Skip to main content Accessibility help
×
Hostname: page-component-78c5997874-94fs2 Total loading time: 0 Render date: 2024-11-10T09:49:56.705Z Has data issue: false hasContentIssue false

10 - Extreme Prematurity: Truth and Justice

Published online by Cambridge University Press:  07 May 2010

Geoffrey Miller
Affiliation:
Yale University, Connecticut
Get access

Summary

In this chapter I will consider some of the ethical issues that surround the management of the extremely preterm infant (EPTI). Such infants are characterized by a gestational age (GA) of less than 28 weeks. However, in practice, within this group, those who give rise to the most ethical concern are the ones who are born at less than 26 weeks. The issues raised by this group are discussed in several chapters in this book and include, in particular, parental rights and responsibilities; the forgoing of life-sustaining treatment; and the usefulness or otherwise of such words as “best interests,” “benefits,” “burdens,” and “futility,” which, incorrectly used, can both cloud and taint a coherent moral approach. I will not repeat these topics, but rather I will highlight the lack of use, misuse, and misinterpretation of empirical data to shape and drive ethical and medical management. This will include perceptions concerning prognosis, delivery room resuscitation, and justice, both distributive and personal.

There is an ongoing concern that continuing to care for and save the lives of EPTIs comes at the inevitable expense – to some babies, families, and society – of disability, emotional trauma, and financial cost. Because mortality and morbidity increase with decreasing GA and weight, it is argued that a line should be drawn on the basis of these measures, such that the provision of active care to a baby born at less than 25 weeks or 600g should be optional. But not only is there uncertainty about the outcome for the individual child, there is also poor understanding of the types of disability that may occur and the accuracy of predicting GA and weight.

Type
Chapter
Information
Pediatric Bioethics , pp. 141 - 148
Publisher: Cambridge University Press
Print publication year: 2009

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
×