Yonsei Med J.  2010 May;51(3):392-397. 10.3349/ymj.2010.51.3.392.

How Respiratory Muscle Strength Correlates with Cough Capacity in Patients with Respiratory Muscle Weakness

Affiliations
  • 1Department of Rehabilitation Medicine, Eulji University Hospital, Daejeon, Korea.
  • 2Department of Rehabilitation Medicine and Rehabilitation Institute of Muscular Disease, Yonsei University College of Medicine, Seoul, Korea. kswoong@yuhs.ac
  • 3Department of Physical Medicine and Rehabilitation, Myongji Hospital, Kwandong University College of Medicine, Seoul, Korea.

Abstract

PURPOSE
The purpose of this study is to investigate how respiratory muscle strength correlates to cough capacity in patients with respiratory muscle weakness.
MATERIALS AND METHODS
Forty-five patients with amyotrophic lateral sclerosis (ALS), 43 with cervical spinal cord injury (SCI), and 42 with Duchenne muscular dystrophy (DMD) were recruited. Pulmonary function tests including forced vital capacity (FVC) and respiratory muscle strength (maximal expiratory pressure, MEP; maximal inspiratory pressure, MIP) were performed. The correlation between respiratory muscle strength and cough capacity was analyzed.
RESULTS
In the SCI group, FVC in a supine position (2,597 +/- 648 mL) was significantly higher than FVC in a sitting position (2,304 +/- 564 mL, p < 0.01). Conversely, in the ALS group, FVC sitting (1,370 +/- 604 mL) was significantly higher than in supine (1,168 +/- 599 mL, p < 0.01). In the DMD group, there was no statistically significant difference between FVC while sitting (1,342 +/- 506 mL) and FVC while supine (1,304 +/- 500 mL). In addition, the MEP and MIP of all three groups showed a significant correlation with peak cough flow (PCF) (p < 0.01, Pearson's correlation analysis). In the SCI group, MIP was more closely correlated with PCF, while in the ALS and DMD groups, MEP was more closely correlated with PCF (p < 0.01, multiple regression analysis).
CONCLUSION
To generate cough flow, inspiratory muscle strength is significantly more important for SCI patients, while expiratory muscle function is significantly more important for ALS and DMD patients.

Keyword

Amyotrophic lateral sclerosis; muscular dystrophy; duchenne; respiratory function tests; spinal cord injuries

MeSH Terms

Adult
Amyotrophic Lateral Sclerosis/*physiopathology
Cough/*physiopathology
Female
Humans
Inspiratory Capacity
Male
Middle Aged
Muscle Strength/*physiology
Muscle Weakness/pathology/*physiopathology
Muscular Dystrophy, Duchenne/*physiopathology
Respiratory Muscles/pathology/*physiopathology
Spinal Cord Injuries/*physiopathology

Cited by  1 articles

A Comparison of Cough Assistance Techniques in Patients with Respiratory Muscle Weakness
Sun Mi Kim, Won Ah Choi, Yu Hui Won, Seong-Woong Kang
Yonsei Med J. 2016;57(6):1488-1493.    doi: 10.3349/ymj.2016.57.6.1488.


