Department of Surgery, Center for Video-endoscopic Surgery, University of Washington, 1959 NE Pacific Street, Box 356410, Seattle, WA 98195, USA.
Surg Endosc. 2010 Jun;24(6):1296-302. doi: 10.1007/s00464-009-0763-1. Epub 2009 Dec 24.
Persistent, activity-limiting pain after laparoscopic ventral or incisional hernia repair (LVIHR) appears to be related to fixation of the implanted mesh. A randomized study comparing commonly used fixation techniques with respect to postoperative pain and quality of life has not previously been reported.
A total of 199 patients undergoing non-urgent LVIHR in our unit between August 2005 and July 2008 were randomly assigned to one of three mesh-fixation groups: absorbable sutures (AS) with tacks; double crown (DC), which involved two circles of tacks and no sutures; and nonabsorbable sutures (NS) with tacks. All operations were performed by one of two experienced surgeons, who used a standardized technique and the same type of mesh and mesh-fixation materials. The severity of the patients' pain was assessed preoperatively and at 2 weeks, 6 weeks and 3 months postoperatively by using a visual analogue scale (VAS). Quality of life (QoL) was evaluated by administering a standard health survey before and 3 months after surgery. Results in the three groups were compared.
The AS, DC, and NS mesh-fixation groups had similar patient demographic, hernia and operative characteristics. There were no significant differences among the groups in VAS scores at any assessment time or in the change in VAS score from preoperative to postoperative evaluations. The QoL survey data showed a significant difference among groups for only two of the eight health areas analyzed.
In this trial, the three mesh-fixation methods were associated with similar postoperative pain and QoL findings. These results suggest that none of the techniques can be considered to have a pain-reduction advantage over the others. Development of new methods for securing the mesh may be required to decrease the rate or severity of pain after LVIHR.
腹腔镜下腹膜前或切口疝修补术(LVIHR)后持续的、活动受限的疼痛似乎与植入网片的固定有关。以前没有报道过比较常用固定技术的随机研究,涉及术后疼痛和生活质量。
2005 年 8 月至 2008 年 7 月期间,我们单位共对 199 例非紧急性 LVIHR 患者进行了随机分组,分为三组:可吸收缝线(AS)+缝合钉;双冠(DC),涉及两圈缝合钉,无缝线;和不可吸收缝线(NS)+缝合钉。所有手术均由两位经验丰富的外科医生之一进行,他们使用标准化技术和相同类型的网片和网片固定材料。使用视觉模拟评分(VAS)评估术前及术后 2 周、6 周和 3 个月患者疼痛的严重程度。在手术前后进行标准健康调查,评估生活质量(QoL)。比较三组结果。
AS、DC 和 NS 网片固定组患者的人口统计学、疝和手术特征相似。在任何评估时间,三组患者的 VAS 评分或从术前到术后评估的 VAS 评分变化均无显著差异。QoL 调查数据显示,在分析的八个健康领域中,仅两组存在显著差异。
在这项试验中,三种网片固定方法与术后疼痛和生活质量相似。这些结果表明,这些技术都没有在减轻疼痛方面具有优势。可能需要开发新的网片固定方法来降低 LVIHR 后疼痛的发生率或严重程度。