Imperial College London
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DrWilliamMan

Faculty of Medicine, National Heart & Lung Institute

Reader in Respiratory Medicine
 
 
 
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Contact

 

+44 (0)1895 828 851w.man

 
 
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Location

 

Harefield HospitalHarefield Hospital

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Summary

 

Publications

Citation

BibTex format

@article{Polkey:2017:10.1016/j.chest.2017.01.015,
author = {Polkey, MI and Man, W},
doi = {10.1016/j.chest.2017.01.015},
journal = {Chest},
pages = {6--7},
title = {Should we get sniffy about Maximal Inspiratory Pressure?},
url = {http://dx.doi.org/10.1016/j.chest.2017.01.015},
volume = {152},
year = {2017}
}
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RIS format (EndNote, RefMan)

TY  - JOUR
AB  - Respiratory muscle weakness either occurs in isolation or as part of a more generalised neuromuscular process.  In the former case this is very often self limiting as, for example, after iatrogenic damage to the phrenic nerve or in the case of neuralgic amyotrophy.  In the latter case patients will usually have evidence of limb muscle involvement and or a known diagnosis (notable exceptions however being Pompe’s disease and about 3% of amyotrophic lateral sclerosis, ALS, presentations).  From this conjecture follow the two main reasons why clinicians request evaluation of inspiratory muscle strength; either to rule-in or rule-out inspiratory muscle weakness as a cause of symptoms or to predict prognosis (or the need for non-invasive ventilation).  MIP has also frequently been used as an outcome measure for trials of inspiratory muscle training.
AU  - Polkey,MI
AU  - Man,W
DO  - 10.1016/j.chest.2017.01.015
EP  - 7
PY  - 2017///
SN  - 1931-3543
SP  - 6
TI  - Should we get sniffy about Maximal Inspiratory Pressure?
T2  - Chest
UR  - http://dx.doi.org/10.1016/j.chest.2017.01.015
UR  - http://hdl.handle.net/10044/1/43924
VL  - 152
ER  -
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