首页> 外文期刊>Journal of minimally invasive gynecology >Low vs Standard Pneumoperitoneum Pressure During Laparoscopic Hysterectomy: Prospective Randomized Trial
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Low vs Standard Pneumoperitoneum Pressure During Laparoscopic Hysterectomy: Prospective Randomized Trial

机译:腹腔镜子宫切除术中低与标准气腹压力:前瞻性随机试验

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Study Objective: To compare the use of low pneumoperitoneum pressure (LPP; 8 mm Hg) vs standard pneumoperitoneum pressure (SPP; 12 mm Hg) during mini-laparoscopic hysterectomy (MLH). Design: Randomized controlled trial (Canadian Task Force classification I). Setting: Tertiary care center. Patients: Forty-two consecutive women scheduled to undergo MLH to treat benign uterine disease. Interventions: Women were randomly selected to undergo MLH using LPP (n = 20) or SPP (n = 22). MLH was performed via 3-mm ancillary ports. Measurements and Main Results: The primary outcome was to evaluate changes in abdominal and shoulder-tip pain via a 100-mm visual analog scale at 1, 3, and 24 hours postoperatively. All procedures were completed via mini-laparoscopy without the need to increase intra-abdominal pressure or convert to conventional laparoscopy or open surgery. Intraoperatively, 1 episode of severe bradycardia occurred in the LPP group, whereas no intraoperative complications were recorded in the SPP group (p = .47). No postoperative complications were recorded (p > .99). Abdominal pain was similar between groups at each time point. Incidence and intensity of shoulder-tip pain at 1 and 3 hours postoperatively was lower in the LPP group than in the SPP group (p < .05), whereas no between-group differences were observed at 24 hours (p > .05). Rescue analgesic requirement did not differ statistically between the LPP and SPP groups (20% vs 41%, respectively; p = .19; odds ratio, 2.7; 95% confidence interval, 0.69-11.08). Conclusion: In experienced hands, use of LPP is safe and feasible. During performance of MLH, compared with SPP, LPP is a simple method that offers advantages of less shoulder-tip pain.
机译:研究目的:比较在小型腹腔镜子宫切除术(MLH)时低气腹压力(LPP; 8 mm Hg)与标准气腹压力(SPP; 12 mm Hg)的使用。设计:随机对照试验(加拿大特别工作组I级)。地点:三级护理中心。患者:预定接受MLH治疗良性子宫疾病的42位连续女性。干预措施:随机选择使用LPP(n = 20)或SPP(n = 22)进行MLH的妇女。 MLH通过3毫米辅助端口进行。测量和主要结果:主要结果是在术后1、3和24小时通过100毫米视觉模拟量表评估腹部和肩尖疼痛的变化。所有程序均通过微型腹腔镜检查完成,而无需增加腹腔内压力或转换为常规腹腔镜检查或开腹手术。术中LPP组发生1次严重心动过缓,而SPP组未见术中并发症(p = .47)。没有记录术后并发症(p> .99)。各时间点各组的腹部疼痛相似。 LPP组术后1和3小时的肩尖疼痛发生率和强度低于SPP组(p <.05),而24小时未观察到组间差异(p> .05)。 LPP组和SPP组的急救镇痛要求无统计学差异(分别为20%和41%; p = .19;优势比为2.7; 95%置信区间为0.69-11.08)。结论:在经验丰富的手中,使用LPP是安全可行的。与SPP相比,MLH在进行MLH期间是一种简单的方法,具有减轻肩尖疼痛的优点。

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