Gordon Paul R, Kerwin James P, Boesen Kelly Green, Senf Janet
College of Medicine, University of Arizona, Tucson, AZ 85724, USA.
Menopause. 2006 Jul-Aug;13(4):568-75. doi: 10.1097/01.gme.0000196595.82452.ca.
To evaluate the effectiveness of a selective serotonin reuptake inhibitor (SSRI) (sertraline) in decreasing hot flashes in a general population of women.
A double-blind, placebo-controlled, crossover trial was conducted in a southwestern urban setting. A total of 102 women aged 40 to 65 who were experiencing hot flashes and not taking any hormone therapy were recruited. After 1 week of baseline hot flash data collection, study participants were randomized to receive placebo or active drug (sertraline 50 mg) for 4 weeks. This intervention was followed by a 1-week washout and cross over to the opposite treatment for 4 weeks. The number and severity of hot flashes were measured.
One hundred two women were enrolled in the study. Five dropped out before providing baseline data. Of the 97 remaining, 52 were randomized to active drug first and 45 to placebo first. Ten dropped out of the study before completing all 10 weeks, leaving 46 in the active drug-first arm and 41 in the placebo-first arm. At baseline, the mean number of hot flashes reported was 45.6 per week (SD = 29.6), ranging from 2 to 148. During the sertraline phase of the study, women experienced five fewer hot flashes per week than they did on the placebo (P = 0.002). The severity of hot flashes was not significantly different; however, the hot flash score (number x average severity) was significantly improved during the sertraline phase.
Sertraline reduced the number of hot flashes and improved the hot flash score relative to placebo and may be an acceptable alternative treatment for women experiencing hot flashes.
评估选择性5-羟色胺再摄取抑制剂(SSRI)(舍曲林)在降低普通女性人群潮热发生率方面的效果。
在西南城市地区进行了一项双盲、安慰剂对照的交叉试验。共招募了102名年龄在40至65岁之间、正在经历潮热且未接受任何激素治疗的女性。在收集1周的基线潮热数据后,研究参与者被随机分为接受安慰剂或活性药物(舍曲林50毫克)治疗4周。此干预之后是1周的洗脱期,然后交叉接受相反的治疗4周。测量潮热的次数和严重程度。
102名女性参与了该研究。5名在提供基线数据前退出。在其余的97名中,52名首先被随机分配到活性药物组,45名首先被随机分配到安慰剂组。10名在完成全部10周之前退出研究,活性药物优先组剩下46名,安慰剂优先组剩下41名。在基线时,报告的潮热平均次数为每周45.6次(标准差=29.6),范围为2至148次。在研究的舍曲林阶段,女性每周经历的潮热次数比服用安慰剂时少5次(P = 0.002)。潮热的严重程度没有显著差异;然而,潮热评分(次数×平均严重程度)在舍曲林阶段有显著改善。
与安慰剂相比,舍曲林减少了潮热次数并改善了潮热评分,对于经历潮热的女性可能是一种可接受的替代治疗方法。