Randomized clinical trial comparing skin closure with tissue adhesives <i>vs </i>subcuticular suture after robotic urogynecologic procedures
Sunetris Fluellen, Kyle Mackey, Karen Hagglund, Muhammad Faisal Aslam
Abstract
BACKGROUND: may be a comparable and safe option for port site closure as compared with subcuticular suture. In this randomized clinical trial, we hypothesized that operative time for skin closure would be less than subcuticular suture during robotic urogynecologic procedures. AIM: To compare skin closure during robotic urogynecologic surgeries for tissue adhesives and subcuticular suture. METHODS: = 25). All procedures and postoperative evaluations were performed by the same board certified Female Pelvic Medicine and Reconstructive Surgeon. Incisional closure time was recorded. Each subject was followed for 12-wk postoperatively. Incision cosmesis was evaluated using the Stony Brook Scar Evaluation Scale. RESULTS: = 0.234, respectively). No statistical demographical differences existed between the two study arms. CONCLUSION: Our study supported our original hypothesis that cyanoacrylate tissue adhesive for port site closure during robotic urogynecolgic procedures uses less time than with subcuticular suture. Our study also supports that tissue adhesive is comparable to cosmetic outcome while not jeopardizing rates of bleeding, infection, or dehiscence.