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)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what is the KCO?

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what are the causes of a high and low KCO?

A

high - alveolar haemorrhage

low - emphysema and interstitial lung disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what is the indication of mediastinoscopy?

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

define bronchiectasis

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what are the causes of bronchiectasis?

A

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

post-infectious: measles, pertussis, recurrent bronchiolitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

diagnosis of CF?

A

sweat sodium and chloride >60 mmol/L

(chloride > sodium usually)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

median age of survival in CF?

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

what lymph nodes are affected in bronchial carcinoma?

A

mediastinal (cannot palpate), supraclavicular and axillary

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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
Q

what are some systemic disease that can present with asthma?

(not atopy)

A

GORD/reflux, vasculitides (polyarteritis nodosa, eGPA Churg-Strauss), ABPA

26
Q

what are some complications of COPD?

A

lung

  • infectious exacerbations
  • fibrosis
  • type II respiratory failure
  • pneumothorax
  • lung CA

systemic

  • secondary polycythaemia
  • cor pulmonale
27
Q

beyond medical therapy, what is helpful in managing COPD?

A

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
Q

what are the common signs of PE on ECG?

A
  • sinus tachycardia
  • right ventricular strain (inverted T waves in V1-4)
  • right bundle branch block

don’t say S1 Q3 T3 first!

29
Q

causes of transudative and exudative pleural effusions

A

transudate - cardiac failure, hypoalbuminaemia (liver and renal failure)

exudate - malignancy and pneumonia

30
Q

where do you send samples of pleural fluid?

A

biochemistry

microbiology

cytology

need a paired sample of serum for protein and LDH

31
Q

Light’s criteria and differentiating pleural effusions

A

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
Q

what are some causes of cor pulmonale?

A

Lung parenchyma

  • COPD
  • bronchiectasis
  • pulmonary fibrosis

pulmonary vasculature

  • pulmonary embolism
  • primary pulmonary hypertension

other - thoracic cage and neuromuscular abnormalities

33
Q

what are the signs of cor pulmonale on chest examination?

A
  • 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
Q

what are the indications for steroid treatment in sarcoidosis ?

A

parenchymal lung disease

uveitis

hypercalcaemia

neurologic or cardiac involvement

35
Q

what are some causes of bihilar lymphadenopathy?

A

benign

  • sarcoidosis
  • tuberculosis
  • hypersensitivity pneumonitis
  • pneumoconioses (silica, beryllium)

malignant

  • bronchial CA (stage N2-3)
  • lymphoma/CLL
  • histiocytosis x (langerhan’s cell histicocytosis)
36
Q

what happens to the TLCO/KCO in IPF?

A

decreased

37
Q

what are the treatment options for IPF?

A

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
Q

what is the correct term for a patient with a large thoracic volume on inspection when you are examining them?

A

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
Q

what are the most important findings when presenting intersitial lung disease?

A
  • supplimental oxygen
  • clubbing and cyanosis
  • fine crackles (+/- apex or base)
40
Q

what are the most important findings when presenting consolidation?

A
  • bronchial breathing (+/- coarse crackles)
  • dull to percussion
  • increased vocal fremitus
41
Q

what are the most important findings when presenting bronchiectasis?

A
  • clubbing
  • sputum
  • coarse crackles
42
Q

what are the most important findings when presenting pleural effusion?

A
  • decreased breath sounds
  • stoney dull to percussion
  • decreased vocal fremitus
43
Q

how do you describe the breathing pattern of somebody with COPD?

A

dyspnoeic, audible wheeze from the end of the bed

purse-lip breathing

prolonged expiratory phase

44
Q

COPD does not cause clubbing.

what should be suspected in a patient with COPD and clubbing?

A

smoking can also cause cancer, which can cause clubbing

investigate for small cell lung CA

45
Q

what is the pathophysiology of COPD?

A

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
Q

what are the causes of COPD and how does this relate to their histological distribution?

A

smoking - mixed centri-/panancinar

alpha1 anti-trypsin - panacinar

coal dust - centriacinar

47
Q

what are the bugs of acute exacerbation of COPD?

A
  • haemophilus influenzae*
  • strep pneumo*
  • moraxella catarrhalis*
48
Q

what are the conditions for LTOT in COPD?

A

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
Q

what are the causes of bronchiectasis?

A

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
Q

what is the gold standard diagnostic test for bronchiectasis?

A

high-resolution chest CT

51
Q

what does the ‘signet ring sign’ represent? (CT)

A

signet ring sign = bronchiectasis

damaged and enlarged bronchus has a larger diameter than the adjacent blood vessel

52
Q

what are the LRTI bugs for bronchiectasis?

A
  • staphylococcus aureus*
  • haemophilus influenzae*
  • pseudomonas aeruginosa*
53
Q

which antibiotic is suitable for treating legionella pneumonia?

A

clarithromycin

… macrolide > quinolone

54
Q

which lung CA is associated with PHTrP?

which lung CA is associated with ectopic ACTH and ADH?

A

PTHrP = squamous cell carcinoma

ADH/ACTH/LEMS = small cell carcinoma

55
Q

what is the rule for calculating the blood gas expected PaO2 from the FiO2?

A

[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
Q

what are the causes of intersitial lung disease/pulmonary fibrosis?

A

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