Resp Flashcards

(66 cards)

1
Q

what is asthma?

A

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.

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2
Q

What causes airway obstruction in asthma?

A

acute: bronchial muscle constriction, mucosal inflammation and swellig and an increased production of mucus.
long term: increase in smooth muscle, damaged cilia,

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3
Q

what is brittle asthma?

A

rapid change between being well to having life-threatening asthma, and repeated exacerbations despite treatment.

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4
Q

what should you do with patients of intermediate risk of asthma?

A

BTS guidelines say spirometry with bronchodilator variability testing (>15% chnage or >200ml change). Could also do histamine test or nitric oxide test

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5
Q

what is bronchiectasis?

A

this is the abnormal widening on bronchi or bronchioles which often leads to mucus build up and recurrent infection.

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6
Q

what are the causes of bronchiectasis?

A

congenital (CF, PCD. hypogammaglobunaemia in CVID), infection (measles pertussis, TB, HIV), inflammation (RA, IBD, sarcoid, asthma), other (idiopathic, bronchial obstruction - tumour or FB).

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7
Q

what is the gold standard investigation for bronchiectasis?

A

HRCT - bronchial dilatation and wall thicking, tramlines, small airways near pleura

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8
Q

What are the symptoms and signs of bronchiectasis?

A

chronic mucopurulent cough and intermittent haemoptysis. On examination may have clubbing, wheeze, and bibasal coarse crackles which improve with coughing.

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9
Q

What is COPD?

A

This is a chronic progressive respiratory disorder characterised by airway obstruction with little to no reversibility. The clinical picture includes chronic bronchitis and emphysema.

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10
Q

what is the definition of chronic bronchitis?

A

cough and sputum on most days for 3 months for two successive years.

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11
Q

how does A1AT deficiency cause COPD?

A

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.

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12
Q

Signs of cor pulmonale>

A

prominent RV heave and loud pulmonary S2

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13
Q

What are the signs of hypercapnia?

A

Bounding pulse, headache, peripheral vasodilation, tremor, papilloedema, confusion, drowsiness, coma

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14
Q

How can interstitial lung disease be classified?

A

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)

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15
Q

Systems of interstitial lung disease?

A

Dyspnoea, dry cough, fatigue, end inspiratory crackles (sound like Velcro)

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16
Q

Causes of apical lung fibrosis?

A

BREAST. Borelliosis (Lyme disease) Radiation EAA Ankylosing spondylitis Sarcoidosis TB

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17
Q

Causes of basal PF?

A

DARSI. Drugs (amiodarone, cyclophosphamide), Asbestosis, RA, Systemic sclerosis, IPF

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18
Q

What is the bode index?

A

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)

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19
Q

What is the management of IPF?

A

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.

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20
Q

what are the CXR signs of IPF?

A

reticulo-nodular shadowing, ground-glass shadowing, honeycombing in late disease

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21
Q

what is EAA caused by?

A

hypersensitivity to moldy hay, bird shit, moldy barley

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22
Q

which paraneoplastic syndromes are associated with small cell lung cancer?

A

ectopic ACTH, SIADH, Lambet-Eaton syndrome

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23
Q

what paraneoplastic syndrome is accoiated with squamous cell lung cancer?

A

PTHrP

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24
Q

how do you stage small cell lung cancer?

