Alvisi Stefania, Lami Alessandra, Baldassarre Maurizio, Lenzi Jacopo, Mancini Ilaria, Seracchioli Renato, Meriggiola Maria Cristina
Gynecology and Physiopathology of Human Reproduction, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy; Department of Medical and Surgical Sciences, Alma Mater Studiorum University of Bologna, Bologna, Italy.
Department of Medical and Surgical Sciences, Alma Mater Studiorum University of Bologna, Bologna, Italy; Center for Applied Biomedical Research, Department of Surgical and Medical Sciences, S. Orsola-Malpighi University Hospital, Alma Mater Studiorum University of Bologna, Bologna, Italy.
J Sex Med. 2022 May;19(5):761-770. doi: 10.1016/j.jsxm.2022.02.027. Epub 2022 Mar 31.
Among treatments for vulvo-vaginal atrophy (VVA), there is a new kind of energy-based device, the non-ablative CO laser.
This study aimed to assess the efficacy and safety of the non-ablative CO laser in menopausal women with VVA as a monotherapy or in association with vaginal estriol or moisturizer.
Seventy-five women with VVA received laser treatment (Laser group), laser plus estriol gel (Laser+E) or laser plus moisturizers (Laser+M). The study protocol consisted of 3 monthly laser sessions (t0, t1, t2) and a gynecological examination at baseline and 1 month after last laser treatment (t3). Objective measures included VHI (Vaginal Health Index) and VuHI (Vulvar Health Index); subjective symptoms of VVA (Dryness, Burning, Itching, Dysuria) evaluated via visual analog scales, sexual function evaluated by FSFI (Female Sexual Function Index), FSDS (Female Sexual Distress Score) and MENQOL (Mopause-specific Quality Of Life). Adverse events and discomfort encountered during the procedure were also assessed.
Primary outcomes were the evaluation of VHI and VuHI and secondary outcomes were changes in VVA symptoms (VAS), sexual function (MENQOL, FSFI, FSDS) and discomfort during the procedure.
Seventy-five women (25 in Laser, 25 in Laser+E and 25 in Laser+M group) completed the study. At t3, mean VHI, VuHI, dryness, burning and itching VAS scores improved significantly with no differences between the groups. The lubrication domain of FSFI improved significantly only in the Laser+M group, while the pain domain improved significantly in all women with no differences between the groups. FSFI and FSDS overall scores and MENQOL sexual domain improved in all women with no significant difference between the groups. The mean score of the pain during the procedure was low at t0 and did not change throughout the study.
This study extends knowledge concerning the effectiveness of a new non-ablative CO laser in post-menopausal women with VVA.
STRENGTHS & LIMITATIONS: This is one of the first studies on this kind of laser and is the first to compare the effectiveness of laser treatment alone or in combination with vaginal estriol or moisturizers. Parameters of VVA and sexual function were evaluated using validated tools. Study limitations include short follow-up time, the limited number of participants and the absence of a sham-controlled group.
Non-ablative CO laser seems to be an effective treatment for VVA in menopausal women. Our preliminary data shows that it can be effective as monotherapy or with adjuvant treatments. Alvisi S, Lami A, Baldassarre M, et al. Short-Term Efficacy and Safety of Non-Ablative Laser Treatment Alone or with Estriol or Moisturizers in Postmenopausal Women with Vulvovaginal Atrophy. J Sex Med 2022;19:761-770.
在外阴阴道萎缩(VVA)的治疗方法中,有一种新型的基于能量的设备,即非剥脱性CO2激光。
本研究旨在评估非剥脱性CO2激光作为单一疗法或与阴道雌三醇或保湿剂联合使用时,治疗绝经后VVA女性的疗效和安全性。
75名VVA女性接受了激光治疗(激光组)、激光加雌三醇凝胶(激光+E组)或激光加保湿剂(激光+M组)。研究方案包括每月进行3次激光治疗(t0、t1、t2),并在基线和最后一次激光治疗后1个月(t3)进行妇科检查。客观指标包括阴道健康指数(VHI)和外阴健康指数(VuHI);通过视觉模拟量表评估VVA的主观症状(干燥、灼烧、瘙痒、排尿困难),通过女性性功能指数(FSFI)、女性性困扰评分(FSDS)和绝经特异性生活质量量表(MENQOL)评估性功能。还评估了手术过程中遇到的不良事件和不适。
75名女性(激光组25名、激光+E组25名、激光+M组25名)完成了研究。在t3时,平均VHI、VuHI、干燥、灼烧和瘙痒的视觉模拟量表评分显著改善,组间无差异。FSFI的润滑领域仅在激光+M组显著改善,而疼痛领域在所有女性中均显著改善,组间无差异。所有女性的FSFI和FSDS总分以及MENQOL性领域均有改善,组间无显著差异。手术过程中的疼痛平均评分在t0时较低,且在整个研究过程中没有变化。
本研究扩展了关于新型非剥脱性CO2激光治疗绝经后VVA女性有效性的知识。
这是关于这种激光的首批研究之一,也是首个比较单独激光治疗或与阴道雌三醇或保湿剂联合使用的有效性的研究。使用经过验证的工具评估了VVA和性功能参数。研究局限性包括随访时间短、参与者数量有限以及缺乏假手术对照组。
非剥脱性CO2激光似乎是治疗绝经后女性VVA的有效方法。我们的初步数据表明,它作为单一疗法或辅助治疗均有效。阿尔维西S、拉米A、巴尔达萨雷M等。非剥脱性激光单独或与雌三醇或保湿剂联合治疗绝经后外阴阴道萎缩女性的短期疗效和安全性。《性医学杂志》2022;19:761 - 770。