Respiratory Flashcards

1
Q

what are the causes of a restrictive picture on FEV1/FVC?

A

fibrosis, obesity, sarcoidosis, pneumoconiosis, interstitial pneumonia, connective tissue disesase, massive pleural effusion, chest wall defects (kyphoscoliosis)

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2
Q

what is the KCO?

A

the gas diffusion coefficient: represents the carbon monoxide diffusing capacity corrected for alveolar volume

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3
Q

how is TLCO measured?

A

a single inspitation of CO held for 10s, then CO measured in the blood.

TLV is measured with a helium dilution test

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4
Q

what are the causes of a high and low KCO?

A

high - alveolar haemorrhage

low - emphysema and interstitial lung disease

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5
Q

what does this flow-volume loop represent?

A

there is a characteristic defect in the expiratory phase of the flow volume loop.

This is commonly seen in intra-thoracic chest disease.

examples include asthma and emphysema

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6
Q

what does this abnormal flow-volume loop represent?

A

there is a characteristic pathological pattern during the inspiratory phase of this flow volume loop.

This typically represents an extra-throacic pathology.

An example would be tracheal obstruction, whereby during inspiration negative pressure the airway obstruction is sucked into the lumen reducing the flow of inspired air

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7
Q

what is the role of USS in respiratory medicine?

A

USS is commonly used to guide pleural drain insertion and pleural aspiration, especially in the case of loculated effusion/empyema

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8
Q

what is broncheoalveolar lavage? indications? complications?

A

BAL - performed during USS guided bronchoscopy. warmed 0.9% saline instilled into the distal airway and aspirated. fuild sent for lab testing.

  • *indications** -
    diagnostic: ?malignancy, ?pneumonia, ?bronchiectasis, ?TB, interstitial lung disease (sarcoid, pneumoconiosis, EAA)
    therapeutic: alveolar proteinosis

complications
transient shadow on CXR, transient hypoxia (give O2), transient fever
infection (rare)

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9
Q

what are the methods for lung biopsy? when are they useful?

A
  • percutaneous needle biopsy* with USS guidance - peripheral tumours located on chest CT
  • transbronchial, performed during bronchoscopy* - interstitial lung disease (sarcoid, IPF)
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10
Q

what is the indication of mediastinoscopy?

A

for visualisation, examination and biopsy of medisatinal lymph nodes/lesions

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11
Q

who should be offered pneumococcal vaccine?

how frequently is the vaccine given?

A
  • adults >65 y/o
  • chronic heart, liver or renal failure patients
  • DM not controlled by diet alone
  • immunosupression: splenectomy, AIDS, chemo or pred >20 mg/OD

every 5 years

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12
Q

what are the complications of pneumonia?

A

lung: respiratory failure (type I), parapneumonic effusion, empyema (pus in pleural space), lung abscess
systemic: hypotension, atrial fibrilation (elderly), sepsis, death, pericarditis/myocarditis, jaundice (co-amox and flucloxacillin)

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13
Q

define bronchiectasis

A

chronic inflammation and insult to the airways leads to thinning and dilatation

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14
Q

what are the causes of bronchiectasis?

A

congenital: CF, ciliary disorders (kartagner’s), PCD

post-infectious: measles, pertussis, recurrent bronchiolitis

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15
Q

how do you manage bronchiectasis?

A

conservative: airway clearance, chest physio and pulmonary rehab

medical:
abx - treat the isolated organism. >3 exac per year, long-term nebs antibiotics

surgical:
lobectomy: maybe considered for localised disease or to control haemoptysis

consider: bronchodilators (co-existant obstructive pathology) or steroids & itraconazole (ABPA)

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16
Q

what is the inheritance of CF?

A

most common autosomal recessive condition

affect 1:2000 live births, 1:25 carry a copy of the gene

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17
Q

diagnosis of CF?

A

sweat sodium and chloride >60 mmol/L

(chloride > sodium usually)

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18
Q

principles of managing CF?

