repsiratory Flashcards

1
Q

what is asthma?

A

chronic inflammatory disorder characterised by recurrent episodes of typical symptoms: wheee, chest tightness, breathlessness, cough + airflow obstruction, hyper responsiveness and airway inflammation

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2
Q

2 types of asthma

A

extrinsic/atopic childhood asthma: triggered by inhalational of allergens

intrinsic/ non-atopic adult onset: progressive and less responsive to therapy

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3
Q

what is an asthma attack?

A

worsened symptoms over a period of hours to days not responsive to patients normal asthma medications

requires either an increase in normal treatments or new more complex treatment

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4
Q

who gets asthma?

A

1 in 12 children
1 in 10 adults
males more than females in childhood then opposite in adults

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5
Q

causes of asthma

A

atopy
genetic
environment: allergen exposure, occupational factors, viral infections, drugs, maternal smoking, hygiene hypothesis

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6
Q

risk factors of asthma

A
personal or family history of atopy
air pollution
obesity
prematurity and low birth weight 
viral infections in early childhood
maternal smoking
smoking
early exposure to broad spec Abc
beta blockers
anti inflammatory drugs
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7
Q

pathophysiology of asthma

A

allergen induced airway inflammation = smooth muscle constriction, thickening of airway wall, basement membrane thickening and mucus and exudate in airway lumen

airway remodelling -

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8
Q

presentation of asthma

A

typical episodic symptoms: breathlessness, chest tightness, cough, wheeze

diurnal variation
reduction on holiday or at home (occupational)
sputum
triggered by cld air, URTI, exercise, pollution, allergen, occupation

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9
Q

signs on examination of asthma

A
tahcypnoea
wheeze - polyphonic
hyperinflated chest
hyper reosnant to percussion
decreased air entry
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10
Q

acute asthma signs

A

severe attack = inability to complete sentences, pulse>110, RR > 25, PEFR 33-55%

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11
Q

investigations for asthma

A

peak flow - diurnal variation
spirometry - does FEV1 improve with bronchodilator?
exercise tests
prednisolone trial
CXR to rule out other causes
skin prick, blood tests and allergen provocation tests to find triggers

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12
Q

treatment of asthma

A

step wise approach

salbutamol
\+ low dose ICS
\+ low dose ICS + LABA
\+ medium dose ICS +LABA
\+high dose ICS + LABA + omalizumab
\+ high dose ICS + LABA + oral corticosteroid + omalizumab
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13
Q

acute asthma treatment

A

O SHIT ME

Oxygen 15L non rebreathe mask
Salbutamol 5mg nebulizer every 15-30min
Hydrocortisone 200mg IV or prednisolone 40mg oral
Ipratropium bromide IV 0.5mg 4-6hts
Theophylline
Magnesium sulphate 2g IV
Extra help
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14
Q

what is COPD

A

progressive lung disease characterised by airflow obstruction with little or no reversibility

chronic bronchitis + emphysema

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15
Q

who gets COPD

A

> 50 yo
insidious onset
more in men
smokers

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16
Q

risk factors for COPD

A

tobacco smoking
occupation exposure - dust, chemicals, noxious gas, particles
air pollution
genetics - homoxygous antitrypsin deficiency?

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17
Q

pathophysiology of COPD

A

damage to lung by 3 mechanisms

  • inflammatory cell activation by cigarrete smoke
  • oxidative stress
  • impaired mucociliary clearance
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18
Q

presentation of COPD

A

progressive SOB
reduced exercise tolerance
persistent cough
chronic sputum production
wt loss, peripheral muscle weakness or wasting
frequent infective exacerbations occur giving purulent sputum

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19
Q

signs on examination of COPD

A

pink puffers - breathlessness is predominant problem, they’re not cyanosed

blue bloaters - hypoventilation, cyanosed, oedematous, CO2 retention

red flag = clubbing - lung cancer until proven otherwise

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20
Q

investigations for COPD

A

gold standard = spirometry
FEV1/FVC ratio <0.7 = presence of persistent airflow limitation

severity classified in terms of effect on lung function

pulse oximetry, CXR, FBC, sputum culture, A antitrypsin, ECG/ECHO

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21
Q

management of COPD

A

smoking cessation
bronchodilators - step wise approach, inhaled tiotropium bormide, short acting beta antagonist, long acting B2 agonist added

corticosteoids

prevention of infectiosn - vaccines

oxygen

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22
Q

complications of COPD

A

exacerbations
respiratory failure
cor pulmonale
lung cancer

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23
Q

what is bronchial carcinoma

A

95% of primary lung tumours
most common malignant tumour in western world
more in men 3:1

