Respiratory Gap Flashcards

1
Q

Factors associated with poor prognosis of Sarcoidosis

A

insidious onset, symptoms > 6 months
absence of erythema nodosum
extrapulmonary manifestations: e.g. lupus pernio, splenomegaly
CXR: stage III-IV features
black African or African-Caribbean ethnicity

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2
Q

Indication of NIV in COPD

A

NIV should be considered in all patients with an acute exacerbation of COPD in whom a respiratory acidosis (PaCO2>6kPa, pH <7.35 ≥7.26) persists despite immediate maximum standard medical treatment

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3
Q

What type of NIV is used in COPD

A

BiPAP

BC

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4
Q

CPAP used in

A

It is used in conditions where the principal pathophysiology is type 1 respiratory failure i.e. pulmonary oedema/covid pneumonitis. It will not be effective in this scenario as the patient needs support with ventilation as well as oxygenation and therefore needs bilevel (i.e. oxygenation and ventilation) support.

also, OSA

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5
Q

HLA associations:

A

HLA-DR1: bronchiectasis
HLA-DR2: systemic lupus erythematous (SLE), Goodpasture
HLA-DR3: autoimmune hepatitis, primary Sjogren syndrome, type 1 diabetes Mellitus, SLE
HLA-DR4: rheumatoid arthritis, type 1 diabetes Mellitus
HLA-B27: ankylosing spondylitis, postgonococcal arthritis, acute anterior uveitis

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6
Q

Situations where oxygen therapy should not be used routinely if there is no evidence of hypoxia

A

Myocardial infarction and acute coronary syndromes
stroke
obstetric emergencies
anxiety-related hyperventilation

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7
Q

Oxygen therapy for COPD patients

A

Prior to availability of blood gases, use a 28% Venturi mask at 4 l/min and aim for an oxygen saturation of 88-92% for patients with risk factors for hypercapnia but no prior history of respiratory acidosis
adjust target range to 94-98% if the pCO2 is normal

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8
Q

Color of venturi mask

A

BLUE = 2-4L/min = 24% O2
WHITE = 4-6L/min = 28% O2
YELLOW = 8-10L/min = 35% O2
RED = 10-12L/min = 40% O2
GREEN = 12-15L/min = 60% O2

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9
Q

Causes of Bilateral Hilar Lymphadenopathy

A

The most common causes of bilateral hilar lymphadenopathy are sarcoidosis and tuberculosis.

Other causes include:
lymphoma/other malignancy
pneumoconiosis e.g. berylliosis
fungi e.g. histoplasmosis, coccidioidomycosis

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10
Q

ABPA story

A

Allergic bronchopulmonary aspergillosis results from an allergy to Aspergillus spores. In the exam questions often give a history of bronchiectasis and eosinophilia.

Features
bronchoconstriction: wheeze, cough, dyspnoea. Patients may have a previous label of asthma
bronchiectasis (proximal)

Investigations
eosinophilia
flitting CXR changes
positive radioallergosorbent (RAST) test to Aspergillus
positive IgG precipitins (not as positive as in aspergilloma)
raised IgE

Management
oral glucocorticoids
itraconazole is sometimes introduced as a second-line agent

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11
Q

What is ABPA

A

Allergic bronchopulmonary aspergillosis results from an allergy to Aspergillus spores. In the exam questions often give a history of bronchiectasis and eosinophilia.

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12
Q

Features of ABPA

A

bronchoconstriction: wheeze, cough, dyspnoea. Patients may have a previous label of asthma
bronchiectasis (proximal)

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13
Q

Rx of ABPA

A

oral glucocorticoids
itraconazole is sometimes introduced as a second-line agent

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14
Q

high-risk characteristics for Pneumothorax

A

Haemodynamic compromise (suggesting a tension pneumothorax)
significant hypoxia
bilateral pneumothorax
underlying lung disease
≥ 50 years of age with significant smoking history
haemothorax

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15
Q

Fitness to fly advice for Pneumothorax

A

absolute contraindication, the CAA suggest patients may travel 2 weeks after successful drainage if there is no residual air. The British Thoracic Society used to recommend not travelling by air for a period of 6 weeks but this has now been changed to 1 week post check x-ray