A

lung

  • chest physio - frequently family/carers know best. usually in the morning, often >1 x per day
  • treat infections, prophylactic Abx, test for pseudomonas colonisation
  • mucolytics (DNase alpha or hypertonic saline)
  • bronchodilators
  • yearly CXR
  • extra: mutation-specific therapy ivacaftor and lumacaftor target the CFTR protein

GI

  • pancreatic enzyme replacement (CREON)
  • fat-soluble vitamin supplements (ADEK)
  • ursodeoxycolic acid for impaired liver function
  • cirrhosis = liver transplant

other

  • CF-related diabetes
  • osteoporosis
  • genetic councilling/fertility
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19
Q

median age of survival in CF?

A

41 years in the UK, though baby born today would expect to live longer

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20
Q

what lymph nodes are affected in bronchial carcinoma?

A

mediastinal (cannot palpate), supraclavicular and axillary

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21
Q

differential diagnosis of nodule on CXR?

A
  • malignancy (1ary or 2ary)
  • abscess
  • granuloma (TB or sarcoid, look for lymphadenopathy)
  • carcinoid tumour, other benign neoplams (hamartoma)
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22
Q

what must be done in the work-up for curative lung tumour resection before surgery?

A

PET-CT for staging

  • N0 no nodes
  • N1 peribronchial or ipsilateral hilum
  • N2 ipsilateral medistinum or subcarinal
  • N3 contralateral mediastinum or hilum, scalene or subcarinal
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23
Q

what is the prognosis for patients with bronchial carcinoma?

A

NSCLC - 50% 2 year survival without spread, 10% with spread

SCLC - 3 months if untreated, 1-1.5 yrs if treated

24
Q

what are the 5 ways aspergillus can affect the lung?

