Comparison of different starting gonadotropin doses (50, 75 and 100 IU daily) for ovulation induction combined with intrauterine insemination
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu klinické zkoušky, srovnávací studie, časopisecké články
PubMed
22736041
PubMed Central
PMC3439605
DOI
10.1007/s00404-012-2414-3
Knihovny.cz E-zdroje
- MeSH
- dospělí MeSH
- endometrium účinky léků MeSH
- folikuly stimulující hormon lidský aplikace a dávkování MeSH
- indukce ovulace metody MeSH
- lidé MeSH
- ovariální folikul účinky léků MeSH
- ovariální hyperstimulační syndrom epidemiologie MeSH
- prospektivní studie MeSH
- rekombinantní proteiny aplikace a dávkování MeSH
- těhotenství mnohočetné statistika a číselné údaje MeSH
- těhotenství MeSH
- úhrn těhotenství na počet žen v reprodukčním věku * MeSH
- umělá inseminace MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mužské pohlaví MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky MeSH
- srovnávací studie MeSH
- Názvy látek
- folikuly stimulující hormon lidský MeSH
- follitropin beta MeSH Prohlížeč
- rekombinantní proteiny MeSH
PURPOSE: To prevent multiple pregnancies the goal of ovulation induction by gonadotropins is to achieve only mono-follicular development. The most important issue is therefore to determine the starting dose. The aim of this study is to compare three different starting doses of follitropin beta to assess the lowest effective dose. METHODS: We evaluated 92 cycles with ovarian stimulation for patients with unexplained infertility, anovulatory disorder or mild male factor. We prospectively divided patients into 50, 75 and 100 IU groups based on patients' response to clomiphene citrate treatment. RESULTS: We performed 87 intrauterine inseminations (95 % of cycles with ovulation induction). Five cycles were cancelled. We achieved 15 pregnancies; total pregnancy rate was 18 %. Pregnancy rate was 22, 10 and 28 % in 50, 75 and 100 IU follitropin beta groups. The average number of follicles was 2.0 ± 0.8, 2.2 ± 1.1 and 2.5 ± 1.8 (ns), total dose of gonadotropins (IU) 483 ± 192, 600 ± 151 and 830 ± 268 (p < 0.001), respectively. We observed one case of twins in 75 and 100 IU treatment group, as well (25 % risk). CONCLUSIONS: This study suggests that based on the dose which was chosen according to clomiphene citrate response, all treatment regimes were effective for ovulation induction. 50 IU of follitropin beta daily is the appropriate starting dose to support ovulation for clomiphene citrate-sensitive women. The disadvantage may be an increased risk of cycle cancellation due to low ovarian response. Daily doses 75 or 100 IU of rFSH increase total consumption of gonadotropins.
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