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16
Q

NICE recommendation for Smoking cessation

A

Nicotine replacement therapy (NRT)
Varenicline
Bupropion

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17
Q

What is Buproprion

A

a norepinephrine-dopamine reuptake inhibitor and nicotinic antagonist
unlike many antidepressants it has a minimal effect on serotonin
should be started 1 to 2 weeks before the patient’s target date to stop
small risk of seizures (1 in 1,000)
contraindicated in epilepsy, pregnancy and breast feeding. Having an eating disorder is a relative contraindication

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18
Q

Buproprion contraindicated in

A

contraindicated in epilepsy, pregnancy and breast feeding. Having an eating disorder is a relative contraindication

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19
Q

who to refer to NHS Stop Smoking Service in Pregnancy

A

All women who smoke, or have stopped smoking within the last 2 weeks, or those with a CO reading of 7 ppm or above should be referred to NHS Stop Smoking Services.

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20
Q

First line for smoking cessation in pregnancy

A

CBT

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21
Q

Varenicline

A

a nicotinic receptor partial agonist

should be started 1 week before the patients target date to stop
the recommended course of treatment is 12 weeks (but patients should be monitored regularly and treatment only continued if not smoking)
has been shown in studies to be more effective than bupropion
nausea is the most common adverse effect. Other common problems include headache, insomnia, abnormal dreams**
varenicline should be used with caution in patients with a history of depression or self-harm. There are ongoing studies looking at the risk of suicidal behaviour in patients taking varenicline
contraindicated in pregnancy and breastfeeding**

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22
Q

Varenicline is contraindicated in

A

contraindicated in pregnancy and breastfeeding

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23
Q

Which one of the following pathophysiological changes is most responsible for emphysema?

A

Destruction of alveolar walls secondary to Proteinases

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24
Q

COPD management

A

photo

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25
Q

criteria to determine whether a patient has asthmatic/steroid responsive features:

A
  • any previous, secure diagnosis of asthma or of atopy
  • a higher blood eosinophil count - note that NICE recommend a full blood count for all patients as part of the work-up
  • substantial variation in FEV1 over time (at least 400 ml)
  • substantial diurnal variation in peak expiratory flow (at least 20%)
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26
Q

Asthma Exacerbation class

A

Moderate:
PEFR 50-75% best or predicted
Speech normal
RR < 25 / min
Pulse < 110 bpm

Severe:
PEFR 33 - 50% best or predicted
Can’t complete sentences
RR > 25/min
Pulse > 110 bpm

Life-Threatening:
PEFR < 33% best or predicted
Oxygen sats < 92%
‘Normal’ pC02 (4.6-6.0 kPa)
Silent chest, cyanosis or feeble respiratory effort
Bradycardia, dysrhythmia or hypotension
Exhaustion, confusion or coma

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27
Q

Predisposing factors for OSA

A

obesity
macroglossia: acromegaly, hypothyroidism, amyloidosis
large tonsils
Marfan’s syndrome

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28
Q

Rx for OSA

A

Management
weight loss
continuous positive airway pressure (CPAP) is first line for moderate or severe OSAHS
intra-oral devices (e.g. mandibular advancement) may be used if CPAP is not tolerated or for patients with mild OSAHS where there is no daytime sleepiness
the DVLA should be informed if OSAHS is causing excessive daytime sleepiness
limited evidence to support use of pharmacological agents

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29
Q

Genotype for A1AT Deficiency

A

For anyone who cannot remember the PiMM, PiSS, PiZZ, remember in an alphabet list, M comes first then S and last Z so… PiMM = normal., PiSS = 50% and PiZZ = Zero.

Also this:
Normal PiMM > PiMS > PiMZ > PiSS > PiSZ > PiZZ Abnormal

PIZZ - last letter in the alphabet - therefore the worst.
PIMM - the best, no carrier, not ill
PiSS – Slow on electrophoresis. Unlikely to be symptomatic.

