BACKGROUND: The presentations of intravenous or depot bromocriptine (b
romocriptine LA or long acting, Pariodel LA(R) and bromocriptine LAR o
r long acting repeteable, Parlodel LAR(R)) have improved the efficacy
and the tolerance of oral bromocriptine. In contrast to bromocriptine
LA, bromocriptine LAR may be repeatedly administered intramuscularly.
METHODS: Five patients with macroprolactinoma and 4 with microprolacti
noma were included in the study. A 50 mg bottle of bromocriptine LAR w
as administered intramuscullarly every month, over a minimum period of
6 months. PRL was determined prior to the study, 1, 3, 7, 14, and 28
days following the initial dose of bromocriptine and thereafter with m
onthly periodicity. RESULTs: The PRL values decreased in those patient
s with macroprolactinomas following the administration of bromocriptin
e LAR; in 2 patients the monthly dosis of bromocriptine LAR was increa
sed to 100 mg since the month after the initial dose PRL remained grea
ter than 200 ng/ml with serum RPL normalizing in most of the patients
at 6 months of treatment. In two of the three patients who presented v
isual changes a clear improvement was observed and in all the cases a
reduction in the size of the macroprolactinoma was found upon CAT cont
rol at 6 months. The PRL values also decreased in the patients with mi
croprolactinomas following administration of bromocriptine LAR, althou
gh the response was not as homogeneous as in the patients with macropr
olactinomas due to that at 6 months 2 patients continued to have sligh
tly elevated serum PRL levels. The microadenoma persisted in the contr
ol CAT at 6 months except in one case. Local and general tolerance to
bromocriptine LAR was very good. CONCLUSIONS: This study indicates goo
d tolerance to bromocriptine LAR, being a therapeutic option in the tr
eatment of macroprolactinomas.