Skip to main content Accessibility help
×
Hostname: page-component-586b7cd67f-t7czq Total loading time: 0 Render date: 2024-11-29T00:09:32.572Z Has data issue: false hasContentIssue false

6 - Diagnosis and treatment of recurrent miscarriage

Published online by Cambridge University Press:  05 July 2014

Rehan Salim
Affiliation:
University College Hospital
Davor Jurkovic
Affiliation:
University College London
Roy Farquharson
Affiliation:
University of Liverpool
Get access

Summary

Introduction

Miscarriage is the most common complication of pregnancy, with as many as 15-20% of clinically recognised pregnancies ending in spontaneous failure. The main causes of miscarriage are sporadic lethal chromosomal abnormalities and these pregnancies are destined to fail from the outset. In fact, if all conceptions were included in the definition of miscarriage, around 40% would end in failure, with the majority occurring before the pregnancy could be clinically recognised.

However, in some couples, miscarriage can be recurrent, which is defined as three consecutive pregnancy losses before fetal viability at 24 weeks of gestation. The prevalence of this condition is approximately 1%. As the most common cause of miscarriage is aneuploidy, which is directly related to maternal age, the risk and prevalence of early pregnancy loss rises with increasing maternal age. The overall prevalence of recurrent miscarriage in the population is higher than would be expected by chance alone. Statistically, the prevalence should be only 0.34%, indicating that in some couples there may be an underlying cause that puts them at higher risk. However, the calculation of the risk of three consecutive losses is based on the assumption that the baseline risk of miscarriage is 15%. This calculation does not take into account the fact that the risk of miscarriage increases with advancing maternal age. For example, the risk of miscarriage in a 40-year-old woman is at least 45% and therefore the expected prevalence of recurrent miscarriage in this age group is approximately 9%.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2011

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×