よむ、つかう、まなぶ。
資料4-2 セトロレリクス酢酸塩 (12 ページ)
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出典情報 | 医薬・生活衛生局が実施する検討会 医療上の必要性の高い未承認薬・適応外薬検討会議(第50回 1/26)《厚生労働省》 |
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Gynecol Reprod Biol 2005; 120: 185-9.
11) Ernesto Escudero, et al. Comparison of two different starting multiple dose gonadotropinreleasing hormone antagonist protocols in a selected group of in vitro fertilization-embryo
transfer patients. Fertil Steril 2004; 81: 562-6.
12) Raffaella Depalo, et al. Endogenous luteinizing hormone concentration and IVF outcome during
ovarian stimulation in fixed versus flexible GnRH antagonist protocols: An RCT. Int J Reprod
BioMed 2018;16:175-82.
13) Molina B. Dayal, et al. The use of lead follicle diameter to initiate gonadotropin-releasing
hormone antagonist does not affect in vitro fertilization clinical pregnancy, implantation, or live
birth rates: a prospective, randomized study. Fertil Steril 2009; 92: 2047-9.
14) Gonadotrophin‐releasing hormone antagonists for assisted reproductive technology. Cochrane
Database Syst Rev 2016; 4: CD006919.
15) Textbook of Assisted Reproduction. Springer; 2020. p90.
16) 生殖医療ガイドライン. 一般社団法人日本生殖医学会; 2021. p29-31.
17) Tomoko Inoue, et al. Cabergoline administration prevents development of moderate to severe
ovarian hyperstimulation syndrome and it contributes to reduction in ovarian volume. Reprod
Med Biol. 2015; 14: 79-84.
18) Nanako Iwami, et al. New trial of progestin‑primed ovarian stimulation using dydrogesterone
versus a typical GnRH antagonist regimen in assisted reproductive technology. Arch Gynecol
Obstet. 2018; 298: 663-71.
19) Takahashi K, et al. GnRH Antagonist Improved Blastocyst Quality and Pregnancy Outcome
After Multiple Failures of IVF/ICSI–ET with a GnRH Agonist Protocol. J Assist Reprod Genet
2004; 21: 317-22.
20) Atsushi Yanaihara, et al. The decrease of serum luteinizing hormone level by a gonadotropinreleasing hormone antagonist following the mild IVF stimulation protocol for IVF and its
clinical outcome. J Assist Reprod Genet (2008) 25:115–118
21)A. Oride, et al. Comparison of human menopausal gonadotropin stimulation with and without
clomiphene for invitro fertilisation in poor-responders. Journal of Obstetrics and Gynaecology,
February 2015; 35: 163–167
12
11) Ernesto Escudero, et al. Comparison of two different starting multiple dose gonadotropinreleasing hormone antagonist protocols in a selected group of in vitro fertilization-embryo
transfer patients. Fertil Steril 2004; 81: 562-6.
12) Raffaella Depalo, et al. Endogenous luteinizing hormone concentration and IVF outcome during
ovarian stimulation in fixed versus flexible GnRH antagonist protocols: An RCT. Int J Reprod
BioMed 2018;16:175-82.
13) Molina B. Dayal, et al. The use of lead follicle diameter to initiate gonadotropin-releasing
hormone antagonist does not affect in vitro fertilization clinical pregnancy, implantation, or live
birth rates: a prospective, randomized study. Fertil Steril 2009; 92: 2047-9.
14) Gonadotrophin‐releasing hormone antagonists for assisted reproductive technology. Cochrane
Database Syst Rev 2016; 4: CD006919.
15) Textbook of Assisted Reproduction. Springer; 2020. p90.
16) 生殖医療ガイドライン. 一般社団法人日本生殖医学会; 2021. p29-31.
17) Tomoko Inoue, et al. Cabergoline administration prevents development of moderate to severe
ovarian hyperstimulation syndrome and it contributes to reduction in ovarian volume. Reprod
Med Biol. 2015; 14: 79-84.
18) Nanako Iwami, et al. New trial of progestin‑primed ovarian stimulation using dydrogesterone
versus a typical GnRH antagonist regimen in assisted reproductive technology. Arch Gynecol
Obstet. 2018; 298: 663-71.
19) Takahashi K, et al. GnRH Antagonist Improved Blastocyst Quality and Pregnancy Outcome
After Multiple Failures of IVF/ICSI–ET with a GnRH Agonist Protocol. J Assist Reprod Genet
2004; 21: 317-22.
20) Atsushi Yanaihara, et al. The decrease of serum luteinizing hormone level by a gonadotropinreleasing hormone antagonist following the mild IVF stimulation protocol for IVF and its
clinical outcome. J Assist Reprod Genet (2008) 25:115–118
21)A. Oride, et al. Comparison of human menopausal gonadotropin stimulation with and without
clomiphene for invitro fertilisation in poor-responders. Journal of Obstetrics and Gynaecology,
February 2015; 35: 163–167
12