A
  • asthma (present in 1-5% of asthmatics)
  • allergic bronchopulmonary aspergillosis
  • aspergilloma
  • invasive aspergillosis
  • extrinsic allergic alveolitis
25
what are some systemic disease that can present with asthma? (not atopy)
GORD/reflux, vasculitides (polyarteritis nodosa, eGPA Churg-Strauss), ABPA
26
what are some complications of COPD?
lung * infectious exacerbations * fibrosis * type II respiratory failure * pneumothorax * lung CA systemic * secondary polycythaemia * cor pulmonale
27
beyond medical therapy, what is helpful in managing COPD?
smoking cessation diet + supplements (often underweight) pulmonary rehabilitation/exercise encouragement LTOT - if resting hypoxaemia and successfully stopped smoking diuretics (co-morbid heart failure) vaccinations - influenza (all) and pneumococcus (\>65 y/o)
28
what are the common signs of PE on ECG?
* sinus tachycardia * right ventricular strain (inverted T waves in V1-4) * right bundle branch block don't say S1 Q3 T3 first!
29
causes of transudative and exudative pleural effusions
transudate - cardiac failure, hypoalbuminaemia (liver and renal failure) exudate - malignancy and pneumonia
30
where do you send samples of pleural fluid?
biochemistry microbiology cytology need a paired sample of serum for protein and LDH
31
Light's criteria and differentiating pleural effusions
transudate protein \<25 g/L exudate protein \>35 g/L 25-35 g/L - pleural fluid protein/serum protein \>0.5 = exudate pleural fluid LDH/serum LDH \>0.6 = exudate
32
what are some causes of cor pulmonale?
**Lung parenchyma** * COPD * bronchiectasis * pulmonary fibrosis **pulmonary vasculature** * pulmonary embolism * primary pulmonary hypertension **other** - thoracic cage and neuromuscular abnormalities
33
what are the signs of cor pulmonale on chest examination?
* prominent P2 * right parasternal heave (RVH) * right heart failure: raised JVP, pulsatile hepatomegaly, oedema +/- pulmonary regurg = Graham Steel murmur (early diastolic) +/- tricuspid regurg = pansystolic murmur
34
what are the indications for steroid treatment in sarcoidosis ?
parenchymal lung disease uveitis hypercalcaemia neurologic or cardiac involvement
35
what are some causes of bihilar lymphadenopathy?
benign * sarcoidosis * tuberculosis * hypersensitivity pneumonitis * pneumoconioses (silica, beryllium) malignant * bronchial CA (stage N2-3) * lymphoma/CLL * histiocytosis x (langerhan's cell histicocytosis)
36
what happens to the TLCO/KCO in IPF?
decreased
37
what are the treatment options for IPF?
supportive care: oxygen, pulmonary rehab, opiates and palliation consideration of lung transplant and current clinical trial involvement **new**: anti-fibrotic drugs *nintedanib* and *pirfenidone* starting to show promise
38
what is the correct term for a patient with a large thoracic volume on inspection when you are examining them?
barrel chest cannot say 'hyperexpanded' becuase you have to measure the chest with a tape measure and compare this to a nomogram for that to be accurate
39
what are the most important findings when presenting intersitial lung disease?
* supplimental oxygen * clubbing and cyanosis * fine crackles (+/- apex or base)
40
what are the most important findings when presenting consolidation?
* bronchial breathing (+/- coarse crackles) * dull to percussion * increased vocal fremitus
41
what are the most important findings when presenting bronchiectasis?
* clubbing * sputum * coarse crackles
42
what are the most important findings when presenting pleural effusion?
* decreased breath sounds * stoney dull to percussion * decreased vocal fremitus
43
how do you describe the breathing pattern of somebody with COPD?
dyspnoeic, audible wheeze from the end of the bed purse-lip breathing prolonged expiratory phase
44
COPD does not cause clubbing. what should be suspected in a patient with COPD and clubbing?
smoking can also cause cancer, which can cause clubbing investigate for small cell lung CA
45
what is the pathophysiology of COPD?
_smoking_ 1. **direct oxidative stress** causes necrosis and apoptosis of the lung parenchyma 2. activates resident macrophages and neutrophils of the airways to release elastases. **proteolytic enzymes \> anti-protease enzymes** leads to destruction of compliant lung & airway tissue and **obstruction**
46
what are the causes of COPD and how does this relate to their histological distribution?
**smoking** - mixed centri-/panancinar **alpha1 anti-trypsin** - panacinar **coal dust** - centriacinar
47
what are the bugs of acute exacerbation of COPD?
* haemophilus influenzae* * strep pneumo* * moraxella catarrhalis*
48
what are the conditions for LTOT in COPD?
MUST * stopped smoking - carboxyhaemoglobin \< 3% AND * PaO2 \< 7.3 kPa OR * PaO2 7.3-8.0 kPa with * secondary polycythaemia * pulmonary hypertension * cor pulmonale * nocturnal deoxygenation
49
what are the causes of bronchiectasis?
**childhood infection** * tuberculosis * pertussis * measles **muco-ciliary dysfunction** * cystic fibrosis * kartagner's * primary ciliary dyskinesia **bronchial obstruction** * endobronchial tumour * foreign body aspiration **fibrosis** * idiopathic pulmonary fibrosis (long-standing) * infection complicated by fibrosis **idiopathic**
50
what is the gold standard diagnostic test for bronchiectasis?
high-resolution chest CT
51
what does the 'signet ring sign' represent? (CT)
signet ring sign = bronchiectasis damaged and enlarged bronchus has a larger diameter than the adjacent blood vessel
52
what are the LRTI bugs for bronchiectasis?
* staphylococcus aureus* * haemophilus influenzae* * pseudomonas aeruginosa*
53
which antibiotic is suitable for treating *legionella* pneumonia?
clarithromycin ... macrolide \> quinolone
54
which lung CA is associated with PHTrP? which lung CA is associated with ectopic ACTH and ADH?
PTHrP = squamous cell carcinoma ADH/ACTH/LEMS = small cell carcinoma
55
what is the rule for calculating the blood gas expected PaO2 from the FiO2?
[FiO2 (%) - 10] = expected PiO2 (kPa) can also be done using the arterial-alveolar (A-a) oxygen gradient, but usually works out to just FiO2 - 10
56
what are the causes of intersitial lung disease/pulmonary fibrosis?
**lung diseases** * IPF * TB/sarcoid * EAA * COPD * pneumoconioses * beryllium * coal * silica * asbestos **rheumatological disease** * SLE * rheumatoid arthritis * MCTD * systemic sclerosis **drugs** * amiodarone * methotrexate * bleomycin * gold * nitrofurantoin **vasculitis** * wegener's * polyarteritis nodosa * goodpasture's * churg-strauss