Skip Navigation

This Article
Right arrow Full Text (PDF)
Right arrow E-Letters: Submit a response to the article
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (39)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Hund, E.
Right arrow Articles by Hacke, W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hund, E.
Right arrow Articles by Hacke, W.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

British Journal of Anaesthesia, Vol 78, Issue 3 274-278, Copyright © 1997 by The Board of Management and Trustees of the British Journal of Anaesthesia


CLINICAL INVESTIGATIONS

Predominant involvement of motor fibres in patients with critical illness polyneuropathy

E. Hund, H. Genzwurker, H. Bohrer, H. Jakob, R. Thiele and W. Hacke
Department of Neurology, Ruprecht-Karls University, 69120 Heidelberg, Germany; Department of Anaesthesia, Ruprecht-Karls University, 69120 Heidelberg, Germany; Department of Cardiac Surgery, Ruprecht-Karls University, 69120 Heidelberg, Germany

Critical illness polyneuropathy (CIP) is a recognized cause of muscle weakness and failure of weaning from a ventilator. In order to characterize the features of CIP, we have examined 28 consecutive surgical patients with severe sepsis using bedside electrophysiology. Of the 28 patients (median APACHE II score 31), 20 developed moderate to severe CIP, as shown by the presence of moderate to severe denervation activity on resting EMG. The median nerve compound muscle action potential (CMAP) amplitudes were reduced to 3.24 (SEM 0.48) mV, while sensory nerve action potential (SNAP) amplitudes obtained from the same nerve were normal (13.1 (1.9) microV). In approximately 50% of these patients, the reduction in CMAP exceeded 50% of the lower limit of normal. Similar results were obtained from stimulation of the ulnar nerve. We conclude that CIP is a major complication in patients with severe sepsis and prolonged artificial ventilation. It predominantly involves motor fibres and thus markedly interferes with weaning from the ventilator.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Neurol. Neurosurg. PsychiatryHome page
J-P Lefaucheur, T Nordine, P Rodriguez, and L Brochard
Origin of ICU acquired paresis determined by direct muscle stimulation
J. Neurol. Neurosurg. Psychiatry, April 1, 2006; 77(4): 500 - 506.
[Abstract] [Full Text] [PDF]


Home page
Am J Crit CareHome page
A. M. Keaveney
Critical Illness Polyneuropathy in Adults After Cardiac Surgery: a Case Study
Am. J. Crit. Care., September 1, 2004; 13(5): 421 - 424.
[Full Text] [PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
S. Deem, C. M. Lee, and J. R. Curtis
Acquired Neuromuscular Disorders in the Intensive Care Unit
Am. J. Respir. Crit. Care Med., October 1, 2003; 168(7): 735 - 739.
[Full Text] [PDF]


Home page
ChestHome page
M. I. Polkey and J. Moxham
Clinical Aspects of Respiratory Muscle Dysfunction in the Critically Ill
Chest, March 1, 2001; 119(3): 926 - 939.
[Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.