Respiratory Flashcards

1
Q

Differentials for Interstitial Lung Disease

A

IREST VIDRO

Idiopathic Pulmonary Fibrosis
Rheumatological Diseases
(RA, SLE, Polymyositis, Dermatomyositis, Sjogren’s, MCTD, Ankylosing Spondylitis, Psoriasis)
Eosinophilic Lung Disease
(Aspergillosis + Medications [nitrofurantoin, sulfasalazine])
Sarcoidosis
Tuberculosis
Vasculitis
Inhaled Agents
(Extrinsic Allergic Alveolitis, Asbestosis, Silicosis, Beryliosis)
Drugs
(Amiodarone, Nitrofurantoin, Bleomycin, MTX, Gold)
Radiation Fibrosis
Other: Tuberous Sclerosis, NFT

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2
Q

Causes of Clubbing

A
3 Respiratory:
- Suppurative Lung Disease (CF + Bronchiectasis)
- Interstitial Lung Disease
- Lung Cancer
3 Cardiac:
- Cyanotic Heart Disease
- Infective Endocarditis
- Myxoma
3 Other:
- Thyroid (Graves)
- GI / IBD / Hepatopulmonary
- Idiopathic
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3
Q

Management of IPF

A

Non-Pharmacological

  • smoking cessation
  • oxygen therapy
  • ordine

Pharmacological
- anti-fibrotic agents (nintendanib + pirfinedone)

Transplant (single or double lung)

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4
Q

Investigations in IPF

A

Bloods - FBC, inflammatory markers (ESR + CRP), Immunoglobulins, ANA, ENA, ANCA, antiGBM, CK, myositis panel, RF, anti-CCP, serum ACE, Precipitins
ABG
CXR - bibasal reticular markings, destruction of parenchyma (honeycombing), bilateral hilar lymphadenopathy, pleural plaques (asbestosis)
Pulmonary Function Tests - FVC/FEV1 ratio (restrictive), FEV1, FVC, TLC, DLCO (reduced = impaired gas exchange)
HRCT
- UIP pattern (subpleural and basal predominance of reticulation, honeycombing with traction bronchiectasis)
- NSIP pattern (reticulation, ground glass changes with traction bronchiectasis - better prognosis)
Bronchoscopy - lavage + biopsy

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5
Q

Causes of Apical Lung Fibrosis

A
BREASTS CLAP
Berylliosis
Radiation
Extrinsic Allergic Alveolitis (Hypersensitivity Pneumonitis)
ABPA - Allergic Bronchopulmonary Aspergillosis
Sarcoidosis
TB
Silicosis

Coal worker’s pneumoconiosis
Langerhans’ Histiocytosis
Ank Spondy
Psoriasis

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