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An extremely patient-friendly and efficient stimulation protocol for assisted reproductive technology in normal and high responders
BACKGROUND: The use of oral progestin has been shown to effectively prevent luteining hormone (LH) surge during ovarian stimulation with daily human menopausal gonadotropin injections. This study was aimed to investigate the efficacy of long-acting follicle stimulating hormone (long-acting FSH; cori...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836459/ https://www.ncbi.nlm.nih.gov/pubmed/29506543 http://dx.doi.org/10.1186/s12958-018-0335-0 |
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author | Huang, Chen-Yu Chen, Guan-Yeu Shieh, Miawh-Lirng Li, Hsin-Yang |
author_facet | Huang, Chen-Yu Chen, Guan-Yeu Shieh, Miawh-Lirng Li, Hsin-Yang |
author_sort | Huang, Chen-Yu |
collection | PubMed |
description | BACKGROUND: The use of oral progestin has been shown to effectively prevent luteining hormone (LH) surge during ovarian stimulation with daily human menopausal gonadotropin injections. This study was aimed to investigate the efficacy of long-acting follicle stimulating hormone (long-acting FSH; corifollitropin alfa, Elonva®) use in progestin-primed ovarian stimulation for normal and high responders undergoing IVF/ICSI. METHODS: This is a retrospective and proof-of-concept study. We developed an extremely patient-friendly protocol to be applied to forty-five normal or high responders, in which a single injection of corifollitropin alfa (Elonva®) was administered and medroxyprogesterone acetate (MPA) was taken orally every day from the day after Elonva injection to the day of trigger. Seven days after Elonva injection, folliculometry and hormone tests were performed, followed by short-acting daily FSH/LH injections, if needed, until the day before trigger. Duration of stimulation, number of injections and visits before trigger, incidence of premature LH surge, the number of oocytes retrieved, fertilization rate, cleavage rate, the rate of day 2 good embryos available, and cumulative ongoing pregnancy rate per retrieval were assessed. RESULTS: The average age of the population was 34.7 years. Duration of stimulation was 9.4 days in average. Before trigger, only 3.6 injection shots and 1.4 visits were needed on average. There was no case of premature LH surge. Number of oocytes retrieved was 13.7, fertilization rate was 79.04%, cleavage rate was 91.11%, and day 2 good embryo rate was 64.34%, in average respectively. There was no case of ovarian hyperstimulation syndrome. The cumulative ongoing pregnancy rate per oocyte retrieval achieved a satisfactory level as 53.1%. CONCLUSIONS: Our protocol consisting of long-acting FSH injection and oral MPA preventing LH surge reduces the number of injections and visits to an extreme and achieves a satisfactory reproductive outcome, and, therefore, is a really patient-friendly and effective approach to ovarian stimulation. |
format | Online Article Text |
id | pubmed-5836459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58364592018-03-07 An extremely patient-friendly and efficient stimulation protocol for assisted reproductive technology in normal and high responders Huang, Chen-Yu Chen, Guan-Yeu Shieh, Miawh-Lirng Li, Hsin-Yang Reprod Biol Endocrinol Research BACKGROUND: The use of oral progestin has been shown to effectively prevent luteining hormone (LH) surge during ovarian stimulation with daily human menopausal gonadotropin injections. This study was aimed to investigate the efficacy of long-acting follicle stimulating hormone (long-acting FSH; corifollitropin alfa, Elonva®) use in progestin-primed ovarian stimulation for normal and high responders undergoing IVF/ICSI. METHODS: This is a retrospective and proof-of-concept study. We developed an extremely patient-friendly protocol to be applied to forty-five normal or high responders, in which a single injection of corifollitropin alfa (Elonva®) was administered and medroxyprogesterone acetate (MPA) was taken orally every day from the day after Elonva injection to the day of trigger. Seven days after Elonva injection, folliculometry and hormone tests were performed, followed by short-acting daily FSH/LH injections, if needed, until the day before trigger. Duration of stimulation, number of injections and visits before trigger, incidence of premature LH surge, the number of oocytes retrieved, fertilization rate, cleavage rate, the rate of day 2 good embryos available, and cumulative ongoing pregnancy rate per retrieval were assessed. RESULTS: The average age of the population was 34.7 years. Duration of stimulation was 9.4 days in average. Before trigger, only 3.6 injection shots and 1.4 visits were needed on average. There was no case of premature LH surge. Number of oocytes retrieved was 13.7, fertilization rate was 79.04%, cleavage rate was 91.11%, and day 2 good embryo rate was 64.34%, in average respectively. There was no case of ovarian hyperstimulation syndrome. The cumulative ongoing pregnancy rate per oocyte retrieval achieved a satisfactory level as 53.1%. CONCLUSIONS: Our protocol consisting of long-acting FSH injection and oral MPA preventing LH surge reduces the number of injections and visits to an extreme and achieves a satisfactory reproductive outcome, and, therefore, is a really patient-friendly and effective approach to ovarian stimulation. BioMed Central 2018-03-05 /pmc/articles/PMC5836459/ /pubmed/29506543 http://dx.doi.org/10.1186/s12958-018-0335-0 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Huang, Chen-Yu Chen, Guan-Yeu Shieh, Miawh-Lirng Li, Hsin-Yang An extremely patient-friendly and efficient stimulation protocol for assisted reproductive technology in normal and high responders |
title | An extremely patient-friendly and efficient stimulation protocol for assisted reproductive technology in normal and high responders |
title_full | An extremely patient-friendly and efficient stimulation protocol for assisted reproductive technology in normal and high responders |
title_fullStr | An extremely patient-friendly and efficient stimulation protocol for assisted reproductive technology in normal and high responders |
title_full_unstemmed | An extremely patient-friendly and efficient stimulation protocol for assisted reproductive technology in normal and high responders |
title_short | An extremely patient-friendly and efficient stimulation protocol for assisted reproductive technology in normal and high responders |
title_sort | extremely patient-friendly and efficient stimulation protocol for assisted reproductive technology in normal and high responders |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836459/ https://www.ncbi.nlm.nih.gov/pubmed/29506543 http://dx.doi.org/10.1186/s12958-018-0335-0 |
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