Respiratory Flashcards

1
Q

Signs or cardiomegaly/cardiac tamponade

A

“Pericardial silhouette enlarged” if more than half of lung width

Better than cardiomegaly cos it may be enlarged due to pericardial effusion/tamponade

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2
Q

Types of pneumothorax

A

Primary spontaneous pneumothorax/PSP:no underlying lung issues

Vs secondary spontaneous pneumothorax(secondary to lung disease eg asthma,COPD)

Traumatic
-iatrogenic(eg from ventilator,central line too far from SCA,biopsy,thorascopy)
-non iatrogenic(eg from stab wounds)

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3
Q

Objective ways to identify a pneumothorax on XR

A

ACCP:distance from apex to cupola >3cm(threshold higher cos of gravity)A for Apex

BTS:interpleural distance at level of hilum> 2cm

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4
Q

How does the lung USUALLY collapse in a pneumothorax

A

The lung usually collapses towards the hilum:unless scarring causee it to collapse un-uniformly(eg scarring in the upper lobe caused by chronic smoking causes it not to collapse towards hilum)

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5
Q

Risk factors for a nodule being benign vs malignant

A

-Size >20mm 50% chance of malignancy

-Borders(spiculations): poorly circumscribed borders more likely to be malignant

-Growth rate(too fast or too slow unlikely)except Small cell carcinoma and lymphoma

-attenuation:solid vs non solid(solid more common but non solid more likely to be malignant)

-calcifications:eccentric most dangerous(tumour grows out from the calcification) vs popcorn central etc

-Location:apex tends to collect more smoke in lung,higher chance of malignant lesions

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6
Q

Signs of Pulmonary Embolism on CXR

A

-Hamptons Hump(wedge shaped infarct)

-Westermark sign(oligaemia:a clarified area distal to a large vessel occluded by a pulmonary embolism,caused by reflex vasoconstriction and impaired vascular is still bc obstruction
-Pallas’s sign:enlarged descending pulmonary artery

-Fleischner sign: Dilated central pulmonary artery

-Meniscus sign: blunting of costophrenic angle

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7
Q

Criteria for differentiating transudative and exudative pleural effusion

A

Lights criteria

Exudative if:
Effusion protein/Serum protein >0.5
OR Effusion LDH/Serum LDH >0.6
OR Effusion LDH > 2/3 laboratory upper limit of serum LDH reference range

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8
Q

Causes of transudative effusion

A

1)Congestive Heart Failure
2)Nephrotic syndrome
3)Chronic Liver disease

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9
Q

Causes of exudative effusion

A

1)Infections
2)Neoplasm

Increased inflammation causes more protein to leak out of pulmonary vessels

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10
Q

Types of interstitial lung disease(restrictive)

A

1.Idiopathic Pulmonary Fibrosis:diagnosis of exclusion
2.Hypersensitivity pneumonitis(chronic)
3.Pneunoconiosis
4.Sarcoidosis
5.Asbestosis:caused by asbestos fibres
6.SLE
7. Rheumatoid arthritis associated ILD
8.Silicosis
9. Drug fibrosis:AMIODARONE BROMOCRIPTINE CYCLOPHOSPHAMIDE METHOTREXATE NITROFURANTOIN

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11
Q

4 Ts of anterior mediastinal masses

A
  1. Thyroid
  2. Thymus
  3. Teratoma
  4. Terrible lymphoma
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12
Q

Medial mediastinal masses

A
  1. Esophageal
  2. Bronchial cysts
  3. Hernia(hiatus?)
  4. Lymph nodes
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13
Q

Posterior Mediastinal masses

A
  1. Aortic Aneurysm
  2. Germ Cell Tumors
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14
Q

Which main bronchus do foreign bodies usually enter and why

A

Right main bronchus as it is oriented more vertically, has a larger diameter and is shorter

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15
Q

Impt qns to ask in any suspected asthma case

A

Interval Symptoms, personal and family history of Atopy, past HD/ICU admissions or invasive intubation

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16
Q

Complications of pneumonia

A

Parapneumonic effusion
Sepsis
Spread to other sites eg meningitis,osteomyelitis
Hemolytic Uremic Syndrome with strep pneumo
Necrotising pneumonia

