Monitoring diaphragm function in a patient with myasthenia gravis: electrical activity of the diaphragm vs. maximal inspiratory pressure
Author:
Publisher
Springer Science and Business Media LLC
Subject
Critical Care and Intensive Care Medicine
Link
http://link.springer.com/content/pdf/10.1186/s40560-017-0262-8.pdf
Reference16 articles.
1. Munoz-Fdez C, Diez-Tejedor E, Frank A, Pino JM, Perez C, Barreiro P. Maximal respiratory pressures in myasthenia gravis—relation to single fiber electromyography. Acta Neurol Scand. 2001;103(6):392–5.
2. Borel CO, Tilford C, Nichols DG, Hanley DF, Traystman RJ. Diaphragmatic performance during recovery from acute ventilatory failure in Guillain-Barre-syndrome and myasthenia-gravis. Chest. 1991;99(2):444–51.
3. Multz AS, Aldrich TK, Prezant DJ, Karpel JP, Hendler JM. Maximal inspiratory pressure is not a reliable test of inspiratory muscle strength in mechanically ventilated patients. Am Rev Respir Dis. 1990;142(3):529–32.
4. Yonis H, Crognier L, Conil JM, Serres I, Rouget A, Virtos M, et al. Patient-ventilator synchrony in neurally adjusted ventilatory assist (NAVA) and pressure support ventilation (PSV): a prospective observational study. BMC Anesthesiol. 2015;15:117.
5. Wolf GK, Walsh BK, Green ML, Arnold JH. Electrical activity of the diaphragm during extubation readiness testing in critically ill children. Pediatr Crit Care Med. 2011;12(6):e220–4.
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