Respiratory Flashcards

1
Q

what two pathologies make up COPD?

A

emphysema

bronchitis

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2
Q

what is emphysema?

A

loss of elastic recoil in the alveoli

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3
Q

what is chronic bronchitis in COPD?

A

mucus

fibrosis/thickening of airways = impaired flow of air

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4
Q

is COPD restrictive or obstructive?

A

obstructive

lung volume is fine but nt able to blow air in/out

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5
Q

in chronic COPD what provides the inspiratory drive?

A

hypoxia

CO2 is permanently high as not able to blow it off, so body becomes desensitised

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6
Q

5 signs/symptoms that indicate COPD?

A
dyspnoea
cough 
wheeze 
odema secondary to heart failure 
tachypnoea 
chest 'tightness'
weight loss 
recurrent infections
exacerbations and better periods
barrel chest 
pursed lip breathing, bent over
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7
Q

3 symptoms of chronic disease that are generally NOT seen in COPD?

A

clubbing
haemoptysis
chest pain

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8
Q

in COPD what does spirometry show?

A

FVC fairly normal
FEV1 is low, less than 80% of expected
FEV1/FVC ratio less than 0.7
poor response to bronchodilators eg salbutamol

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9
Q

what might a chest x ray show in COPD?

A

only see severe disease
enlarged lungs
bullae (air pockets)
flattened diaphragm

excludes cancer and infection

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10
Q

what part of the lung is most affected in alpha 1 antitrypsin deficiency?

A

the bottom
panacinar
use a CT or CXR to see this

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11
Q

what is TCLO and what does it tell you?

A

transfer factor for carbon monoxide
low in COPD
high in asthma

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12
Q

what is first line for COPD?

A

smoking cessation
short acting b2 agonist eg salbutamol
or short acting anti muscarinic eg ipratropium bromide
vaccinations

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13
Q

what is second line for COPD?

A

long acting b2 agonist + long acting antimuscarinic

eg oladaterol/tiotropium combo

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14
Q

what is third line for COPD, or 2nd line for COPD with asthmatic features?

A

inhaled corticosteroid (eg beclomethasone) + LABA (eg salmeterol)

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15
Q

when is ipratropium bromide contraindicated?

A

closed angle glaucoma

urinary retention eg BPH

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16
Q

side effects of ipratropium bromide / antimuscarinics?

A
arrythmia
dizziness 
blurred vision
glaucoma 
G| upset
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17
Q

side effects of salbutamol?

A

tachycardia, arrythmia

hypokalaemia esp in diabetes

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18
Q

an example of a long acting beta 2 agonist?

A

salmeterol

oladaterol

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19
Q

what drugs interact syngerstically with steroids?

A

beta agonists
steroids = increased expr of beta2receptor
beta agonist = increased expression of steroid receptor

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20
Q

as well as relax smooth muscle, what else do beta 2 agonists do?

A

reduce histamine release

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21
Q

what is pirfenidone?

A

antifibrotic

for advanced resp conditions

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22
Q

what is theophylline?

A

phosphodiesterase inhibitor
bronchodilation
reduces reactivity to histamine

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23
Q

what is carbocysteine?

A

mucolytic

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24
Q

type 1 vs type 2 resp failure?

A

type 1 = low O2

type 2 = low O2 high CO2, resp acidosis

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25
Q

how can you tell if a respiratory acidosis is chronic?

A

the bicarbonate will be raised, kidneys trying to compensate, but this can’t happen immediately so you only see it in chronic

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26
Q

5 triggers for asthma?

A
infection
exercise
cold air 
dust
damp
pollen
emotion
tobacco
beta blockers
aspirin
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27
Q

what kind of hypersensitivity reaction is asthma?

A

type 3 / type 1

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28
Q

what cells/molecules are involved in asthma?

A

cytokines = IgE and mast cells
mast cells release histamine, prostaglandins, leukotrienes
and attract eosinophils

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29
Q

what happens in the late response of asthma?

A

immune mediators damage the epithelium

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30
Q

why is airflow reduced in asthma?

