Abstract

BackgroundThe aim of this theoretical study is to explore the cost-effectiveness of aneuploidy screening in a UK setting for every woman aged under the age of 40 years when fresh and vitrified-warmed embryos are transferred one at a time in a first full cycle of assisted conception.MethodsIt is envisaged that a 24-chromosome genetic test for aneuploidy could be used to exclude embryos with an abnormal test result from transfer, or used only to rank embryos with the highest potential to be viable; the effect on cumulative outcome is assessed. The cost associated with one additional live birth event and one clinical miscarriage avoided is estimated, and the time taken to complete a cycle considered. The numbers of individual woman for whom testing is likely to be beneficial or detrimental is also evaluated.ResultsAdding aneuploidy screening to a first treatment cycle is unlikely to result in a higher chance of a live birth event, and can be detrimental for some women. Premature termination of a clinical trial is likely to be biased in favour of genetic testing. Testing is likely to be an expensive way of reducing the chance of clinical miscarriage and shortening treatment time without a substantial reduction in the cost of testing, and is likely to benefit a minority of women. Selecting out embryos is likely to reduce the treatment time for women whether or not they have a baby, whilst ranking embryos only to reduce the time for those that have a child and not for those who need another stimulated cycle.ConclusionsAdding aneuploidy screening to IVF treatment for women under the age of 40 years is unlikely to be beneficial for most women. To achieve an unbiased assessment of the cost-effectiveness of genetic testing for aneuploidy, clinical trials need to take account of women who still have embryos available for transfer at the end of the study period. Specifying the proportions of women for whom testing is likely to be beneficial and detrimental may help better inform couples who might be considering adding aneuploidy screening to their treatment cycle.

Highlights

  • The aim of this theoretical study is to explore the cost-effectiveness of aneuploidy screening in a UK setting for every woman aged under the age of 40 years when fresh and vitrified-warmed embryos are transferred one at a time in a first full cycle of assisted conception

  • Intention-to-treat outcomes Table 3 shows the number of clinical miscarriages and live birth events following a fresh transfer and each vitrified-warmed (FET) attempt, and the cumulative rates without premature trial termination

  • The effect of testing on the cumulative clinical miscarriage rate (CCMR) and the cumulative live birth rate (CLBR) for 1000 women started is shown in Figs. 1 and 2 respectively

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Summary

Introduction

The aim of this theoretical study is to explore the cost-effectiveness of aneuploidy screening in a UK setting for every woman aged under the age of 40 years when fresh and vitrified-warmed embryos are transferred one at a time in a first full cycle of assisted conception. The current National Institute for Health and Care Excellence (NICE) guideline covering diagnosing and treating fertility problems in the UK recommends state-funding and single embryo transfer (fresh or cryopreserved) in the first full IVF cycle for women under 37 years, and if there are one or more top-quality embryos for women aged 37 to 39 years [2]. Selecting embryos with the highest potential for implantation offers the potential to transfer one embryo at a time in the fewest possible number of transfer procedures to optimise a woman’s chance of achieving a healthy singleton live birth event and reduce the risk of miscarriage due to chromosome aneuploidy. Others have argued for a more pragmatic approach to circumnavigate protracted delay in introducing the highest quality treatment for patients [5]

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