Ovarian stimulation with daily late follicular phase administration of low-dose human chorionic gonadotropin for in vitro fertilization: a prospective, randomized trial

Detalhes bibliográficos
Autor(a) principal: Serafini, Paulo
Data de Publicação: 2006
Outros Autores: Yadid, Isaac, Motta, Eduardo L. A. [UNIFESP], Alegretti, Jose R., Fioravanti, Joyce, Coslovsky, Marcio
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1016/j.fertnstert.2006.02.110
http://repositorio.unifesp.br/handle/11600/29160
Resumo: Objective: Evaluate the effectiveness of a new ovarian stimulation (OS) protocol before IVF.Design: Prospective centers.Setting: Private centers.Patient(s): Three hundred and twenty-three intended-to-treat women candidates for IVF.Intervention(s): Patients were divided into three groups and administered the following treatments: group A, recombinant hFSH from day 3 until follicles reached 13-14mm, when recombinant hFSH was lowered to 75 IU daily and daily injections of 200 IU of hCG and a GnRH antagonist were administered until final maturation; group B, recombinant hFSH and a GnRH antagonist; group C, recombinant hFSH and a GnRH agonist.Main Outcome Measure(s): Primary outcome was the number of mature oocytes. Secondary outcomes included average initial and total recombinant hFSH dosage, serum E-2 level on day of ovulation, number of oocytes retrieved, fertilization, number of top-quality embryos, endometrial thickness, implantation rate, pregnancy rate (PR), and incidence of ovarian hyperstimulation syndrome (OHSS).Result(s): the numbers of oocytes retrieved, mature oocytes, fertilization, top-quality embryos, and embryos transferred were comparable in all groups. Implantation rate, PR, and incidence of OHSS were also comparable. the total dose of recombinant hFSH was significantly lower in group A (1,674.7 +/- 59.4 IU. vs. 2,197.9 +/- 77.8 IU in group B and 2,156.7 +/- 80.9 IU in group C).Conclusion(s): This new OS protocol permits follicles and oocytes to fully develop, helps generate top-quality embryos, avoids premature ovulation, establishes clinical pregnancies, reduces administration of recombinant hFSH, minimizes costs, and does not increase the chances of OHSS.
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spelling Ovarian stimulation with daily late follicular phase administration of low-dose human chorionic gonadotropin for in vitro fertilization: a prospective, randomized trialovarian stimulationin vitro fertilizationlow-dose hCGObjective: Evaluate the effectiveness of a new ovarian stimulation (OS) protocol before IVF.Design: Prospective centers.Setting: Private centers.Patient(s): Three hundred and twenty-three intended-to-treat women candidates for IVF.Intervention(s): Patients were divided into three groups and administered the following treatments: group A, recombinant hFSH from day 3 until follicles reached 13-14mm, when recombinant hFSH was lowered to 75 IU daily and daily injections of 200 IU of hCG and a GnRH antagonist were administered until final maturation; group B, recombinant hFSH and a GnRH antagonist; group C, recombinant hFSH and a GnRH agonist.Main Outcome Measure(s): Primary outcome was the number of mature oocytes. Secondary outcomes included average initial and total recombinant hFSH dosage, serum E-2 level on day of ovulation, number of oocytes retrieved, fertilization, number of top-quality embryos, endometrial thickness, implantation rate, pregnancy rate (PR), and incidence of ovarian hyperstimulation syndrome (OHSS).Result(s): the numbers of oocytes retrieved, mature oocytes, fertilization, top-quality embryos, and embryos transferred were comparable in all groups. Implantation rate, PR, and incidence of OHSS were also comparable. the total dose of recombinant hFSH was significantly lower in group A (1,674.7 +/- 59.4 IU. vs. 2,197.9 +/- 77.8 IU in group B and 2,156.7 +/- 80.9 IU in group C).Conclusion(s): This new OS protocol permits follicles and oocytes to fully develop, helps generate top-quality embryos, avoids premature ovulation, establishes clinical pregnancies, reduces administration of recombinant hFSH, minimizes costs, and does not increase the chances of OHSS.Huntington Ctr Reprod Med, São Paulo, BrazilHuntington Ctr Reprod Med, Rio de Janeiro, BrazilCtr Human Reprod Hosp & Matern Santa Joana, São Paulo, BrazilUniversidade Federal de São Paulo, Paulista Sch Med, Dept Gynecol, São Paulo, BrazilUniversidade Federal de São Paulo, Paulista Sch Med, Dept Gynecol, São Paulo, BrazilWeb of ScienceElsevier B.V.Huntington Ctr Reprod MedCtr Human Reprod Hosp & Matern Santa JoanaUniversidade Federal de São Paulo (UNIFESP)Serafini, PauloYadid, IsaacMotta, Eduardo L. A. [UNIFESP]Alegretti, Jose R.Fioravanti, JoyceCoslovsky, Marcio2016-01-24T12:41:29Z2016-01-24T12:41:29Z2006-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion830-838http://dx.doi.org/10.1016/j.fertnstert.2006.02.110Fertility and Sterility. New York: Elsevier B.V., v. 86, n. 4, p. 830-838, 2006.10.1016/j.fertnstert.2006.02.1100015-0282http://repositorio.unifesp.br/handle/11600/29160WOS:000241165400009engFertility and Sterilityinfo:eu-repo/semantics/openAccesshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policyreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2016-01-24T10:41:29Zoai:repositorio.unifesp.br/:11600/29160Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652016-01-24T10:41:29Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Ovarian stimulation with daily late follicular phase administration of low-dose human chorionic gonadotropin for in vitro fertilization: a prospective, randomized trial