A

bronchoconstriction & mucus

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31
Q

is asthma reversible?

A

initially, yes
over time inflammatory reactions mean the basement membrane becomes thicker and fibrosed, = permanently reduced diameter, then it is not reversible

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32
Q

what does an asthma attack look like?

A
trigger
worsening SOB 
tachynoea 
using accessory muscles 
tachycardia
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33
Q

what is the wheeze like in asthma?

A

polyphonic
bilateral
widespread
episodic

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34
Q

what does spirometry show in asthma?

A

FVC fairly normal
FEV1 is low, less than 80% of expected
FEV1/FVC ratio less than 0.7
improves with bronchodilators eg salbutamol
- 12% increase in FEV1, 200ml increase in vol
worsens with histamine/metacholine challenge, which causes hyperreactivity

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35
Q

what is FENO, how is it used?

A

fractional exhaled nitrogen oxide
more than 40 is pos
can be used in investigation of asthma

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36
Q

what is first line for asthma?

A

SABA eg salbutamol

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37
Q

what is second line for asthma?

A

inhaled corticosteroid eg beclamethosone

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38
Q

what are some third line options for asthma?

A
  1. montelukast
  2. laba eg salmeterol (need to be taking saba too)

theophylline
lama
more steroid

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39
Q

what is montelukast?

A

a leukotriene antagonist

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40
Q

what is a problem with theophylline?

A

it has a very narrow TI

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41
Q

NICE treatment for severe asthma attack in hospital?

A

salbutamol (nebulised)
ipratropium bromide nebulised
oral predisolone or IV hydrocortisone

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42
Q

in asthma exacerbation what is the ABG like?

A

initially low pCO2, as trying to get enough oxygen in - alkalosis
normal co2 means pt is getting tired of compensatory breathing, this is a bad sign

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43
Q

what are the two most common kinds of non small cell lung cancer?

A
squamous cell (central)
adenocarcinoma (peripheral) - from mucus secreting cells
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44
Q

what cells is small cell lung cancer from?

A
kulchitsky cells 
(neuroendocrine)
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45
Q

which is generally worse, small cell or non small cell lung cancer?

A

small cell, as it tends to cause paraneoplastic syndromes

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46
Q

5 clinical presentations of lung cancer?

A
SOB
cough
haemoptysis
clubbing 
recurrent infection 
lymphadenopathy - supraclavicular 
fever, weight loss, night sweats, lethargy
pleuritic chest pain 
wheeze
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47
Q

what is the wheeze like in lung cancer?

A

fixed monophonic

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48
Q

a recurrent laryngeal nerve palsy could be caused by a ______ tumour and would result in __________

A

lung

hoarse voice

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49
Q

a phrenic nerve palsy caused by a lung tumour would cause ______ weakness and this would manifest as _______

A

diagphragm

SOB

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50
Q

what is pembertons sign?

A

bilateral arm elevation = facial oedema

shows the vena cava is being occluded by a lump in the neck, eg enlarged thyroid or lung cancer

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51
Q

what is Horners syndrome?

A

unilateral ptosis, anhydrosis, myosis

caused by pancoast tumour in the apex of the lung pressing on the sympathetic ganglion

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52
Q

what is lambert-eaton myasthenic syndrome?

A

the body produces antibodies against small cell cancer
the antibodies also attack voltage gated calcium channels
proximal weakness, diplopia, ptosis, dysphagia

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53
Q

what hormone does squamous cell lung cancer commonly release and what is the effect of this?

A

PTH
hypercalcaemia
osteomalacia

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54
Q

two molecules that small cell lung cancer commonly releases that cause paraneoplastic syndromes?

A
ADH = SIADH = hyponatraemia 
AcTH = cushings
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55
Q

what is an important cause of limbic encephalitis?

A

small cell lung cancer releases antibodies to the limbic system
= memory loss, hallucinations and seizures
anti Hu antibodies

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56
Q

3 features of lung cancer seen on a chest x ray?

A

hilar enlargement
circular peripheral opacity
unilateral pleural effusion
lung collapse

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57
Q

how might you obtain a biopsy in lung cancer?

