Department of Surgery, Vanderbilt University Medical Center, 1161 21St Avenue South, D-5203 Medical Center North, Nashville, TN, 37232, USA.
Institute for Health Technologies and Interventions, Weill Cornell College of Medicine, New York, NY, USA.
Surg Endosc. 2023 Jul;37(7):5583-5590. doi: 10.1007/s00464-022-09739-0. Epub 2022 Nov 1.
Use of macroporous synthetic mesh in contaminated ventral hernia repair has become more frequent. The objective of this study is to compare the outcomes of ventral incisional hernia repair with permanent synthetic mesh in contaminated fields to those in a clean field.
The Abdominal Core Health Quality Collaborative registry, a prospectively updated longitudinal hernia-specific national database, was retrospectively queried for adults who underwent open ventral incisional hernia repair using light or medium-weight synthetic mesh and classified as clean (CDC Class I) or contaminated (CDC Class II/III). Univariate analysis was used to compare demographic information, hernia characteristics, and operative details. Odds ratios (OR) were calculated using multivariable logistic regression for the primary outcome of 30-day surgical site infection (SSI) and secondary outcomes of 30-day surgical site occurrence (SSO), SSO requiring procedural intervention (SSO-PI), and clinical recurrence at one year.
7219 cases met criteria for inclusion; 13.2% of these were contaminated. 83.4% of patients had follow-up data at 30 days and 20.8% at 1 year. The adjusted OR for 30-day SSI in contaminated fields compared to clean was 2.603 (95% CI 1.959-3.459). OR for 30-day SSO was 1.275 (95% CI 1.017-1.600) and 2.355 (95%CI 1.817-3.053) for 30-day SSO-PI. OR for recurrence at one year was 1.489 (95%CI 0.892-2.487). Contaminated cases had higher rates of mesh infection (3.9% vs 0.8%, p < 0.001) and mesh removal (7.3 vs 2.5%, p < 0.001) at 1 year.
After adjusting for baseline differences, patients undergoing ventral incisional hernia repair using light or midweight synthetic mesh in contaminated fields have higher odds of 30-day SSI, SSO, and SSO-PI than those performed in clean wounds. The odds of recurrence did not statistically differ and further studies with long-term outcomes are needed to better evaluate the best treatment options for this patient population.
在污染的腹侧疝修复中使用大孔合成网的情况越来越多。本研究的目的是比较污染场和清洁场使用永久性合成网进行腹侧切口疝修复的结果。
腹核心健康质量协作注册处是一个前瞻性更新的纵向疝特异性国家数据库,对使用轻或中重量合成网进行开放腹侧切口疝修复的成年人进行了回顾性查询,并分为清洁(CDC Ⅰ级)或污染(CDC Ⅱ/Ⅲ级)。使用单变量分析比较人口统计学信息、疝特征和手术细节。使用多变量逻辑回归计算 30 天手术部位感染(SSI)的主要结局和次要结局的比值比(OR),包括 30 天手术部位事件(SSO)、需要手术干预的 SSO(SSO-PI)和 1 年临床复发。
7219 例符合纳入标准;其中 13.2%为污染。83.4%的患者在 30 天和 20.8%在 1 年有随访数据。与清洁场相比,污染场 30 天 SSI 的调整 OR 为 2.603(95%CI 1.959-3.459)。30 天 SSO 的 OR 为 1.275(95%CI 1.017-1.600),30 天 SSO-PI 的 OR 为 2.355(95%CI 1.817-3.053)。1 年复发的 OR 为 1.489(95%CI 0.892-2.487)。污染病例在 1 年时的网感染率(3.9%比 0.8%,p<0.001)和网去除率(7.3%比 2.5%,p<0.001)更高。
在调整基线差异后,在污染部位使用轻或中重量合成网进行腹侧切口疝修复的患者,其 30 天 SSI、SSO 和 SSO-PI 的发生几率高于在清洁伤口中进行手术的患者。复发的几率没有统计学差异,需要进一步进行长期结局的研究,以更好地评估该患者群体的最佳治疗选择。