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INTRODUCTION

Dyspnoea is the subjective sensation of breathlessness that is excessive for any given level of physical activity.

Important causes of dyspnoea

  • Asthma (image 47)

  • COPD (image 135)

  • Heart failure (image 291)

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Table D10 Comparison of distinguishing features between dyspnoea due to heart disease and to lung disease

Lung disease

Heart disease

History of respiratory disease

History of hypertension, cardiac ischaemia or valvular heart disease

Slow development

Rapid development

Present at rest

Mainly on exertion

Productive cough common

Cough uncommon, and then ‘dry’

Aggravated by respiratory infection

Usually unaffected by respiratory infection

Table D11Dyspnoea: diagnostic strategy model

KEY INVESTIGATIONS FOR DYSPNOEA

  • Pulmonary function tests including pulse oximetry

  • CXR

  • FBE/ESR/CRP

  • Arterial blood gases

  • Cardiac, e.g. ECG, echocardiography

PULMONARY FUNCTION TESTS

Figure D12

Spirograms showing normal, obstructive and restrictive patterns

Figure D13

Maximum expiratory and inspiration flow volume curves with examples of relative changes of patterns with respiratory disease

INTERSTITIAL LUNG DISEASES

Interstitial lung diseases comprise a group of disorders that have the common features of inflammation and fibrosis of the interalveolar septum, representing a non-specific reaction of the lung to injury of various causes. Causes of pulmonary infiltration include:

  • sarcoidosis

  • idiopathic pulmonary fibrosis

  • hypersensitivity pneumonitis (extrinsic allergic alveolitis)

  • lymphangitis carcinomatosis

  • drug induced (e.g. nitrofurantoin, cytotoxics)

Common clinical features:

  • dyspnoea and dry cough (insidious onset)

  • slowly progressive dyspnoea over months to years

  • fine inspiratory crackles at lung base

  • finger clubbing

  • PFTs:

    • – restrictive ventilatory deficit

    • – decrease in gas transfer factor

  • characteristic X-ray changes

Sarcoidosis

Clinical features:

  • may be asymptomatic (one-third)

  • onset usually 3rd or 4th decade (but any age)

  • bilateral hilar lymphadenopathy (on CXR)

  • cough

  • fever, malaise, arthralgia

  • erythema nodosum

  • ocular lesions (e.g. anterior uveitis)

  • other multiple organ lesions (uncommon)

  • overall mortality 2–5%

Diagnosis

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