A

percutaneous

or with an ultrasound guide bronchoscopy

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58
Q

how can you scan the body to look for cancer?

A

PET-CT

higher uptake of glucose tracer where there is more cancer

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59
Q

treatment for non small cell lung cancer?

A

surgery can often be curative

adjuvant or palliative chemo/radio

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60
Q

treatment for small cell lung cancer?

A

generally not curative

platinum based chemo + radiotherapy

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61
Q

5 risk factors for pulmonary embolism?

A
immobility eg flight
recent surgery
pregnancy
oestrogens 
malignancy
polycythaemia 
thrombophilia eg antiphospholipid syndrome 
inflam conditions eg SLE
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62
Q

5 clinical manifestations of pulmonary embolism?

A
hypoxia -- cyanosis
SOB
haemoptysis
tachycardiaa
tachypnoea
pleuritic chest pain
hypotension
pyrexial
right parasternal heave 
syncope
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63
Q

investigations in ?PE?

A

CXR to exclude pneumothorax, pneumonia
well’s score - is PE likely?
- yes – do a CTPA
- no – do a d dimer – if d dimer raised – do a CTPA

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64
Q

if you want to do a CTPA for PE but it is contraindicated what can you do instead?
when would CTPA be contraindicated?

A

ventilation-perfusion scan - shows good ventilation poor perfusion
CTPA contraind if allergy to contrast or severe kidney failure

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65
Q

what would ABG show in PE?

A

low oxygen - as blood cannot get to the alveoli to pick up the oxygen
resp alkalosis - as co2 is being blown off

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66
Q

management of PE? - 5

A
supportive - admission, analgaesia, oxygen 
enoxaparin 
alteplase - if PE is large 
surgical embelectomy
vena cava filter
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67
Q

in pregnant patients at a high risk of PE, what is the best prophylaxis?/

A

heparin

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68
Q

where does lung cancer commonly metastasise to?

A
brain
bone
liver
adrenals
lymph
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69
Q

where does secondary lung cancer usually come from?

A
breast
prostate
colon
bladder
neuroblastoma
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70
Q

who is TB most common in?

A

people moving from outside of UK esp s asia, subsaharan africa
immunocomp
alcoholic
homeless, ivdu

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71
Q

what is TB’s waxy capsule made of?

A

mycolic acid

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72
Q

how does latent TB arise?

A

the immune system forms a granuloma around the bacteria

but the granuloma does not succeed in killing it and instead actually seals off the bacteria and protects it

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73
Q

what is it called when latent TB reactivates?

A

secondary TB

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74
Q

what is milliary TB?

A

Disseminated infection

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75
Q

what is a ‘cold abscess’?

A
TB forms a colony in the lymph
this is often what allows it to spread
painless lump in lymph 
usually in the neck
no surrounding inflammation
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76
Q

how does TB usually spread between people?

A

through inhaled drops oof infected saliva

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77
Q

5 presentations of pulmonary TB?

A
fatigue, night sweats, weight loss, fever
cold abscess
cough/haemoptysis 
dyspnoea
clubbing
crackles
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78
Q

how does the mantoux test work?

A

inject tuberculin
if there is more than 5mm induration of skin after 72 hours it is pos
the person has had TB and the imune system has generated a response against the ag

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79
Q

what alternative to mantoux test checks for immune response to TB?

A

IGRA - interferon gamma release assay
looks to interferon alpha in response to tb antigen
(quantiferon is an igra test)

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80
Q

tb on a chest x ray:

  • 3 features of primary TB?
  • 2 features of reactivated TB?
A
GHON COMPLEX 
Primary: pleural effusion
patchy consolidation 
lymphadenopathy 
dense homogenous opacity

secondary: nodular consolidations
cavitations at the top of the lung

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81
Q

what are TB on culture?

A

acid fast bacilli

red on ziehl-neilson stain

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82
Q

what is the usual management of TB and what are some side effects?

