Pearlstein T B, Stone A B
Department of Psychiatry and Human Behavior, Brown University, Providence, RI 02906.
J Clin Psychiatry. 1994 Aug;55(8):332-5.
The safety and efficacy of fluoxetine in the short-term treatment of late luteal phase dysphoric disorder (LLPDD) have been shown in several studies, but its efficacy and safety over more than a few cycles have not been demonstrated.
Sixty-four women with prospectively confirmed LLPDD were treated with fluoxetine for a mean of 18.6 months. Response was determined by clinical interview and Clinical Global Impressions rating within the first three cycles, and subjects were followed clinically every 3 to 6 months. Medication dose was titrated on the basis of side effects and response. Women who had been treated for at least 1 year were asked to discontinue medication to reassess the need for treatment.
Sixty women were able to tolerate at least 1 month of treatment. Of these, 57% (N = 34) remained on 20 mg/day and 37% (N = 22) received 40 mg/day. Fifty-two percent (N = 31) achieved remission (CGI score = 1); 48% (N = 29) achieved a partial remission of symptoms (CGI score = 2). The most common side effect was sexual dysfunction, which occurred in 17% of women (N = 10). Symptoms recurred in most women after treatment discontinuation and remitted again with reinstitution of treatment. An earlier age at onset of LLPDD or a prior episode of major depression was associated with achieving only partial remission of symptoms.
These results support the findings of the double-blind studies of fluoxetine treatment for LLPDD. Fluoxetine is an effective and well-tolerated treatment for this condition when used over time. Approximately half of those treated achieved complete remission of their symptoms, while the others experienced significant improvement. This study also lends further support to the effectiveness of serotonergic agents in the treatment of premenstrual symptoms.
多项研究已表明氟西汀在治疗黄体后期烦躁障碍(LLPDD)短期疗效及安全性,但尚未证实其在多个周期以上的疗效及安全性。
64例经前瞻性确诊的LLPDD女性患者接受氟西汀治疗,平均治疗时间为18.6个月。在前三个周期内通过临床访谈和临床总体印象评分来确定疗效,并且每3至6个月对患者进行一次临床随访。根据副作用和疗效调整药物剂量。已接受至少1年治疗的女性被要求停药以重新评估治疗需求。
60名女性能够耐受至少1个月的治疗。其中,57%(n = 34)维持20mg/天的剂量,37%(n = 22)接受40mg/天的剂量。52%(n = 31)达到缓解(临床总体印象评分=1);48%(n = 29)症状部分缓解(临床总体印象评分=2)。最常见的副作用是性功能障碍,17%的女性(n = 10)出现该症状。大多数女性在停药后症状复发,重新开始治疗后症状再次缓解。LLPDD发病年龄较早或既往有重度抑郁发作史的女性仅出现部分症状缓解。
这些结果支持了氟西汀治疗LLPDD的双盲研究结果。长期使用氟西汀治疗LLPDD有效且耐受性良好。约一半接受治疗的患者症状完全缓解,其他患者症状也有显著改善。本研究进一步支持了血清素能药物在治疗经前症状方面的有效性。