2-octyl cyanoacrylate with interrupted sutures vs continuous suturing in adult male circumcision
A randomized controlled pilot trial
DOI:
https://doi.org/10.5489/cuaj.9692Keywords:
Adult circumcision, Wound closure, 2-octyl cyanoacrylate, Continuous sutures, Randomized controlled trialAbstract
Introduction: This randomized controlled pilot study evaluated the use of 2-octyl cyanoacrylate (2-OCA) combined with four interrupted sutures vs. continuous suturing for wound closure in adult male circumcision. While continuous sutures are the current standard at the Men’s Health Clinic Manitoba, 2-OCA has demonstrated superior results in the context of cosmesis, postoperative pain, and operative time, as shown in pediatric populations. The primary objective was to assess cosmetic satisfaction. Secondary outcomes included operative time, postoperative pain, and complications.
Methods: A non-blinded, randomized controlled pilot study was conducted at a single ambulatory urology surgical center. Twenty patients undergoing circumcision were randomly assigned to receive either 2-OCA with four interrupted sutures or continuous suturing for wound closure. Data collected included demographic information, intraoperative time, postoperative pain, adverse events, and cosmetic satisfaction at six and 12 weeks.
Results: Cosmetic satisfaction at six and 12 weeks was similar between groups, both with a median of 5 (highly satisfied). Mean procedure time was shorter in the 2-OCA group compared to the continuous suture group (28.7 vs. 34.3 min, p=0.037). Postoperative pain was low in both groups and did not differ significantly; however, wound dehiscence occurred in 50% of 2-OCA cases, prompting early study termination.
Conclusions: Although 2-OCA with interrupted sutures may offer faster procedures and comparable cosmetic results, the observed complications do not support its routine use in adult circumcision. Larger, blinded trials are needed to further evaluate the safety of tissue adhesives and address current study limitations, including small sample size, non-blinded design, and reliance on patient-reported outcomes.
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