Caruso S, Iraci M, Cianci S, Casella E, Fava V, Cianci A
Department of General Surgery and Medical Surgical Specialties, Gynecological Clinic of the Policlinico Universitario, Via S.Sofia 78, 95124, Catania, Italy.
Research Group for Sexology, Catania, Italy.
J Endocrinol Invest. 2015 Nov;38(11):1211-8. doi: 10.1007/s40618-015-0383-7. Epub 2015 Sep 4.
The aim of the study was to evaluate the effects of dienogest (DNG) on quality of life (QoL) and sexual function of women affected by endometriosis pain.
Fifty-four women constituted the study group and were given 2 mg/daily DNG; 48 women were given non-steroidal anti-inflammatory drugs and constitut ed the control group. To define the endometriosis-associated pelvic pain, the Visual Analogic Scale (VAS) was used. The Short Form-36 (SF-36), the Female Sexual Function Index (FSFI) and the Female Sexual Distress Scale (FSDS) were used to assess the QoL, the sexual function and the sexual distress, respectively. The study included two follow-ups at 3 and 6 months.
Pain improvement was observed in the study group at 3 (p < 0.05) and 6 months (p < 0.001) of treatment. At the 1st follow-up, women reported QoL improvements in some functions (p < 0.05); at the 2nd follow-up, they reported improvement in all categories (p < 0.001). The FSFI score did not change at the 1st follow-up (p = NS). On the contrary, at the 2nd follow-up, it improved with respect to the baseline (p < 0.05). At the 2nd follow-up, the FSFI score had risen to 27.8 (p < 0.001) and the FSDS score had dropped to 11.3 (p < 0.001). No change was observed in the control group (p = NS).
The progressive reduction of the pain syndrome reported by women over the treatment period could contribute to improve the QoL and sexual life of women on DNG.
本研究旨在评估地诺孕素(DNG)对受子宫内膜异位症疼痛影响的女性生活质量(QoL)和性功能的影响。
54名女性组成研究组,每日服用2mg DNG;48名女性服用非甾体抗炎药,组成对照组。采用视觉模拟评分法(VAS)定义与子宫内膜异位症相关的盆腔疼痛。分别使用简短健康调查问卷(SF-36)、女性性功能指数(FSFI)和女性性困扰量表(FSDS)评估生活质量、性功能和性困扰。该研究包括在3个月和6个月时的两次随访。
在治疗3个月(p<0.05)和6个月(p<0.001)时,研究组的疼痛得到改善。在第一次随访时,女性报告某些功能的生活质量有所改善(p<0.05);在第二次随访时,她们报告所有类别均有改善(p<0.001)。FSFI评分在第一次随访时没有变化(p=无显著性差异)。相反,在第二次随访时,相对于基线有所改善(p<0.05)。在第二次随访时,FSFI评分升至27.8(p<0.001),FSDS评分降至11.3(p<0.001)。对照组未观察到变化(p=无显著性差异)。
在治疗期间,女性报告的疼痛综合征逐渐减轻,这可能有助于改善服用DNG的女性的生活质量和性生活。