The protective effect of cilostazol on transverse rectus abdominis myocutaneous flap in rats
dc.authorscopusid | 57209119427 | |
dc.authorscopusid | 16024976400 | |
dc.authorscopusid | 16416838000 | |
dc.authorscopusid | 13611402200 | |
dc.contributor.author | Özdemir, Ayfer | |
dc.contributor.author | Orhan, Erkan | |
dc.contributor.author | Altun, Serdar | |
dc.contributor.author | İnözü, Emre | |
dc.date.accessioned | 2022-05-11T14:36:52Z | |
dc.date.available | 2022-05-11T14:36:52Z | |
dc.date.issued | 2017 | |
dc.department | Fakülteler, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Plastik, Rekonstrüktif ve Estetik Cerrahi Ana Bilim Dalı | |
dc.description.abstract | Objective: Transverse Rectus Abdominis Myocutaneous (TRAM) flap is commonly used in breast reconstruction. The aim of this study is to demonstrate the effects of cilostazol on TRAM flap viability in a rat TRAM model. Methods: Twenty-four Wistar rats were used. They were divided into four groups. Rats in Group 1 were applied TRAM flap. In Group 2, cilostazol 30 mg/kg was administered to rats via oral gavage 3 hours before the flap surgery. After the flap surgery, cilostazol 30mg/kg was administered via oral gavage twice a day for 7 days. In Group 3 before the flap surgery, cilostazol 30 mg/kg was administered via oral gavage twice a day for 7 days, and treatment continued for 7 more days after the flap surgery. In Group 4 before the flap surgery, cilostazol 30 mg/kg was administered via oral gavage twice a day for 7 days and treatment was discontinued after the flap surgery. Result: The mean necrosis rate in Group 1 was 41.69%, in Group 2 it was 27.0%, in Group 3 it was 6.66%, and in Group 4 it was 11.2%. The necrosis rate in Group 1 was found to be statistically significantly higher than other groups (p < .01), the necrosis rate in Group 2 was found to be statistically significant higher than Groups 3 and 4 (p < .01), and the necrosis rate in Group 4 was found to be statistically significant higher than Group 3 (p < .01). Conclusion: Cilostazol treatment seemed to increase the viability of TRAM flap, especially when administered as adjuvant therapy. | |
dc.identifier.doi | 10.1080/2000656X.2016.1237958 | |
dc.identifier.endpage | 222 | |
dc.identifier.issn | 2000-656X | |
dc.identifier.issn | 2000-6764 | |
dc.identifier.issue | 3 | en_US |
dc.identifier.pmid | 27707079 | |
dc.identifier.scopus | 2-s2.0-84990174347 | |
dc.identifier.scopusquality | Q2 | |
dc.identifier.startpage | 217 | |
dc.identifier.uri | https://doi.org/10.1080/2000656X.2016.1237958 | |
dc.identifier.uri | https://hdl.handle.net/20.500.11776/8450 | |
dc.identifier.volume | 51 | |
dc.identifier.wos | WOS:000401517600011 | |
dc.identifier.wosquality | Q4 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.indekslendigikaynak | PubMed | |
dc.institutionauthor | Orhan, Erkan | |
dc.language.iso | en | |
dc.publisher | Taylor & Francis Ltd | |
dc.relation.ispartof | Journal of Plastic Surgery and Hand Surgery | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | TRAM flap | |
dc.subject | cilostazol | |
dc.subject | flap viability | |
dc.subject | Endothelial Growth-Factor | |
dc.subject | Tram Flap | |
dc.subject | Musculocutaneous Flap | |
dc.subject | Intermittent Claudication | |
dc.subject | Model | |
dc.subject | Reconstruction | |
dc.subject | Inhibitor | |
dc.subject | Viability | |
dc.subject | Ischemia | |
dc.subject | Flow | |
dc.title | The protective effect of cilostazol on transverse rectus abdominis myocutaneous flap in rats | |
dc.type | Article |
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