A

R - rifampicin - red tears/urine, cyp induction - 6 months
I - isoniazid - lupus, peripheral neuropathy - 6 months
P - pyrazinamide - gout, hepatitis - 2 months
E - ethambutol - eye probs eg colour blind - 2 months

steroids

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83
Q

is TB a notifiable disease?

A

yes

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84
Q

what is the most common cause of community acquired pneumonia?

A

strep pneumoniae

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85
Q

what is the second most common cause of community acquired pneumonia?

A

haemophilus influenzae

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86
Q

pseudomonas causes pneumonia in who?

A

cystic fibrosis

bronchiectasis

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87
Q

what syndrome can legionella pneumophilia cause, alongside pneumonia?

A

SIADH

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88
Q

what extra-respiratory syndromes does mycoplasma pneumoniae present with?

A
erythema multiformae (target rash)
neuro symptoms
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89
Q

in exams a bird owner with a cough and infection is usually infected with

A

chlamydia psittaci

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90
Q

what is ‘lung consolidation’?

A

lung is full o stuff (water, mucus) not air

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91
Q

what is aspiration pneumonia caused by?

A

foreign material in the lungs

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92
Q

‘q fever’ is most often seen in farmers, what is it caused by?

A

coxiella burnetti

93
Q

5 symptoms of pneumonia?

A
SOB 
productive cough 
haemoptysis 
pleuritic chest pain 
delirium
sepsis - fever tachycardia tachypnoea hypotension etc
94
Q

5 signs of pneumonia?

A
fever, tachycardia, tachypnoea
hypotension
bronchial/harsh breath sounds equally loud on inspiration/expiration
dullness to percuss
crackles
95
Q

what system is used to consider how risky a patients pneumonia will be? what does it consider? what score warrants admission?

A
CURB-65 
C - confusion
U - uraemia
R - resp rate high
B - bp less than 90/ or /60
over 65

consider admit if score of 2 or more
3 or more – intensive care

96
Q

3 antibiotics commonly used in pneumonia?

A

co amoxiclav

amoxicillin
doxycycline
clarithromycin - -mycin = macrolide. usually co amoxiclav + -mycin for hosp treatment
ceftriaxone

97
Q

what antibiotic works against MRSA?

A

Vancomycin

98
Q

what is an empyma?

A

infected pulmonary effusion

99
Q

3 complications of pneumonia?

A
ARDS
sepsis
lung abscess
pleural effusion
empyma
death
100
Q

where is the division between the upper and lower respiratory tract?

A

vocal chords

101
Q

5 parts of the upper resp tract (that might get infected!)

A
nasal passages 
sinuses
pharynx 
larynx, above vocal cords 
tonsils 
eustachian tube
102
Q

is tonsilitis usually caused by a bacteria or virus?

A

virus

103
Q

3 features that suggest a tonsilitis is bacterial, not viral?

A

fever
tonsillar exudate
no cough
tender anterior cervical lymph nodes

104
Q

some microbiology of strep pyogenes?

A

lancefield group a
beta haemolytic
catalase neg

105
Q

presentation of tonsilitis?

A
usually associated with pharyngitis 
red inflamed sore tonsils
sore throat
pain on swallowing 
fever
malaise
headache
106
Q

first line drug for bacterial tonsilitis?

A

penicillin V

107
Q

what is otitis media?

A

inflammation of the ‘middle ear’

commonly infection of the eustachian tube following urt inf

108
Q

4 bacteria that cause most upper resp tract infections?

A

strep pneumoniae
h influenzae
moraxella catarrhalis
staph aureus

109
Q

5 presenting signs/symptoms of otitis media?

A
ear pain  
hearing loss 
loss of balance
inflamed/perforated tympanic membrane
middle ear effusion
otorrhea (discharge)
110
Q

1st and 2nd line treatments for otitis media and sinusitis?

A

1 - amoxicillin

2 - co amoxiclav

111
Q

what could you use instead of penicillin/amoxicillin if pt is allergic to penicillin?

A

clarithromycin

112
Q

is sinusitis usually bacterial or viral?

A

viral

eg rhinovirus

113
Q

presentation of sinusitis? 4

A
purulent rhinorrhoea 
face pain
headache
fever
voice changes 
change in smell/taste
cough
114
Q

differences between copd and asthma?

