2013, Number 07
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Ginecol Obstet Mex 2013; 81 (07)
Clinical comparison of alpha dihidroergocriptina against cabergolina in the treatment of the fibrocystic mastopathy
Castillo-Huerta E, Garibay-Valencia M, Mirabent-González F
Language: Spanish
References: 23
Page: 370-376
PDF size: 583.30 Kb.
ABSTRACT
Background: Fibrocystic breast disease is one of the most
frequent conditions of the breast among women from 30 to
49 years, with a frequency of about 60%, hence the interest
in studying and treating it with the most advanced and
effective resources.
Objective: To compare the efficacy and adverse events of
alpha dihydroergocryptine with cabergoline in patients with
fibrocystic breast disease.
Material and Methods: A prospective, longitudinal, open,
comparative study between alpha-dihydroergocryptine and
cabergoline, made in the service of Gynecology and Obstetrics
at the Dr. Miguel Silva General Hospital in Morelia,
Michoacán. 171 patients diagnosed with fibrocystic breast
disease were randomly assigned to the alpha-dihydroergocryptine
or the cabergoline group. Assessments were made
at baseline and every month subsequently. The following
symptoms were evaluated: breast tenderness, breast pain,
lumps and nipple discharge. The concentrations of prolactin
were determined and an ultrasound was performed at
baseline and at 3 and 6 months, patients were questioned
about adverse events.
Results: 171 patients were included (81 treated with alpha-dihydroergocryptine
and 90 with cabergoline); 156 completed
the study. The age limits were 18 and 51 years. The evolution
time prior to study entry was 17.71 ± 18.3 months for the
alpha-dihydroergocryptine group and 18.57 ± 20.35 for the
cabergoline group. 15 patients discontinued treatment due
to adverse events (8 of the alpha-dihydroergocryptine group
and 7 of the cabergoline group). The most common adverse
event was headache.
Conclusions: In this study alpha-dihydroergocryptine was
better tolerated and had better clinical response compared
with cabergoline; breast pain and breast tenderness disappeared
within the first month of treatment. Adverse events
were similar for both treatments.
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