PIMZ: carrier and unlikely to develop emphysema if a non-smoker

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30
Q

A1AT Features

A

located on chromosome 14
inherited in an autosomal recessive / co-dominant fashion*
Features

Lungs: panacinar emphysema, most marked in lower lobes
Liver: cirrhosis and hepatocellular carcinoma in adults, cholestasis in children

Investigations
A1AT concentrations
spirometry: obstructive picture

Management:
- no smoking
- supportive: bronchodilators, physiotherapy
- intravenous alpha1-antitrypsin protein concentrates
** - surgery: lung volume reduction surgery, lung transplantation**

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31
Q

Klebsiella pneumoniae is a Gram——— bacilli?/cocci? that is part of the normal ——

A

Klebsiella pneumoniae is a Gram-negative rod that is part of the normal gut flora

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32
Q

Red currant Jelly sputum is caused by

A

Klebsiella

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33
Q

Klebsiella is common in

A

Alcoholics and Diabetics

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34
Q

Spirometry in A1At

A

Obstructive

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35
Q

Causes of Upper zone pulmonary fibrosis:

A

Causes of upper zone pulmonary fibrosis:

CHARTS

Coal workers pneumoconiosis
Hypersensitivity pneumonitis, histiocytosis
Ankylosing spondylitis
Radiation
Tuberculosis
Silicosis, sarcoidosis

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36
Q

Causes of lower zone pulmonary fibrosis

A

ACID

Asbestosis
C- connective tissue diseases (e.g. rheumatoid arthritis)
Idiopathic pulmonary fibrosis
Drugs (e.g. methotrexate)

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37
Q

Type of hypersensitivity in Extrinsic Allergic Alveolitis

A

It is thought to be largely caused by **immune-complex mediated tissue damage (type III hypersensitivity) **although delayed hypersensitivity (type IV) is also thought to play a role in EAA, especially in the chronic phase.

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38
Q

Examples of Extrinsic Allergic Alveolitis

A

bird fanciers’ lung: avian proteins from bird droppings

farmers lung: spores of Saccharopolyspora rectivirgula from wet hay (formerly Micropolyspora faeni)

malt workers’ lung: Aspergillus clavatus
mushroom workers’ lung: thermophilic actinomycetes*

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39
Q

BAL Finding of Extrinsic Allergic Alveolitis
Blood finding of EAA

A

bronchoalveolar lavage: lymphocytosis
blood: NO eosinophilia

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40
Q

What is TLCO

A

The transfer factor describes the rate at which a gas will diffuse from alveoli into blood. Carbon monoxide is used to test the rate of diffusion. Results may be given as the total gas transfer (TLCO) or that corrected for lung volume (transfer coefficient, KCO)

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41
Q

Relation Between TLCO and KCO

A

TLCO = KCO x Alveolar volume (VA)

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42
Q

Granulomatosis with Polyangitis also known as

A

Wegner’s Granulomatosis

It commonly affects the;
upper respiratory tract (chronic sinusitis)
lungs (haemoptysis due to pulmonary haemorrhage, leading to raised TLCO), and kidneys (glomerulonephritis causing proteinuria and haematuria). The presence of c-ANCA is strongly associated with GPA

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43
Q

Causes of a raised TLCO

A

asthma
pulmonary haemorrhage (e.g. granulomatosis with polyangiitis, Goodpasture’s)

left-to-right cardiac shunts
polycythaemia
hyperkinetic states
male gender, exercise

blood flow barabe jara lungs e tara shobai TLCO barabe

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44
Q

Causes of a lower TLCO

A

pulmonary fibrosis
pneumonia
pulmonary emboli
pulmonary oedema
emphysema
anaemia
low cardiac output

active lung volume jodi kome jay- or blood flow jodi kome

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45
Q

Features of ASD

A

The fixed splitting of the second heart sound and the systolic murmur at the left upper sternal edge are classic clinical signs of an ASD

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45
Q

TLCO in chronic bronchitis- normal/raised/decreased

A

Normal

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46
Q

TLCO in emphysema- normal/raised/decreased

A

Decreased

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46
Q

Relation of TLCO vs KCO

A

TLCO = KCO x Alveolar volume (VA)

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47
Q

Small Cell Lung Cancer Associated with

A

Hyponatremia

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48
Q

How to diagnose Asthma in Children

A

Children 5-16 years
all children should have spirometry with a bronchodilator reversibility (BDR) test
+
a FeNO test should be requested if there is normal spirometry or obstructive spirometry with a negative bronchodilator reversibility (BDR) test

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49
Q

i am a simple man, i see cherry red lesion i choose ———-
i see alcoholic or diabetic with pneumonia i choose ——–
i see pneumonia in immunosupprssed, without or with less chest findings i ——-
i see fever, retroorbital headache, rash, thrombocytopenia, in a travellar i choose ——
i see pleural plaques i choose ——
i see….
i seee….