A

copd: non reversible, interval symptoms

115
Q

emphysema vs bronchitis presentation?

A

emphysema = pink puffer - pursed lips, bent over, skinny,

blue bloater = reactive pulmonary vasoconstriction, overweight, productive cough, hypertension

116
Q

what is the most common interstitial lung disease?

A

idiopathic pulmonary fibrosis

117
Q

what kind of spirometry does silicosis and aspestosis have?

A

restrictive

118
Q

presentation of silicosis and asbestosis?

A

dry cough
dyspnoea

generally quiet, not crackly chest

119
Q

what systems are affected by granulomatosis with polyangiitis?

A
ELK
ENT  - conjunctivitis, ear infections (ent involvement separates it from goodpastures)
Lung  - cough/dyspnoea/wheeze 
Kidney - haematuria
general malaise, fever etc
120
Q

what investigation for staging lung cancer?

A

CT chest, liver, adrenals

121
Q

on CXR what is the difference between the consolidation inn tb and pneumonia?

A

TB - in the middle

pneumonia - at the bottom

122
Q

what are the most common causes of hosp acquired pneumonia?

A

aerobic gram neg bacilli eg
pseudomonas
klebsiella
e coli

123
Q

first line imaging for ?lung cancer or ?TB?

A

chest x ray

124
Q

in a non smoker what lung cancer is most common??

A

adenocarcinoma

125
Q

What is the most common form of pulmonary fibrosis?

A

idiopathic

126
Q

5 aetiologies of pulmonary fibrosis?

A
idiopathic
ra/sle/annkylosing spondylitis/other connective tissue diseases
vasculitis eg goodpastures 
aspergillus/TB infection 
drugs eg amiodarone, methotrexate 
aspiration
sarcoidosis
127
Q

presentation of pulmonary fibrosis?

A

dry cough
SOB
fine bilateral crackles when you listen to chest

wheeze
haemoptysis 
chest pain
clubbing 
cor pulmonale
128
Q

what kind of spirometry is seen in pulmonary fibrosis?

A

restrictive - so reduced fvc

because fibrosis prevents the lung from expanding

129
Q

what investigation for pulmonary fibrosis?

A

chest CT is best but can do x ray if not available

ground glass appearance - irregular peripheral opacities

130
Q

how is DCLO affected in pulmonary fibrosis?

A

reduced

as gas exchange is impaired

131
Q

2 drugs for pulmonary fibrosis?

A

pirfenidone/nintendinab - anti fibrotic

132
Q

what is the epidemiology of sarcoidosis?

A

female
black and scandinavian
young adults/60+

133
Q

what is the pathophysiology of sarcoidosis?

& what type of hypersensitivity?

A

type 4 hypersensitivity
unknown antigen
granuloma
pulmonary fibrosis and nodules

134
Q

what cells make up the granulomas in sarcoidosis?

A

macrophage in the center

t cells on the edges

135
Q

what is the most common location for the granulomas in sarcoidosis?

A

the hilar lymph node, where the bronchi meets the lung

136
Q

symptoms of pulmonary sarcoidosis?

A

cough
gradual onset progressive dyspnoea
mediastinal lymphadenopathy

137
Q

5 extrapulmonary effects of sarcoidosis?

A
systemic - fever, weight loss, fatigue 
skin - erythema nodosum, lupus pernio 
joints - polyarthralgia
eye - uveitis, conjunctivitis 
heart - bundle branch block
hypercalcaema 
liver - nodules, cirrhosis, cholestasis
nervous system - diabetes insipidus, bells palsy
138
Q

treatment for sarcoidosis?

A

generally resolves spontaneously
1st line = prednisolone
2nd line = methotrexate/azathiopurine

139
Q

blood tests in sarcoidosis? - 3

A

raised serum ACE
raised serum calcium
raised serum soluble il2 receptor

140
Q

what is gold standard investigation for sarcoidosis and what will you see?