24
Q

types of bronchial carcinoma

A

small cell 20-30% - in endocrine cells, repsonds to chemo, mets common, poor prognosis

non-small cell (squamous, large cell, adenocarcinoma) -

25
risk factors for bronchial carcinoma
smoking urban areas passive smoking exposure to asbestos and possibly also contact with arsenic, chromium, ron oxides and products of coal combustion
26
presentation of bronchial carcinoma
local effects of tumour - cough, chest pain, haemoptysis, breathlessness spread within chest - pain and bone fractures, pancoasts tumour - horners syndrome, spread to LRL nerve - coarseness and bovine cough, metastatic disease - bone, brain are common non metastatic manifestations, - finger clubbing, malaise, lethargy, weightloss, lymphadenopathy
27
investigations of bronchial carcinoma
confirm diagnosis y CXR determine histology by biopsy via bronchoscopy or tranthoracic FNA assess spread of tumour by PET CT
28
treatment of bronchial carcinoma
non-small cell lung cancer - surgeyr, neoadjuvant chemo, radiotherapy small cell - chemo and radiotherpay for limited disease, just chemo for extensive disease, very poor prognosis
29
causes of pneumothorax
tension penumothorax - pleural tear acts as one way valve for air. unilateral increase in intrapleural pressure spontaneous - tall, young and thin men, rwuslt of rupture of a pleural bleb (congenital defect in connective tissue of alveolar wall) secondary - pneumothorax associated with underlying lung disease (COPD)
30
presentation of Pnuemothorax
sudden onset of pleuritic chest pain and breathlessness
31
signs on examination of pneumothorax
reduced breath sounds | hyperessonant percussion
32
investigations of pneumothorax
standard PA chest XR to confirm diagnosis CT differentiates emphysematous bullae from pneumothoracies and prevent potentially dangerous aspiration CT detects small pneumothoracies
33
treatment of pneumothorax
if breathless aspirate air if failure to re-expand lung intercostal tube drainage if still no re expansion after 48hrs , then surgery pleurectomy or pleurodesis
34
causes of pleural effusion - unilateral
transudate - protein <30g/L - caused by imbalance of hydrostatic forces - heart failure, hypoalbuminaemia, constrictive pericarditis, hypothyroidism, ovarian fibroma exudate >30mg protein - infection, malignancy, PE with infarction, connective tissue disease,
35
presentation of pleural effusion
may be asymptomatic if small but breathless if large reduced chest wall movements stony dull to percussion absent breath sounds reduced vocal resonance`
36
investigations of pleural effusion
CXR - mensicus visible on erect diagnostic pleural fluid aspiration - appearance noted and sent to cytology contrast enahnced CT if diagnosis remains unclear pleural biopsy - for tissue diagnosis
37
treatment of pleural effusion
exudates - drain transudates - treat underlying causes malignant effusions - treat by aspiration followed by installation of sclerosing agent into pleural space - talc, tetracycline, bleomycin
38
cuases of lobar pneumonia
inflammation of lungs caused by bacteria classified anatomically - lobar, bronchopneumonia TB also is cause can be caused by aspiration of vomit and radiotherapy
39
risk factors of lobar pneumonia
``` underlying lung disease smoking alcohol abuse immunosuppression other chronic illness ```
40
presentation of lobar pneumonia
pyrexia, respiratory symptoms (cough, sputum, pleurisy, dyspnoea), signs of consolidation and pleural rub,
41
important history questions for pneumonia
``` contact with bird (psittacosis) farm animals recent stays in large hotels chronic alcohol abuse IV drug abuse contact with other patients with pneumonia ```
42
signs on examination of pneumonia
CURB 65 Confusion Urea >7mmol/L Respiratory rate >30/min Blood pressure <90/<60
43
investigations for pneumonia
``` CXR - only this if outpatient sputum blood tests serology ABG urine ```
44
treatment of pneumonia
pleuritic pain = analgesia hypoxaemia = oxygen fluids physiotherapy HAP: coamoxiclav 3x daily or more severe cases use second generatio cephalosporin metronidazole dded in those at risk of anaerobic infection antibiotic treatment adjusted after MC+S results
45
causes of PE
most common = DVT in lower limb | other sources - tumours, fat, amniotic fluid, sepsis, foreign bodies, air
46
risk factors of PE
``` DVT prev DVT or PE active cancer recent surgery hospitalisation lower limb trauma immobilisation pregnancy ```
47
presentation of PE
dyspnoea tachypnoea pleuritic chest pain features of DVT
48
signs on examination of PE
``` tahcycardia haemoptysis syncope hypotension crepitations cough or fever ```
49
investigations for PE
wells score CXR, ABG, ECG ddimer for exclusion spiral CT with IV contrast radionuclide lung scan (demonstrates areas of ventilated lung with perfusion defects)
50
treatment of PE
high flow oxygen if hypoxemic thrombolysis for massive embolism surgical embolectomy occasionally if thrombolysis contraindicated or ineffective analgesia prevention of further: LMWH, oral warfarin
51
who gets pulmonary fibrosis
late 60s | more common in males
52
what is pulmonary fibrosis
restrictive lung disease patchy fibrosis of the interstitium and minimal or absent inflammation, acute fibroblastic proliferation and collagen deposition
53
risk factors of pulmonary fibrosis
cigarette smoking viral infections exposure to environmental pollutants, inc silica and hard metal dusts bacteria and animal proteins and gases and fumes use of certain meds genetics GORD
54
presentation of pulmonary fibrosis
progressive breathlessness and non-productive cough eventually, resp failure, pul hypertension and cor pulmonale finger clubbing in 2/3 and fine inspiratory basal crackles heard on auscultation acute form = hamman-rich syndrome
55
investigations of pulmonary fibrosis
CXR appearances are initially of a ground glass appearance progressing to fibrosis and a honeycomb lung changes mostly in lower lung zones high res CT most sensitive imaging blood tests: hypoxaemia with normal PacO2 autoantibodies such as antinuclear factor and rheumatoid factor in 1/3 histological confirmation is required in some patients
56
treatment of pulmonary fibrosis
large doses of prednisolone daily azathioprine and cyclophosphamide can be tried single lung transplantation now an established treatment in some patients