Resp 1 Flashcards

1
Q

What is FEV1?

A

Maximal inspiration and maximal exhalation as fast as possible

Fraction of the total forced vital capacity expired in 1 second = FEV1

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

What is a normal/average FEV1 as a percentage?

A

Healthy individuals can expire approx. - 80% of vital capacity in one second

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

What is FVC?

A

forced vital capacity

the total amount of air forcibly expired

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

What is FEF25?

A

flow at point when 25% of total volume to be exhaled has been exhaled

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

What can FEV1/FVC ratio tell you?

A

IF ratio is below 0.7 = airway obstruction

IF ratio is high i.e. normal but the FVC is low = airway restriction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are examples of obstructive respiratory disorders?

A

obstructive = reduction in airflow

  1. COPD
  2. Asthma
  3. Bronchiectasis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are examples of restrictive respiratory disorders?

A

restrictive = reduction in lung volume

  1. Interstitial lung disease
  2. Scoliosis
  3. Neuromuscular cause
  4. Marked obesity
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What would you see in terms of pO2 and pCO2 in Type 1 Respiratory Failure?

A

pO2 is low
pCO2 is low or normal

Type 1 = 1 change = low pO2 + normal/low CO2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What would you see in terms of pO2 and pCO2 in Type 2 Respiratory Failure?

A

pO2 is low
pCO2 is high

Type 2 = 2 changes = low pO2 + high pCO2

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

What are causes of Type 1 respiratory failure?

A

low ambient oxygen

ventilation-perfusion mismatch (P.E.)

Alveolar hypoventilation (neuromuscular disease)

Shunt (right to left shunt)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are causes of Type 2 respiratory failure?

A

Increased airway resistance (COPD, asthma, suffocation)

Reduced breathing effort (drugs, brainstem, extreme obesity)

Decrease in the area of the lung available for gas exchange

Neuromuscular (GBS, MND)

Deformation (kyphoscoliosis, ankylosing spondylitis, flail chest)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What are some signs of hypercapnoea?

A
bounding pulse
flapping tremor
confusion
drowsiness
reduced consciousness
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is COPD? What 3 conditions are associated with it?

A

disease state characterized by airflow limitation that is not fully reversible

Chronic bronchitis - mucous secretion which blocks airways

Emphysema - loss of elasticity and airway collapse during expiration

Bronchiolitis - inflammation and scarring cause the small airways to narrow

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

What are some causes of COPD?

A

SMOKING

chronic exposure to - pollutants at work, outdoor air pollution, inhalation of smoke from biomass fuels

Alpha-1-antitrypsin deficiency (early onset COPD)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

How would you investigate COPD?

A

Spirometry - FEV1/FVC ratio <0.7

Pulse oximetry - low oxygen saturation

ABG - hypercapnia, hypoxia and resp acidosis

CXR - hyperinflation, pneumonia, pneumothorax

FBC - raised haematocrit

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How would you treat COPD?

A

SABA/SAMA

if no asthma/steroid responsiveness - add LABA + LAMA

if asthma/steroid responsive - add LABA + ICS

if either still uncontrolled add what’s missing

  • LABA + LAMA + ICS
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What is emphysema?

A

Dilation and destruction of the lung tissue distal to terminal bronchioles

Leads to expiratory airflow limitation and air trapping

Patients with emphysema referred to as pink puffers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What is chronic bronchitis?

A

airway narrowing and airflow limitation - hypertrophy and hyperplasia of mucus secreting glands of bronchial tree, bronchial wall inflammation and mucosal oedema

Patients with chronic bronchitis referred to as blue bloaters

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

What causes COPD patients to be described as pink puffers? How do they become blue bloaters?

A

low-normal PaCO2 due to increasing alveolar ventilation in an attempt to correct their hypoxia

In short term, rise is CO2 leads to stimulation of respiration - longer term = patients insensitive to CO2 = dependent on hypoxaemia to drive ventilation

these patients start to retain fluid and become cyanosed = blue bloaters

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

How does COPD present?

A

productive cough with white or clear sputum, wheeze and breathlessness - many years of a smokers cough

hypertension, osteoporosis, depression, weight loss

breathless at rest, prolonged expiration, chest expansion is poor and lungs are hyperinflated (barrel chest)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

What is extrinsic allergic alveolitis?

A

Type of Interstitial Lung Disease - cellular infiltrates and extracellular matrix deposition in the lung distal to the terminal bronchiole

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

What are some types/causes of extrinsic allergic alveolitis?

A

Farmers lung - MOST COMMON - exposure to mouldy hay

Bird/pigeon fanciers lung - exposure to avian proteins in droppings

Cheese-workers lung - exposure to mouldy cheese

Humidifier fever - contaminated humidifying systems in the air conditioners

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

How would extrinsic allergic alveolitis present?

