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首页> 外文期刊>American Journal of Obstetrics and Gynecology >Evaluating ureteral patency in the post-indigo carmine era: a randomized controlled trial
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Evaluating ureteral patency in the post-indigo carmine era: a randomized controlled trial

机译:评估靛蓝胭脂红地区的输尿管通畅:随机对照试验

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摘要

Background Many gynecologic, urologic, and pelvic reconstructive surgeries require accurate intraoperative evaluation of ureteral patency. Objective We performed a randomized controlled trial to compare surgeon satisfaction with 4 methods of evaluating ureteral patency during cystoscopy at the time of benign gynecologic or pelvic reconstructive surgery: oral phenazopyridine, intravenous sodium fluorescein, mannitol bladder distention, and normal saline bladder distention. Study Design We conducted an unblinded randomized controlled trial of the method used to evaluate ureteral patency during cystoscopy at time of benign gynecologic or pelvic reconstructive surgery. Subjects were randomized to receive 200 mg oral phenazopyridine, 25 mg intravenous sodium fluorescein, mannitol bladder distention, or normal saline bladder distention during cystoscopy. The primary outcome was surgeon satisfaction with the method, assessed via a 100-mm visual analog scale with 0 indicating strong agreement and 100 indicating strong disagreement with the statement. Secondary outcomes included comparing visual analog scale responses about ease of each method and visualization of ureteral jets, bladder mucosa and urethra, and operative information, including time to surgeon confidence in the ureteral jets. Adverse events were evaluated for at least 6 weeks after the surgical procedure, and through the end of the study. All statistical analyses were based on the intent-to-treat principle, and comparisons were 2-tailed. Results In all, 130 subjects were randomized to phenazopyridine (n?= 33), sodium fluorescein (n?= 32), mannitol (n?= 32), or normal saline (n?= 33). At randomization, patient characteristics were similar across groups. With regard to the primary outcome, mannitol was the method that physicians found most satisfactory on a visual analog scale. The median (range) scores for physicians assessing ureteral patency were 48 (0-83), 20 (0-82), 0 (0-44), and 23 (3-96) mm for phenazopyridine, sodium fluorescein, mannitol, and normal saline, respectively ( P Conclusion The use of mannitol during cystoscopy to assess ureteral patency provided surgeons with the most overall satisfaction, ease of use, and superior visualization without affecting surgery or cystoscopy times. There were no differences in adverse events, including incidence of urinary tract infections. ]]>
机译:背景技术许多妇科,泌尿科和盆腔重建植物需要准确地对输尿管通畅的术语评估。目的我们进行了随机对照试验,将外科医生满意与4种评估输尿管间隔在良同经或盆腔重建手术期间评估输尿管通畅的方法进行比较:口服苯吡啶,静脉注射钠血液,甘露醇膀胱疼痛和生理盐水膀胱脱离。研究设计我们对用于评估患有患者患者患者患者在良同经理或盆腔重建手术期间的方法的方法进行了未结合的随机对照试验。受试者被随机化以获得200mg口服苯吡啶,25mg静脉内荧光素,甘露醇膀胱疼痛或膀胱镜检查期间的生理盐水囊肿。主要结果是与该方法的外科医生满足,通过100毫米视觉模拟规模评估,0表示强烈的协议,100表示​​与声明有着强烈的分歧。二次结果包括比较视觉模拟规模对易于每种方法的响应和输尿管喷射器,膀胱粘膜和尿道的可视化以及手术信息,包括外科医生对输尿管喷射的时间的时间。在外科手术后至少6周评估不良事件,并通过研究结束。所有统计分析都基于意图原则,并且比较是2尾。结果,将130个受试者随机化为苯基吡啶(N?= 33),荧光素(N?= 32),甘露醇(N?= 32)或生理盐水(n?= 33)。在随机化时,患者的特征在群体中相似。关于主要结果,甘露醇是医生在视觉模拟规模上发现最令人满意的方法。评估输尿管通畅的医生的中位数(范围)分数为48(0-83),20(0-82),0(0-44)和23(3-96)mm,用于苯基吡啶,荧光素,甘露醇和甘露醇和分别正常盐水(P结论在膀胱镜检查期间使用甘露醇,评估输尿管通畅提供外科医生,具有最整体满意度,易用性和卓越的可视化,而不会影响手术或膀胱镜检查时间。不良事件没有差异,包括发病事件,包括发病率尿路感染。]]>

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