A

i am a simple man, i see cherry red lesion i choose lung carcinoid.
i see alcoholic or diabetic with pneumonia i choose klebsiella.
i see pneumonia in immunosupprssed, without or with less chest findings i choose pneumocystis jiroveci.
i see fever, retroorbital headache, rash, thrombocytopenia, in a travellar i choose** dengue.
i see pleural plaques i choose
no follow up.**
i see….
i seee….

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50
Q

Lung carcinoid Bronch finding

A

Cherry red ball lesion

51
Q

bronchiolitis obliterans

A

bronchiolitis obliterans
progressive dyspnoea
obstructive pattern on spirometry
centrilobular nodules, bronchial wall thickening is seen on CT

can be a presentation of Rheumatoid lung disease

52
Q

Why use ICS in COPD

A

reduced exacerbations

53
Q

SCC of Lungs associated with

A

sQuamous cell Carcinoma
–> The sound of K points to:
 HyperCalcemia (elevated PTHrP)
 Cavitating lesions

think like SCC
smoking
Calcium
Cavity

54
Q

D/d of Cavitary lesion in the Xray

A

Differential
abscess (Staph aureus, Klebsiella and Pseudomonas)
squamous cell lung cancer
tuberculosis
Wegener’s granulomatosis
pulmonary embolism
rheumatoid arthritis
aspergillosis, histoplasmosis, coccidioidomycosis

55
Q

Lung cancer associations

Small Cell
SCC
Adeno

A

Small cell - SVC obstruction
Squamous cell - cavity
Adeno - trousseau syndrome and clubbing

56
Q

Psittacosis should be suspected in a combination of——

A

Psittacosis should be suspected in a combination of typical fever with a history of bird contact (reported in 84%) or a presentation with pneumonia and severe headache or organomegaly and failure to respond to penicillin-based antibiotics.

57
Q

Rx of Psittacosis

A

Treatment:
1st-line: tetracyclines e.g. doxycycline
2nd-line: macrolides e.g. erythromycin

58
Q

Contraindication to Lung cancer surgery

A

assess general health
stage IIIb or IV (i.e. metastases present)
FEV1 < 1.5 litres is considered a general cut-off point
*
malignant pleural effusion
tumour near hilum
vocal cord paralysis
SVC obstruction

59
Q

Risk factors for lunh cancer

A

smoking
+

asbestos - increases risk of lung ca by a factor of 5
arsenic
radon
nickel
chromate
aromatic hydrocarbon
cryptogenic fibrosing alveolitis

Factors that are NOT related
coal dust

NARCOS
Nickel
Asbestos, Arsenic, Aromatic HC
Radon
Cryptogenic FA
Omitt
Smoking

60
Q

Dx Criteria for ARDS

A

acute onset (within 1 week of a known risk factor)
pulmonary oedema: bilateral infiltrates on chest x-ray (‘not fully explained by effusions, lobar/lung collapse or nodules)
non-cardiogenic (pulmonary artery wedge pressure needed if doubt)
pO2/FiO2 < 40kPa (300 mmHg)

61
Q

Asbestos exposure can cause

A

Pleural Plaque
Pleural Thickening
Asbestosis
Mesothelioma
Lung Cancer

62
Q

Rx for Mesothelioma

A

Palliative Chemo.

Little role for Radio and Surgery

63
Q

Most dangerous form of Mesothelioma

A

Crocidolite (blue) asbestos is the most dangerous form.

64
Q

Spirometry findings in Asbestosis
Gas Transfer in Asbestosis

A

lung function tests show a restrictive pattern with reduced gas transfer

65
Q

What feature of lung metastasis is found in chondrosarcoma or osteosarcoma

A

Calcification

66
Q

Type of metastatic features

A

Miliary: Kidney on its side => battleship => cannonball metastases with miliary (military) pattern. M for melanoma
Haemorrhagic: cHoriocarcinoma + angio (blood) sarcoma
Adenocarcinoma: Alveolar spread (=> consolidation)
Calcification: lots of calcium in cartilage/bones - osteosarcoma + chondrosarcoma
Cavitation: we love VQ scanning for the lungs - caV =? sQuamous

67
Q

Indication for placement of chest tube in Pleural Effusion?
Indication for ventilation and intubation in Asthma?
Indication for LTOT in COPD?
Contraindication for lung cancer resection?Indication for NIV in COPD?

