School of Women's and Children's Health, UNSW Sydney, New South Wales, Australia.
School of Clinical Sciences, Monash University, Melbourne, Victoria, Australia.
JAMA. 2021 Oct 12;326(14):1381-1389. doi: 10.1001/jama.2021.14892.
Postmenopausal vaginal symptoms are common and frequently detrimental to a woman's quality of life. Fractional carbon dioxide vaginal laser is increasingly offered as a treatment, but the efficacy remains unproven.
To determine the efficacy of fractional carbon dioxide laser for treatment of vaginal symptoms associated with menopause.
DESIGN, SETTING, AND PARTICIPANTS: A double-blind, randomized, sham-controlled trial with 12-month follow-up was undertaken at a single tertiary referral hospital in Sydney, Australia. Enrollment commenced on September 19, 2016, with final follow-up on June 30, 2020. Participants were postmenopausal women with vaginal symptoms substantive enough to seek medical treatment. Of 232 participants approached, 85 were randomized.
Three treatments using a fractional microablative carbon dioxide laser system performed 4 to 8 weeks apart, with 43 women randomized to the laser group and 42 to the sham group.
The co-primary outcomes were symptom severity assessed using a visual analog scale (VAS; range, 0-100; 0 indicates no symptoms and 100 indicates the most severe symptoms) and the Vulvovaginal Symptom Questionnaire (VSQ; range, 0-20; 0 indicates no symptoms and 20 indicates the most severe symptoms) at 12 months. The minimal clinically important difference was specified as a 50% decrease in both VAS and VSQ severity scores. There were 5 prespecified secondary outcomes, including quality of life (range, 0-100; higher scores indicate better quality of life), the Vaginal Health Index Score (range, 5-25; higher scores indicate better health), and vaginal histology (premenopausal or postmenopausal status).
Of 85 randomized participants (mean [SD] age, 57 [8] years), 78 (91.7%) completed the 12-month follow-up. From baseline to 12 months, there was no significant difference between the carbon dioxide laser group and the sham group in change in symptom severity (VAS score for overall vaginal symptoms: -17.2 vs -26.6; difference, 9.4 [95% CI, -28.6 to 47.5]; VAS score for the most severe symptom: -24.5 vs -20.4; difference -4.1 [95% CI, -32.5 to 24.3]; VSQ score: -3.1 vs -1.6; difference, -1.5 [95% CI, -5.9 to 3.0]). There were no significant differences between the laser and sham group in the mean quality of life score (6.3 vs 1.4; difference, 4.8 [95% CI, -3.9 to 13.5]) and Vaginal Health Index Score (0.9 vs 1.3; difference, -0.4 [95% CI, -4.3 to 3.6]) or in histological comparisons between laser and sham treatment groups. There were 16 adverse events in the laser group and 17 in the sham group, including vaginal pain/discomfort (44% vs 68%), spotting, discharge, and lower urinary tract symptoms. No severe adverse events were reported in either group.
Among women with postmenopausal vaginal symptoms, treatment with fractional carbon dioxide laser vs sham treatment did not significantly improve vaginal symptoms after 12 months.
Australian and New Zealand Clinical Trials Registry: ACTRN12616001403426.
绝经后阴道症状很常见,且常对女性的生活质量造成负面影响。越来越多的医生推荐使用二氧化碳阴道激光治疗这些症状,但该疗法的疗效尚未得到证实。
确定二氧化碳阴道激光治疗绝经后阴道症状的疗效。
设计、地点和参与者:这是一项为期 12 个月的随访的、单中心、双盲、随机、假对照试验,在澳大利亚悉尼的一家三级转诊医院进行。招募工作于 2016 年 9 月 19 日开始,最终随访于 2020 年 6 月 30 日结束。参与者为有足够阴道症状寻求治疗的绝经后女性。在接触的 232 名参与者中,85 名被随机分组。
使用二氧化碳微剥脱激光系统进行 3 次治疗,每次治疗间隔 4 至 8 周,43 名参与者被随机分配到激光组,42 名参与者被分配到假激光组。
主要终点是使用视觉模拟量表(VAS;范围为 0-100;0 表示无症状,100 表示最严重的症状)和阴道症状问卷(VSQ;范围为 0-20;0 表示无症状,20 表示最严重的症状)在 12 个月时评估的症状严重程度。最小临床重要差异指定为 VAS 和 VSQ 严重程度评分均降低 50%。有 5 个预先指定的次要结局,包括生活质量(范围为 0-100;分数越高表示生活质量越好)、阴道健康指数评分(范围为 5-25;分数越高表示健康状况越好)和阴道组织学(绝经前或绝经后状态)。
在 85 名随机参与者(平均[标准差]年龄为 57[8]岁)中,有 78 名(91.7%)完成了 12 个月的随访。从基线到 12 个月,二氧化碳激光组与假激光组在症状严重程度变化方面无显著差异(阴道整体症状的 VAS 评分:-17.2 对-26.6;差异为 9.4[95%置信区间(CI),-28.6 至 47.5];最严重症状的 VAS 评分:-24.5 对-20.4;差异为-4.1[95%CI,-32.5 至 24.3];VSQ 评分:-3.1 对-1.6;差异为-1.5[95%CI,-5.9 至 3.0])。激光组和假激光组的生活质量评分(6.3 对 1.4;差异为 4.8[95%CI,-3.9 至 13.5])和阴道健康指数评分(0.9 对 1.3;差异为-0.4[95%CI,-4.3 至 3.6])或激光和假激光治疗组之间的组织学比较均无显著差异。激光组有 16 例不良事件,假激光组有 17 例,包括阴道疼痛/不适(44%对 68%)、阴道出血、分泌物和下尿路症状。两组均无严重不良事件报告。
在有绝经后阴道症状的女性中,与假激光治疗相比,二氧化碳阴道激光治疗在 12 个月后并未显著改善阴道症状。
澳大利亚和新西兰临床试验注册中心:ACTRN12616001403426。