A

4-6 hrs post exposure

fever
rigors
myalgia
dry cough
dyspnoea
crackles
chest-tightness

resolution occurs within 24-48 hrs following removal of antigen

subacute attacks happen with less severe and more gradual onset symptoms - improvement takes weeks and months

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

How would you manage extrinsic allergic alveolitis?

A

avoid antigen

corticosteroid taper - prednisolone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

What are some examples of occupational lung disorders?

A

Coal-workers pneumoconiosis
Silicosis - stonemasons, sand-blasters, pottery and ceramic workers
Asbestosis - roofing, insulation and fireproofing
Byssinosis - cotton mills
Berylliosis - aerospace industry, atomic reactors and electrical devices

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

What are complications of coal-workers pneumoconiosis?

A

Simple pneumoconiosis - can progress to PMF

Progressive massive fibrosis - develop round fibrotic masses, Rheum factor and anti-nuclear antibodies are both often present in serum of patients with asbestosis/silicosis

27
Q

What are characteristic findings on CXR of silicosis and coal worker’s pneumoconiosis?

A

Progressive upper zone non-calcified, small, rounded opacities - ‘egg shell calcification’

Progressive upper zone linear interstitial fibrosis

28
Q

What is bronchiectasis?

A

chronic infection of the bronchi and bronchioles leading to permanent dilation of these airways

bronchial walls become inflamed, thickened and irreversibly damaged

29
Q

What can cause bronchiectasis?

A
pneumonia
TB
measles, whooping cough
bronchiolitis
cystic fibrosis

foreign body
tumour
HIV

30
Q

How would bronchiectasis present?

A
usually lower lobes affected
chronic cough with foul smelling purulent sputum - intermittent haemoptysis
finger clubbing
wheeze
infection
chest pain
recurrent exacerbations
31
Q

How would you investigate bronchiectasis?

A
CXR
CT
FBC
sputum culture and sensitivity
serum alpha-1 antitrypsin
sweat chloride test
bronchosopy
32
Q

How would you manage bronchiectasis?

A

exercise and improved nutrition
airway clearance therapy - postural drainage, percussion, vibration

salbutamol inhaled
hypertonic saline inhaled
azithromycin

33
Q

What is sarcoidosis?

A

type of interstitial lung disease - cellular and extracellular matrix deposition in lung distal to the terminal bronchiole = alveolar/capillary interface

multi-system granulomatous disorder of unknown cause

34
Q

How does sarcoidosis present?

A

20-40% incidental

fever
weight loss
fatigue
erythema nodosum
polyarthralgia

bilateral hilar lymphadenopathy
dry cough
progressive dyspnoea
chest pain

hepatomegaly, splenomegaly,conjunctivitis, glaucoma, anterior uveitis, bell’s palsy

35
Q

How would you stage sarcoidosis?

A

CXR
Stage 0 - normal
Stage 1 - bilateral hilar lymphadenopathy
Stage 2 - Pulmonary infiltrates with BHL
Stage 3 - Pulmonary infiltrates without BHL
Stage 4 - Progressive pulmonary fibrosis, bulla formation and bronchiectasis

36
Q

How would you treat sarcoidosis?

A

Oral/inhaled corticosteroid
MTX

end-stage - lung transplant

topical corticosteroid for cutaneous disease

37
Q

What is idiopathic pulmonary fibrosis?

A

most common of the idiopathic pulmonary pneumonias

patchy fibrosis of the interstitium and minimal or absent inflammation, acute fibroblastic proliferation and collagen deposition

38
Q

What are some risk factors/causes of Idiopathic Pulmonary fibrosis?

A
cigarette smoking
infectious agents (CMV, Hep C, EBV)
Occupational dust exposure
Drugs (MTX, imipramine)
GORD
Genetic predisposition
39
Q

How would idiopathic pulmonary fibrosis present?

A
Dry cough
Exertional dyspnoea
Malaise
Weight loss
Arthralgia
Cyanosis
Finger clubbing
Fine bi-basal end-inspiratory crackles
40
Q

How would you investigate idiopathic pulmonary fibrosis?

A

CXR - basilar, peripheral, bilateral, asymmetrical reticular opacities

high-res CT - honeycombing

41
Q

How would you treat idiopathic pulmonary fibrosis?

A

anti-fibrotic - pirfenidone
lung transplant
acute exarcebation - high dose corticosteroid - prednisolone

42
Q

What is normal mean pulmonary artery pressure (mPAP)? What is pulmonary hypertension defined as?

A

Normal = 14 +/- 3 mmHg

mPAP of above 25mmHg as measured at right heart catheterisation and secondary right ventricular failure

43
Q

What are causes of pulmonary hypertension?

