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腹带对腹腔镜切口疝修补术后疼痛的影响——腹腔内补片修补术的多中心、随机先导试验(ABIHR-I)。

The Effect of an Abdominal Binder on Postoperative Pain After Laparoscopic Incisional Hernia Repair–A Multicenter, Randomized Pilot Trial (ABIHR-I) of the Intraperitoneal Onlay-Mesh Technique.

机构信息

Department of General, Abdominal, Vascular, and Transplant Surgery, Magdeburg University Hospital; Center for Obesity and Metabolic Surgery, Helios Hospital Berlin-Buch; Department of General, Visceral, and Cancer Surgery, Helios Hospital Berlin-Buch; Department of Pediatrics, Stanford University, School of Medicine, Stanford, USA; Department of Surgery, Oberhavel Hospital Oranienburg.

出版信息

Dtsch Arztebl Int. 2021 Sep 17;118(37):607-613. doi: 10.3238/arztebl.m2021.0250. Epub 2021 Sep 24.

Abstract

BACKGROUND

Incisional hernias with apertures measuring less than 7 cm can generally be treated adequately with the laparoscopic intraperitoneal onlay-mesh (IPOM) technique. The wearing of an abdominal binder after surgery is often recommended in order to promote wound healing and prevent recurrent herniation. We carried out a multicenter, randomized pilot trial to evaluate the utility of abdominal binders.

METHODS

The trial was conducted from May 2019 to December 2020. Persons with a laparoscopic IPOM procedure for treatment of an incisional hernia were included in the trial and randomized preoperatively (1:1). The patients in the abdominal binder group wore an abdominal binder during the day for 14 days after surgery, while those in the control group wore no binder. The primary endpoint was pain at rest on postoperative days 1, 2, and 14, as measured on a visual analog scale. The secondary endpoints were overall subjective well-being, the rates of wound infection, recurrence, and complications, mobility, and the rate and size of postoperative seromas (on postoperative days 1, 2, and 14).

RESULTS

Forty patients were included. Three were excluded because of conversion to an open surgical technique. The biometric and perioperative data of the abdominal binder group (n = 18) and the control group (n = 19) did not differ to any statistically significant extent. The patients in the binder group had significantly less postoperative pain (F [dfn, dfd]) 4.44, 95% confidence interval [1; 35]; p = 0.042).The patients in the binder group also had better overall subjective well-being and a higher rate of postoperative seroma formation, but these differences did not reach statistical significance. There was less limitation of mobility than in the control group; however, this difference also did not attain statistical significance.

CONCLUSION

An abdominal binder may reduce pain after incisional hernia repair with the IPOM technique. The postoperative use of analgesic medication was not measured.

摘要

背景

对于孔径小于 7cm 的切口疝,通常可以通过腹腔镜腹腔内补片修补术(IPOM)技术进行充分治疗。手术后常建议佩戴腹部束带,以促进伤口愈合和防止复发疝。我们进行了一项多中心、随机试点试验,以评估腹部束带的实用性。

方法

该试验于 2019 年 5 月至 2020 年 12 月进行。将接受腹腔镜 IPOM 手术治疗切口疝的患者纳入试验并进行术前(1:1)随机分组。腹部束带组患者在术后第 1、2 和 14 天白天佩戴腹部束带 14 天,而对照组患者不佩戴束带。主要终点是术后第 1、2 和 14 天静息时的疼痛程度,通过视觉模拟评分法测量。次要终点是整体主观舒适度、伤口感染、复发和并发症的发生率、活动能力以及术后血清肿的发生率和大小(术后第 1、2 和 14 天)。

结果

共纳入 40 例患者,其中 3 例因转为开放手术而被排除。腹部束带组(n=18)和对照组(n=19)的生物统计学和围手术期数据无统计学显著差异。与对照组相比,束带组患者术后疼痛明显减轻(F[dfn,dfd]4.44,95%置信区间[1;35];p=0.042)。束带组患者整体主观舒适度更好,术后血清肿形成率更高,但这些差异无统计学意义。与对照组相比,束带组患者的活动受限程度较低;然而,这种差异也没有达到统计学意义。

结论

在 IPOM 技术修复切口疝后,腹部束带可能会减轻疼痛。未测量术后使用镇痛药的情况。

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