Asthma Flashcards

1
Q

Triggers

A
  • cold air
  • dust mites
  • pollen/animal fur/dust mites
  • smoke/fumes/pollution
  • NSAIDs
  • emotion e.g. stress/laughter
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2
Q

Pathology of asthma

A

immune condition mediated by IgE
IgE formed in response to a trigger.
Re-exposure to the allergen casues this specific IgE on mast cells, causing an inflammatory response:
-Histamine, prostaglandins, leukotrienes and eosinophils infiltrate the airway
-goblet cells over-produce mucous
-T lymphocytes produce cytokines that potentiates the inflammatory response
-This cascade causes bronchospasm - hyper-responsive smooth muscle on airway to narrow

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3
Q

Diagnosis of asthma

A
  • No single test can diagnose asthma
  • Combination of history, examination, tests to access the probability of asthma
  • Diagnosis is through lung function testing and reversibility tests with either a SABA or an corticosteroid
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4
Q

Lung function tests to help diagnose asthma

A

-FVC
-FEV1
-FEV1:FVC ratio
-PEFR
FeNo

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5
Q

Define FVC

A

Forced vital capacity

Total volume expelled by the lungs

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6
Q

Define FEV1

A

Forced expiratory volume exhaled in first second of FVC

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7
Q

FEV1:FVC ratio normal values

improvement?

A

Normal 0.7
Below this indicates obstruction
Obstruction is reversible in asthmatic patients whom should see an increase of 400ml to lung capacity after taking salbutamol

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8
Q

PEFR

A

Peak expiratory flow rate
Done via peak flow meter
Maximum rate of airflow which can be achieved during a sudden forced expiration from a position of full inspiration

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9
Q

What do you do with the spirometry results?

A

Compare against predicted values for those patients that took it
Based on: age, height, race and sex

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10
Q

Uncontrolled asthma has what spirometry test results?

What happens after administration of salbuatmol?

A

Decrease if PEF and FEV1 in uncontrolled asthma

400mL increase in lung capacity after salbutamol administration

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11
Q

FeNO

A

Functional exhaled nitric oxide
indicates airway inflammation
elevated levels in asthma patients

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12
Q

Other non-spirometry tests

A

Blood eosinophils - inflammation
allergies
IgE levels

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13
Q

Presentation of asthma

A

wheezing
shortness of breath (dysponea
coughing - particularly at night and on waking
triggers from allergens
if severe - cyanosis, drowsiness, difficulty speaking full sentences

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14
Q

aims of asthma treatment

A
  • control symptoms, including nocturnal and exercise-induced exacerbations
  • Reduce reliance on rescue therapy
  • Prevent exacerbations
  • Achieve best possible lung function: FEV1 and/or PEF >80% predicted or best
  • minimising side effects of medication
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15
Q

“Control” of asthma is defined as

A
  • no daytime symptoms
  • no nighttime symptoms
  • no need for rescue medication
  • no limitations on activity, including exercise
  • no exacerbations
  • normal lung function: FEV1 and/or PEF >80% predicted or best
  • minimal side effects of treatment
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16
Q

Non-pharmacological management of asthma

A
  • Avoiding triggers
  • stop smoking
  • lose weight if obese
  • avoid exercise in cold air
  • minimise occupational stimuli
  • avoid NSAIDs and Beta-blockers (including eye drops)
  • Hollistic remedies (immunotherapy, Buteytco breathing technique)
  • Breast feeding
  • -air ionisers
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17
Q

Treatment of chronic ashtma

A
  • inhaled (with spacer/nebuliser) and oral routes of administration
  • this makes side effects and ADRs more common due to the route being more systemic
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18
Q

Reliever

A

SABA e.g. salbutamol
produces quick symptomatic relief
Normally PRN

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19
Q

Preventer

A

Corticosteroids i.e. beclomethasone
Act on underlying inflammation
Usually PRN

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20
Q

Controller

A

:LABA e.g. salmeterol

Slow onset, long-acting, usually BD

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21
Q

Nebulisers

A

Vaporise aqueous solution of drug (normally salbutamol or ipratropium) to mist for inhalation through a mask or mouthpiece
They offer high dose delivery and are particularly useful in acte or chronic/severe asthma as
co-ordination not needed
Often used in hospitals

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22
Q

B2-agonists

A

Caause smooth muscle relaxation and enhance mucociliary clearance

  • SABA
  • LABA
  • 3rd line controllers
23
Q

SABAs
2 examples
onset and duration

A

Salbutamol and terbutaline
Onset 1-5minutes
Duration 4-6 hours
1st line relievers offer quick symptomatic relief

