resp Flashcards

(48 cards)

1
Q

causes of pleural effusion

A

exudate (protein > 35g/dl): infection (pneumonia), inflammation (SLE, rheumatoid arthritis), malignancy (lung cancer, mets)
transudate (protein < 25g/dl): cardiac, liver, renal failure

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2
Q

causes of ILD

A

idiopathic pulmonary fibrosis
occupational / environmental: extrinsic allergic alveolitis / pneumoconiosis
drugs: methotrexate, amiodarone
inflammatory: SLE, RA, sarcoidosis, ank spond, systemic sclerosis
other: radiation

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3
Q

ILD investigations

A

bloods: FBC, CRP/ESR,
serology: RF, ANA, anti-CCP, anti-Jo
lung function tests (restrictive pattern)
CXR (initial)
high-res CT → honeycombing
bronchoscopy + biopsy (diagnostic)

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4
Q

definition of COPD

A

emphysema + chronic bronchitis
emphysema = enlargement of alveolar spaces
chronic bronchitis = chronic productive cough for at least 3mths/year for at least 2 years

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5
Q

signs of hyperexpansion

A
reduced cricosternal distances (normal = 3 fingers) 
tracheal tug
barrel chest
reduced chest expansion 
loss of cardiac dullness
displaced liver edge
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6
Q

signs on examination for COPD

A
hyperexpansion
hyperresonance
reduced breath sounds + vocal resonance 
coarse crackles 
expiratory wheeze
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7
Q

causes type 1 resp failure

A
ventilation perfusion mismatch:
pneumonia
PE
pulmonary oedema 
asthma
ARDS
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8
Q

causes type 2 resp failure

A

resp disease: COPD, asthma, pneumonia, obstructive sleep apnoea
reduced resp drive: sedatives, CNS tumour / trauma
neuromuscular disease: guillain-barre, myasthenia gravis
thoracic wall disease: flail chest, kyphoscoliosis

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9
Q

pulmonary embolism ECG findings

A

S1Q3T3
deep S waves in lead I
deep Q waves in lead III
inverted T waves in lead III

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10
Q

management suspected pulmonary embolism

A

Well’s score:
4 or less = PE unlikely → D-dimer → immediate CTPA + admission if +ve
5 or more = PE likely → admission + immediate CTPA

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11
Q

management confirmed pulmonary embolism

A
  1. LMWH (tinzaparin 175units/kg once daily SC) / fondaparinux for > 5 days / until INR > 2 for > 24hrs
    for 6mths for pts w active cancer
  2. start warfarin within 24hrs
    continue for at least 3mths and reassess whether should be continued
    continue for >3mths if unprovoked PE
  3. thrombolysis for massive PE w haemodynamic instability: tPa, streptokinase
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12
Q

management stable COPD

A
  1. short acting bronchodilator: SABA (salb) / SAMA (ipratropium)
    • long acting bronchodilator: LABA (salmeterol), LAMA (tiotropium)
    • inhaled corticosteroid (combined inhalers if poss)
      long-term oxygen therapy
      surg: lung volume reduction surg / transplant
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13
Q

management acute COPD

A

ABCDE

  1. neb salb / ipratropium
  2. oxygen if sats < 90 (aim for 88-92%) via venturi
  3. oral steroids 5 days
  4. NIV (BiPAP) if respiratory insufficiency
  5. antibiotics if infective exacerbation
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14
Q

management acute asthma

A
ABCDE 
oxygen: high-flow 15L via non-rebreathe mask 
neb 5mg salb (oxygen-driven / via spacer) 
oral pred 40mg (5 days) 
neb ipratropium
IV magnesium sulphate 
IV aminophylline 
intubation + ventilation
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15
Q

management stable asthma

A
  1. PRN inhaled SABA (salb)
    • BD inhaled low-dose CS (beclamethasone)
    • inhaled LABA (salmeterol)
      if not effective consider: increased steroid dose, LTRA (montelukast), SR theophylline, oral beta-agonist
  2. daily oral steroids
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16
Q

indications for NIV (BiPAP)

A

COPD w respiratory acidosis 7.25-7.35
type 2 respiratory failure (neuromuscular disease or chest wall deformities)
failure of CPAP for pulmonary oedema

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17
Q

indications for CPAP

A

chronic severe obstructive sleep apnoea

type 1 respiratory failure e.g. acute pulmonary oedema

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18
Q

ILD management

A

cons: MDT approach, smoking cessation, pulmonary rehabilitation
med: anti-fibrotic drugs e.g. pirfenidone, nintedanib
steroids (exacerbation fo Sx)
LTOT
surgery: lung transplant (curative)

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19
Q

signs on examination ILD

A

clubbing

fine end-inspiratory crepitations

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20
Q

causes of upper lobe fibrosis

A
ROTAS:
radiation
occupational: EAA / pneumoconiosis 
TB 
ank spond
sarcoidosis
21
Q

causes of lower lobe fibrosis

A
DR CIA: 
drugs: methotrexate, amiodarone
connective tissue disease e.g. RA, SLE 
idiopathic pulmonary fibrosis 
asbestos
22
Q

indications for pneumonectomy

A
primary lung cancer
pulmonary metastases 
traumatic lung injury 
bronchiectasis 
infection: TB, fungal
23
Q

indications for lobectomy

A

primary lung cancer
lung volume reduction (COPD)
bronchiectasis
infection: TB (upper lobe), fungal

