Clinical outcomes of potential high responders after individualized FSH dosing based on anti-Müllerian hormone and body weight
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
34756645
DOI
10.1016/j.rbmo.2021.08.024
PII: S1472-6483(21)00423-5
Knihovny.cz E-resources
- Keywords
- Anti-Müllerian hormone (AMH), Individualized FSH dosing, Ovarian response, Risk of OHSS,
- MeSH
- Anti-Mullerian Hormone blood MeSH
- Adult MeSH
- Fertilization in Vitro methods MeSH
- Follicle Stimulating Hormone, Human administration & dosage MeSH
- Ovulation Induction adverse effects MeSH
- Humans MeSH
- Ovarian Hyperstimulation Syndrome blood etiology MeSH
- Birth Rate MeSH
- Progesterone blood MeSH
- Recombinant Proteins administration & dosage MeSH
- Retrospective Studies MeSH
- Pregnancy MeSH
- Body Weight physiology MeSH
- Pregnancy Rate MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Pregnancy MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Anti-Mullerian Hormone MeSH
- Follicle Stimulating Hormone, Human MeSH
- follitropin alfa MeSH Browser
- follitropin delta MeSH Browser
- Progesterone MeSH
- Recombinant Proteins MeSH
RESEARCH QUESTION: How does the efficacy and safety of individualized follitropin delta dosing compare with conventional dosing for ovarian stimulation in potential high responders? DESIGN: Retrospective analysis of 153 potential high responders identified on the basis of baseline serum anti-Müllerian hormone (AMH) levels above 35 pmol/l, who were originally randomized to an individualized fixed dose of follitropin delta based on AMH and body weight (n = 78) or to a daily starting dose of 150 IU follitropin alfa (n = 75). RESULTS: At the end of stimulation, patients treated with individualized follitropin delta or conventional follitropin alfa had 12.1 ± 7.0 and 18.3 ± 7.0 (P < 0.001) follicles measuring 12 mm or wider, and 27.3% and 62.7% had serum progesterone levels higher than 3.18 nmol/l (P < 0.001), respectively. Overall number of oocytes in these two respective arms was 9.3 ± 6.7 and 17.9 ± 8.7 (P < 0.001), and the ongoing pregnancy rate per started cycle after fresh blastocyst transfer was 28.2% and 24.0%. The risk of ovarian hyperstimulation syndrome (OHSS) for all cases was three times higher in the conventional follitropin alfa arm at 16.0% versus 5.1% with individualized follitropin delta treatment (P = 0.025) and 26.7% versus 7.7% (P = 0.001) for early moderate or severe OHSS, preventive interventions for early OHSS, or both. CONCLUSIONS: Treatment with individualized follitropin delta provides an improved efficacy-safety balance in women with high ovarian reserve, as it normalizes the ovarian response and decreases the risk of OHSS without compromising the chance of pregnancy.
Ferring Pharmaceuticals Global Biometrics Kay Fiskers Plads 11 Copenhagen DK 2300 Denmark
Ginemed Calle Farmaceutico Murillo Herrera 3 Sevilla 41010 Spain
IRCCS San Raffaele Hospital Via Olgettina 60 Milan 20132
IVF Cube Fertility Clinic Evropská 423 Prague 160 00 Czech Republic
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