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Updated: Apr 26, 2026

Fertility Preservation Through Oocyte Vitrification: Clinical and Laboratory Perspectives
Published on: September 16, 2021
Dopamine agonists in prevention of ovarian hyperstimulation syndrome
Miro Kasum1, Hrvoje Vrčić1, Patrik Stanić1
1a Department of Obstetrics and Gynaecology, University Hospital Centre Zagreb, School of Medicine, University of Zagreb Zagreb Croatia.
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.
Insights
Dopamine agonists like cabergoline effectively prevent moderate and early-onset ovarian hyperstimulation syndrome (OHSS). Treatment should start around human chorionic gonadotrophin (hCG) injection, especially for high-risk patients.
Area of Science:
- Reproductive Endocrinology
- Pharmacology
- Obstetrics & Gynecology
Background:
- Ovarian hyperstimulation syndrome (OHSS) is a potential complication of assisted reproductive technologies.
- Dopamine agonists are frequently used to prevent OHSS, but optimal regimens vary.
- Existing literature shows inconsistent findings regarding the efficacy of different dopamine agonists and protocols.
Purpose of the Study:
- To review and analyze the effectiveness of various dopamine agonists in preventing OHSS.
- To identify optimal timing, dosage, and duration for dopamine agonist therapy in OHSS prevention.
- To evaluate the efficacy of dopamine agonists for early-onset versus late-onset OHSS.
Main Methods:
- Systematic review of clinical trials investigating dopamine agonists (cabergoline, quinagolide, bromocriptine) for OHSS prevention.
- Analysis of variations in treatment protocols, including timing, dosage, and duration.
- Comparison of OHSS incidence rates between dopamine agonist groups and placebo groups.
Main Results:
- Dopamine agonists demonstrated significant efficacy in preventing moderate and early-onset OHSS (9.41%) compared to placebo (21.45%).
- Efficacy for preventing late-onset OHSS was not confirmed.
- Optimal regimens identified include 0.5 mg of cabergoline for 8 days or 2.5 mg of rectal bromocriptine for 16 days.
Conclusions:
- Dopamine agonists are effective in preventing early-onset and moderate OHSS.
- Initiating treatment on the day of human chorionic gonadotrophin (hCG) injection or slightly before is recommended.
- Dopamine agonists should be considered for patients at high risk of OHSS or with a history of the syndrome.
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