Programa de Pós-Graduação em Ciências da Saúde: Ginecologia e Obstetrícia, Grupo de Pesquisa: Climatério e Menopausa, Serviço de Ginecologia e Obstetrícia, Hospital de Clínicas de Porto Alegre, Faculdade de Medicina, Universidade Federal Do Rio Grande Do Sul, Porto Alegre, Brasil.
Department of Obstetrics and Gynecology, Faculty of Medicine, Aragón Health Research Institute, University of Zaragoza, Zaragoza, Spain.
Gynecol Endocrinol. 2020 Mar;36(3):247-251. doi: 10.1080/09513590.2019.1658189. Epub 2019 Sep 3.
Low doses of sulpiride have been used off-label to treat menopausal hot slashes in Southern Brazil despite limited scientific evidence. This randomized controlled trial aimed at assessing the effects of sulpiride as compared to placebo on the frequency and severity of hot flashes. Postmenopausal women, aged 47-62, were recruited from the Menopause Clinic at Hospital de Clínicas de Porto Alegre, Rio Grande do Sul, Brazil, between March 2016 and January 2017. After a baseline assessment of 4 weeks, women were included if they had at least a mean of five moderate to severe hot flashes per day and then randomized to receive for 8 weeks either placebo (= 14) or sulpiride 50 mg/d (= 14). The number and severity of hot flashes were evaluated after the 8-week intervention. A generalized estimating equations (GEE) model with Bonferroni correction was used to simultaneously assess the frequency and severity of hot flashes. Baseline frequency and severity of hot flashes/day were similar in both groups. Sulpiride significantly reduced the total weekly mean of hot flash frequency (GEE, =.019) and the total weekly mean of severity scores (GEE, =.09, =.006, ≤.0001) after 4 and 8 weeks of treatment. Treatment with sulpiride 50 mg/d significantly reduced the frequency and severity of hot flashes. Further studies are needed to confirm its benefits and related mechanisms of action.
尽管科学证据有限,巴西南部仍有医生将低剂量舒必利(sulpiride)超适应证用于治疗更年期热潮红。本随机对照试验旨在评估舒必利与安慰剂相比对热潮红频率和严重程度的影响。
2016 年 3 月至 2017 年 1 月,巴西南里奥格兰德州阿雷格里港临床医院的更年期诊所招募了年龄在 47-62 岁之间的绝经后女性。经过 4 周的基线评估,如果每天至少有 5 次中度至重度热潮红,且平均严重程度至少为 3 分,则将这些女性纳入研究,并随机分为 8 周的安慰剂组(= 14 例)或舒必利 50mg/d 组(= 14 例)。干预 8 周后评估热潮红的次数和严重程度。采用广义估计方程(GEE)模型和 Bonferroni 校正同时评估热潮红的频率和严重程度。两组的基线热潮红频率和严重程度相似。舒必利治疗 4 周和 8 周后,每周平均总热潮红频率(GEE,= 0.019)和每周平均总严重程度评分(GEE,= 0.09,= 0.006,= 0.0001)均显著降低。舒必利 50mg/d 治疗可显著降低热潮红的频率和严重程度。还需要进一步的研究来证实其益处及其相关作用机制。