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盐酸帕罗西汀治疗早泄。

Treatment of premature ejaculation with paroxetine hydrochloride.

作者信息

McMahon C G, Touma K

机构信息

Australian Centre for Sexual Health, St. Luke's Hospital, Sydney.

出版信息

Int J Impot Res. 1999 Oct;11(5):241-245; discussion 246. doi: 10.1038/sj.ijir.3900415.

Abstract

AIMS OF THIS STUDY

To evaluate the efficacy of chronic and 'on demand' administration of paroxetine hydrochloride in the drug treatment of premature ejaculation (PE).

MATERIALS AND METHODS

Ninety-four normally potent men, aged 18-61 y (mean 39 y) with premature ejaculation were treated between January 1996 and March 1997, with oral paroxetine hydrochloride, a selective serotonin re-uptake inhibitor (SSRI). All men were either married or in a stable relationship. Sixty-four out of ninety-four men (Group A) were initially treated with paroxetine hydrochloride 20 mg administered once daily. Those men who responded with improved ejaculatory control within four weeks, were then treated with 'on-demand' paroxetine hydrochloride (20 mg) administered 3-4 h prior to planned intercourse. The remaining 33 out of 94 men (Group B) were initially treated with 'on-demand' paroxetine hydrochloride 20 mg administered 3-4 h prior to planned intercourse.

RESULTS

The mean pre-treatment ejaculatory latency time (ELT) of both group A and B was 0.4 min (range 0-1 min) in 205 intercourses at a frequency of 0.4 intercourses per week. In group A after four weeks of daily administration of paroxetine, the mean ELT was 4.5 min (range 1-anejac.) in 761 intercourses at a frequency of 2.4 intercourses per week. Fifty-three out of sixty-one men in group A regarded their ejaculatory control as improved and were then treated with 'on-demand' paroxetine, achieving an ELT of 3.9 min (range 0-10) in 608 intercourses at a frequency of 2.6 intercourses per week. Thirty-six men in this group of 53 regarded that they had maintained improved ejaculatory control with a mean ELT of 5.5 min (range 2-20 min) after a further four weeks of treatment (P < 0.001). The remaining 17 men reported a recurrence of poor ejaculatory control with a mean ELT of 0.7 min (range 0-2 min). In group B with initial 'on-demand' paroxetine after a mean of 4.5 weeks of treatment, the mean ELT was 1.5 min (range 0-5 min) in 298 intercourses at a frequency of 2.2 intercourses per week. Adverse effects were only recorded in men taking daily paroxetine and included anejaculation in 5 out of 61, inhibited orgasm in 3 out of 61 and reduced libido on 3 out of 61. Erectile dysfunction was not reported and 'on demand' paroxetine was not associated with any adverse effects.

CONCLUSIONS

Paroxetine hydrochloride appears to be a useful agent in the pharmacological treatment of premature ejaculation when administered on a chronic, an 'on-demand' basis following chronic treatment or initial 'on demand' basis.

摘要

本研究目的

评估盐酸帕罗西汀长期及“按需”给药在早泄药物治疗中的疗效。

材料与方法

1996年1月至1997年3月,对94名18 - 61岁(平均39岁)患有早泄的性功能正常男性,使用选择性5-羟色胺再摄取抑制剂(SSRI)盐酸帕罗西汀进行口服治疗。所有男性均已婚或处于稳定恋爱关系。94名男性中的64名(A组)最初接受每日一次20mg盐酸帕罗西汀治疗。在四周内射精控制得到改善的男性,随后在计划性交前3 - 4小时接受“按需”盐酸帕罗西汀(20mg)治疗。94名男性中的其余33名(B组)最初在计划性交前3 - 4小时接受“按需”20mg盐酸帕罗西汀治疗。

结果

A组和B组在每周0.4次性交频率的205次性交中,治疗前平均射精潜伏期(ELT)为0.4分钟(范围0 - 1分钟)。A组在每日服用帕罗西汀四周后,在每周2.4次性交频率的761次性交中,平均ELT为4.5分钟(范围1 - 无射精)。A组61名男性中有53名认为其射精控制得到改善,随后接受“按需”帕罗西汀治疗,在每周2.6次性交频率的608次性交中,ELT为3.9分钟(范围0 - 10)。在这53名男性中,36名认为在进一步治疗四周后他们仍保持射精控制改善,平均ELT为5.5分钟(范围2 - 20分钟)(P < 0.001)。其余17名男性报告射精控制再次变差,平均ELT为0.7分钟(范围0 - 2分钟)。B组最初“按需”服用帕罗西汀,在平均4.5周的治疗后,在每周2.2次性交频率的298次性交中,平均ELT为1.5分钟(范围0 - 5分钟)。仅在每日服用帕罗西汀的男性中记录到不良反应,61名中有5名无射精,61名中有3名性高潮受抑制,61名中有3名性欲降低。未报告勃起功能障碍,“按需”服用帕罗西汀未出现任何不良反应。

结论

盐酸帕罗西汀在长期给药、长期治疗后“按需”给药或最初“按需”给药时,似乎是早泄药物治疗中的一种有效药物。

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