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Unusual features in chronic inflammatory demyelinating polyneuropathy: Good outcome after prolonged ventilatory support

Severe respiratory muscle paralysis and ventilatory failure is rare in chronic inflammatory demyelinating polyneuropathy (CIDP). We report a 14 year child who presented with respiratory failure, bulbar and multiple cranial nerves involvement along with bilateral phrenic nerve paralysis. He was diagn...

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Autores principales: Jha, Sanjeev, Ansari, MK, Sonkar, KK, Paliwal, VK
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3159356/
https://www.ncbi.nlm.nih.gov/pubmed/21897683
http://dx.doi.org/10.4103/0976-3147.83586
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author Jha, Sanjeev
Ansari, MK
Sonkar, KK
Paliwal, VK
author_facet Jha, Sanjeev
Ansari, MK
Sonkar, KK
Paliwal, VK
author_sort Jha, Sanjeev
collection PubMed
description Severe respiratory muscle paralysis and ventilatory failure is rare in chronic inflammatory demyelinating polyneuropathy (CIDP). We report a 14 year child who presented with respiratory failure, bulbar and multiple cranial nerves involvement along with bilateral phrenic nerve paralysis. He was diagnosed with CIDP after electrophysiological evaluation. He required AMBU ventilation for about 4 months (including domiciliary use), after which he recovered significantly. Along with several unusual features of CIDP, this report highlights good example of steady basic intensive care to save lives and rewarding outcome of prolonged respiratory support, provided by AMBU ventilation which is a rather primitive, but inexpensive device.
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spelling pubmed-31593562011-09-06 Unusual features in chronic inflammatory demyelinating polyneuropathy: Good outcome after prolonged ventilatory support Jha, Sanjeev Ansari, MK Sonkar, KK Paliwal, VK J Neurosci Rural Pract Case Report Severe respiratory muscle paralysis and ventilatory failure is rare in chronic inflammatory demyelinating polyneuropathy (CIDP). We report a 14 year child who presented with respiratory failure, bulbar and multiple cranial nerves involvement along with bilateral phrenic nerve paralysis. He was diagnosed with CIDP after electrophysiological evaluation. He required AMBU ventilation for about 4 months (including domiciliary use), after which he recovered significantly. Along with several unusual features of CIDP, this report highlights good example of steady basic intensive care to save lives and rewarding outcome of prolonged respiratory support, provided by AMBU ventilation which is a rather primitive, but inexpensive device. Medknow Publications 2011 /pmc/articles/PMC3159356/ /pubmed/21897683 http://dx.doi.org/10.4103/0976-3147.83586 Text en Copyright: © Journal of Neurosciences in Rural Practice http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Jha, Sanjeev
Ansari, MK
Sonkar, KK
Paliwal, VK
Unusual features in chronic inflammatory demyelinating polyneuropathy: Good outcome after prolonged ventilatory support
title Unusual features in chronic inflammatory demyelinating polyneuropathy: Good outcome after prolonged ventilatory support
title_full Unusual features in chronic inflammatory demyelinating polyneuropathy: Good outcome after prolonged ventilatory support
title_fullStr Unusual features in chronic inflammatory demyelinating polyneuropathy: Good outcome after prolonged ventilatory support
title_full_unstemmed Unusual features in chronic inflammatory demyelinating polyneuropathy: Good outcome after prolonged ventilatory support
title_short Unusual features in chronic inflammatory demyelinating polyneuropathy: Good outcome after prolonged ventilatory support
title_sort unusual features in chronic inflammatory demyelinating polyneuropathy: good outcome after prolonged ventilatory support
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3159356/
https://www.ncbi.nlm.nih.gov/pubmed/21897683
http://dx.doi.org/10.4103/0976-3147.83586
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