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The optimal duration of progesterone supplementation in pregnant women after IVF/ICSI: a meta-analysis

BACKGROUND: Progesterone supplementation after in vitro fertilisation/intracytoplasmic sperm injection (IVF/ICSI) can improve the rates of clinical pregnancy and live birth, but the optimal duration of treatment remains controversial. The objective of this meta-analysis was to investigate the effect...

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Autores principales: Liu, Xi-Ru, Mu, Hua-Qiao, Shi, Qi, Xiao, Xiao-Qiu, Qi, Hong-Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551800/
https://www.ncbi.nlm.nih.gov/pubmed/23237065
http://dx.doi.org/10.1186/1477-7827-10-107
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author Liu, Xi-Ru
Mu, Hua-Qiao
Shi, Qi
Xiao, Xiao-Qiu
Qi, Hong-Bo
author_facet Liu, Xi-Ru
Mu, Hua-Qiao
Shi, Qi
Xiao, Xiao-Qiu
Qi, Hong-Bo
author_sort Liu, Xi-Ru
collection PubMed
description BACKGROUND: Progesterone supplementation after in vitro fertilisation/intracytoplasmic sperm injection (IVF/ICSI) can improve the rates of clinical pregnancy and live birth, but the optimal duration of treatment remains controversial. The objective of this meta-analysis was to investigate the effects of early progesterone cessation on pregnancy outcomes in women undergoing IVF/ICSI. METHODS: We searched MEDLINE, EMBASE, the Cochrane Central Register of Controlled Trials (CENTRAL), the Chinese biomedicine (CBM) literature database, and the Wanfang database. The final search was performed in July 2012. All available randomised trials that compared the effects of early progesterone cessation with progesterone continuation during early pregnancy after IVF/ICSI were included. The main outcome measures were live birth rate, miscarriage rate and ongoing pregnancy rate. Fixed or random-effects models were chosen to calculate the risk ratio (RR). RESULTS: Six eligible studies with a total of 1,201 randomised participants were included in the final analysis. No statistically significant differences were detected between patients who underwent early progesterone cessation and those who received progesterone continuation for luteal phase support in terms of live birth rate (RR: 0.95, 95% CI: 0.86–1.05), miscarriage rate (RR: 1.01, 95% CI: 0.74–1.38) or ongoing pregnancy rate (RR: 0.97, 95% CI: 0.90–1.05). These results did not change after a sensitivity analysis. CONCLUSIONS: The currently available evidence suggests that progesterone supplementation beyond the first positive hCG test after IVF/ICSI might generally be unnecessary, although large-scale randomised controlled trials are needed to strengthen this conclusion.
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spelling pubmed-35518002013-01-24 The optimal duration of progesterone supplementation in pregnant women after IVF/ICSI: a meta-analysis Liu, Xi-Ru Mu, Hua-Qiao Shi, Qi Xiao, Xiao-Qiu Qi, Hong-Bo Reprod Biol Endocrinol Review BACKGROUND: Progesterone supplementation after in vitro fertilisation/intracytoplasmic sperm injection (IVF/ICSI) can improve the rates of clinical pregnancy and live birth, but the optimal duration of treatment remains controversial. The objective of this meta-analysis was to investigate the effects of early progesterone cessation on pregnancy outcomes in women undergoing IVF/ICSI. METHODS: We searched MEDLINE, EMBASE, the Cochrane Central Register of Controlled Trials (CENTRAL), the Chinese biomedicine (CBM) literature database, and the Wanfang database. The final search was performed in July 2012. All available randomised trials that compared the effects of early progesterone cessation with progesterone continuation during early pregnancy after IVF/ICSI were included. The main outcome measures were live birth rate, miscarriage rate and ongoing pregnancy rate. Fixed or random-effects models were chosen to calculate the risk ratio (RR). RESULTS: Six eligible studies with a total of 1,201 randomised participants were included in the final analysis. No statistically significant differences were detected between patients who underwent early progesterone cessation and those who received progesterone continuation for luteal phase support in terms of live birth rate (RR: 0.95, 95% CI: 0.86–1.05), miscarriage rate (RR: 1.01, 95% CI: 0.74–1.38) or ongoing pregnancy rate (RR: 0.97, 95% CI: 0.90–1.05). These results did not change after a sensitivity analysis. CONCLUSIONS: The currently available evidence suggests that progesterone supplementation beyond the first positive hCG test after IVF/ICSI might generally be unnecessary, although large-scale randomised controlled trials are needed to strengthen this conclusion. BioMed Central 2012-12-13 /pmc/articles/PMC3551800/ /pubmed/23237065 http://dx.doi.org/10.1186/1477-7827-10-107 Text en Copyright ©2012 Liu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Liu, Xi-Ru
Mu, Hua-Qiao
Shi, Qi
Xiao, Xiao-Qiu
Qi, Hong-Bo
The optimal duration of progesterone supplementation in pregnant women after IVF/ICSI: a meta-analysis
title The optimal duration of progesterone supplementation in pregnant women after IVF/ICSI: a meta-analysis
title_full The optimal duration of progesterone supplementation in pregnant women after IVF/ICSI: a meta-analysis
title_fullStr The optimal duration of progesterone supplementation in pregnant women after IVF/ICSI: a meta-analysis
title_full_unstemmed The optimal duration of progesterone supplementation in pregnant women after IVF/ICSI: a meta-analysis
title_short The optimal duration of progesterone supplementation in pregnant women after IVF/ICSI: a meta-analysis
title_sort optimal duration of progesterone supplementation in pregnant women after ivf/icsi: a meta-analysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551800/
https://www.ncbi.nlm.nih.gov/pubmed/23237065
http://dx.doi.org/10.1186/1477-7827-10-107
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