title Ovarian stimulation with daily late follicular phase administration of low-dose human chorionic gonadotropin for in vitro fertilization: a prospective, randomized trial
spellingShingle Ovarian stimulation with daily late follicular phase administration of low-dose human chorionic gonadotropin for in vitro fertilization: a prospective, randomized trial
Serafini, Paulo
ovarian stimulation
in vitro fertilization
low-dose hCG
title_short Ovarian stimulation with daily late follicular phase administration of low-dose human chorionic gonadotropin for in vitro fertilization: a prospective, randomized trial
title_full Ovarian stimulation with daily late follicular phase administration of low-dose human chorionic gonadotropin for in vitro fertilization: a prospective, randomized trial
title_fullStr Ovarian stimulation with daily late follicular phase administration of low-dose human chorionic gonadotropin for in vitro fertilization: a prospective, randomized trial
title_full_unstemmed Ovarian stimulation with daily late follicular phase administration of low-dose human chorionic gonadotropin for in vitro fertilization: a prospective, randomized trial
title_sort Ovarian stimulation with daily late follicular phase administration of low-dose human chorionic gonadotropin for in vitro fertilization: a prospective, randomized trial
author Serafini, Paulo
author_facet Serafini, Paulo
Yadid, Isaac
Motta, Eduardo L. A. [UNIFESP]
Alegretti, Jose R.
Fioravanti, Joyce
Coslovsky, Marcio
author_role author
author2 Yadid, Isaac
Motta, Eduardo L. A. [UNIFESP]
Alegretti, Jose R.
Fioravanti, Joyce
Coslovsky, Marcio
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Huntington Ctr Reprod Med
Ctr Human Reprod Hosp & Matern Santa Joana
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Serafini, Paulo
Yadid, Isaac
Motta, Eduardo L. A. [UNIFESP]
Alegretti, Jose R.
Fioravanti, Joyce
Coslovsky, Marcio
dc.subject.por.fl_str_mv ovarian stimulation
in vitro fertilization
low-dose hCG
topic ovarian stimulation
in vitro fertilization
low-dose hCG
description Objective: Evaluate the effectiveness of a new ovarian stimulation (OS) protocol before IVF.Design: Prospective centers.Setting: Private centers.Patient(s): Three hundred and twenty-three intended-to-treat women candidates for IVF.Intervention(s): Patients were divided into three groups and administered the following treatments: group A, recombinant hFSH from day 3 until follicles reached 13-14mm, when recombinant hFSH was lowered to 75 IU daily and daily injections of 200 IU of hCG and a GnRH antagonist were administered until final maturation; group B, recombinant hFSH and a GnRH antagonist; group C, recombinant hFSH and a GnRH agonist.Main Outcome Measure(s): Primary outcome was the number of mature oocytes. Secondary outcomes included average initial and total recombinant hFSH dosage, serum E-2 level on day of ovulation, number of oocytes retrieved, fertilization, number of top-quality embryos, endometrial thickness, implantation rate, pregnancy rate (PR), and incidence of ovarian hyperstimulation syndrome (OHSS).Result(s): the numbers of oocytes retrieved, mature oocytes, fertilization, top-quality embryos, and embryos transferred were comparable in all groups. Implantation rate, PR, and incidence of OHSS were also comparable. the total dose of recombinant hFSH was significantly lower in group A (1,674.7 +/- 59.4 IU. vs. 2,197.9 +/- 77.8 IU in group B and 2,156.7 +/- 80.9 IU in group C).Conclusion(s): This new OS protocol permits follicles and oocytes to fully develop, helps generate top-quality embryos, avoids premature ovulation, establishes clinical pregnancies, reduces administration of recombinant hFSH, minimizes costs, and does not increase the chances of OHSS.
publishDate 2006
dc.date.none.fl_str_mv 2006-10-01
2016-01-24T12:41:29Z
2016-01-24T12:41:29Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.fertnstert.2006.02.110
Fertility and Sterility. New York: Elsevier B.V., v. 86, n. 4, p. 830-838, 2006.
10.1016/j.fertnstert.2006.02.110
0015-0282
http://repositorio.unifesp.br/handle/11600/29160
WOS:000241165400009
url http://dx.doi.org/10.1016/j.fertnstert.2006.02.110
http://repositorio.unifesp.br/handle/11600/29160
identifier_str_mv Fertility and Sterility. New York: Elsevier B.V., v. 86, n. 4, p. 830-838, 2006.
10.1016/j.fertnstert.2006.02.110
0015-0282
WOS:000241165400009
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Fertility and Sterility
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
eu_rights_str_mv openAccess
rights_invalid_str_mv http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.format.none.fl_str_mv 830-838
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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