Parents’ Report of Child’s Response to Sibling’s Death in a Neonatal or Pediatric Intensive Care Unit
JoAnne M. Youngblut, Phd, and Dorothy Brooten, Phd
Parents’ Report of Child’s Response to Sibling’s Death in a Neonatal or Pediatric Intensive Care Unit: Read Article
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Learning Objectives

At the completion of this program, you will be able to:
  • Describe the study’s objective and the demographics of the subjects studied.
  • Identify 6 themes that emerged about the surviving children of deceased siblings.
  • State the major limitation of this study.

Continuing Education Information

CE ID: A132262
Total Contact Hours: 1.00
Pharma Hours: 0.0
Synergy Cat: B
Test Expires: 11/1/2016

Description

A child’s death affects all members of the family. Few studies have focused on the contribution of the environment in the neonatal or pediatric intensive care unit to surviving children’s reactions following their siblings’ deaths. In this study, children’s responses in the first 7 months after their siblings’ deaths in the neonatal or pediatric intensive care unit differed with the child’s age, parents’ race/ethnicity, and the unit where the sibling died.

Publication/Sponsor Information


American Journal of Critical Care is an official publication of the American Association of Critical-Care Nurses (AACN), and copyright belongs to AACN. No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording or by any information storage retrieval system without permission of AACN. For all permission requests, please contact the Copyright Clearance Center, Customer Service, 222 Rosewood Drive, Danvers, MA 01923. (978) 750-8400. The statements and opinions contained herein are solely those of individual contributors and not of the editors, AACN, or The InnoVision Group. The editors, AACN, and The InnoVision Group assume that articles emanating from a particular institution are submitted with the approval of the requisite authority, including all matters pertaining to human studies and patient privacy requirements.

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