Pain and convalescence following laparoscopic ventral hernia repair.

Danish medical bulletin Pub Date : 2011-12-01
Jens Ravn Eriksen
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In Study I - a prospective descriptive study - 35 patients were prospectively included and underwent LVHR. Scores of pain, quality of life, convalescence, fatigue, and general well-being were obtained from each patient. Follow-up was six months. Average pain from postoperative day (POD) 0-2 and POD 0-6 measured on a 0-100 mm visual analogue scale (VAS) was 61 and 48, respectively. Pain scores reached preoperative values at POD 30. The incidence of severe chronic pain was 7%. No parameter predicted postoperative pain significantly. Significant correlations were found between pain, and general well-being (rS= -0.8, p < 0.001), satisfaction (rS= -0.67, p < quality of life score (rS= -0.63, p < 0.001) six months postoperatively. Patients resumed normal daily activity at POD 14. In Study II - a randomised experimental study in pigs - nine pigs were operated laparoscopically with insertion of two different meshes fixed with either FS or tacks. All pigs were euthanized on POD 30. The primary outcome parameter was strength of ingrowth between the mesh and the anterior abdominal wall. A mechanical peel test was performed for each tissue sample. The secondary outcome parameters were grade and strength of adhesions to the mesh, shrinkage and displacement/folding of the mesh and histological parameters. All nine pigs survived without complications until sacrifice. No meshes were displaced from their initial position at autopsy, but in two cases mesh folding was observed. No significant difference in strength of ingrowth was found between different fixation methods or mesh types. Furthermore, no significant difference was found in grade or strength of adhesions or any histological parameters. In Study III - a randomised, controlled, double-blinded, multicenter trial - 40 patients with umbilical hernia defects between 1.5-5 cm, were randomly assigned to receive FS or titanium tacks for mesh fixation in LVHR. Patients, care givers and those assessing the outcomes were blinded to group assignment. The primary outcome was average pain from POD 0-2 (VAS score). Secondary outcome parameters were fatigue, general well-being and time to resume normal daily activity. Follow-up was one month for all. Patients in the FS group reported significantly less pain at POD 0-2 (median VAS 38 (range 6-98) vs. 60 (18-96), p = 0.01). Absolute VAS score difference between groups was 20 mm (95% CI 4-35 mm) at activity, and 19 mm (95% CI 3-34 mm) at rest. Patients in the FS group reported significantly less discomfort from POD 0-2 and POD 0-10, compared with the tack group. No significant difference was found in fatigue score between groups. No significant difference in hospital stay, hernia diameter, or morphine consumption in the post anesthesia care unit was found between groups. Patients in the FS group resumed normal daily activity at POD 7 (1-66) versus POD 18 (1-95) in the tack group (p = 0.03). 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引用次数: 0

Abstract

Severe pain is usual after laparoscopic ventral hernia repair (LVHR). Mesh fixation with titanium tacks may play a key role in the development of acute and chronic pain and alternative fixation methods should therefore be investigated. This PhD thesis was based on three studies and aimed too: 1) assess the intensity and impact of postoperative pain by detailed patient-reported description of pain and convalescence after LVHR (Study I), 2) evaluate the feasibility of fibrin sealant (FS) for mesh fixation in an experimental pig model (Study II), and 3) investigate FS vs. tacks for mesh fixation in LVHR in a randomised, double-blinded, clinical controlled study with acute postoperative pain as the primary outcome (Study III). In Study I - a prospective descriptive study - 35 patients were prospectively included and underwent LVHR. Scores of pain, quality of life, convalescence, fatigue, and general well-being were obtained from each patient. Follow-up was six months. Average pain from postoperative day (POD) 0-2 and POD 0-6 measured on a 0-100 mm visual analogue scale (VAS) was 61 and 48, respectively. Pain scores reached preoperative values at POD 30. The incidence of severe chronic pain was 7%. No parameter predicted postoperative pain significantly. Significant correlations were found between pain, and general well-being (rS= -0.8, p < 0.001), satisfaction (rS= -0.67, p < quality of life score (rS= -0.63, p < 0.001) six months postoperatively. Patients resumed normal daily activity at POD 14. In Study II - a randomised experimental study in pigs - nine pigs were operated laparoscopically with insertion of two different meshes fixed with either FS or tacks. All pigs were euthanized on POD 30. The primary outcome parameter was strength of ingrowth between the mesh and the anterior abdominal wall. A mechanical peel test was performed for each tissue sample. The secondary outcome parameters were grade and strength of adhesions to the mesh, shrinkage and displacement/folding of the mesh and histological parameters. All nine pigs survived without complications until sacrifice. No meshes were displaced from their initial position at autopsy, but in two cases mesh folding was observed. No significant difference in strength of ingrowth was found between different fixation methods or mesh types. Furthermore, no significant difference was found in grade or strength of adhesions or any histological parameters. In Study III - a randomised, controlled, double-blinded, multicenter trial - 40 patients with umbilical hernia defects between 1.5-5 cm, were randomly assigned to receive FS or titanium tacks for mesh fixation in LVHR. Patients, care givers and those assessing the outcomes were blinded to group assignment. The primary outcome was average pain from POD 0-2 (VAS score). Secondary outcome parameters were fatigue, general well-being and time to resume normal daily activity. Follow-up was one month for all. Patients in the FS group reported significantly less pain at POD 0-2 (median VAS 38 (range 6-98) vs. 60 (18-96), p = 0.01). Absolute VAS score difference between groups was 20 mm (95% CI 4-35 mm) at activity, and 19 mm (95% CI 3-34 mm) at rest. Patients in the FS group reported significantly less discomfort from POD 0-2 and POD 0-10, compared with the tack group. No significant difference was found in fatigue score between groups. No significant difference in hospital stay, hernia diameter, or morphine consumption in the post anesthesia care unit was found between groups. Patients in the FS group resumed normal daily activity at POD 7 (1-66) versus POD 18 (1-95) in the tack group (p = 0.03). No recurrences were observed. No adverse events or side effects were observed. No significant differences in predefined complications were found between groups. In conclusion, pain is a significant clinical problem after LVHR with impact on general well-being, quality of life and patient satisfaction. This issue must have first priority in future ventral hernia repair research. It is now documented, that the simple application of fibrin glue instead of titanium tacks for mesh fixation in LVHR of defects < 5 cm significantly reduced acute pain, discomfort and the period of convalescence. Long-term follow-up will show the value of FS fixation in terms of chronic pain and recurrence. As FS potentially may solve many of the outcome problems associated with LVHR, future studies should include larger hernia defects including large incisional hernias, as the operative technique may be different.

