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微创泌尿妇科手术后的肠道功能:一项前瞻性随机对照试验。

Bowel function after minimally invasive urogynecologic surgery: a prospective randomized controlled trial.

作者信息

McNanley Anna, Perevich Mare, Glantz Chris, Duecy Erin E, Flynn Michael K, Buchsbaum Gunhilde

机构信息

Department of Obstetrics and Gynecology, University of Rochester Medical Center, Rochester, NY, USA.

出版信息

Female Pelvic Med Reconstr Surg. 2012 Mar-Apr;18(2):82-5. doi: 10.1097/SPV.0b013e3182455529.

DOI:10.1097/SPV.0b013e3182455529
PMID:22453316
Abstract

OBJECTIVES

The goals of this study were to assess the effect of a standardized postoperative bowel regimen of over-the-counter medications on (1) time to first bowel movement (BM) and (2) pain level associated with first BM in subjects undergoing minimally invasive urogynecologic surgery.

METHODS

Eligible patients scheduled to undergo minimally invasive urogynecologic surgery were offered participation. Enrolled subjects were randomized by computerized schedule. Demographic and perioperative data were collected. Subjects completed a validated questionnaire preoperatively and postoperatively assessing preexisting constipation, frequency and consistency of bowel movements, use of pain medications, mean daily pain level (using visual analog scale), stool consistency, and pain associated with first postoperative bowel movement. The control group was instructed to take docusate sodium twice daily postoperatively. The treatment group took docusate sodium plus Miralax, fiber wafers, and bisacodyl suppositories as directed by protocol. Wilcoxon or t testing was used to compare continuous variables; χ testing was used for categorical relationships, and backward-elimination multiple regression was used to assess independent effects.

RESULTS

Seventy-two subjects were enrolled and randomized. Twelve subjects withdrew, leaving 60 (30 per group) completing the study. There were no statistically significant differences between groups in baseline characteristics. Mean (SD) age was 63 (9) years for the control group and 58 (10) for the study group (P = 0.06). Mean pelvic organ prolapse stage was III in each group. The mean (SD) operating room time was 198 (65) minutes for the controls and 216 (74) for the study subjects. Sixty-five percent underwent robot-assisted surgery (50% hysterectomy and 63% sacrocolpopexy). Ninety-eight percent of surgeries were performed under general anesthesia.Before adjustment, the mean (SD) time to first BM was 77 (24) hours in controls versus 64 (21) in the study patients (P = 0.03). Using multiple regression, baseline frequency of defecation (1-2 BMs/wk) was directly associated with the time to first BM (added 25.2 hours; P = 0.009) and being in the study group was inversely associated (first BM, 11.7 hours sooner; P = 0.04). No other variables were retained.There was no difference in pain associated with first postoperative BM (visual analog scale, 3.6 (3.2) vs 3.7 (2.8); P = 0.98), but those with prior complaints of vaginal or rectal splinting had higher pain scores (1.9 and 2.8 points higher, respectively; P = 0.04 for both). There was a trend toward higher pain scores with higher postoperative daily narcotic intake (P = 0.06). No other variables were retained.There was a significant difference in recorded compliance between control versus study regimens (94% vs 81%, respectively; P = 0.002).

CONCLUSIONS

Mean time to first postoperative BM after minimally invasive urogynecologic surgery is more than 3.5 days with use of docusate sodium alone and is only slightly shorter when combination therapy is used. First BM after surgery is considered to be painful despite the use of medications. Future studies targeting postoperative discomfort/pain with defecation could target preoperative bowel regimens or more aggressive postoperative interventions. Regimens should remain simple to increase compliance.

摘要

目的

本研究的目的是评估一种标准化的非处方药物术后肠道方案对接受微创泌尿妇科手术患者的(1)首次排便时间和(2)与首次排便相关的疼痛程度的影响。

方法

邀请计划接受微创泌尿妇科手术的符合条件的患者参与。通过计算机化日程安排对入选的受试者进行随机分组。收集人口统计学和围手术期数据。受试者在术前和术后完成一份经过验证的问卷,评估术前存在的便秘情况、排便频率和稠度、止痛药物的使用、平均每日疼痛程度(使用视觉模拟量表)、大便稠度以及与术后首次排便相关的疼痛。对照组被指示术后每天服用两次多库酯钠。治疗组按照方案指示服用多库酯钠加聚乙二醇、纤维片和比沙可啶栓剂。使用Wilcoxon检验或t检验比较连续变量;使用χ检验分析分类关系,并使用向后排除多元回归评估独立效应。

结果

72名受试者被纳入并随机分组。12名受试者退出,剩余60名(每组30名)完成研究。两组在基线特征方面无统计学显著差异。对照组的平均(标准差)年龄为63(9)岁,研究组为58(10)岁(P = 0.0。每组的平均盆腔器官脱垂分期均为III期。对照组的平均(标准差)手术室时间为198(65)分钟,研究对象为216(74)分钟。65%的患者接受了机器人辅助手术(50%为子宫切除术,63%为骶骨阴道固定术)。98%的手术在全身麻醉下进行。在进行调整之前,对照组首次排便的平均(标准差)时间为77(24)小时,研究组患者为64(21)小时(P = 0.03)。使用多元回归分析,排便的基线频率(每周1 - 2次排便)与首次排便时间直接相关(增加25.2小时;P = 0.009),而在研究组中则呈负相关(首次排便提前11.7小时;P = 0.04)。未保留其他变量。术后首次排便相关的疼痛无差异(视觉模拟量表,分别为3.6(3.2)和3.7(2.8);P = 0.98),但之前有阴道或直肠夹闭主诉的患者疼痛评分更高(分别高1.9分和2.8分;两者P = 0.04)。术后每日麻醉剂摄入量越高,疼痛评分有升高趋势(P = 0.06)。未保留其他变量。对照组与研究组方案的记录依从性存在显著差异(分别为94%和8%;P = 0.002)。

结论

仅使用多库酯钠时,微创泌尿妇科手术后首次排便的平均时间超过3.5天,联合治疗时仅略短。尽管使用了药物,但术后首次排便仍被认为是疼痛的。未来针对排便后术后不适/疼痛的研究可以针对术前肠道方案或更积极的术后干预措施。方案应保持简单以提高依从性。

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