Reference

1. McCool FD. Global physiology and pathophysiology of cough: ACCP evidence-based clinical practice guidelines. Chest. 2006. 129:1 Suppl. 48S–453.
2. Kang SW, Kang YS, Sohn HS, Park JH, Moon JH. Respiratory muscle strength and cough capacity in patients with Duchenne muscular dystrophy. Yonsei Med J. 2006. 47:184–190.
Article
3. McCool FD, Leith DE. Pathophysiology of cough. Clin Chest Med. 1987. 8:189–195.
Article
4. Schramm CM. Current concepts of respiratory complications of neuromuscular disease in children. Curr Opin Pediatr. 2000. 12:203–207.
Article
5. Brain JD, Proctor DF, Reid L. Respiratory defense mechanisms. 1977. New York: M. Dekker.
6. Braun SR, Giovannoni R, O'Connor M. Improving the cough in patients with spinal cord injury. Am J Phys Med. 1984. 63:1–10.
7. Sivasothy P, Brown L, Smith IE, Shneerson JM. Effect of manually assisted cough and mechanical insufflation on cough flow of normal subjects, patients with chronic obstructive pulmonary disease (COPD), and patients with respiratory muscle weakness. Thorax. 2001. 56:438–444.
Article
8. Inkley SR, Oldenburg FC, Vignos PJ Jr. Pulmonary function in Duchenne muscular dystrophy related to stage of disease. Am J Med. 1974. 56:297–306.
Article
9. Lechtzin N, Wiener CM, Shade DM, Clawson L, Diette GB. Spirometry in the supine position improves the detection of diaphragmatic weakness in patients with amyotrophic lateral sclerosis. Chest. 2002. 121:436–442.
Article
10. Varrato J, Siderowf A, Damiano P, Gregory S, Feinberg D, McCluskey L. Postural change of forced vital capacity predicts some respiratory symptoms in ALS. Neurology. 2001. 57:357–359.
11. Wade OL, Gilson JC. The effect of posture on diaphragmatic movement and vital capacity in normal subjects with a note on spirometry as an aid in determining radiological chest volumes. Thorax. 1951. 6:103–126.
Article
12. Baydur A, Adkins RH, Milic-Emili J. Lung mechanics in individuals with spinal cord injury: effects of injury level and posture. J Appl Physiol. 2001. 90:405–411.
Article
13. Winslow C, Rozovsky J. Effect of spinal cord injury on the respiratory system. Am J Phys Med Rehabil. 2003. 82:803–814.
Article
14. Szeinberg A, Tabachnik E, Rashed N, McLaughlin FJ, England S, Bryan CA, et al. Cough capacity in patients with muscular dystrophy. Chest. 1988. 94:1232–1235.
15. Smith PE, Calverley PM, Edwards RH, Evans GA, Campbell EJ. Practical problems in the respiratory care of patients with muscular dystrophy. N Engl J Med. 1987. 316:1197–1205.
16. Estenne M, De Troyer A. The effects of tetraplegia on chest wall statics. Am Rev Respir Dis. 1986. 134:121–124.
17. Estenne M, Heilporn A, Delhez L, Yernault JC, De Troyer A. Chest wall stiffness in patients with chronic respiratory muscle weakness. Am Rev Respir Dis. 1983. 128:1002–1007.
18. McCool FD, Tzelepis GE. Inspiratory muscle training in the patient with neuromuscular disease. Phys Ther. 1995. 75:1006–1014.
Article
19. Kang SW, Shin JC, Park CI, Moon JH, Rha DW, Cho DH. Relationship between inspiratory muscle strength and cough capacity in cervical spinal cord injured patients. Spinal Cord. 2006. 44:242–248.
20. Koessler W, Wanke T, Winkler G, Nader A, Toifl K, Kurz H, et al. 2 Years' experience with inspiratory muscle training in patients with neuromuscular disorders. Chest. 2001. 120:765–769.
21. Griggs RC, Bushby K. Continued need for caution in the diagnosis of Duchenne muscular dystrophy. Neurology. 2005. 64:1498–1499.
Article
22. Brooks BR, Miller RG, Swash M, Munsat TL. World Federation of Neurology Research Group on Motor Neuron Diseases. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000. 1:293–299.
Article
23. Wilson SH, Cooke NT, Edwards RH, Spiro SG. Predicted normal values for maximal respiratory pressures in caucasian adults and children. Thorax. 1984. 39:535–538.
Article
24. Gozal D. Pulmonary manifestations of neuromuscular disease with special reference to Duchenne muscular dystrophy and spinal muscular atrophy. Pediatr Pulmonol. 2000. 29:141–150.
Article
25. Kang SW. Pulmonary rehabilitation in patients with neuromuscular disease. Yonsei Med J. 2006. 47:307–314.
Article
26. Simonds AK, Muntoni F, Heather S, Fielding S. Impact of nasal ventilation on survival in hypercapnic Duchenne muscular dystrophy. Thorax. 1998. 53:949–952.
Article
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