SSRI-INDUCED SEXUAL DYSFUNCTION - FLUOXETIME, PAROXETINE, SERTRALINE,AND FLUVOXAMINE IN A PROSPECTIVE, MULTICENTER, AND DESCRIPTIVE CLINICAL-STUDY OF 344 PATIENTS
Al. Montejogonzalez et al., SSRI-INDUCED SEXUAL DYSFUNCTION - FLUOXETIME, PAROXETINE, SERTRALINE,AND FLUVOXAMINE IN A PROSPECTIVE, MULTICENTER, AND DESCRIPTIVE CLINICAL-STUDY OF 344 PATIENTS, Journal of sex & marital therapy, 23(3), 1997, pp. 176-194
The authors analyzed the incidence of sexual dysfunction (SD) with dif
ferent selective serotonin reuptake inhibitors (SSRIs; fluoxetine, flu
voxamine, paroxetine, and sertraline) and hence the qualitative and qu
antitative changes in SD throughout time in a prospective and multicen
ter study. Outpatients (192 women and 152 men; age = 39.6+/-11.4 years
) under treatment with SSRIs were interviewed with an SD questionnaire
designed for this purpose by the authors and that included questions
about the following: decreased libido, delayed orgasm or anorgasmia, d
elayed ejaculation, inability to ejaculate, impotence, and general sex
ual satisfaction. Patients with the following criteria were included:
normal sexual function before SSRI intake, exclusive treatment with SS
RIs or treatment associated with benzodiazepines, previous heterosexua
l or self-erotic current sexual practices. Excluded were patients with
previous sexual dysfunction, association of SSRIs with neuroleptics,
recent hormone intake, and significant medical illnesses. There was a
significant increase in the incidence of SD when physicians asked the
patients direct questions (58%) versus when SD was spontaneously repor
ted (14%). There were some significant differences among different SSR
Is: paroxetine provoked more delay of orgasm or ejaculation and more i
mpotence than fluvoxamine, fluoxetine and sertraline (chi(2), p < .05)
. Only 24.5% of the patients had a good tolerance of their sexual dysf
unction. Twelve male patients who suffered from premature ejaculation
before the treatment preferred to maintain delayed ejaculation, and th
eir sexual satisfaction, and that of their partners, clearly improved.
Sexual dysfunction was positively correlated with dose. Patients expe
rienced substantial improvement in sexual function when the dose was d
iminished or the drug was withdrawn. Men showed more incidence of sexu
al dysfunction than women, but women sexual dysfunction was more inten
se than men's. In only 5.8% of patients, the dysfunction disappeared c
ompletely within 6 months, but 81.4% showed no improvement at all by t
he end of this period. Twelve of 15 patients experienced total improve
ment when the treatment was changed to moclobemide (450-600 mg/day), a
nd 3 of 5 patients improved when treatment was changed to amineptine (
200 mg/day).