腹腔镜腹疝修补术后的疼痛与康复。
重度疼痛是腹腔镜腹疝修复(LVHR)后常见的。钛钉网状固定可能在急性和慢性疼痛的发展中起关键作用,因此应该研究其他固定方法。这篇博士论文基于三项研究,目的也是:1)通过详细的患者报告的LVHR后疼痛和康复描述来评估术后疼痛的强度和影响(研究I), 2)评估纤维蛋白密封剂(FS)在实验猪模型中用于网状固定的可行性(研究II),以及3)在随机、双盲的LVHR中研究FS与钉钉的网状固定。以急性术后疼痛为主要结局的临床对照研究(研究III)。研究I是一项前瞻性描述性研究,前瞻性纳入35例患者并行LVHR。对每位患者进行疼痛评分、生活质量评分、康复评分、疲劳评分和总体幸福感评分。随访6个月。术后0-100 mm视觉模拟评分(VAS) 0-2和0-6日均疼痛分别为61和48。POD 30时疼痛评分达到术前值。重度慢性疼痛发生率为7%。没有参数能显著预测术后疼痛。术后6个月疼痛与总体幸福感(rS= -0.8, p < 0.001)、满意度(rS= -0.67, p <生活质量评分(rS= -0.63, p < 0.001)存在显著相关性。患者在POD 14恢复正常的日常活动。在第二项研究中——一项猪的随机实验研究——9头猪接受腹腔镜手术,植入两种不同的网片,用FS或大头针固定。所有猪均在POD 30上实施安乐死。主要结局参数是补片与前腹壁之间的生长强度。对每个组织样本进行机械剥离试验。次要结局参数是网片粘附的等级和强度,网片的收缩和位移/折叠以及组织学参数。所有9头猪在祭祀前都没有出现并发症。解剖时没有网格从初始位置移位,但在两例中观察到网格折叠。不同固定方式和网片类型间长入强度无显著差异。此外,在粘连的等级或强度或任何组织学参数上没有发现显著差异。研究III是一项随机、对照、双盲、多中心试验,40名脐疝缺陷在1.5-5厘米之间的患者被随机分配接受FS或钛钉用于LVHR的补片固定。患者、护理人员和评估结果的人员对小组分配不知情。主要终点为POD 0-2的平均疼痛(VAS评分)。次要结局参数是疲劳、总体幸福感和恢复正常日常活动的时间。随访时间为一个月。FS组患者在POD 0-2时报告的疼痛明显减轻(VAS中位数38(范围6-98)比60 (18-96),p = 0.01)。两组间的绝对VAS评分差异在活动时为20 mm (95% CI 4-35 mm),在休息时为19 mm (95% CI 3-34 mm)。与tack组相比,FS组患者报告POD 0-2和POD 0-10的不适明显减少。各组间疲劳评分无显著差异。两组间在住院时间、疝直径或麻醉后护理单元吗啡用量方面无显著差异。FS组患者在POD 7(1-66)恢复正常的日常活动,而tack组患者在POD 18(1-95)恢复正常活动(p = 0.03)。未见复发。未观察到不良事件或副作用。两组间预诊并发症无显著差异。总之,疼痛是LVHR术后显著的临床问题,影响患者的总体幸福感、生活质量和满意度。这一问题在今后腹疝修补研究中必须优先考虑。目前有文献报道,在缺陷< 5 cm的LVHR中,简单应用纤维蛋白胶代替钛钉进行补片固定,可显著减少急性疼痛、不适和恢复期。长期随访将显示FS固定在慢性疼痛和复发方面的价值。由于FS可能解决LVHR相关的许多预后问题,由于手术技术可能不同,未来的研究应包括更大的疝缺陷,包括大切口疝。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Danish medical bulletin
Danish medical bulletin 医学-医学:内科
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