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LetterCorrespondence

Considerations About the Effect of Cough Assist on Laryngeal Function in Neurologic Disease

Antonio M Esquinas and Giuseppe Fiorentino
Respiratory Care November 2018, 63 (11) 1459; DOI: https://doi.org/10.4187/respcare.06547
Antonio M Esquinas
Intensive Care Unit Hospital Morales Meseguer Murcia, Spain
MD PhD
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Giuseppe Fiorentino
UOC di Fisiopatologia e Riabilitazione AO Ospedali dei Colli Napoli Naples, Italy
MD
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To the Editor:

We read with interest the work by Andersen et al1 about transnasal laryngoscopy during mechanical insufflation-exsufflation in amyotrophic lateral sclerosis (ALS). We believe the following should be considered.

First, the larynx is a complex structure that cannot simply be thought of as a passive valve through which one may insufflate and exsufflate the lungs with similar responses in all, particularly not in patients with intrinsic laryngeal weaknesses and reduced motor control. Given the nature of ALS, with its combination of upper and lower motor neuron signs, glottic narrowing in patients with ALS could be the infranuclear paralytic type, the supranuclear nonparalytic type, or a combination of the two. Vocal cord abductor paresis and laryngospasm in ALS are rarely described in the neurologic literature and autopsy studies.2

During exsufflation in all patients with neuromuscular disorders, including ALS, there was constriction of the hypopharynx, an exaggeration of the findings seen in patients without neuromuscular disorders to a varying degree. Constriction seemed very pronounced in subjects with hypotonic bulbar weakness. Clearly, airway closure on both insufflation and exsufflation is a major limitation in applying mechanical insufflation-exsufflation and is likely to be distressing in those patients most severely affected. Andersen et al1 showed that adduction of supraglottic structures limits insufflation in patients with bulbar neuromuscular disease, including ALS. They surmise that upper airway reflexes may be hyper-regulated to prevent aspiration of foreign material into the airways, which will stimulate glottis closure, with the collapse of more floppy supraglottic structures.3

Second, mechanical insufflation-exsufflation has been increasingly used in individuals with neuromuscular weakness, despite the lack of large randomized trials, although there is cumulative evidence that mechanical insufflation-exsufflation increases cough peak flow and, in combination with noninvasive ventilation, can prolong survival. The literature varies regarding appropriate settings of inspiratory and expiratory pressures, which range from 20 to 60 cm H2O in positive and negative pressures. Noninvasive ventilation and mechanical insufflation-exsufflation are reported to be less effective in patients with bulbar involvement, and those with spastic upper motor neuron weakness are least likely to tolerate mechanical insufflation-exsufflation because upper airway collapse and/or spasm may be generated. In particular, gradual development of bulbar dysfunction may influence the extent to which a successful use of mechanical insufflation-exsufflation is to be expected.4

Third, in patients with bulbar symptoms, noninvasive ventilation and mechanical insufflation-exsufflation should be managed individually, with the expectation that settings and interventions may need to be modified with disease progression. In patients with ALS, the clinical response to noninvasive use of mechanical insufflation-exsufflation is variable, which indicates a certain motor dysfunction of the upper airways. In some cases, the effect of mechanical insufflation-exsufflation seems to be reduced in parallel to disease progression and deteriorating bulbar dysfunction. It is difficult to predict beforehand which individuals will succeed because there are no evidence-based predictive factors.

Treatment failure with mechanical insufflation-exsufflation in patients with bulbar symptoms is likely to be caused primarily by laryngeal adduction during insufflation, predominantly at the supraglottic level. This response precludes air filling of the lungs during insufflation, which causes discomfort and subsequent inefficient exsufflation. A similar approach is appropriate in starting noninvasive ventilation; high inspiratory pressures may generate airway closure, and so pressure should be gently titrated upward.5

The main methodological problem in the study was the gradual increase in pressure during the intervention to familiarize the subjects to the feeling of mechanical insufflation-exsufflation. This could be a confounding factor; the subjects become familiarized with the feeling of mechanical insufflation-exsufflation through experience and modification of movements according to the theory of motor learning. Randomizing the intervention sequences could prevent this issue, but, in clinical settings, pressures are always increased gradually to be as gentle as possible for patients.

Individually customized settings for pressure and flow can improve and extend the use of noninvasive mechanical insufflation-exsufflation in ALS, and flexible laryngoscopy can be an efficient tool in selected patients who do not respond as expected. When we increase our understanding of these issues, we can, it is hoped, develop better clinical instructions, more fine-tuned settings, or even new functions for mechanical insufflation-exsufflation devices.

  • Copyright © 2018 by Daedalus Enterprises

References

  1. 1.↵
    1. Andersen TM,
    2. Sandnes A,
    3. Fondenes O,
    4. Nilsen RM,
    5. Tysnes OB,
    6. Heimdal JH,
    7. et al
    . Laryngeal responses to mechanically assisted cough in progressing amyotrophic lateral sclerosis. Respir Care 2018;63(5):538–549.
    OpenUrlAbstract/FREE Full Text
  2. 2.↵
    1. van der Graaff MM,
    2. Groiman W,
    3. Westermann EJ,
    4. Boogaardt HC,
    5. Koelman H,
    6. van der Kool AJ,
    7. et al
    . Vocal cord function in amyotrophic lateral sclerosis: four cases and a review of the literature. Arch Neurol 2009;66(11):1329–1333.
    OpenUrlCrossRefPubMed
  3. 3.↵
    1. Andersen T,
    2. Sandnes A,
    3. Brekka AK,
    4. Hilland M,
    5. Clemm H,
    6. Fondenes O,
    7. et al
    . Laryngeal response patterns influence the efficacy of mechanical assisted cough in amyotrophic lateral sclerosis. Thorax 2017;72(3):221–229.
    OpenUrlAbstract/FREE Full Text
  4. 4.↵
    1. Sayas Catalán J,
    2. Jiménez Huerta I,
    3. Benavides Mañas P,
    4. Luján M,
    5. López-Padilla D,
    6. Arias Arias E,
    7. et al
    . Videolaryngoscopy with non- invasive ventilation in subjects with upper-airway obstruction. Respir Care 2017;62(2):222–230.
    OpenUrlAbstract/FREE Full Text
  5. 5.↵
    1. Sancho J,
    2. Servera E,
    3. Díaz J,
    4. Marín J
    . Efficacy of mechanical insufflation-exsufflation un medically stable patients with amyotrophic lateral sclerosis. Chest 2004;125(4):1400–1405.
    OpenUrlCrossRefPubMed
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Respiratory Care: 63 (11)
Respiratory Care
Vol. 63, Issue 11
1 Nov 2018
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Considerations About the Effect of Cough Assist on Laryngeal Function in Neurologic Disease
Antonio M Esquinas, Giuseppe Fiorentino
Respiratory Care Nov 2018, 63 (11) 1459; DOI: 10.4187/respcare.06547

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Considerations About the Effect of Cough Assist on Laryngeal Function in Neurologic Disease
Antonio M Esquinas, Giuseppe Fiorentino
Respiratory Care Nov 2018, 63 (11) 1459; DOI: 10.4187/respcare.06547
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