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一项多中心、开放标签研究,旨在评估使用经皮雌二醇/醋酸炔诺酮疗法治疗绝经症状和体征的女性的满意度和绝经后生活质量。

A multicenter, open-label study to evaluate satisfaction and menopausal quality of life in women using transdermal estradiol/norethindrone acetate therapy for the management of menopausal signs and symptoms.

作者信息

Adler George, Young Douglas, Galant Ron, Quinn Laura, Witchger Mary Sue, Maki Kevin C

机构信息

Florida GYN Group, Orlando, Florida, USA.

出版信息

Gynecol Obstet Invest. 2005;59(4):212-9. doi: 10.1159/000084346. Epub 2005 Mar 7.

Abstract

AIM

This multicenter, open-label, single-arm study evaluated subject satisfaction and improvements in menopausal quality of life among menopausal women using the CombiPatch transdermal system consisting of 17beta-estradiol 0.05 mg plus norethindrone acetate 0.14 mg in a matrix patch formulation.

METHODS

The 193 postmenopausal women between the ages of 45 and 65 years who comprised the modified intent-to-treat population (at least one patch and one efficacy assessment) were required to have reported at least five daily moderate-to-severe hot flashes and episodes of nocturnal sweating upon study entry for at least 1 month and applied one patch twice a week for 12 weeks. At weeks 0, 6, and 12, the women completed the Menopause-Specific Quality of Life (MENQOL) Questionnaire and, as a secondary study outcome, reported the scale of their application site discomfort. During weeks 1-12, they also kept diary records of number and severity of hot flashes and four other menopausal symptoms. Skin tolerance and adherence of the transdermal system were evaluated at weeks 6 and 12 by qualified evaluators. At week 6 and the end of the study, both subjects and physicians rated their satisfaction with the system.

RESULTS

Among women in the modified intent-to-treat population, transdermal 17beta-estradiol plus norethindrone acetate significantly reduced the mean daily number of moderate-to-severe hot flashes experienced by women from 4.1 at week 1 to 0.6 at week 12 (p < 0.0001). The mean ratings of headache severity, insomnia, and vaginal irritation/dryness also improved significantly by week 6 and were maintained at week 12. At week 12, 92.4% of the subjects and 97.3% of the physicians reported that they were 'satisfied' or 'very satisfied' with the transdermal hormone delivery system.

CONCLUSIONS

The results of this study compare favorably with previous placebo-controlled studies of transdermal hormone therapy in managing menopausal signs and symptoms. Furthermore, quality of life was significantly improved by the transdermal hormone therapy system, and both subjects and physicians reported high levels of satisfaction.

摘要

目的

本多中心、开放标签、单臂研究评估了使用由0.05毫克17β - 雌二醇加0.14毫克醋酸炔诺酮组成的基质贴片剂型的复方贴片经皮系统的绝经后女性的受试者满意度和绝经生活质量的改善情况。

方法

构成改良意向性治疗人群(至少使用一片贴片并进行一次疗效评估)的193名45至65岁的绝经后女性,在研究入组时需报告至少1个月以来每天至少有5次中度至重度潮热和夜间出汗发作,并每周两次应用一片贴片,持续12周。在第0、6和12周,这些女性完成绝经特异性生活质量(MENQOL)问卷,作为次要研究结果,报告她们应用部位不适的程度。在第1至12周期间,她们还记录潮热及其他四种绝经症状的发作次数和严重程度的日记。在第6周和第12周由合格评估人员评估经皮系统的皮肤耐受性和粘贴性。在第6周和研究结束时,受试者和医生都对该系统的满意度进行评分。

结果

在改良意向性治疗人群的女性中,经皮给予17β - 雌二醇加醋酸炔诺酮显著降低了女性经历的中度至重度潮热的平均每日发作次数,从第1周的4.1次降至第12周的0.6次(p < 0.0001)。头痛严重程度、失眠以及阴道刺激/干燥的平均评分在第6周时也显著改善,并在第12周时保持。在第12周时,92.4%的受试者和97.3%的医生报告他们对经皮激素递送系统“满意”或“非常满意”。

结论

本研究结果与先前关于经皮激素疗法治疗绝经症状和体征的安慰剂对照研究相比具有优势。此外,经皮激素疗法系统显著改善了生活质量,受试者和医生均报告高度满意。

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