Section of Minimally Invasive Surgery, Department of Surgery, NorthShore Center for Simulation and Innovation, NorthShore University HealthSystem, 2650 Ridge Ave, Evanston, IL, 60201, USA.
Northwestern University Feinberg School of Medicine, Evanston, IL, 60201, USA.
Surg Endosc. 2019 Aug;33(8):2670-2679. doi: 10.1007/s00464-018-6555-8. Epub 2019 Jan 9.
It remains unclear whether use of self-fixating mesh during laparoscopic inguinal hernia repair (LIHR) impacts postoperative quality of life (QoL). We hypothesize patients receiving self-fixating mesh during totally extraperitoneal (TEP) LIHR will report less pain and improved QoL compared to those receiving non-fixating mesh.
An IRB-approved, single-blinded randomized controlled trial was conducted. Patients with primary, unilateral inguinal hernias were randomized to receive either non-fixating (control) or self-fixating mesh. Clinical visits were conducted 3 weeks and 1 year after LIHR. A validated Surgical Outcomes Measurement System (SOMS) instrument was used to assess patients' QoL preoperatively and postoperatively along with Carolinas Comfort Scale (CCS) at 3 weeks and 1 year after surgery. Comparisons between self-fixating and non-fixating mesh groups were made using Chi-square, Wilcoxon rank-sum or independent samples t tests.
Two hundred and seventy patients were enrolled (137 non-fixating vs 133 self-fixating). Preoperatively, there was no difference in mean age, BMI, or median hernia duration between groups (57.9 vs 56.6 years, p = 0.550; 26.1 vs 26.8, p = 0.534; 3.0 vs 3.0 months, p = 0.846). Median operative times (34 vs 34 min, p = 0.545) and LOS were similar. More patients in the non-fixating group received tacks (43 vs 19, p = 0.001). Patients receiving non-fixating mesh recorded better mean SOMS scores for the first 3 days following surgery (Day 1: p = 0.005; Day 2: p = 0.002; Day 3: p = 0.024, Table 1) indicating less pain. No differences in pain were seen 3 weeks or 1 year postoperatively. There were zero recurrences found during clinical follow-up in either of the groups.
Patients receiving self-fixating mesh report worse postoperative pain in the first 2-3 days than those receiving non-fixating mesh. The groups showed no differences across QoL metrics (SOMS and CCS) at 3 weeks or 1 year postoperatively. Self-fixating mesh does not appear to positively impact QoL after TEP LIHR.
目前尚不清楚腹腔镜腹股沟疝修补术(LIHR)中使用自固定网片是否会影响术后生活质量(QoL)。我们假设在完全腹膜外(TEP)LIHR 中接受自固定网片的患者与接受非固定网片的患者相比,疼痛更少,生活质量更高。
一项经 IRB 批准的单盲随机对照试验。将原发性单侧腹股沟疝患者随机分为非固定(对照组)或自固定网片组。LIHR 后 3 周和 1 年进行临床随访。使用经过验证的手术结果测量系统(SOMS)仪器评估患者术前和术后的 QoL,并在术后 3 周和 1 年使用卡罗莱纳舒适度量表(CCS)进行评估。使用卡方检验、Wilcoxon 秩和检验或独立样本 t 检验比较自固定网片组和非固定网片组之间的差异。
共纳入 270 例患者(非固定组 137 例,自固定组 133 例)。术前两组患者的平均年龄、BMI 或中位疝持续时间无差异(57.9 岁 vs 56.6 岁,p=0.550;26.1 岁 vs 26.8 岁,p=0.534;3.0 个月 vs 3.0 个月,p=0.846)。中位手术时间(34 分钟 vs 34 分钟,p=0.545)和 LOS 相似。非固定组中更多的患者使用了钉(43 例 vs 19 例,p=0.001)。接受非固定网片的患者在术后前 3 天的 SOMS 评分平均更高(第 1 天:p=0.005;第 2 天:p=0.002;第 3 天:p=0.024,表 1),提示疼痛较轻。术后 3 周和 1 年时疼痛无差异。两组在临床随访中均未发现复发。
与接受非固定网片的患者相比,接受自固定网片的患者在术后第 2-3 天报告的疼痛更严重。两组在术后 3 周和 1 年的 QoL 指标(SOMS 和 CCS)上均无差异。在 TEP LIHR 后,自固定网片似乎不会对 QoL 产生积极影响。