Visceral Surgery Department, Limoges University Hospital, Limoges, France.
Univ. Limoges, CNRS, XLIM, UMR 7252, 87000, Limoges, France.
Surg Endosc. 2021 Feb;35(2):702-709. doi: 10.1007/s00464-020-07435-5. Epub 2020 Feb 14.
Biological acellular porcine dermis mesh, such as Permacol™, has been used since 2009 to treat abdominal incisional hernias in a septic context. This study investigated the risk factors for incisional hernia recurrence after biological mesh augmentation.
Over a period of 6 years from February 2009 to February 2015, 68 patients underwent surgery. The mesh was placed intraperitoneally with closure of the anterior fascia in 27 cases (39.7%). The biological mesh was placed in the retromuscular pre-fascial plane in 1 case (1.5%) and pre-aponeurotic plane in 1 case (1.5%). Closure of the anterior fascia was not achieved in 39 cases, including 20 cases in which the mesh was placed intraperitoneally (intraperitoneal bridging group, 29.4%) and 19 cases in which the mesh was placed between the edges of the fascia (inlay bridging group, 27.9%). There were 37 cases of postoperative surgical site infections (54.4%), and Clavien-Dindo morbidity staging indicated stage I-II and III-IV complications in 19.1% and 44.1% of the cases, respectively. The recurrence rate was 61.8%, and the mortality rate was 0%. The rate of recurrence was significantly lower in the «fascia approximated» group (37%), p = 0.001). Univariate analyses of risk factors for procedural failure indicated an increased risk of recurrence in cases of postoperative surgical site infections, complications of Clavien-Dindo grade III or higher, an absent fascial closure in front of the mesh (OR = 8.69), an operating time longer than 180 min, and a VHWG score higher than 2. After logistic regression, the risk factors for recurrence were postoperative infections (OR = 6.2), placement of bridged biological mesh (OR = 22.3), and postoperative morbidity grade III or higher (OR = 16.7).
Patients with postoperative surgical site infections are at an increased risk for recurrence, and bridged mesh placements lack efficacy. Overall, this study challenges the purported advantage of biologics in treating incisional hernia repairs.
自 2009 年以来,Permacol™ 等生物去细胞猪皮网已用于治疗感染环境下的腹部切口疝。本研究调查了生物网增强修补术后切口疝复发的危险因素。
在 2009 年 2 月至 2015 年 2 月的 6 年期间,68 名患者接受了手术。在 27 例(39.7%)中,网片被置于腹膜内,前筋膜关闭。1 例(1.5%)和 1 例(1.5%)将生物网置于肌肉后筋膜前平面和腱膜前平面。39 例未完成前筋膜关闭,其中 20 例网片置于腹膜内(腹膜内桥接组,29.4%),19 例网片置于筋膜边缘之间(内插桥接组,27.9%)。术后发生 37 例手术部位感染(54.4%),Clavien-Dindo 发病率分期显示 19.1%和 44.1%的病例分别为 I-II 期和 III-IV 期并发症。复发率为 61.8%,死亡率为 0%。在“筋膜接近”组(37%),复发率显著降低,p=0.001)。对手术失败危险因素的单因素分析表明,术后手术部位感染、Clavien-Dindo 分级 III 或更高并发症、网片前无筋膜关闭(OR=8.69)、手术时间长于 180 分钟、VHWG 评分高于 2 等情况下,复发风险增加。经逻辑回归分析,复发的危险因素是术后感染(OR=6.2)、桥接生物网放置(OR=22.3)和术后 III 级或更高发病率(OR=16.7)。
术后发生手术部位感染的患者复发风险增加,桥接网片缺乏疗效。总的来说,这项研究对生物制品治疗切口疝修复的所谓优势提出了挑战。