Stimulation goals in a hyper-responder |
1. The target number of oocytes to be collected in a stimulation cycle for IVF in an anticipated hyper-responder is 15–19. |
2. For a potential hyper-responder, I would rather achieve a hyper-response and freeze all than aim for a fresh transfer |
Treatment protocol in an anticipated hyper-responder |
3. GnRH agonists should be avoided for pituitary suppression in anticipated hyper-responders performing IVF. |
4. I do not use any specific algorithm to estimate the starting dose for an IVF cycle |
5. The preferred starting dose in the first IVF stimulation cycle of an anticipated hyper-responder of average weight is 150 IU/day. |
6. Body weight should be considered to determine the daily gonadotropin dosage for an anticipated hyper-responder undergoing IVF. |
7. Increasing the starting gonadotropin dose in the first IVF cycle of an anticipated hyper-responder is recommended if her weight is above 80 kg |
Cycle modifications in response to a hyper-response |
8. I decrease gonadotropin dosage in the middle of an IVF cycle if the patient seems to hyper-respond based on serum estradiol levels and/or number of growing follicles > 10mm. |
9. Under the risk of hyper-response during stimulation, I would not trigger one to two days before the patient reaches my usual trigger criteria. |
10. I do not use coasting to decrease the risk of OHSS. |
Use of adjuvants during the stimulation of a hyper-responder |
11. I add metformin before/during ovarian stimulation to anticipated hyper-responders only if the woman has PCOS and is insulin resistant. |
12. I do not add any adjuvants from the first day of stimulation to a potential hyper-responder. |
13. During ovarian stimulation, I do not add any adjuvant if the patient seems to hyper-respond based on serum estradiol levels and/or number of growing follicles > 10 mm. |
Choice of trigger in a hyper-responder |
14. On the day of ovulation trigger, if the number of follicles > 10 mm and the estradiol levels are discordant, I would decide to use a GnRH agonist trigger alone based on the number of follicles > 10 mm. |
15. There is no minimal estradiol level on the day of trigger that would require agonist trigger alone |
16. On the day of ovulation trigger, the minimal number of follicles > 10 mm that would require agonist trigger alone (in an antagonist cycle) is 18 |
OHSS prevention and the use of dopaminergic agent |
17. In the case of a hyper-response, a dopaminergic agent should be used only if hCG will be used as a trigger (including dual/double trigger) with or without a fresh transfer. |
18. For maximal effectiveness, cabergoline 0.5 mg for OHSS prevention should be started on the day of trigger. |
19. For maximal effectiveness in OHSS prevention, cabergoline 0.5 mg should be continued for 7 days. |
20. In a woman with a hyper-response, triggered with hCG, the only interventions I would add to prevent OHSS are freeze all and the use of cabergoline. |
21. In a woman with a hyper-response, triggered with GnRH agonist the only interventions I would add to prevent OHSS is freeze all. |
22. If a hyper-response occurred after a trigger that included hCG I would always freeze all |
23. After using a GnRH agonist trigger due to a perceived risk of OHSS, I would not consider a luteal phase rescue with hCG and attempt a fresh transfer regardless of the number of oocytes collected. |
FET protocol in a hyper-responder |
24. My choice of FET protocol is not influenced by the fact that the patient is a hyper-responder. |
25. In cases of freeze all due to an OHSS risk, I perform an FET cycle in the immediate first menstrual cycle. |
OHSS management |
26. I would recommend admission following a hyper-response after the diagnosis of severe OHSS. |