Ovarian stimulation with daily late follicular phase administration of low-dose human chorionic gonadotropin for in vitro fertilization: a prospective, randomized trial
Autor(a) principal: | |
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Data de Publicação: | 2006 |
Outros Autores: | , , , , |
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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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 |
_version_ |
1814268368974249984 |