Resp Flashcards
(66 cards)
what is asthma?
asthma is a chronic respiratory disorder characterised by recurrent episodes of dyspnoea, cough and wheeze caused by reversible airway obstruction, which occurs due to hyper-responsiveness to stimuli.
What causes airway obstruction in asthma?
acute: bronchial muscle constriction, mucosal inflammation and swellig and an increased production of mucus.
long term: increase in smooth muscle, damaged cilia,
what is brittle asthma?
rapid change between being well to having life-threatening asthma, and repeated exacerbations despite treatment.
what should you do with patients of intermediate risk of asthma?
BTS guidelines say spirometry with bronchodilator variability testing (>15% chnage or >200ml change). Could also do histamine test or nitric oxide test
what is bronchiectasis?
this is the abnormal widening on bronchi or bronchioles which often leads to mucus build up and recurrent infection.
what are the causes of bronchiectasis?
congenital (CF, PCD. hypogammaglobunaemia in CVID), infection (measles pertussis, TB, HIV), inflammation (RA, IBD, sarcoid, asthma), other (idiopathic, bronchial obstruction - tumour or FB).
what is the gold standard investigation for bronchiectasis?
HRCT - bronchial dilatation and wall thicking, tramlines, small airways near pleura
What are the symptoms and signs of bronchiectasis?
chronic mucopurulent cough and intermittent haemoptysis. On examination may have clubbing, wheeze, and bibasal coarse crackles which improve with coughing.
What is COPD?
This is a chronic progressive respiratory disorder characterised by airway obstruction with little to no reversibility. The clinical picture includes chronic bronchitis and emphysema.
what is the definition of chronic bronchitis?
cough and sputum on most days for 3 months for two successive years.
how does A1AT deficiency cause COPD?
A1AT blocks elastase , therefore a deficiency causes excessive elastase, which in turn breaks down elastin in the alveolar wall. this occurs all over the lung (panacinar pattern) unlike in smoking which has a centrilobular pattern.
Signs of cor pulmonale>
prominent RV heave and loud pulmonary S2
What are the signs of hypercapnia?
Bounding pulse, headache, peripheral vasodilation, tremor, papilloedema, confusion, drowsiness, coma
How can interstitial lung disease be classified?
Into 3 groups:
Known cause - occupational, environmental (asbestososis, coal workers lung), drugs (DMARDS, Biologics, SSRIs, chemotherapy, amiodarone), infections (TB, fungal, severe pneumonia), hypersensitivity reactions (EAA)
Associated systemicndisease (RA, sarcoidosis, UC, sjorens, SLE)
Idiopathic (IPF, cryptogenic fibrosing alveolitos)
Systems of interstitial lung disease?
Dyspnoea, dry cough, fatigue, end inspiratory crackles (sound like Velcro)
Causes of apical lung fibrosis?
BREAST. Borelliosis (Lyme disease) Radiation EAA Ankylosing spondylitis Sarcoidosis TB
Causes of basal PF?
DARSI. Drugs (amiodarone, cyclophosphamide), Asbestosis, RA, Systemic sclerosis, IPF
What is the bode index?
It is a predictor of survival in COPD. looks at BMI, obstruction (FEV1 % of predicted), Dyspnoea (on the MRC scale - 1-5) , Exercise capacity (6 minute walk distance)
What is the management of IPF?
Conservative - MDT including ILD specialist nurse, patient support groups (Action for Pulmonary Fibrosis), patient education, smoking cessation.
Medical - PPI if symptomatic, Pirfenidone (anti-fibrotic drug), NAC is sometimes used
Surgical - lung transplant.
what are the CXR signs of IPF?
reticulo-nodular shadowing, ground-glass shadowing, honeycombing in late disease
what is EAA caused by?
hypersensitivity to moldy hay, bird shit, moldy barley
which paraneoplastic syndromes are associated with small cell lung cancer?
ectopic ACTH, SIADH, Lambet-Eaton syndrome
what paraneoplastic syndrome is accoiated with squamous cell lung cancer?
PTHrP
how do you stage small cell lung cancer?
limited - in one hemithorax and supraclavicular LN only
extensive - spread beyond the above