Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2016 Jun;31(3):383-90.
doi: 10.1007/s00455-015-9687-1. Epub 2016 Jan 23.

Voluntary Cough Airflow Differentiates Safe Versus Unsafe Swallowing in Amyotrophic Lateral Sclerosis

Affiliations

Voluntary Cough Airflow Differentiates Safe Versus Unsafe Swallowing in Amyotrophic Lateral Sclerosis

Emily K Plowman et al. Dysphagia. 2016 Jun.

Abstract

Dysphagia and aspiration are prevalent in amyotrophic lateral sclerosis (ALS) and contribute to malnutrition, aspiration pneumonia, and death. Early detection of at risk individuals is critical to ensure maintenance of safe oral intake and optimal pulmonary function. We therefore aimed to determine the discriminant ability of voluntary cough airflow measures in detecting penetration/aspiration status in ALS patients. Seventy individuals with ALS (El-Escorial criteria) completed voluntary cough spirometry testing and underwent a standardized videofluoroscopic swallowing evaluation (VFSE). A rater blinded to aspiration status derived six objective measures of voluntary cough airflow and evaluated airway safety using the penetration-aspiration scale (PAS). A between groups ANOVA (safe vs. unsafe swallowers) was conducted and sensitivity, specificity, area under the curve (AUC) and likelihood ratios were calculated. VFSE analysis revealed 24 penetrator/aspirators (PAS ≥3) and 46 non-penetrator/aspirators (PAS ≤2). Cough volume acceleration (CVA), peak expiratory flow rise time (PEFRT), and peak expiratory flow rate (PEFR) were significantly different between airway safety groups (p < 0.05) and demonstrated significant discriminant ability to detect the presence of penetration/aspiration with AUC values of: 0.85, 0.81, and 0.78, respectively. CVA <45.28 L/s/s, PEFR <3.97 L/s, and PEFRT >76 ms had sensitivities of 91.3, 82.6, and 73.9 %, respectively, and specificities of 82.2, 73.9, and 78.3 % for identifying ALS penetrator/aspirators. Voluntary cough airflow measures identified ALS patients at risk for penetration/aspiration and may be a valuable screening tool with high clinical utility.

Keywords: Amyotrophic lateral sclerosis; Aspiration; Cough; Deglutition; Deglutition disorders; Screen.

PubMed Disclaimer

Conflict of interest statement

Authors' Conflict of Interest: None.

Figures

Figure 1
Figure 1
Example of voluntary cough spirometry waveform depicting derived objective measures. Four temporal measures that include inspiratory phase duration, compression phase duration, expiratory phase duration and peak expiratory flow rate (PEFR) are shown. In addition, measures of peak inspiratory flow rate (PIFR) and peak expiratory flow rate (PEFR) are identified. Cough volume acceleration (CVA) is not depicted but is calculated by dividing PEFRT by PEFR (i.e. CVA=PEFR/PEFRT).
Figure 2
Figure 2
Videofluoroscopic image and voluntary cough airflow waveform examples from an ALS patient who demonstrated safe swallowing (PAS=1, Figure 2A) and an ALS patient who aspirated without a cough response (PAS=8, Figure 2B). The aspirator demonstrated a smaller peak inspiratory flow rate (PIFR), a longer compression phase duration (CPD), and a smaller peak expiratory flow rate (PEFR). Asp= aspiration.
Figure 3
Figure 3
Receiver operator curves (ROC) for voluntary cough airflow measures that were significant to identify penetrator/aspirators (PAS ≥3).

References

    1. Chen A, Garrett CG. Otolaryngologic presentations of amyotrophic lateralsclerosis. Otolaryngol Head Neck Surg. 2005;132(3):500–504. doi:S0194599804018753[pii]10.1016/j.otohns.2004.09.092. - PubMed
    1. Chio A, Logroscino G, Hardiman O, Swingler R, Mitchell D, Beghi E, Traynor BG, Eurals C. Prognostic factors in ALS: A critical review. Amyotroph Lateral Scler. 2009;10(5-6):310–323. doi: 10.3109/17482960802566824. - DOI - PMC - PubMed
    1. Kuhnlein P, Gdynia HJ, Sperfeld AD, Lindner-Pfleghar B, Ludolph AC, Prosiegel M, Riecker A. Diagnosis and treatment of bulbar symptoms in amyotrophic lateral sclerosis. Nat Clin Pract Neurol. 2008;4(7):366–374. doi:ncpneuro0853[pii]10.1038/ncpneuro0853. - PubMed
    1. Paris G, Martinaud O, Petit A, Cuvelier A, Hannequin D, Roppeneck P, Verin E. Oropharyngeal dysphagia in amyotrophic lateral sclerosis alters quality of life. J Oral Rehabil. 2013;40(3):199–204. doi: 10.1111/joor.12019. - DOI - PubMed
    1. Yang R, Huang R, Chen D, Song W, Zeng Y, Zhao B, Zhou D, Shang HF. Causes and places of death of patients with amyotrophic lateral sclerosis in south-west China. Amyotroph Lateral Scler. 2011;12(3):206–209. doi: 10.3109/17482968.2011.572979. - DOI - PubMed

Publication types

MeSH terms