Long term:
Lung fibrosis
Bronchiectasis

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17
Q

Pathogens in atypical pneumonia

A

Mycoplasma and chlamydia pneumoniae

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18
Q

Causes s of bronchiectasis

A

Focal
1.Post infectious
2. Mechanical
3. Aspiration
4. Tumor
5. Lymph nodes

Systemic
Immunodeficiency acquired and congenital
Cystic fibrosis
Ciliary abnormalities eg kartegener
Congenital lobar emphysema
Idiopathic

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19
Q

Coryzal symptoms

A

Fever, rhinorrhea, cough, sore throat

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20
Q

Croup triad

A
  1. Loss of voice/laryngitis
  2. Barking cough
  3. Strider
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21
Q

Ideal method for administering high flow O2 in acute respiratory distress

A

Non rebreather mask> venturi and nasal prongs

22
Q

Causes of ILD

A

Idiopathic
Rheumatological
Drug related
Pneumoconiosis

23
Q

Function of incentive spirometer

A

Patient to breathe in as deeply and as slowly aa possible-> helps expand the lungs and prevent atelactasis

24
Q

How to ddx between pleural effusion and fibrothorax

A

Tracheal deviation in pleural effusion?

25
Q

Causes of upper lobe lung fibrosis

A

STAR

Sarcoidosis
TB
ABPA
Radiation

26
Q

Causes of lower lobe lung fibrosis

A

RADIO

Rheum(RA, scleroderma, Dermatomyositis, systemic sclerosis)
Asbestosis
Drugs
Idiopathic
Others

27
Q

Treatment of interstitial lung disease

A

Non pharm
-pt education
-smoking cessation
- vaccinations

Pharm
-Fibrinolytics eg perfenidone, nintedanib

Non pharm
-Lung transplant

28
Q

Key invx in case of interstitial lung disease

A
  1. CXR
  2. HRCT
  3. ABG
  4. Lung function test
29
Q

3 common pathogens causing COPD exacerbation

A
  1. Strep pneumo
  2. HIB
  3. Moraxella Catarrhalis
30
Q

eosinophilia count cutoff for starting ICS in COPD exacerbation

A

> 300

31
Q

GOLD grade vs ABE

A

Grade is for prognosis

ABE is for management

32
Q

2 causes of white out lung

A

Pleural effusion(trachea pushed contralateral) and lung collapse(trachea pushed ipsilateral)

33
Q

Paraneoplastic syndromes a/w small cell lung ca

A

SIADH, Lambert Eaton, Cushings

34
Q

Common sites of lung mets

A

Liver, adrenals, bone and brain

35
Q

Malignancy most associated with asbestosis

A

Malignant Mesothelioma

36
Q

Things to send for pleural fluid studies

A

Cytology - cancer cells
Cell counts - neutrophilic or lymphocytic
ADA - local context can be TB or some tumours
Culture & sensitivity
Protein
LDH
pH, glucose
pH <7.2, glucose > 2.2 means complicated parapneumonic effusion → need chest tube insertion

37
Q

Ddx of massive pleural effusion

A

1) Malignancy
2) Parapneumonic
3) Tuberculous
4) Transudate eg hepatoc hydrothorax

38
Q

Definitive treatment of massive hemoptysis

A

Bronchial Artery Embolization

39
Q

cutoff for complicated pleural effusion

A

pH <7.2

40
Q

ai

A
41
Q
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42
Q
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43
Q

n invx for suspected pulmonary embolism depending on suspicion

A

CTPA(high sus)
D Dimer(low sus)
US Lower Limbs

44
Q

Diagnosis of pulmonary arterial hypertension(PAH)

A

Via Swan Ganz catheter

> 25mm at rest
35mm during exercise

45
Q

mx of asthma exacerbation

A

nebs in 1:2:1 ratio(salb NS ipratropium)
PO or IV corticosteroids
Magnesium sulphate

46
Q

Common cause of hypoK in asthma patients

A

Iatrogenic due to beta agonist

47
Q

pulmonary hypertension treatment

A

ambrisentan and sildenafil
Oxygen therapy

48
Q

Rheumatological causes of ILD at bases

A

RA, Systemic sclerosis, dermatomyositis

49
Q

Causes of upper Lobe ILD: STAR

A

Sarcoidosis
Tuberculosis
ABPA/Ankylosing Spondylitis
Radiation

50
Q

Causes of lower lobe ILD: RAID

A

Rheumatological( RA, Scleroderma, Dermatomyositis)
Asbestosis
Idiopathic Pulmonary Fibrosis
Drugs( Methotrexate, Cyclophosphamide, Azathioprine)

51
Q
A