Clinical signs of pulmonary fibrosis
Inspection: clubbing, central cyanosis, tachypnoea
Auscultation: fine end-inspiratory crackles which do not alter with coughing
Signs of associated AI disease e.g. RA, SLE, systemic sclerosis
Signs of treatment e.g. Cushingoid
Discoloured grey skin - amiodarone as cause
Investigations for pulmonary fibrosis
Bloods: ESR, RF, ANA
CXR: reticulonodular changes, loss of definition of heart borders, small lungs
ABG: type I respiratory failure
Lung function tests: FEV1/FVC >0.8 (restrictive), low TLC (small lungs)
Bronchoalveolar lavage: exclude infection prior to immunosuppressant use)
HRCT: distribution aids diagnosis
Lung biopsy
Treatment for pulmonary fibrosis
If inflammatory –> immunosuppression (steroids)
If UIP - pirfenidone (antifibrotic agent)
Single lung transplant
Causes of basal lung fibrosis
Usual interstitial pneumonia (UIP)
Asbestosis
Connective tissue disease
Aspiration
Clinical signs for bronchiectasis
Room: sputum pot +++
Gen: cachexia and tachypnoea
Hands: clubbing
Chest: mixed character crackles that alter with coughing, occasional squeaks and wheeze
Cor pulmonale: SOB, raised JVP, RV heave, loud P2
Investigation for bronchiectasis
Sputum culture and cytology
CXR: tramlines and ring shadows
HRCT thorax: signet ring sign (thickened dilated bronchi larger than adjacent vascular bundle)
To find specific cause:
Immunoglobulins - hypogammaglobulinaemia
Aspergillus RAST/skin prick testing - ABPA (upper lobe)
Rheumatoid serology
Saccharine ciliary motility test (nose to taste buds in 30mins) - Kartagener’s
Genetic screening - CF
Hx of IBD
Causes of bronchiectasis
Congenital: Kartagener’s and CF
Childhood infection: measles and TB
Immune OVERactivity: ABPA and IBD associated
Immune UNDERactivity: hypogammaglobulinaemia, CVID
Aspiration: chronic alcoholics and GORD, localised to right lower lobe
Treatment for bronchiectasis
Physio - active cycle breathing
Prompt abx therapy for exacerbations
Long-term treatment with low-dose azithromycin 3x week
Bronchodilators/inhaled corticosteroids if airflow obstruction
If localised –> surgery
Complications of bronchiectasis
Cor pulmonale Secondary amyloidosis (dip urine for protein) Massive haemoptysis (mycotic aneurysm)
Clinical signs of old TB
Inspection:
Palpation:
Percussion:
-dull percussion but present tactile vocal remits
Auscultation:
-crackles and bronchial breathing
Historical techniques to treat TB
Plombage: insertion of polystyrene balls into the thoracic cavity
Phrenic nerve crush: diaphragm paralysis
Thoracoplasty: rib removal but lung not resected
Apical lobectomy
Serious side effects of TB drugs
Rifampicin: hepatitis, increased metabolism of OCP
Isoniazid: peripheral neuropathy (treat with pyridoxine) and hepatitis
Pyrazinamide: hepatitis
Ethambutol: retro-bulbar neuritis and hepatitis
What to tell patients about to commence TB therapy
Causes of apical fibrosis
TRASH
Clinical signs of lobectomy
Inspection:
Palpation:
Lower lobectomy: dull percussion note over lower zone + absent breath sounds
Upper lobectomy: normal exam OR hyper-resonant percussion note over upper zone and dull percussion at base where hemidiaphragm has lifted
Clinical signs of pneumonectomy
Inspection:
-Thoracotomy scar
Palpation:
Percussion:
Auscultation:
Clinical signs of single lung transplant
Thoracotomy scar
Normal exam on side of scar
May have signs on opposite hemithorax
Clinical signs of double lung transplant
Clamshell incision - from on axilla, along line of lower ribs, up to the xiphisternum to other axilla
Indications for single lung transplant
‘Dry lung’ conditions: COPD, pulmonary fibrosis
Indications for double lung transplant
‘Wet lung’ conditions: CF, bronchiectasis, pulmonary hypertension
Clinical signs of COPD
Inspection:
Palpation:
-Hyperexpanded
Percussion:
-Resonant with loss of cardiac dullness
Auscultation:
Clinical signs of cor pulmonale
Investigations for COPD
ABG: type II respiratory failure
Bloods: high WCC (infection), low A1AT (younger patients/FH), low albumin (severity)
CXR: hyper-expanded and/or pneumothorax
Spirometry: low FEV1, FEV1/FVC <0.7 (obstructive)
Gas transfer: low TLCO
Possible COPD treatments
-Long-term oxygen therapy: 2-4L/min via nasal prongs for at least 15hrs a day
Surgical: