2010
DOI: 10.1097/aln.0b013e3181f70f3d
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Neostigmine/Glycopyrrolate Administered after Recovery from Neuromuscular Block Increases Upper Airway Collapsibility by Decreasing Genioglossus Muscle Activity in Response to Negative Pharyngeal Pressure

Abstract: Neostigmine/glycopyrrolate, when administered after recovery from neuromuscular block, increases upper airway collapsibility and impairs genioglossus muscle activation in response to negative pharyngeal pressure. Reversal with acetylcholinesterase inhibitors may be undesirable in the absence of neuromuscular blockade.

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Cited by 101 publications
(69 citation statements)
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“…On the other hand, the "well-meant" pre-emptive antagonism of merely suspected residual muscle relaxation is likely to do more harm than good. Cholinesterase inhibitors can impair neuromuscular transmission, threatening the integrity of the upper airway (17). In view of its pathophysiological mechanism, any residual neuromuscular blockade has implications similar to those of inadequately treated myasthenia gravis for the integrity and function of the upper airway (12, 13, 16, 36, e50).…”
Section: Figurementioning
confidence: 99%
“…On the other hand, the "well-meant" pre-emptive antagonism of merely suspected residual muscle relaxation is likely to do more harm than good. Cholinesterase inhibitors can impair neuromuscular transmission, threatening the integrity of the upper airway (17). In view of its pathophysiological mechanism, any residual neuromuscular blockade has implications similar to those of inadequately treated myasthenia gravis for the integrity and function of the upper airway (12, 13, 16, 36, e50).…”
Section: Figurementioning
confidence: 99%
“…(9) Bunun yanında yeterli derecede antagonize edilmezlerse postoperatif dönemde rekürarizasyona neden olup, hava yolu obstrüksiyonu, hipoventilasyon ve hipoksiye neden olabilmektedirler. (10) Bu komplikasyonlar özellikle miyastenia gravisli hastalarda daha belirgindir. Nondepolarizan kas gevşeticiler genellikle kolinesteraz enzim inhibitörleri (neostigmin, pridostigmin vb.)…”
Section: Discussionunclassified
“…However, we designed our study to investigate the exclusive effect of the timing of administration of the reversal agent and rule out the effect of the dose. Another reason was to determine whether blockade induced by neostigmine [19,20] occurs in this situation (and we confirm that it does not). Another limitation of this study was that the perceptions of loss of TOF or DBS-fade were subjective.…”
Section: Discussionmentioning
confidence: 99%