24
Q

differentials for thoracotomy scar

A
pneumonectomy 
lobectomy 
lung transplant 
chest wall resection 
oesophagectomy
25
indications for lung transplant
``` COPD ILD cystic fibrosis alpha1-antitrypsin deficiency pulmonary HTN bronchiectasis ```
26
differentials for coarse crackles vs fine crackles
corase: bronchiectasis, COPD, pneumonia fine: ILD, pulmonary oedema, pneumonia, atelectasis
27
differentials for wheeze
asthma / COPD bronchiectasis anaphylaxis foreign body
28
signs on examination bronchiectasis
``` clubbing coarse crackles high-pitched inspiratory squeaks monophonic wheeze rhonchi (low-pitched rattling due to secretions in bronchial airways) ```
29
causes of bronchiectasis
idiopathic post-infective: TB, measles, ABPA genetic: a1antitrypsin, cystic fibrosis, Kartagener's bronchial obstruction: malignancy, foreign body, lymphadenopathy connective tissue disease: RA, sjogren's EDS, marfan
30
management bronchiectasis
cons: airway clearance therapy (postural drainage, percussion, vibration) pulmonary rehabilitation med: ABx for acute exacerbations long-term macrolide if >2 / year bronchodilators / theophylline if trial shows improvement LTOT surg: resection of bronchiectatic areas of lung lung transplant
31
investigations bronchiectasis
bedside: sputum culture bloods: FBC, U&Es alpha1 antitrypsin screen for immunodeficiency / connective tissue disease aspergillus markers cystic fibrosis testing imaging: CXR high-res CT is diagnostic (ring shadows, tramlines) other: lung function testing (obstructive)
32
types of lung cancer
non-small cell: squamous cell: PTHrP → Ca adenocarcinoma: non-smokers large cell small cell: ectopic hormone production (ADH, ACTH, PTH, GnRH)
33
presentation pancoasts tumour
apical lung tumour → compression of structures: brachial plexus → hand muscle wasting arteries → oedema of arms sympathetic ganglion → Horner's syn (ptosis, miosis, anhydrosis) SVC → facial swelling / flushing, difficulty breathing small cell tumours → ectopic hormone production (ACTH, ADH, PTH)
34
investigations lung cancer
``` bloods: FBC, U+Es, LFTs, bone profile CXR, contrast CT PET-CT → distant mets bronchoscopy + biopsy lung function testing (?fit for surg) ```
35
complications of old TB
aspergilloma in old TB cavity bronchiectasis (lymph node causes obstruction) risk of bronchial carcinoma
36
causes of consolidation
fluid: pulmonary oedema pus: pneumonia blood: pulmonary haemorrhage cells: malignancy
37
pneumonia severity score + resulting action
confusion urea > 7 resp rate > 30 BP < 90/60 (either systolic OR diastolic) age > 65 1: community management 2: community management if sats > 90 + normal CXR 3: admit 4: consider ITU 5: manage in ITU (30% mortality at 30 days)
38
types of pneumothorax
spontaneous: no precipitating event traumatic: penetrating / blunt chest injury tension: one-way valve → air entry during inspiration (emergency)
39
management pneumothorax
primary: no underlying lung disease < 2cm / no SOB: conservative, discharge w advice + follow-up CXR > 2cm / SOB: aspiration 2nd ICS MCL w large-bore cannula failure → chest drain: 5th ICS MAL ``` secondary: underlying lung disease e.g. asthma, COPD, cystic fibrosis admit for > 24hrs < 1cm: oxygen + analgesia + observation 1-2cm: aspiration >2cm / > 50years: chest drain ```
40
borders of safe triangle (for chest drain)
base of axilla lat border pec major ant border latissimus dorsi 5th ICS / line superior to horizontal level of nipple
41
signs on examination pneumothorax
reduced chest expansion hyperressonance absent / reduced breath sounds + TVF tracheal deviation from affected side in tension pneumothorax
42
management recurrent pleural effusion
recurrent aspiration pleurodesis: insertion of temporary chest drain + talc (sclerosing agent) indwelling pleural catheter opioids relieve dyspnoea
43
management pneumonia
ABCDE oxygen, analgesia, fluids ABx: mild: 5 days oral amox (macrolide if allergic / atypical) mod: 7-10 days oral / IV amox + macrolide severe: IV co-amox + macrolide repeat CXR in 6wks post-resolution
44
mechanism of BiPAP
iPAP > ePAP iPAP: ventilates ePAP: recruits collapsed / underventilated alveoli
45
causes of tracheal deviation
pulls towards: lobar / lung collapse, pneumonectomy, pulmonary hypoplasia pushes away: tension pneumothorax, massive pleural effusion, large thoracic mass, diaphragmatic hernia
46
management of anaphylaxis (incl dose)
``` IM adrenaline 0.5mg 1:1000 IV hydrocortisone 200mg neb salb IV chlorphenamine 10mg + IV fluids if shock ```
47
management hospital acquired pneumonia
< 5 days: co-amox / cefuroxime > 5 days: tazocin / ciprofloxacin pseudomonas: tazocin MRSA: vancomycin
48
causes of ARDS
pulmonary: trauma, pneumonia, inhalation of smoke / soot | extra-pulmonary: sepsis, DIC, pancreatitis