Cleveland Clinic Center for Abdominal Core Health, Digestive Diseases and Surgery Institute, Cleveland Clinic, The Cleveland Clinic Foundation, Cleveland, Ohio.
Comprehensive Hernia Center, Department of Surgery, University of South Carolina School of Medicine Greenville, Greenville.
JAMA Surg. 2020 May 1;155(5):380-387. doi: 10.1001/jamasurg.2020.0034.
Despite rapid adoption of the robotic platform for inguinal hernia repair in the US, to date, no level I trials have ever compared robotic inguinal hernia repair to laparoscopic repair. This multicenter randomized clinical trial is the first to compare the robotic platform to laparoscopic approach for minimally invasive inguinal hernia repair.
To determine whether the robotic approach to inguinal hernia repair results in improved postoperative outcomes compared with traditional laparoscopic inguinal hernia repairs.
DESIGN, SETTING, AND PARTICIPANTS: This multicenter, single-blinded, prospective randomized clinical pilot study was conducted from April 2016 to April 2019, with a follow-up duration of 30 days in 6 academic and academic-affiliated sites. Enrolled in this study were 113 patients with a unilateral primary or recurrent inguinal hernia. After exclusions 102 remained for analysis.
Standard laparoscopic transabdominal preperitoneal repair or robotic transabdominal preperitoneal repair.
Main outcomes included postoperative pain, health-related quality of life, mobility, wound morbidity, and cosmesis. Secondary outcomes included cost, surgeon ergonomics, and surgeon mental workload. A primary outcome was not selected because this study was designed as a pilot study. The hypothesis was formulated prior to data collection.
A total of 102 patients were included in the study (54 in the laparoscopic group, mean [SD] age, 57.2 [13.3] years and 48 [88.9%] male; 48 in the robotic group, mean [SD] age, 56.1 [14.1] years and 44 [91.6%] male). There were no differences at the preoperative, 1-week, or 30-day points between the groups in terms of wound events, readmissions, pain as measured by the Visual Analog Scale, or quality of life as measured by the 36-Item Short Form Health Survey. Compared with traditional laparoscopic inguinal hernia repair, robotic transabdominal preperitoneal repair was associated with longer median (interquartile range) operative times (75.5 [59.0-93.8] minutes vs 40.5 [29.2-63.8] minutes, respectively; P < .001), higher median (interquartile range) cost ($3258 [$2568-$4118] vs $1421 [$1196-$1930], respectively; P < .001), and higher mean (SD) frustration levels on the NASA Task Load Index Scale (range, 1-100, with lower scores indicating lower cognitive workload) (32.7 [23.5] vs 20.1 [19.2], respectively; P = .004). There were no differences in ergonomics of the surgeons between the groups as measured by the Rapid Upper Limb Assessment instrument.
Results of this study showed no clinical benefit to the robotic approach to straightforward inguinal hernia repair compared with the laparoscopic approach. The robotic approach incurred higher costs and more operative time compared with the laparoscopic approach, with added surgeon frustration and no ergonomic benefit to surgeons.
ClinicalTrials.gov Identifier: NCT02816658.
重要性:尽管机器人平台在美国已迅速用于腹股沟疝修补术,但迄今为止,尚无任何一级临床试验将机器人腹股沟疝修补术与腹腔镜修补术进行比较。这项多中心随机临床试验是首次比较机器人平台与腹腔镜方法在微创腹股沟疝修补术中的应用。
目的:确定机器人腹股沟疝修补术与传统腹腔镜腹股沟疝修补术相比,术后结果是否有所改善。
设计、地点和参与者:这项多中心、单盲、前瞻性随机临床试验于 2016 年 4 月至 2019 年 4 月进行,在 6 个学术和学术附属机构进行,随访时间为 30 天。共纳入 113 例单侧原发性或复发性腹股沟疝患者。排除后,102 例患者仍纳入分析。
干预措施:标准腹腔镜经腹腹膜前修补术或机器人经腹腹膜前修补术。
主要结局和测量指标:主要结局包括术后疼痛、健康相关生活质量、活动能力、伤口发病率和美容效果。次要结局包括成本、外科医生的人体工程学和外科医生的心理工作量。未选择主要结局,因为这项研究设计为试点研究。假设在数据收集之前就已经提出。
结果:共有 102 例患者纳入研究(腹腔镜组 54 例,平均[标准差]年龄 57.2[13.3]岁,男性 48 例[88.9%];机器人组 48 例,平均[标准差]年龄 56.1[14.1]岁,男性 44 例[91.6%])。两组在术前、1 周和 30 天时的伤口事件、再入院、视觉模拟评分(VAS)测量的疼痛或 36 项简短健康调查(SF-36)测量的生活质量方面均无差异。与传统腹腔镜腹股沟疝修补术相比,机器人经腹腹膜前修补术的中位(四分位距)手术时间更长(分别为 75.5[59.0-93.8]分钟和 40.5[29.2-63.8]分钟;P<0.001)、中位(四分位距)成本更高(分别为 3258[2568-4118]美元和 1421[1196-1930]美元;P<0.001)、美国国家航空航天局任务负荷指数量表(范围 1-100,得分越低表示认知工作量越低)上的平均(标准差)挫败感水平更高(分别为 32.7[23.5]和 20.1[19.2];P=0.004)。两组外科医生的人体工程学测量,使用快速上肢评估工具,结果无差异。
结论和相关性:本研究结果显示,与腹腔镜方法相比,机器人方法在直疝修补术中没有明显的临床优势。与腹腔镜方法相比,机器人方法的成本和手术时间更高,外科医生的挫败感更高,且没有为外科医生带来人体工程学优势。
试验注册:ClinicalTrials.gov 标识符:NCT02816658。