A

pH<7.2 - Indication for placement of chest tube in Pleural Effusion.

PH <7.35 - Indication for ventilation and intubation in Asthma.

PO2<7.3 - Indication for LTOT.

FEV1 <1.5 - Contraindication for lung cancer resection.
96 MetaMegaly - 28 Nov 22

pH 7.25-7.35 - Indication for NIV in COPD.

68
Q

Signs of Life Threatening Asthma

A

PEFR < 33% best or predicted
Oxygen sats < 92%
‘Normal’ pC02 (4.6-6.0 kPa)
Silent chest, cyanosis or feeble respiratory effort
Bradycardia, dysrhythmia or hypotension
Exhaustion, confusion or coma

69
Q

Commonest chemical for occupaitonal asthma

A

Isocyanate

70
Q

Inv for occupational asthma

A

Serial measurements of peak expiratory flow are recommended at work and away from work.

Referral should be made to a respiratory specialist for patients with suspected occupational asthma.

71
Q

Risk factor for TB

A

Silicosis

72
Q

Occupations at tisk of silicosis

A

Mining
slate works
foundries
potteries

73
Q

Causes of Bronchiectasis

A

post-infective: tuberculosis, measles, pertussis, pneumonia
cystic fibrosis
bronchial obstruction e.g. lung cancer/foreign body
immune deficiency: selective IgA, hypogammaglobulinaemia
allergic bronchopulmonary aspergillosis (ABPA)
ciliary dyskinetic syndromes: Kartagener’s syndrome, Young’s syndrome
yellow nail syndrome

74
Q

Lofgrens Syndrome

A

This patient is suffering from Lofgren’s syndrome - a pattern of sarcoidosis symptoms encompassing **fever, joint pain, erythema nodosum, lymphadenopathy and bilateral hilar lymphadenopathy. **

Needs monitoring only

75
Q

Contraindication of Surgical Resection of Lung Cancer

A

ROPE

Reduced FEV1 <1.5,
Obstruction of the SVC
Paralysis of vocal cords
Effusion (malignant)

+
tumour near hilum

76
Q

Insertion of a chest drain is relatively contraindicated in patients with any of the:

A

Insertion of a chest drain is relatively contraindicated in patients with any of the following:
INR > 1.3
Platelet count < 75
Pulmonary bullae
Pleural adhesions

77
Q

Removal of Chest Drain

A

Removal of the chest drain is dependent upon the indication for insertion:
- In cases of fluid drainage from the pleural cavity, the drain should be removed when there has been no output for > 24 hours and imaging shows resolution of the fluid collection.
- In cases of pneumothorax, the drain should be removed when it is no longer bubbling spontaneously or when the patient coughs and ideally when imaging shows resolution of the pneumothorax.
- Drains inserted in cases of penetrating chest injury should be reviewed by the specialist to confirm an appropriate time for removal.

78
Q

What to do if Re explansion Pulmonary edema is suspected

A

Re-expansion pulmonary oedema may be preceded by the onset of a cough and/or shortness of breath. In the event of concerns regarding re-expansion pulmonary oedema, the chest drain should be clamped and an urgent chest x-ray should be obtained

79
Q

How to avoid re expansion pulmonary pulmonary edema

A

To avoid re-expansion pulmonary oedema, it is recommended that the drain tubing should be clamped regularly in the event of rapid fluid output i.e. drain output should not exceed 1L of fluid over a short period of time (less than 6 hours)

80
Q

Drugs causing Fibrosis

A

drug-induced:

Be-DAMN
Bleomycin
Dopamine agonists
Amiodarone
Methotrexate
Nitrofurantoin

lower zone

81
Q

Kartagener’s syndrome (also known as primary ciliary dyskinesia) features

A

dextrocardia or complete situs inversus
bronchiectasis
recurrent sinusitis
subfertility (secondary to diminished sperm motility and defective ciliary action in the fallopian tubes)

