Elimination of Radiographic Confirmation For Small-Bowel Feeding Tubes in Critical Care
Jan Powers, RN, PhD, CCRN, CCNS, CNRN, Mary H. Fischer, RN, MSN,CCRN, PCCN, CHFN, ACNS, Mary Ziemba-Davis, BA, Jamie Brown, RN, MSN, CCRN, and Donna M. Phillips, RN, BSN, CCRN, CNRN, CNML
Elimination of Radiographic Confirmation For Small-Bowel Feeding Tubes in Critical Care: Read Article
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Learning Objectives

At the completion of this program, you will be able to:
  • Describe the indications for using small-bowel feeding tubes for nutritional support.
  • Identify the benefits of using a bedside electromagnetic placement device for small-bowel feeding tube placement.
  • Discuss the verification methods for small-bowel feeding tube placement.

Continuing Education Information

CE ID: A132263
Total Contact Hours: 1.00
Pharma Hours: 0.0
Synergy Cat: A
Test Expires: 11/1/2016

Description

A variety of techniques are used for placement of small-bowel feeding tubes. Standard practice at the study institution is for postpyloric placement using an electromagnetically guided placement device (EMPD). EMPD placement is performed by bedside nurses trained in the placement technique and may reduce radiograph exposures and time to initiation of enteral nutrition.

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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