Yao J, Liao X J, Mao W M, Wu W J, Yu Y Y, Yang G G
Department of Anal-Colorectal Surgery, Hangzhou Third People's Hospital Clinical College of Anhui Medical University, Hangzhou 310009, China.
Zhonghua Wei Chang Wai Ke Za Zhi. 2019 Jul 25;22(7):656-661. doi: 10.3760/cma.j.issn.1671-0274.2019.07.010.
To explore the safety and feasibility of colonoscopy - assisted transanal minimally invasive surgery via glove port (CA-TAMIS-GP) in the treatment of early rectal tumors. A total of 67 patients evaluated as early rectal tumors (adenoma limited within mucosal layer) with diameter ≤4.0 cm at Department of Anal-Colorectal Surgery, Hangzhou Third People's Hospital from July 2013 to March 2017 were prospectively enrolled in the study. Benign tumors were diagnosed by preoperative imaging in all the patients with the distance to anal edge of 4 to 20 cm. Patients were randomly divided into treatment group and the control group according to the random number table. The treatment group (=32) underwent CA-TAMIS-GP, including 19 males and 13 females with mean age of (55.6±11.2) years and mean tumor size of (3.3±0.4) cm, while the control group (=35) underwent endoscopic submucosal dissection (ESD, control group), including 20 males and 15 females with mean age of (52.9±12.3) years and mean tumor size of (3.4±0.5) cm. Differences of baseline data between two groups were not significant (all >0.05). The specific method of CA-TAMIS-GP was as follows: a surgical rubber glove sleeve (No.6) was passed through the anal device; the glove was fixed at the anvil device; after fully expanding the anus, the anal sac was placed into the anus with the fingers outside; then, the cuff and the anal sac were sutured and fixed to the perianal; a well-tight glove path was established; the ultrasonic scalpel, grasper and the colonoscopy lens connected to the host platform and the electric negative pressure suction were inserted into the three finger sleeves respectively and fixed by rubber band or silk thread; the laparoscopic instruments such as the grasper and the ultrasonic scalpel were used for pulling, grasping, cutting, electrocoagulation, suturing and other operations to complete the resection of rectal lesions. Efficacy, postoperative complication and operative cost, etc. between two groups were compared using the student's test, chi-square tests, and Fisher's exact test. Operations of two groups were completed successfully without conversion to laparotomy. Histopathologic examination showed all specimens had negative margins with the surgical resection of the layer to the submucosa, and showed no significant differences between two groups (>0.05). Compared to the control group, the operation time was shorter [(49.5±14.6) minutes vs.(66.1±17.6) minutes, =-4.235, <0.001], and the intraoperative hemorrhage was less [(4.2±1.6) ml vs. (6.2±2.1) ml, =-4.349, <0.001] in the treatment group with significant differences. In the treatment group, 6 patients had mild anal pain or discomfort after operation, and 1 patient in the control group showed anal foreign body sensation. The difference was statistically significant [18.8% (6/32) vs. 2.9% (1/35), =0.048]. The incidence of postoperative hematochezia in the treatment group was lower than that in the control group [9.4% (3/32) vs. 20.0% (7/35), =0.310] without significant difference. The cost of consumables in the treatment group was (1586.9±204.4) yuan, which was lower than (7694.4±1123.2) yuan in control group, and the difference was statistically significant (=-30.880, <0.001). All the patients were followed up for 6 to 36 months after operation, and no recurrence or long-term complication occurred in the treatment group, while 1 case developed local recurrence in the control group. CA-TAMIS-GP is a safe and effective method for early rectal tumors with simple and economical characteristics, which broadens the application of colonoscopy.
探讨经手套端口结肠镜辅助经肛门微创手术(CA-TAMIS-GP)治疗早期直肠肿瘤的安全性和可行性。2013年7月至2017年3月,前瞻性纳入杭州市第三人民医院肛肠外科67例经评估为早期直肠肿瘤(腺瘤局限于黏膜层)、直径≤4.0 cm的患者。所有患者均通过术前影像学诊断为良性肿瘤,距肛缘4至20 cm。根据随机数字表将患者随机分为治疗组和对照组。治疗组(n = 32)接受CA-TAMIS-GP,其中男性19例,女性13例,平均年龄(55.6±11.2)岁,平均肿瘤大小(3.3±0.4)cm;对照组(n = 35)接受内镜黏膜下剥离术(ESD,对照组),其中男性20例,女性15例,平均年龄(52.9±12.3)岁,平均肿瘤大小(3.4±0.5)cm。两组基线数据差异无统计学意义(均P>0.05)。CA-TAMIS-GP的具体方法如下:将一个手术橡胶手套袖套(6号)穿过肛门装置;将手套固定在吻合器装置上;充分扩肛后,将肛门囊经手指放入肛门外;然后,将袖带和肛门囊缝合固定于肛周;建立一个密闭的手套通道;将超声刀、抓钳和连接主机平台的结肠镜镜头以及电动负压吸引器分别插入三个手指套内,并用橡皮筋或丝线固定;使用抓钳和超声刀等腹腔镜器械进行牵拉、抓取、切割、电凝、缝合等操作,完成直肠病变切除。采用t检验、卡方检验和Fisher确切概率法比较两组的疗效、术后并发症及手术费用等。两组手术均顺利完成,未中转开腹。病理检查显示所有标本手术切除至黏膜下层切缘阴性,两组间差异无统计学意义(P>0.05)。与对照组相比,治疗组手术时间更短[(49.5±14.6)分钟 vs.(66.1±17.6)分钟,t = -4.235,P<0.001],术中出血更少[(4.2±1.6)ml vs.(6.2±2.1)ml,t = -4.349,P<0.001],差异有统计学意义。治疗组6例患者术后有轻度肛门疼痛或不适,对照组1例患者有肛门异物感。差异有统计学意义[18.8%(6/32) vs. 2.9%(1/35),P = 0.048]。治疗组术后便血发生率低于对照组[9.4%(3/32) vs. 20.0%(7/35),P = 0.310],差异无统计学意义。治疗组耗材费用为(1586.9±204.4)元,低于对照组的(7694.4±1123.2)元,差异有统计学意义(t = -30.880,P<0.001)。所有患者术后随访6至36个月,治疗组无复发或远期并发症发生,对照组1例出现局部复发。CA-TAMIS-GP是一种治疗早期直肠肿瘤安全有效的方法,具有操作简单、经济的特点,拓宽了结肠镜的应用范围。