82
Q

dextrocardia or complete situs inversus
bronchiectasis
recurrent sinusitis
subfertility (secondary to diminished sperm motility and defective ciliary action in the fallopian tubes)dextrocardia or complete situs inversus

A

Kartagener’s syndrome (also known as primary ciliary dyskinesia) features

83
Q

Contraindication to lung transplant in CF

A

chronic infection with Burkholderia cepacia is an important CF-specific contraindication to lung transplantation

84
Q

Drug used for CF

A

Lumacaftor/Ivacaftor (Orkambi)

  • is used to treat cystic fibrosis patients who are homozygous for the delta F508 mutation
  • lumacaftor increases the number of CFTR proteins that are transported to the cell surface
  • ivacaftor is a potentiator of CFTR that is already at the cell surface, increasing the probability that the defective channel will be open and allow chloride ions to pass through the channel pore
85
Q

What are the altitude related disorders

A

acute mountain sickness (AMS)
High altitude pulmonary oedema (HAPE)
High altitude cerebral oedema (HACE).

86
Q

Management of HAPE

A

descent
nifedipine, dexamethasone, acetazolamide, phosphodiesterase type V inhibitors*
oxygen if available

87
Q

Management of HACE

A

descent
dexamethasone

88
Q

Predention of AMS

A

Prevention and treatment of AMS
the risk of AMS may actually be positively correlated to physical fitness
gain altitude at no more than 500 m per day
acetazolamide (a carbonic anhydrase inhibitor) is widely used to prevent AMS and has a supporting evidence base
it causes a primary metabolic acidosis and compensatory respiratory alkalosis which increases respiratory rate and improves oxygenation
treatment: descent

89
Q

How does Acetazolamide prevent AMS

A

acetazolamide (a carbonic anhydrase inhibitor) is widely used to prevent AMS and has a supporting evidence base
it causes a primary metabolic acidosis and compensatory respiratory alkalosis which increases respiratory rate and improves oxygenation
treatment: descent

90
Q

Classical Presentation of Churg Strauss

A

The diagnosis here is eosinophilic granulomatosis with polyangiitis (EGPA), formerly known as Churg-Strauss syndrome. This is evidenced by the history of asthma, allergic rhinitis, presentation with mononeuritis multiplex (the most common vasculitic manifestation of EGPA) and eosinophilia. Classically, pANCA is positive in this condition and used to aid diagnosis.

(conversely-
ECG— granulomatosis with polyengitis e cANCA positive.
okhane sinusitis thakena.

91
Q

Indications for steroids in Sarcoidosis

A

patients with chest x-ray stage 2 or 3 disease who are symptomatic. Patients with asymptomatic and stable stage 2 or 3 disease who have only mildly abnormal lung function do not require treatment
hypercalcaemia
eye, heart or neuro involvement

92
Q

XRay finding of Silicosis

A

The typical chest X-ray findings in chronic silicosis are multiple and small well-rounded nodules, particularly in the upper zone. As the disease progresses the hilar retracts upwards and cavitation can occur leading to the potential for a secondary tuberculosis infection. Classically, eggshell calcification is seen on imaging.

93
Q

Genetics of CF

A

Cystic fibrosis (CF) is an autosomal recessive disorder causing increased viscosity of secretions (e.g. lungs and pancreas). It is due to a defect in the cystic fibrosis transmembrane conductance regulator gene (CFTR), which codes a cAMP-regulated chloride channel

94
Q

Occupational Asthma caused by

A

isocyanates - the most common cause
example occupations include spray painting and foam moulding using adhesives
platinum salts
soldering flux resin
glutaraldehyde
flour
epoxy resins
proteolytic enzymes

95
Q

Initial NIV Setup for COPD

A

Recommended initial settings for bi-level pressure support in COPD
Expiratory Positive Airway Pressure (EPAP): 4-5 cm H2O
Inspiratory Positive Airway Pressure (IPAP): RCP advocate 10 cm H20 whilst BTS suggest 12-15 cm H2O
back up rate: 15 breaths/min
back up inspiration:expiration ratio: 1:3

