Resp Flashcards
(53 cards)
How might lung function change in patient with transplanted lung with IPF?
Lung function could show worsening restrictive pattern suggesting native lung is worsening fibrosis
Or could start to show obstructive pattern if they’re developing bronchiolitis obliterans
Most common type of chronic lung rejection after transplant?
Bronchioloitis obliterans
Spirometry for ILD
Restrictive pattern
Reduced FEV and FVC with preserved ratio
Reduced total lung capacity and transfer factor
Causes of restrictive spirometry
Plural disease, motor neuron disease, obesity, and kyphoscoliosis
Causes of upper zone lung fibrosis
Ankylosing spondylitis
ABPA
TB
radiation
silicosis and sarcoidosis
Causes of lower zone lung fibrosis
IPF, asbestosis, RA, SLE/Sjogren’s
Surgical sieve for long fibrosis
Auto immune
occupational/environmental
drugs
post infective
smoking
other systemic disorders e.g. sarcoid vasculitis IBD
Why don’t we use suction for pneumothorax?
Risk of pulmonary oedema re-expansion
Indication for VATS procedure
Lobectomy or wedge resection, bullectomy, lung reduction, pleurectomy, biopsy
Indications for surgical management of pneumothorax
Recurring pneumothorax or ongoing air leak despite drain
Indications for surgical management of pneumothorax
Recurring pneumothorax or ongoing air leak despite drain
Pros and cons of VAT versus open thoracotomy
That is less invasive, less pain less wound infection
That has slightly higher risk of recurrent pneumothorax
What is ABPA?
Fungal infection in asthmatics/ CF/ immunosuppressed due to sensitivity to aspergillosis antigen
Increased asthma exacerbations, weight loss, sinusitis = ?
APBA
ABPA CT findings
Bronchiectatic changes, centrilobular nodules, tree in bud appearance
Peak flow pattern in asthma
Low peak flow in am and diurnal variation
How does spirometry differ in asthma compared to COPD?
Both obstructive with reduced FEV and preserved FVC
Asthma shows reversibility ie improvement of at least 15%
Gas transfer is reduced in COPD
Common organisms in cystic fibrosis
In children staph aureus
Adults pseudomonas and non tv mycobacterium
burkholderia which is bad prognosis and contraindication to lung transplant
Management of CF
MDT!
1. Daily transfer physio including postural drainage.
2. Nebulisers including mucolytics e.g. hypertonic saline and recombinase
3. Azithromycin and regular courses of antibiotics.
4. Pancreatic enzymes and fat soluble vitamins.
5. Nutritional supplements or NGO peg feeding.
6. CFTR modulator Med is.
7. Insulin therapy
How is cystic fibrosis diagnosed?
Screening with the Guthrie test as newborn and then go onto test for the commonest CFTR mutations and perform a sweat test
Indications for pneumonectomy
Trauma
Cancer
Chronic infections eg TB or fungal
How can you differentiate between an exudate and transudate on a plural tap?
Using lights criteria if protein levels are between 25 and 35
Indications for lung transplant
2 wet 2 dry
Cystic fibrosis bronchiectasis pulmonary hypertension pulmonary fibrosis
COPD single rather than double transplant
Complications of lung transplant
Acute: hyper acute rejection and infection.
Chronic: bronchiolitis obliterans and skin malignancy or lymphoproliferative