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Frozen blastocyst embryo transfer using a supplemented natural cycle protocol has a similar live birth rate compared to a programmed cycle protocol

  • Assisted Reproduction Technologies
  • Published:
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Abstract

Purpose

The purpose of this study is to compare outcomes for a supplemented natural cycle with a programmed cycle protocol for frozen blastocyst transfer.

Methods

A retrospective analysis was performed of frozen autologous blastocyst transfers, at a single academic fertility center (519 supplemented natural cycles and 106 programmed cycles). Implantation, clinical pregnancy, miscarriage, and live birth and birth weight were compared using Pearson’s Chi-squared test, T-test, or Fisher’s exact test.

Results

There was no significant difference between natural and programmed frozen embryo transfers with respect to implantation (21.9 vs. 18.1 %), clinical pregnancy (35.5 vs. 29.2 %), and live birth rates (27.7 vs. 23.6 %). Mean birth weights were also similar between natural and programmed cycles for singletons (3354 vs. 3340 g) and twins (2422 vs. 2294 g)

Conclusion

Frozen blastocyst embryo transfers using supplemented natural or programmed protocols experience similar success rates. Patient preference should be considered in choosing a protocol.

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Acknowledgments

The authors wish to thank the Society for Assisted Reproductive Technology and its members for providing the clinical information, which allowed this analysis to be performed.

Funding

This study was funded by Award Number P01 HD 065647 from the National Institute of Child Health and Human Development.

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Authors

Corresponding author

Correspondence to Ruth B. Lathi.

Additional information

Capsule Supplemented natural cycle with hCG trigger and luteal progesterone support is equivalent to hormone replacement cycles for frozen blastocyst transfer.

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Lathi, R.B., Chi, YY., Liu, J. et al. Frozen blastocyst embryo transfer using a supplemented natural cycle protocol has a similar live birth rate compared to a programmed cycle protocol. J Assist Reprod Genet 32, 1057–1062 (2015). https://doi.org/10.1007/s10815-015-0499-x

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  • DOI: https://doi.org/10.1007/s10815-015-0499-x

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