腹腔镜腹股沟疝气修补术中 N-丁基-2-氰基丙烯酸酯粘合剂与可吸收钉:多中心随机临床试验

C. Petro, B. Poulose, M. Rosen, A. Carbonell, A. G. El-Ghazzawy, J. Warren, E. Lo Menzo, A. Prabhu, D. Krpata, S. Szomstein, Vimal K. Narula, Crystal F. Totten, Kelly R. Haisley, Andrew C. Bernard, Henrik O. Berdel, Jessica K. Reynolds, Zachary D. Warriner, J. S. Roth
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Roth","doi":"10.1097/as9.0000000000000462","DOIUrl":null,"url":null,"abstract":"\n \n We aimed to determine whether n-butyl-2-cyanoacrylate (NB2C) adhesive is a safe and effective mechanism for nonpenetrating mesh and peritoneal fixation during laparoscopic groin hernia repair.\n \n \n \n Chronic pain after laparoscopic groin hernia repair has been associated with penetrating fixation, but there had been no US Food and Drug Administration–approved devices for nonpenetrating fixation in this context.\n \n \n \n Patients undergoing laparoscopic transabdominal preperitoneal (TAP) or totally extraperitoneal (TEP) groin hernia repair with mesh at 1 of 5 academic medical centers were randomized to mesh (TAP/TEP) and peritoneal (TAP) fixation with NB2C adhesive or absorbable tacks. The primary outcome was improvement in pain (visual analog scale [VAS]) at 6 months. The noninferiority margin was 0.9 (α = 0.025; β = 80%). 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引用次数: 0

摘要

我们的目的是确定在腹腔镜腹股沟疝修补术中,2-氰基丙烯酸正丁酯(NB2C)粘合剂是否是一种安全有效的非穿透性网片和腹膜固定机制。 腹腔镜腹股沟疝修补术后的慢性疼痛与穿透性固定有关,但在这种情况下还没有美国食品药品管理局批准的非穿透性固定装置。 在 5 家学术医疗中心中的 1 家接受腹腔镜经腹膜前 (TAP) 或全腹膜外 (TEP) 腹股沟疝修补术的患者随机接受了网片固定(TAP/TEP)和使用 NB2C 粘合剂或可吸收大头针进行腹膜固定(TAP)。主要结果是6个月时疼痛(视觉模拟量表[VAS])的改善情况。非劣效度为 0.9(α = 0.025;β = 80%)。复发、成功使用设备、生活质量和不良事件(AEs)发生率是次要结果。 从2019年到2021年,284名患者被随机分配到NB2C粘合剂或可吸收粘合剂中(n = 142/142)。患者和疝气特征具有可比性,65%的患者采用TAP方法进行了修复。在意向性治疗分析和按协议分析中,NB2C 粘合剂在 6 个月时的 VAS 改善差异不劣于可吸收粘合剂(0.25 [95% CI, -0.33 to 0.82]; P = 0.013; 0.22 [95% CI, -0.36 to 0.80], noninferiority P = 0.011)。在复发、成功使用每种装置固定网片和腹膜、生活质量和其他 VAS 疼痛评分等次要结果方面没有差异。不良反应和严重不良反应的发生率也相当。 NB2C粘合剂在腹腔镜腹股沟疝修补术中用于网片固定和腹膜闭合是安全有效的。
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N-Butyl-2-Cyanoacrylate Adhesive Versus Absorbable Tacks in Laparoscopic Groin Hernia Repair: A Multicenter Randomized Clinical Trial
We aimed to determine whether n-butyl-2-cyanoacrylate (NB2C) adhesive is a safe and effective mechanism for nonpenetrating mesh and peritoneal fixation during laparoscopic groin hernia repair. Chronic pain after laparoscopic groin hernia repair has been associated with penetrating fixation, but there had been no US Food and Drug Administration–approved devices for nonpenetrating fixation in this context. Patients undergoing laparoscopic transabdominal preperitoneal (TAP) or totally extraperitoneal (TEP) groin hernia repair with mesh at 1 of 5 academic medical centers were randomized to mesh (TAP/TEP) and peritoneal (TAP) fixation with NB2C adhesive or absorbable tacks. The primary outcome was improvement in pain (visual analog scale [VAS]) at 6 months. The noninferiority margin was 0.9 (α = 0.025; β = 80%). Recurrence, successful use of the device, quality of life, and rates of adverse events (AEs) were secondary outcomes. From 2019 to 2021, 284 patients were randomized to either NB2C adhesive or absorbable tacks (n = 142/142). Patient and hernia characteristics were comparable, and 65% were repaired using a TAP approach. The difference in VAS improvement at 6 months with NB2C adhesive was not inferior to absorbable tacks in intention-to-treat and per-protocol analyses, respectively (0.25 [95% CI, −0.33 to 0.82]; P = 0.013; 0.22 [95% CI, −0.36 to 0.80], noninferiority P = 0.011). There were no differences in secondary outcomes including recurrence, successful use of each device to fixate the mesh and peritoneum, quality of life, and additional VAS pain scores. Rates of adverse and serious AEs were also comparable. NB2C adhesive is safe and effective for mesh fixation and peritoneal closure during laparoscopic groin hernia repair.
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