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Pretreatment with estrogen does not affect IVF-ICSI cycle outcome compared with no pretreatment in GnRH antagonist protocol: a prospective randomized trial.
Cédrin-Durnerin, Isabelle; Guivarc'h-Levêque, Anne; Hugues, Jean-Noël.
Afiliação
  • Cédrin-Durnerin I; Service de Médecine de la Reproduction, Hôpital Jean Verdier, Assistance Publique-Hôpitaux de Paris, Université Paris XIII, Bondy, France. isabelle.cedrin-durnerin@jvr.ap-hop-paris.fr
Fertil Steril ; 97(6): 1359-64.e1, 2012 Jun.
Article em En | MEDLINE | ID: mdl-22464760
ABSTRACT

OBJECTIVE:

To assess effects of estrogen pretreatment in GnRH antagonist protocol.

DESIGN:

Prospective, randomized multicenter study.

SETTING:

Ten private or university-based centers. PATIENT(S) A total of 472 patients undergoing IVF/ICSI. INTERVENTION(S) Randomization by sealed envelopes to receive 17ß-estradiol (4 mg/d) or no pretreatment before daily recombinant FSH administration started on the first day of estrogen discontinuation or on cycle day 2 in nonpretreated women. MAIN OUTCOME MEASURE(S) The primary outcome measure was the number of retrieved oocytes. Secondary efficacy variables included total FSH dose, cycle duration, and outcome. RESULT(S) The mean numbers of retrieved oocytes (10.9 ± 5.7 vs. 10.2 ± 5.6) and obtained embryos (5.5 ± 3.7 vs. 4.8 ± 3.7) were not significantly different between women allocated to estrogen pretreatment (n = 238) and no pretreatment (n = 234). Total FSH amount (1,557 ± 408 vs. 1,389 ± 347 IU) and stimulation duration (10.8 ± 1.4 vs. 10.0 ± 1.5 days) were slightly but significantly increased in pretreated patients. Positive pregnancy tests, ultrasound pregnancy rate, and delivery rate per cycle were similar (36%, 33%, and 26.6%, respectively, vs. 38.2%, 35.4%, and 30%). CONCLUSION(S) These data confirm that estrogen pretreatment is associated with requirement of higher FSH doses and longer duration of stimulation without any significant increase in the number of retrieved oocytes. However, estrogen does not affect cycle outcome and therefore might be used in clinical practice for programming IVF retrievals during working days. CLINICAL TRIALS REGISTRATION NUMBER NCT01489852.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Indução da Ovulação / Fertilização in vitro / Hormônio Liberador de Gonadotropina / Injeções de Esperma Intracitoplásmicas / Estradiol / Hormônio Foliculoestimulante Tipo de estudo: Clinical_trials / Guideline / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Fertil Steril Ano de publicação: 2012 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Indução da Ovulação / Fertilização in vitro / Hormônio Liberador de Gonadotropina / Injeções de Esperma Intracitoplásmicas / Estradiol / Hormônio Foliculoestimulante Tipo de estudo: Clinical_trials / Guideline / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Fertil Steril Ano de publicação: 2012 Tipo de documento: Article País de afiliação: França
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