96
Q

LTOT in COPD

A

Offer LTOT to patients with a pO2 of < 7.3 kPa or to those with a pO2 of 7.3 - 8 kPa and one of the following:
secondary polycythaemia
peripheral oedema
pulmonary hypertension

97
Q

Factors shifting Ox disscoaiaton curve to right

A

Causes Raised oxygen delivery:
Raised acidity
Raised temp
Raised 2-3 DPG

98
Q

Factors shifting Ox disscoaiaton curve to Left

A

shifts Left - Lower oxygen delivery
Lower acidity
Low temp
Low 2-3 DPG
+
HbF, methaemoglobin, carboxyhaemoglobin

99
Q

Transudative Pleural Effusion Meaning

A

Transudate (< 30g/L protein)

100
Q

Causes of Transudative Effusion

A

Transudate (< 30g/L protein)
(remember Transudate: all the failures (hypothroid, heart failures, liver failure, liver failure) + meigs syndrome…. it kinda works)

Trans der kom thake + tara fail kore

heart failure (most common transudate cause)
hypoalbuminaemia
liver disease
nephrotic syndrome
malabsorption
hypothyroidism
Meigs’ syndrome

101
Q

Exudatiove Effusion meaning

A

Exudate (> 30g/L protein)

102
Q

Causes of exudative effusion

A

Exudate (> 30g/L protein)
infection
pneumonia (most common exudate cause),
tuberculosis
subphrenic abscess
connective tissue disease
rheumatoid arthritis
systemic lupus erythematosus
neoplasia
lung cancer
mesothelioma
metastases
pancreatitis
pulmonary embolism
Dressler’s syndrome
yellow nail syndrome

103
Q

Malignancy causes —— type of effusion

A

Exudative

104
Q

Indications for corticosteroid treatment for sarcoidosis are

A

parenchymal lung disease, uveitis, hypercalcaemia and neurological or cardiac involvement

105
Q

Paraneoplastic Features of Lung Cancer

A

Small> at the level of head
Squamous> at the level of neck
Adenocarcinoma> at the level of breast

Small cell- AAL
ADH
ACTH - not typical, hypertension, hyperglycaemia, hypokalaemia, alkalosis and muscle weakness are more common than buffalo hump etc
Lambert-Eaton syndrome

Squamous cell
parathyroid hormone-related protein (PTH-rp) secretion causing hypercalcaemia
clubbing
hypertrophic pulmonary osteoarthropathy (HPOA)
hyperthyroidism due to ectopic TSH

Adenocarcinoma
gynaecomastia
hypertrophic pulmonary osteoarthropathy (HPOA)

106
Q

Paraneoplastic feature of small cell lung cancer

A

Small> at the level of head
Squamous> at the level of neck
Adenocarcinoma> at the level of breast

Small cell- AAL
ADH- Hyponatremia
ACTH - not typical, hypertension, hyperglycaemia, hypokalaemia, alkalosis and muscle weakness are more common than buffalo hump etc- CUshing
Lambert-Eaton syndrome

107
Q

Paraneoplastic feature of SCC

A

Squamous cell
parathyroid hormone-related protein (PTH-rp) secretion causing hypercalcaemia
clubbing
hypertrophic pulmonary osteoarthropathy (HPOA)
hyperthyroidism due to ectopic TSH

108
Q

Respiratory acidosis may be caused by a number of conditions

A

Respiratory acidosis

Respiratory acidosis may be caused by a number of conditions:
COPD
decompensation in other respiratory conditions e.g. life-threatening asthma / pulmonary oedema
neuromuscular disease
obesity hypoventilation syndrome
sedative drugs: benzodiazepines, opiate overdose

109
Q

Benzo and Opiate Overdose causes

A

Resp Acidosis

110
Q

Poor Prognosis of Pneumonia

A

High Urea >7
Now Sodium <130

111
Q

Lights Criteria for Pleural Effusion

A

Light’s criteria was developed in 1972 to help distinguish between a transudate and an exudate. The BTS recommend using the criteria for borderline cases:
exudates have a protein level of >30 g/L, transudates have a protein level of <30 g/L
if the protein level is between 25-35 g/L, Light’s criteria should be applied. An exudate is likely if at least one of the following criteria are met:
pleural fluid protein divided by serum protein >0.5
pleural fluid LDH divided by serum LDH >0.6
pleural fluid LDH more than two-thirds the upper limits of normal serum LDH

To remember values for proten LDH
Protein = penta >0.5 exudate
LdH =hexa =6 = >0.6 ratio exudate

112
Q

When is Lights criteria for Pleural Effusion Applicable

A

if the protein level is between 25-35 g/L, Light’s criteria should be applied.

