The object of this study was to investigate a possible pharmacological
effect of fluoxetine on haemostatic function, with special attention
on primary haemostasis, in order to explain haemorrhagic complications
reported in some treated, depressed patients. The haemostatic functio
n of depressive patients, who required fluoxetine therapy, was studied
before and after 1 month of treatment with fluoxetine 20 or 40 mg dai
ly. Exclusion criteria were: pregnancy, initial abnormal haemostatic f
unction, history of coagulation abnormalities, treatment with drugs th
at interfere with haemostasis, and recent fluoxetine therapy. The foll
owing tests were performed: prothrombin time, partial thromboplastin t
ime, thrombin time, plasma fibrinogen, platelet counts, bleeding time,
platelet aggregation induced by ADP, epinephrine, ristocetin, collage
n, arachidonic acid, and plasma determination of fluoxetine and norflu
oxetine levels. Statistical analysis was performed by Wilcoxon paired
sample, one-tailed test (alpha=0.05). Among 18 patients included, only
eight completed the trial. The single statistically significant diffe
rence was a decreased velocity in platelet aggregation induced by epin
ephrine without increased bleeding time. The results failed to demonst
rate any compromised haemostatic function after 20 mg daily fluoxetine
therapy in patients with initial haemostatic function. However, the r
esults suggest possible effects of fluoxetine on platelet adrenorecept
ors. (C) 1998 John Wiley & Sons, Ltd.