A

ultrasound guided biopsy of mediastinal lymph nodes

non caseating granuloma with epitheloid cells

141
Q

on a chest x ray in sarcoidosis what would you see?

A

hilar lymphadenopathy

bilateral lung exudate

142
Q

what is lofgrens syndrome and what condition is it most commonly associated with?

A

sarcoidosis

triad of bilateral hilar lymphadenopathy, polyarthritis and erythema nodosum

143
Q

what is bronchiectasis?

A

widening of the bronchioles and build up of mucus

144
Q

5 aetiologies of bronchiectasis?

A
young syndrome 
cf
infection eg tb, pneumonia, hiv, pertussis 
bronchial obstruction eg tumour 
rheumatoid arthritis/uc 
alpha 1 antitrypsin deficiency
copd
145
Q

why is there increased risk of infection in bronchiectasis?

A

because the cilia are damaged so cannot clear the mucus+infection as easily

146
Q

is bronchiectasis an obstructive or restrictive disease?

A

obstructive, the main problem is that mucus obstructs the airways

147
Q

why is there pulmonary hypertension in bronchiectasis?

A

in response to hypoxia the pulmonary vessels constrict in an attempt to divert flow to somewhere with better airflow

148
Q

5 clinical presentations of bronchiectasis?

A
persistent productive cough
purulous sputum which is foul smelling and dark green (usually has been sat around in the lung for a long time before it can be coughed up)
intermittent haemoptysis
SOB
clubbing
wheeze 
coarse inspiratory crepitations 
prone to respiratory infections
149
Q

what does the chest x ray show in bronchiectasis?

A

cystic shadows

dilated and thickened bronchi and bronchioles

150
Q

how to manage the mucus in bronchiectasis?

A

mucolytic eg carbocysteine

flutter valve for mucus drainage

151
Q

what population is at greatest risk of cystic fibrosis?

A

caucasian

152
Q

what is the mutation in cf and what is the effect of it?

A

mutation in CFTR protein
= lack of cl- into mucus secretions
= thick and sticky mucus

153
Q

5 clinical presentations of CF?

A
Failure to thrive 
cough - haemoptysis/thick sputum 
wheeze 
recurrent resp inf 
bronchiectasis 
pancreatic insufficiency = steatorrhoea and diabetes 
gall stones, cholestasis
male infertility
nasal polyps
cyanosis
clubbing 
bilateral coarse crackles
154
Q

what is the test for CF in newborns? how does it work?

A

Guthrie
detects raised trypsinogen
trypsinogen raised in response to pancreatic damage

155
Q

what is the gold standard CF test?

A

sweat test
inject pilocarpine to stimulate sweat production
salty sweat = cf, sweat glands are opposite so cl- cannot be absorbed from the sweat

156
Q

two methods of genetic testing for CF during pregnancy?

A

amniocentesis

chorionic villus sampling

157
Q

management for CF?

A

chest physio
antibiotics - acute or prophylactic
mucolytics eg dornase alpha
bronchodilators eg salbutamol
fat soluble vitamin supplement
ursodeoxycholic acid to improve bile flow
ivacaftor or lunacaftor depending on mutation

158
Q

what is a pleural effusion?

A

fluid in the pleural cavity

159
Q

exudative vs transudative effusion?

A
transudative = low protein, less than 3
exudative = high protein, more than 3
160
Q

3 aetiology of transudative pleural effusion?

A

transudative is caused by movement of fluid eg

congestive heart failure
low albumin
hypothyroid
peritoneal dialysis

161
Q

3 aetiologies of exudative pleural effusion?

A

exudative caused by inflammation, which means both fluid and proteins can move

lung cancer
pneumonia
tb
RA
SLE and other autoimmune 
pulmonary embolism
162
Q

clinical presentation of pleural effusion?

A
SOB
cough
pleuritic chest pain
stony dull to percussion
reduced chest expansion
superior raspy breathing 
tracheal and mediastinal deviation, if severe
163
Q

investigation for pleural effusion?

A

chest drain/pleural effusion, test the fluid for culture, protein/LDH, appearance, cell count

chest xray

164
Q

what does the chest x ray in pleural effusion show?

