Interstitial Lung Disease
Thank you for asking me to examine Harry who presented with SOB. I would have like to have completed my examination by taking pulse oximetry and peak flow measurements.
My salient findings were basal / apical predominant fine inspiratory crepitations, which are consistent with interstitial lung disease.
I will now present my findings in full before commenting on potential aetiology, severity and complications.
The patient was comfortable at rest with normal/increased WOB with/without evidence of accessory muscle use. There was no evidence of CO2 narcosis with no asterixis. There was / was not supplemental oxygen. The patient had a dry/loose/productive cough on prompting. There was / was no sputum cup at the bedside.
The respiratory rate was ___, and the pulse was ___ and regular/irregular.
On examination of the hands, there was / was not clubbing, nicotine staining, or peripheral cyanosis.
On examination of the face, there was / was not conjunctive pallor, ptosis, or central cyanosis.
The trachea was midline / displaced with/without tracheal tug. There was / was not cervical, supraclavicular or axillary lymphadenopathy.
On inspection of the chest, there was / was no obvious deformity with / without kyphoscoliosis, pectus carinatum, pectus excavatum. There were / were not previous surgical scars. There were / were not radiotherapy skin changes.
Chest expansion was reduced / normal and symmetrical / asymmetrical.
Percussion showed normal / reduced resonance.
On auscultation, there was fine inspiratory crepitations throughout the lower / middle / upper lobes bilaterally with/with no added wheeze. Vocal resonance was / was not normal.
In regard to cardiovascular complications, there was / was not evidence of pulmonary hypertension and right heart dysfunction. More specifically, there was / was not a left parasternal heave, a palpable P2, an elevated JVP with prominent A-waves, or peripheral oedema.
In regard to potential aetiology of this lower/upper zone fibrosis, there were/were not:
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Upper: features of sarcoidosis, cystic fibrosis, ankylosing spondylitis, or radiation
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Lower: features of rheumatoid arthritis or scleroderma
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The presence of clubbing suggests idiopathic pulmonary fibrosis
In terms of findings suggestive of a particular treatment:
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There was / was not signs of steroid complications, such as a Cushingoid appearance, bruising, skin atrophy, cataracts, or proximal myopathy.
In summary, Harry is a patient who presented with SOB. My findings are suggestive of basal/apical predominant interstitial lung disease with/without evidence of pulmonary hypertension or cor pulmonale, and no evidence of complications of long-term steroid use. I could no elicit a specific aetiology.
My differentials are:
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HF
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Bronchiectasis - coarse
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Atelectasis
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COPD - early, coarse
Assuming this is ILD, my differentials for the ILD are....
I would proceed from here by:
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Confirming the diagnosis and assessing severity with a CXR, HRCT, ABG and RFTs. I would also like to complete a 6-minute walk test.
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Assessing for aetiology by taking a history, including exposure history and drug history.
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Completing an assessment of complications with a TTE to assess for pulmonary hypertension and right ventricular function, and if on steroids, a HbA1c, osteoporosis screen, and CV risk profile.
What are the causes of upper and lower lobe ILD?
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Upper:
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Coal workers pneumoconiosis
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Histiocytosis
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Allergic bronchopulmonary aspergillosis, and hypersensitivity pneumonitis
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Ankylosing spondylitis
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Radiation
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Tuberculosis
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Sarcoidosis
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Silicosis
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Lower:
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Idiopathic interstitial pneumonias includes:
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IPF
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Non-specific interstitial pneumonia
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Cryptogenic organising pneumonia
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Desquamative interstitial pneumonia
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CTD/Rheumatological
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RA, Scleroderma, dermatomyositis
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Other - drugs (MTX, bleomycin, nitrofurantoin)
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Asbestosis
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Aspiration
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AAT deficiency
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How would you interpret these RFTs?
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KCO is corrected for volume (in simple terms for exam)
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Learn how to interpret RFTs.
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FER < 0.7
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FVC < 70% restrictive
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TLC < 80% is restrictive
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DLCO 76% to 140% normal (< 40% is severe)
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