Department of General, Visceral, Endocrine and Transplant Surgery, Cantonal Hospital of St. Gallen, St. Gallen, Switzerland.
Department of Surgery, Paracelsus Medical University, Salzburg, Austria.
Colorectal Dis. 2021 Oct;23(10):2627-2636. doi: 10.1111/codi.15817. Epub 2021 Sep 4.
This study assessed the impact of a prophylactic, 3D funnel-shaped intraperitoneal mesh on the rate of parastomal hernia after abdominoperineal rectum resection with permanent end colostomy.
Data from 76 patients receiving permanent end colostomy after abdominoperineal rectum resection between 2013 and 2018 were collected retrospectively. Occurrences of parastomal hernia and reoperation rate due to parastomal hernia in patients with and without a prophylactic mesh were compared by univariate, multivariate, and propensity score-adjusted analyses.
Twenty-two (28.9%) of the 76 included patients received a prophylactic mesh. The mean follow-up was 39.3 ± 23.8 months. Mesh implantation reduced the incidence of parastomal hernia to 9.1% (n = 2) compared to 42.6% (n = 23) in patients without a prophylactic mesh. The propensity score-adjusted hazard ratio (HR) was 0.14 (95% confidence interval (CI): 0.04-0.48, p = 0.001). No reoperations due to parastomal hernia were needed in patients who received a prophylactic mesh, while nine patients without mesh (16.7%) required parastomal hernia repair (HR = 0.09, 95% CI: 0.00-1.76, p = 0.015). Mesh implantation was not associated with increased short-term morbidity (Clavien-Dindo grade > 2, 31.8% vs. 40.7%, p = 0.468) or 30-day mortality (4.5% vs. 3.8%, p = 1.000).
Prophylactic implantation of a 3D funnel-shaped intraperitoneal mesh is a safe and effective method to prevent parastomal hernia in patients requiring permanent end colostomy. Mesh placement significantly reduces reoperations due to parastomal hernia.
本研究评估了预防性、3D 漏斗形腹腔内补片对接受经腹会阴直肠切除术后永久性末端结肠造口术患者发生造口旁疝的影响。
回顾性收集了 2013 年至 2018 年间接受经腹会阴直肠切除术后永久性末端结肠造口术的 76 例患者的数据。通过单因素、多因素和倾向评分调整分析比较了有和无预防性补片患者中造口旁疝的发生和因造口旁疝再次手术的发生率。
76 例患者中有 22 例(28.9%)接受了预防性补片。平均随访时间为 39.3±23.8 个月。与未接受预防性补片的患者(42.6%,n=23)相比,补片组的造口旁疝发生率降低至 9.1%(n=2)。倾向评分调整后的风险比(HR)为 0.14(95%置信区间(CI):0.04-0.48,p=0.001)。接受预防性补片的患者无一例因造口旁疝需要再次手术,而未使用补片的 9 例患者(16.7%)需要进行造口旁疝修复(HR=0.09,95%CI:0.00-1.76,p=0.015)。补片植入与短期并发症(Clavien-Dindo 分级>2,31.8%与 40.7%,p=0.468)或 30 天死亡率(4.5%与 3.8%,p=1.000)无关。
预防性植入 3D 漏斗形腹腔内补片是预防接受永久性末端结肠造口术患者发生造口旁疝的一种安全有效的方法。补片放置显著降低了因造口旁疝再次手术的发生率。