A

blunting of the costophrenic angle
fluid in the lung fissures
meniscus at the bottom
tracheal and mediastinal deviation

165
Q

management of pulmonary effusion?

A

antibiotics
diuretics
pleural aspiration or chest drain
small may spontaneously resolve

166
Q

2 complications of pulmonary effusion?

A

empyema

trapped lung

167
Q

in exams what is a common epidemiology/type of patient for pneumothorax?

A

a tall young male with sudden onset shortness of breath while playing sport

168
Q

what conditions is spontaneous pneumothorax more likely in?

A

marfans
rheumatoid arthritis
etc

169
Q

some causes of iatrogenic pneumothorax?

A

central line insertion
mechanical ventillation
lung biopsy

170
Q

presentation of pneumothorax?

A
sudden onset SOB / pain / cough
cyanosis
tachycardia
tachypnoea 
reduced breath sounds 
hyper resonance 
pleuritic chest pain
171
Q

first line investigation for pneumothorax?

A

erect chest x ray - see a visible rim with no lung markings

172
Q

gold standard investigation for pneumothorax?

A

ct thorax

allows you to see smaller pneumothorax and measure them more effectively than a cxr

173
Q

when would a pneumothorax not need management?

A

less than 2cm with no SOB

174
Q

management of pneumothorax? 3

A

high flow oxygen
insert a chest drain at 5th intercostal space on the mid axillary line
aspiration

175
Q

what can you do for recurrent pneumothorax?

A

surgery to remove the pleura or stick the visceral and parietal layers together

176
Q

where is the air in pneumothorax?

A

in the pleural space (between visceral and parietal pleura)

177
Q

what is a tension pneumothorax caused by?

A

trauma

one way valve

178
Q

clinical presentation of tension pneumothorax?

A
decreased air entry
unequal lung expansion
tachycardia
hypotension
trachial deviation
hyperresonance
179
Q

management of tension pneumothorax?

A

large bore canula
2nd intercostal space
mid clavicular line

180
Q

at what pressure is pulmonary hypertension diagnosed?

A

25mmHg

181
Q

what are the 5 groups of aetiology of pulmonary hypertension?

A
  1. primary - eg SLE
  2. left sided heart failure - eg MI, systemic hypertension
  3. chronic lung disease - eg COPD - reactive vasoconstriction
  4. pulmonary vascular disease eg PE
  5. miscellaneous eg sarcoidosis, vasculitis
182
Q

what is the effect on the lungs of hypertension?

A

thickening of alveolar and capillary membranes

= reduced gas exchange

183
Q

what is cor pulmonale?

A
increased pressure in the lung vessels
backs up into right ventricle
= rv hypertrophy 
= backpressure into veins 
= systemic oedema
184
Q

clinical presentation of pulmonary hypertension?

A
SOB worse when flat / on excercise - orthopnoea 
syncope 
tachycardia
raised jvp
hepatomegaly
peripheral oedema 
chest pain
heart murmur
185
Q

what does an ECG show in pulmonary hypertension?

A

large R waves on the right V1-V3
large S waves on left V4-V6
right axis deviation
right bundle branch block

186
Q

a blood test that would show heart pathology in pulmonary hypertension?

A

NT - pro - BNP

187
Q

3 drugs for primary pulmonary hypertension?

A

IV prostanoid eg epoprostenol
endothelin receptor antagonist eg macitenan
pde-5 inhibitor eg sildenafil

188
Q

3 complications of pulmonary hypertension?

A

resp failure
heart failure
arrythmia

189
Q

how many points do you need on the well’s score for pe to be likely?

A

if wells is more than 4 PE could be likely

190
Q

gold standard test for pulmonary hypertension?

A

right heart catheterisation

this is a way of measuring the pulmonary BP

191
Q

Bird fanciers lung, farmers lung and malt workers lung are all examples of

A

hypersensitivity pneumonitis

192
Q

what type of hypersensitivity reaction is hypersensitivity pneumonitis?

A

type 3

over time – type 4

193
Q

what happens to the lung in hypersensitivity pneumonitis?