A

limited - in one hemithorax and supraclavicular LN only

extensive - spread beyond the above

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25
what causes a bovine cough?
RLN palsy
26
what causes wrist pain in lung cancer?
hypertrophic pulmonary osteoarthropathy
27
what are in the indications for a 2ww CXR?
``` >40 and 2 of: - previous moker cough fatigue sob chest pain weight loss LoA or any age and unexplained: clubbing recurrent chest infection supraclav or cervical LN chest signs suggestive of lung cancer thrombocytosis. ```
28
what is a raised hemidiaphragm suggestive of on CXR?
phrenic nerve damage or lobar collapse (in lung cancer)
29
Pancoast's tumour can invade which structures?
sympathetic chain (Horner's), brachial plexus (hand pain and paralysis), RLN (hoarseness), subclavian artery, brachicephalic vein, phrenic nerve.
30
where is the air in a pneumothorax?
in the pleural space
31
what are the borders of the area in which a chest drain can be safley inserted?
lat border of pec major, lateral edge of lat dorsi, 5th IC space and base of axilla
32
when can someone with a pneumothorax fly?
2w after clear CXR
33
what drugs are used in chemical pleurodesis?
minocycline or talc via chest drain
34
what investigations would you do in allergic bronchopulmonary aspergillosis?
sputum: aspergillus Bloods: FBC (eosinophilia), serum precipitants (igG asperigullus), aspergilus igE RAST test, aspergillus skin test
35
who gets invasive aspergillosis?
immunocompromised or those exposed to massive amount of spores
36
what is treatment for invasive aspergillosis?
IV Voriconazole
37
who gets chronic pulmonary aspergillosis?
those patients with underlying lung diseases
38
how does chronic pulmonary aspergillosis present?
it sort of mimics caner - weight loss, haemoptysis, LoA, chronic productive cough, sweats, malaise
39
how do you investigate suspected chronic pulmonary aspergillosis?
sputum culture, aspergillus-specific serum precipitins, CXR
40
what does an asperigilloma look like on CXR?
round opacity in pre-existing cavity (secondary to TB, sarcoid)
41
what is the treatment for aspergilloma?
only treat if symptomatic - transexamic acid, surgical exicision
42
who gets bronchopneumonia, what is it and what causes it?
bronchopneumonia occurs surroudning airways. It tends to affect elderly patients or those with COPD. assoiacted with low virulence pathogen like staph / strep.
43
what causes lobar pneumonia in past cases?
strep pneumoniae (90%)
44
what are the symptoms of an atypical CAP?
1st: fever, malaise, myalgia 2nd: dyspnoea, dry cough, D&V, hepatitis
45
weird symptoms of legionella?
hyponatraemia, LFT derrangement
46
what is first-line drug for Tx of legionella?
fluoroquinolone
47
chlamydia psittaci is associated with which animal?
birds
48
Klebsiella is seen most commonly in which patient population?
alcoholics
49
what colour is the sputum in klebsiella?
it's like red-current jelly. haemoptysis is also seen.
50
in which pneumonia is hypoxia usually sene to be disproportionate to CXR changes?
Pneumocystis jiroveci
51
what are the causative bacteria in HAP?
S. aureus, Pseudomas aeruinosa, eneterobacteria
52
what pneumonia is associated with rapid deterioration, lung cavitation and MOF?
Panton-Valentine Leukocidin S aureus
53
there is bilateral cavitating lesions with fluid levels on the CXR, what is the most likely causative organism?
Staph aureus
54
viral causes of pneumonia?
adenovirus, coronavirus, flu.
55
what are the signs on chest examination of consolidation?
reduced expansion, dull to percussion, increased vocal fremitus, bronchial breathing
56
what can CURB-65 score be used for?
prognosis as well as determining severity, as well as what antibiotics to give and how long for.
57
what media is TB cultured on?
Lowenstein-Jensen medium
58
what is the drug treatment regime for standard TB?
6 months of rifampacin, isoniazid and pyridoxdine, 2 months of pyraziamide and ethmabutol
59
what is the treatment for latent TB?
9m of isoniazid monotherapy.
60
what are the side effects of rifampacin?
orange secretions (R - Red-orange secretions / youll be picin colours) , hepatotoxicity, resistance to OCP
61
which TB drugs can cause sidedroblastic anaemia?
Isoniazid and pyrazinamide (the ones with the Zs in)
62
what side effects does isoniazid have?
peripheral neuropathy, rash, hepatotoxicty, CNS effects, sideroblastic anaemia
63
what are the side effects of Pyrazinamide?
arthralgia, hyperuricaemia, gout, hepatotoxicty, rash, sideroblastic anaemia
64
what are the side effects of ethambutol?
E is for eyes - optic neuritis, Red-green colour blindness, vertical nystagmus. also peripheral neuropathy. avoid in renal disease!
65
what does the pulmonary artery pressure have to be above in order to classify as pulmonary hypertension?
>25mmHg
66
what's the tretament for pulmonary hypertension?
conservative - use POCO (pregnancy is high risk), pulmonary rehab, annual flu vaccination, monitor for heart failure of valve disease (TR and PR) medical - high dose CCBs (diltiazem, nifedipine), prostaglandins (prostacyclin), sildenafil), anticoagulation for all (warfarin)