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Minimizing ancillary ports size in gynecologic laparoscopy: a randomized trial.

机译:在妇科腹腔镜检查中最小化辅助端口的尺寸:一项随机试验。

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STUDY OBJECTIVE: To evaluate the feasibility, safety, and effect on postoperative pain of laparoscopy for the management of adnexal masses by downsizing ancillary trocars from 5- to 3-mm. DESIGN: Randomized, controlled trial (Canadian Task Force classification I). SETTING: Gynecologic department of a university hospital PATIENTS: A total of 102 women with an adnexal mass scheduled for gynecologic laparoscopic procedures were randomized to undergo laparoscopy using either conventional 5-mm ancillary trocars (n=52) or 3-mm instruments (n=50). Preoperative suspicion of malignancy, deep infiltrating endometriosis, and indications for hysterectomy or myomectomy were considered as exclusion criteria. INTERVENTIONS: Laparoscopic procedures for the treatment of benign adnexal masses. MEASUREMENTS AND MAIN RESULTS: Both groups were similar in patient age, body mass index, history of abdominal surgery, and type of procedures. Intraoperative complications occurred in no patient (0%) in the 3-mm group and in two patients (3.8%) in the 5-mm group (p=.49). Conversion from 3- to 5-mm instrumentation was necessary in one procedure. No difference was found in the operative time between the 3-mm and the 5-mm groups (54 min [range 15-175 min] vs 50 min [range 20-150 min], p=.89). The severity of incisional pain was evaluated with a 100-mm visual analog scale at 1, 3, and 24 hours after surgery. Postoperative pain was significantly lower in the 3-mm than in the 5-mm group 1 hour after laparoscopy (20 [range 0-60] vs 32.5 [range 0-80], p=.04). The proportion of women requiring analgesia before discharge, the timing of analgesic requirement, and the total amount of medication in the first 24 hours after surgery were similar in the two groups. CONCLUSION: Three-millimeter ancillary trocars can safely replace traditional-size equipment for the management of adnexal masses without a negative impact on the surgeon's ability to perform gynecologic laparoscopy and are associated with less immediate postoperative pain.
机译:目的:通过将辅助套管针的尺寸从5mm缩小至3mm,以评估腹腔镜手术治疗附件肿块的可行性,安全性以及对腹腔镜手术后疼痛的影响。设计:随机对照试验(加拿大工作组I级)。地点:一所大学医院的妇产科患者:总共102名计划行妇科腹腔镜手术的附件肿物的女性被随机分配使用传统的5毫米辅助套管针(n = 52)或3毫米器械(n = 50)。术前怀疑恶性肿瘤,深层浸润性子宫内膜异位以及子宫切除术或子宫肌瘤切除术的适应症被视为排除标准。干预:腹腔镜手术治疗良性附件肿块。测量和主要结果:两组患者年龄,体重指数,腹部手术史和手术类型相似。 3毫米组中无患者(0%)发生手术并发症,而5毫米组中2例患者(3.8%)发生术中并发症(p = .49)。从一个3毫米仪器到5毫米仪器的转换是必要的。 3 mm和5 mm组之间的手术时间没有差异(54分钟[15-175分钟]与50分钟[20-150分钟],p = .89)。在手术后1、3和24小时,使用100 mm的视觉模拟量表评估切口疼痛的严重程度。腹腔镜检查后1小时,3-mm组的术后疼痛明显低于5mm组(20 [范围0-60] vs 32.5 [范围0-80],p = .04)。两组中出院前需要镇痛的妇女比例,镇痛要求的时间以及术后头24小时的用药总量相似。结论:三毫米辅助套管针可以安全地代替传统尺寸的设备来处理附件肿块,而不会对外科医生进行妇科腹腔镜检查的能力产生负面影响,并且术后疼痛较少。

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