in Groups 20 and 30.ConclusionsPECS type-1 block using 20ml of 0.25% bupivacaine can provide effective analgesia after breast augmentation surgery.Level of Evidence IVThis journal requires that authors assign a level of evidence to each article. For a full description of these evidence-based medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266.en_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectPECS Type-1 Blocken_US
dc.subjectBreast Augmentationen_US
dc.subjectPostoperative Analgesiaen_US
dc.titleThe efficacy of different volumes on ultrasound-guided type-I pectoral nerve block for postoperative analgesia after subpectoral breast augmentation: a prospective, randomized, controlled studyen_US
dc.typearticleen_US
dc.relation.journalAesthetic Plastic Surgeryen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Anesteziyoloji ve Reanimasyon Ana Bilim Dalıen_US
dc.authorid0000-0002-3245-6614en_US
dc.authorid0000-0002-5580-5960en_US
dc.authorid0000-0003-0811-4945en_US
dc.identifier.volume43en_US
dc.identifier.issue2en_US
dc.identifier.startpage297en_US
dc.identifier.endpage304en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1007/s00266-019-01322-8en_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record