Manejo Racional de Psicofármacos en la Mujer - IGBA
Manejo Racional de Psicofármacos en la Mujer - IGBA
Manejo Racional de Psicofármacos en la Mujer - IGBA
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Continuous or intermitt<strong>en</strong>t dosing with sertraline<br />
for pati<strong>en</strong>ts with severe prem<strong>en</strong>strual syndrome<br />
or prem<strong>en</strong>strual dysphoric disor<strong>de</strong>r.<br />
Xiao S<br />
Am J Psychiatry 2004 Feb;161(2):343-51.<br />
OBJECTIVE: The authors compared the efficacy and acceptability of continuous versus intermitt<strong>en</strong>t<br />
treatm<strong>en</strong>t with a selective serotonin reuptake inhibitor in wom<strong>en</strong> with severe prem<strong>en</strong>strual syndrome<br />
and <strong>de</strong>termined the effects of postm<strong>en</strong>strual symptom severity and <strong>de</strong>pression history as covariates of<br />
the treatm<strong>en</strong>t response. METHOD: Pati<strong>en</strong>ts who met symptom criteria and reported impaired<br />
functioning after three scre<strong>en</strong>ing cycles were randomly assigned to three cycles of double-blind,<br />
p<strong>la</strong>cebo-controlled treatm<strong>en</strong>t with continuous (full-cycle dosing) or intermitt<strong>en</strong>t (luteal-phase dosing)<br />
sertraline. The <strong>de</strong>sign was stratified for severity of postm<strong>en</strong>strual symptoms and history of major<br />
<strong>de</strong>pression. Flexible sertraline dose was 50-100 mg/day. Outcome measures were the Daily Symptom<br />
Rating Form score and pati<strong>en</strong>t global ratings of functioning. RESULTS: Both sertraline groups<br />
improved significantly more than the p<strong>la</strong>cebo group as assessed by total prem<strong>en</strong>strual Daily<br />
Symptom Rating Form scores for 3 treatm<strong>en</strong>t months. Daily Symptom Rating Form factors that were<br />
significantly more improved in the sertraline groups were mood and physical symptoms. Sertraline<br />
improvem<strong>en</strong>t occurred swiftly in the first month of treatm<strong>en</strong>t. Gradual p<strong>la</strong>cebo improvem<strong>en</strong>t was<br />
simi<strong>la</strong>r to sertraline in the third month. Subjects with higher postm<strong>en</strong>strual symptoms before<br />
treatm<strong>en</strong>t remained more symptomatic regardless of the dosing regim<strong>en</strong>. A history of major<br />
<strong>de</strong>pression was not associated with treatm<strong>en</strong>t response. More sertraline-treated subjects reported<br />
improved functioning in the domains of family re<strong>la</strong>tionships, social activities, and sexual activity.<br />
CONCLUSIONS: Prem<strong>en</strong>strual dosing does not differ from continuous dosing with sertraline in<br />
prem<strong>en</strong>strual syndrome treatm<strong>en</strong>t. Higher levels of postm<strong>en</strong>strual symptoms limit treatm<strong>en</strong>t response<br />
and are important to <strong>de</strong>fine in treatm<strong>en</strong>t of prem<strong>en</strong>strual syndrome.