Dopamine agonists in prevention of ovarian hyperstimulation syndrome |
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Authors: | Miro Kasum Hrvoje Vrčić Patrik Stanić Davor Ježek Slavko Orešković Lidija Beketić-Orešković |
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Affiliation: | 1. Department of Obstetrics and Gynaecology, University Hospital Centre Zagreb, School of Medicine, University of ZagrebZagrebCroatia;2. Department of Histology and Embryology, School of Medicine, University of ZagrebZagrebCroatia;3. Department of Oncology, Clinical Hospital Centre Sisters of Mercy, School of Medicine, University of ZagrebZagrebCroatia |
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Abstract: | The aim of this review is to analyze the efficacy of different dopamine agonists in the prevention of ovarian hyperstimulation syndrome (OHSS). Cabergoline, quinagolide and bromocriptine are the most common dopamine agonists used. There are wide clinical variations among the trials in the starting time (from the day of human chorionic gonadotrophin (hCG) to the day following oocyte retrieval); the duration of the treatment (4–21 days), the dose of cabergoline (0.5?mg or 0.25?mg orally) and in the regimens used. At present, the best known effective regimen is 0.5?mg of cabergoline for 8 days or rectal bromocriptine at a daily dose of 2.5?mg for 16 days. Dopamine agonists have shown significant evidences of their efficacy in the prevention of moderate and early-onset OHSS (9.41%), compared with a placebo (21.45%), which cannot be confirmed for the treatment of late OHSS. It would be advisable to start with the treatment on the day of hCG injection or preferably a few hours earlier. The use of dopamine agonists should be indicated in patients at high risk of OHSS, as well as in patients with a history of previous OHSS even without evident signs of the syndrome. |
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Keywords: | Dopamine agonist ovarian hyperstimulation syndrome prevention |
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