Holland Michael A, Joyce John S, Brennaman Lisa M, Drobnis Erma Z, Starr Julie A, Foster Raymond T
Department of Obstetrics and Gynecology, Baylor Scott & White Health, Temple, TX.
Female Pelvic Med Reconstr Surg. 2019 Jan/Feb;25(1):76-81. doi: 10.1097/SPV.0000000000000514.
Pelvic floor hypertonic disorder is characterized by an involuntary spasm of the levator ani muscles and is associated with several clinical syndromes. Several treatment options have been described; however, treatment efficacy data are limited. The objective of this study was to determine the efficacy of intravaginal diazepam for the treatment of pelvic pain secondary to levator ani muscle spasm in comparison to placebo.
Adult women with complaints of pelvic pain, who were noted to have levator ani muscle spasm on physical examination, were approached for enrollment in a double-blind, placebo-controlled, randomized clinical trial. Eligible participants were randomized to receive 10-mg diazepam capsules or identical-appearing placebo capsules. The primary outcome was the change in pain scores measured by a 100-mm visual analog scale at 4 weeks. Several validated questionnaires were similarly assessed as secondary outcomes.
In total, 49 women were randomized (25 in the diazepam arm and 24 in the placebo arm). At 4 weeks, 35 women returned for follow-up and had complete data available analysis. There was no difference in visual analog scale scores between the treatment groups after 4 weeks (50 vs 39 mm, for diazepam and placebo, respectively; P = 0.36). There were also no differences noted in the questionnaire scores.
It is unlikely that self-administered intravaginal diazepam suppositories promote an improvement in the 100-mm visual analog scale of 20 mm or more or other substantial symptom improvement in women with pelvic floor hypertonic disorder.
盆底高张性疾病的特征是肛提肌不自主痉挛,并与多种临床综合征相关。已有多种治疗方案被描述;然而,治疗效果数据有限。本研究的目的是确定与安慰剂相比,阴道内使用地西泮治疗肛提肌痉挛继发盆腔疼痛的疗效。
招募有盆腔疼痛主诉且体格检查发现肛提肌痉挛的成年女性,参与一项双盲、安慰剂对照、随机临床试验。符合条件的参与者被随机分配接受10毫克地西泮胶囊或外观相同的安慰剂胶囊。主要结局是4周时用100毫米视觉模拟量表测量的疼痛评分变化。几个经过验证的问卷也作为次要结局进行了类似评估。
共有49名女性被随机分组(地西泮组25名,安慰剂组24名)。4周时,35名女性返回进行随访并提供了完整的数据用于分析。4周后,治疗组之间的视觉模拟量表评分没有差异(地西泮组和安慰剂组分别为50毫米和39毫米;P = 0.36)。问卷评分也没有差异。
对于盆底高张性疾病的女性,自行阴道内使用地西泮栓剂不太可能使100毫米视觉模拟量表评分提高20毫米或更多,也不太可能使其他症状有实质性改善。