113
Q

Causes of Pulmonary Eosinophilia

A

WE LATCHED onto pulm eosinophilia:

WEgener’s
Loffler’s (transient rxn to parasites, self limiting)
ABPA
Tropical pulm eosinophilia
Churg-Strauss
Hypereosinophilic syndrome
Eosinophilic pneumonia
Drugs - nitro, sulfonamides

114
Q

You have lung cancer but you have never smoked. What type is it?

A

Adeno

Good way to remember:
‘How’d you get lung ca when you don’t smoke?’
‘Adeno’

115
Q

Define PH

A

Pulmonary hypertension may be defined as a sustained elevation in mean pulmonary arterial pressure of greater than 20 mmHg at rest

116
Q
A

Group 1: Pulmonary arterial hypertension (PAH)
- idiopathic
*
- familial
- associated conditions: collagen vascular disease, congenital heart disease with systemic to pulmonary shunts, HIV**, drugs and toxins, sickle cell disease
- persistent pulmonary hypertension of the newborn

Group 2: Pulmonary hypertension with left heart disease
- left-sided atrial, ventricular or valvular disease such as left ventricular systolic and diastolic dysfunction, mitral stenosis and mitral regurgitation

Group 3: Pulmonary hypertension secondary to lung disease/hypoxia
- COPD
- interstitial lung disease
- sleep apnoea
- high altitude

Group 4: Pulmonary hypertension due to thromboembolic disease

Group 5: Miscellaneous conditions
- lymphangiomatosis e.g. secondary to carcinomatosis or sarcoidosis

117
Q

causes of resp alkalosis

A

anxiety leading to hyperventilation
pulmonary embolism
salicylate poisoning*
CNS disorders: stroke, subarachnoid haemorrhage, encephalitis
altitude
pregnancy

118
Q

Pneumothorax in menstruating lady

A

Catamenial pneumothorax is the cause of 3-6% of spontaneous pneumothoraces occurring in menstruating women. It is thought to be caused by endometriosis within the thorax.

119
Q

Spirometry and TLCO in Cryptogenic Pneumonia

A

Lung function tests are most commonly restrictive but can be obstructive or normal. The transfer factor is reduced.

120
Q

Which parameter of the lung volume curve is reduced in obesity

A

ERV

121
Q

All Lung Volume Curve issues

A

Inspiratory capacity = Tidal volume + Inspiratory reserve volume

Expiratory reserve volume may be significantly reduced in obese patients

Vital capacity: 4,500ml in males, 3,500ml in females

Vital capacity is the maximum volume of air that can be expired after a maximal inspiration

Functional residual capacity = Expiratory reserve volume + Residual volume

Total lung capacity is the sum of vital capacity + residual volume

122
Q

——— should be suspected in the presentation of dyspnoea and hypoxaemia around 72 hours postoperatively

A

Atelectasis

123
Q

Indication of Chest Drain in Pleural Effusion

A

Pleural infection

All patients with a pleural effusion in association with sepsis or a pneumonic illness require diagnostic pleural fluid sampling
if the fluid is purulent or turbid/cloudy a chest tube should be placed to allow drainage
if the fluid is clear but the pH is less than 7.2 in patients with suspected pleural infection a chest tube should be placed

124
Q

is the investigation of choice for upper airway compression

A

Flow volume loop is the investigation of choice for upper airway compression

125
Q

malt workers’ lung caused by
Farmers lung caused by

A

malt workers’ lung: Aspergillus clavatus
farmers lung: spores of Saccharopolyspora rectivirgula from wet hay (formerly Micropolyspora faeni)

126
Q

Dietary advice for CF

A

The correct answer is High calorie and high fat with pancreatic enzyme supplementation for every meal. Patients with cystic fibrosis (CF) have an increased energy requirement due to the chronic inflammation and i