A
Pulmonary embolism
Veno-occlusive disease
COPD
Chronic lung disorders
Kyphoscoliosis
Poliomyelitis
Myasthenia gravis
Obstructive sleep apnoea
Morbid obesity
Mitral stenosis
Congenital heart disease
Familial
44
Q

How would pulmonary hypertension present?

A

exertional dyspnoea
lethargy
fatigue

ankle swelling
chest pain

syncope
oedema
abdominal pain
right parasternal heave

45
Q

In advanced pulmonary hypertension, what are the features of right heart failure (cor pulmonale)?

A
elevated jugular venous pressure
hepatomegaly
pulsatile liver
peripheral oedema
ascites
pleural effusion
46
Q

How would you investigate pulmonary hypertension?

A

CXR - peripheral vascular markings, pulmonary artery shadows

ECG - RVH, right axis deviation, right atrial enlargement

Transthoracic Doppler echocardipgraphy

right heart catheterisation

47
Q

How would you treat pulmonary hypertension?

A
Nifedipine
Warfarin
Furosemide
Digoxin
Prostanoid - inhaled Iloprost
48
Q

What is a pleural effusion?

A

excessive accumulation of fluid in the pleural space (in between the parietal and visceral pleura)

49
Q

What are some transudate causes of pleural effusion?

A

Transparent = less protein = pleural fluid protein 30g/L

Heart Failure
Constrictive pericarditis
Fluid overload
Cirrhosis
Hypoalbunaemia
Nephrotic syndrome
Hypothyroidism
50
Q

What are some exudate causes of pleural effusion?

A

Exudate = exudes proteins = >30g/L

Pneumonia
Malignancy
TB
Pulmonary infarction
Lymphoma
Mesothelioma
Asbestos exposure
51
Q

How would a pleural effusion present?

A
Can be asymptomatic
Shortness of breath on exertion
Dyspnoea
Pleuritic chest pain
Cough
Loss of weight
Chest expansion reduced on side of effusion

Trachea may be deviated away from effusion
Stony dull percussion
Decreased tactile vocal fremitus

52
Q

How would you diagnose pleural effusion?

A

Chest X-ray - blunting of costophrenic angles
Pleural USS - fluid in the pleural space
LDH and protein in pleural fluid and serum - to identify exudate
RBC count, WBC count, cytology, glucose and culture of pleural fluid
CRP

53
Q

How would you manage pleural effusion?

A

dependent on cause

thoracentesis

pleurodesis - adhesion of visceral and parietal pleura

infection - amoxicillin or clindamycin

54
Q

What can cause upper zone fibrosis?

A

CHARTS

C - Coal worker's pneumoconiosis
H - Histiocytosis/ hypersensitivity pneumonitis
A - Ankylosing spondylitis
R - Radiation
T - Tuberculosis
S - Silicosis/sarcoidosis
55
Q

What can cause lower zone fibrosis?

A

idiopathic pulmonary fibrosis
most connective tissue disorders (except ankylosing spondylitis) e.g. SLE
drug-induced: amiodarone, bleomycin, methotrexate
asbestosis

56
Q

Investigations for sarcoidosis?

A
CXR
FBC - anaemia and leukopenia (secondary to splenic or bone marrow involvement)
Peak flow
ECG
LFTs - elevated
calcium - hypercalcaemia
57
Q

Investigations of EAA?

A

Immunological response to causative agent - antibody IgG

FBC - leucytosis
ESR - elevated

CXR/CT chest - ground-glass shadowing, poorly defined micronodules

Pulmonary function test - restrictive

Diffusing lung capacity of CO - decreased

58
Q

Asthma pathophysiology?

A

Airway hyper-responsiveness

Bronchial inflammation - t lymphocytes, mast cells, eosinophils - oedema, smooth muscle hypertrophy, mucus plugging and epithelial damage

Mediated by elevated IgE serum levels

59
Q

What medications shouldn’t be given to asthmatics?

A

Aspirin

NSAIDs

beta-blocker

60
Q

Presentation of asthma?

A
intermittent dyspnoea
wheeze
nocturnal cough
sputum
symptoms worse at night
bilateral expiratory polyphonic wheezes
61
Q

What would indicate acute severe asthma?

A

PEF 33-50% of predicted
Respiratory rate >25
HR >110
inability to complete sentences in one breath

62
Q

What would indicate acute life-threathening asthma?

A

PEF <33 %
SpO2 <92%
PaO2 < 8kPa

'normal' PaCO2
altered conscious level
exhaustion
arrhythmia
hypotension
cyanosis
silent chest
poor resp effort
63
Q

What would indicate near fatal asthma?

A

Raised PaCo2 and or requiring mechanical ventilation and raised inflation pressures

64
Q

What is step-wise management of Asthma?

A

SABA

Low-dose ICS (beclomethasone/budesonide)
Add LABA (salmeterol)
Increase ICS dose or add LTRA (Montelukast)