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Revision as of 14:15, 26 September 2012

Restrictive lung disease
ICD-9 518.89

Restrictive Lung Disease Microchapters

Overview

Classification

Acute respiratory distress syndrome
Hypersensitivity pneumonitis
Occupational lung diseases
Pleural Effusion
Interstitial lung disease
Sarcoidosis
Neuromuscular diseases
Scoliosis
Muscular dystrophy
Amyotropic lateral sclerosis (ALS)
Myasthenia gravis

Spirometry Findings in Various Lung Conditions

Approach to Lung Disorders

Differentiating Restrictive Lung Disease from other Diseases

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]

Overview

Restrictive lung diseases are a category of respiratory disease characterized by a loss of lung compliance,[1] causing incomplete lung expansion and increased lung stiffness.

Complete Differential Diagnosis for Restrictive Lung Disease

Pathophysiology

The underlying process is usually pulmonary fibrosis (scarring of the lung). As the disease progresses, the normal lung tissue is gradually replaced by scar tissue interspersed with pockets of air. This can lead to parts of the lung having a honeycomb-like appearance.

Causes and classification

Restrictive lung diseases may be due to specific causes which can be intrinsic to the parenchyma of the lung, or extrinsic to it.[2]

Intrinsic

  • Many cases of restrictive lung disease are idiopathic (have no known cause). Examples are:

Extrinsic

Quadriplegia can be a cause of restrictive lung disease.[3]

Clinical Presentation

The main symptoms are:

Diagnosis

  • In restrictive lung disease, both the FEV1 and FVC are reduced so the FEV1/FVC ratio is normal or even increased in contrast to obstructive lung disease where this ratio is reduced. The values for residual volume and total lung capacity are generally decreased in restrictive lung disease[4].

References

  1. Sharma, Sat. "Restrictive Lung Disease". Retrieved 2008-04-19.
  2. "eMedicine - Restrictive Lung Disease : Article by Sat Sharma". Retrieved 2008-11-21.
  3. Walker J, Cooney M, Norton S (1989). "Improved pulmonary function in chronic quadriplegics after pulmonary therapy and arm ergometry". Paraplegia. 27 (4): 278–83. PMID 2780083. Unknown parameter |month= ignored (help)
  4. "www.spirXpert.com".
  5. Brack T, Jubran A, Tobin MJ (2002). "Dyspnea and decreased variability of breathing in patients with restrictive lung disease". Am. J. Respir. Crit. Care Med. 165 (9): 1260–4. PMID 11991875. Unknown parameter |month= ignored (help)

Related Chapters

Additional Resources

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  • Baydur A. Respiratory muscle strength and control of ventilation in patients with neuromuscular disease. Chest. Feb 1991;99(2):330-8.
  • Bjoraker JA, Ryu JH, Edwin MK, et al. Prognostic significance of histopathologic subsets in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. Jan 1998;157(1):199-203.
  • Douglas WW, Ryu JH, Swensen SJ, et al. Colchicine versus prednisone in the treatment of idiopathic pulmonary fibrosis. A randomized prospective study. Members of the Lung Study Group. Am J Respir Crit Care Med. Jul 1998; 158(1): 220-5.
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