Skip to main content Accessibility help
×
Hostname: page-component-77c89778f8-sh8wx Total loading time: 0 Render date: 2024-07-16T14:10:38.308Z Has data issue: false hasContentIssue false

10 - The treatment of azoospermia with surgery and ICSI

from Part 2 - Implications of the new technologies

Published online by Cambridge University Press:  09 August 2009

T. D. Glover
Affiliation:
University of Leeds
C. L. R. Barratt
Affiliation:
University of Birmingham
Get access

Summary

ICSI for oligoasthenospermia

Before 1992, male infertility had been considered in most cases to be untreatable. Then came a surprisingly neat solution: ICSI, i.e the injection of a single spermatozoon into a single egg. Since the publication of the first papers on ICSI for oligozoospermia in 1992 and 1993, an intense flurry of scientific effort has been dedicated to extending its application to virtually every type of male infertility (Palermo et al., 1992; Van Steirteghem et al., 1993; Silber, 1995; Silber et al., 1995a). First it was confirmed that the most severe cases of oligoasthenoteratospermia enjoyed the same success rates as mild cases of male factor infertility and that these pregnancy rates were no different from those of couples where men with normal spermatozoa were undertaking conventional IVF (Nagy et al., 1995a). Next, it was discovered that it does not really matter how the spermatozoon is pretreated prior to ICSI, and that any method for aspirating the spermatozoon into an injection pipette and transferring it into the oocyte is adequate (Liu et al., 1994a). In fact, no sperm defect precluded success with the ICSI technique. Any fertilization failure was always related either to poor egg quality or to sperm nonviability (Liu et al., 1995). It appeared that there was no negative effect on the pregnancy rate with ICSI even with the most severe morphological sperm defects, the most severe reduction in motility, or with the tiniest number of spermatozoa in the ejaculate (‘pseudoazoospermia’) (see Tables 10.1 and 10.2).

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 1999

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 coreplatform@cambridge.org 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
×