A

fibrosis – impaired gas exchange, loss of elasticity

non caseating granulomas

194
Q

what part of the lung is most affected in hypersensitivity pneumonitis?

A

top

195
Q

presentation of acute hypersensitivity pneumonitis?

A

fever, rigors
cough
dyspnoea
headache

196
Q

presentation of chronic hypersensitivity pneumonitis?

A
progressive cough
progressive dyspnoea 
fatigue
cyanosis
resp failure
weight loss 
clubbing
197
Q

what do you see on biopsy with hypersensitivity pneumonitis?

A

non caseating granuloma

198
Q

management of hypersensitivity pneumonitis?

A

steroids

remove trigger

199
Q

what do you see on imaging in hypersensitivity pneumonitis?

A

diffuse infiltrate
ground glass (fibrosis)
bronchiectasis

200
Q

what are the antibodies to in goodpastures?

A

type 4 collagen

which is in glomerular basement membranes

201
Q

presentation of goodpastures? - 5

A
cough
SOB
haemoptysis
haematuria
proteinuria
oliguria
hypertension 
anorexia
myalgia/arthralgia
lethargy
fever
202
Q

best investigation for goodpastures, what do you see?

A

kidney biopsy
immunoflorescence - iGg associated with glomerulus
crescents
inflammation

203
Q

what is DCLO in goodpastures?

A

high

204
Q

management of goodpastures?

A

plasmaphoresis
steroids
cyclophosphamide

205
Q

what is the most common ANCA vasculitis?

A

granulomatosis with polyangiitis

206
Q

which ANCA antibody is usually associated with granulomatosis with polyangiitis?

A

cANCA

207
Q

what do you see on chest imaging of granulomatosis with polyangiitis?

A

nodules
fluffy alveolar haemorrhage
cavitating lesions
consolidation

208
Q

mesothelioma is associated with

A

asbestos!

209
Q

what is mesothelium?

A

epithelium that forms lining ie pleura, peritoneum, pericardium etc

210
Q

what molecule does mesothelioma express?

A

calretinin

211
Q

presentation of mesothelioma?

A
history to suggest
clubbing
sob
pleuritic chest pain 
harmoptysis
fever, weight loss etc
212
Q

which part of the lung is fibrosed in mesothelioma?

A

lower

213
Q

polo mint sign on CT is associated with what condition?

A

PE

214
Q

bronchus sign on CT indicates what lung pathology?

A

bronchogenic cancer

215
Q

tree in bud sign on CT indicates what lung pathology?

A

pneumonitis, bronchiolitis

216
Q

split pleura sign on CT indicates what lung pathology?

A

exudative, malignant or infected pleural effusion

217
Q

signet ring sign on CT indicates what lung pathology?

A

bronchiectasis

218
Q

what is the most common type of lung cancer?

A

squamous

219
Q

what is the most common lung cancer in non smokers?

A

adenocarcinoma

220
Q

complications of bronchiectasis?

A

empyema
respirator failure
repeated inf = worsening lung function
pneumothorax from repeated coughing

221
Q

what is the microbiology of h influenzae?

A

small
gram neg
cocco-bacillus

222
Q

risk factors for pneumothorax?

A

smoking
trauma
previous pneumothorax
mechanical ventilation

223
Q

how long after admission is it called hospital acquired pneumonia?

A

48hrs

224
Q

what type of hypersensitivity is goodpastures?

A

type 2

225
Q

what is gold standard for TB diagnosis?

A

sputum culture

226
Q

what is the most common cause of pneumonia in bronchiectasis?

A

h influenzae

227
Q

which sinus is most prone to infection and what are the symptoms of that?

A

maxillary, because it drains from the top
forehead and cheek tenderness
worse when leaning forward

228
Q

is cystic fibrosis restrictive or obstructive?

A

obstructive

229
Q

3 Indicators of good asthma control?

A
no  night time symptoms 
inhaler used no more than 3x per week
no breathing difficulties, cough or wheeze on most days 
able to exercise without symptoms 
normal lung function test