24
Q

LABAs
2 examples
onset and duration

A

Salmeterol

  • onset 10-20 minutes
  • duration 12hours

Formoterol
-onset 1-3 minutes
duration 12 hours

25
B2 agonists ADRS
- fine tremor - nervous tension - headache - peripheral vasodilation - tachycardia - hypokalaemia
26
Corticosteroids
2nd line preventers | Anti-inflammatory reducing bronchial hyper-response
27
ICS | 3 examples
``` Inhaled corticosteroids Beclomethasone Budesonide Ciclesonide Available in combination with LABA ICS are classed as either low, medium or high doses ```
28
Oral corticosteroids
Prenisolone Usually 40-50mg for 5 days for acute attacks 40-50mg =minimum effective dose in step 5
29
IV corticosteroid
Hydrocortisone used in acute severe situations suppresses inflammatory processes
30
When are corticosteroids indicated?
- exacerbation of asthma in last 2 years - using inhaled B2 agnoist >3times/week - symptomatic >3times/week - waking one night a week due to symptoms
31
Inahled corticocosteroid ADRs | and solutions
-hoarseness or dysphonia (difficulty speaking) if this happens, use spacer/dry powder - oral candidiasis -rinse mouth after use or use spacer - adrenal suppression - only in sustained doses >1500mcg Beclomethasone daily
32
Oral corticosteroid ADRs
-hypertension -osteoporosis -skin thinning -hyperglycaemia -adrenal suppression -moon face -acne which is why for oral corticosteroids, we use the lowest dose that will control symptoms for the shortest time possible
33
Leukotriene antagonists | examples
- 3rd/4th line controller/preventer - oral montelukast and zafirlukast - antagonise bronchoconstriction, airway oedema and mucous production
34
ADRs for leukotriene antagonists
- abdominal pain - headache - thirst - rash - sleep disturbances/CNS effects
35
Cromones
Necocromil - preventer in 5-12 year olds | -mast cell stabilisers, inhibits mediator (histamine) release from mast cells
36
Cromones ADRs
- nausea and vomiting - bitter taste - dispepsia
37
Immunosuppressants
-Methotrexate -ciclosporin -gold specialist use - used rarely
38
Methylxanthines - how they work
Think INTERACTIONS and ADRs! phosphodiesterase inhibitors that inhibit leukotriene synthesis and therefore inhibit inflammation and bronchoconstriction 3rd/4th line controller/preventer therapy
39
Methylxanthine examples
- oral: theophylline - IV/oral - aminophylline (salt of theophylline) - Narrow therapeutic index - SR preparations available to give predictable effect - Brand MUST remain constant
40
Therapeutic range for methylxanthines
10-20mg/L
41
Side effects of methylxanthines dependent on plasma concentrations
- <20mg/L - nausea, diarrhoea, nervousness, headache - >20mg/L vomiting, insomnia, arrhythmias - >35mg/L - hyperglycaemi, arrhythmias, convulsions, death
42
Methylxanthine clearance affected by
CYP450 metabolism - CCF (congestive heart failure) - liver disease - obesity
43
How to work out methylxanthine dose
by IBW (ideal body weight)
44
Methylxanthine interactions
1) enzyme inhibitors - these interactions can lead to toxicity e. g. - cimetidine - erythromycin - allopurinol - ciprofloxacin 2) enzyme induction - these interactions can lead to sub-therapeutic doses e. g. - carbamazepine - rifampicin - phenytoin - smoking - alcohol
45
Anti IgE monoclonal antibodies
-Omalizumab inhibits binding of IgE to mast cell receptors, therefore preventing inflammatory response to triggers -licensed as add-on therapy in adults and children>12yrs for severe, persistent asthma -S/C injection every 2-4 weeks -only initiated by specialist centres -patients must fulfil specific NICE criteria -discontinue after 16 weeks if inadequate response (4-8 injections)
46
Outline the BTS/SIGN guidelines for adult management of acute+severe asthma
Patients should be reviewed every 3-6 months with a view of stepping down treatment Steps If asthma suspected, give SABA PRN 1) Monitored initiation of low dose ICS ↓ 2) Add LABA (LABA+low dose ICS as combo inhaler) ↓ 3)Additional add on therapies -No response to LABA→stop LABA, consider ↑ICS dose -Benefit from LABA but control still bad→continue LABA, ↑ICS to medium dose OR Continue LABA and ICS and consider a trial of a LTRA, SR Theophylline or LAMA ↓ 4) High dose therapies Refer to specialist care Consider trials of: -↑ICS up to high dose -Adding on a 4th drug e.g. LTRA, SR theophylline, B2-agonist tablet, LAMA ↓ 5) Continuous or frequent use of oral steroids -refer to specialist care -use daily steroid tablet in the lowest dose providing adequate control -Maintain high dose ICS -consider other treatments to minimise use of steroid tablets NB- SABA PRN is on ALL steps
47
Outline the management of chronic and acute asthma in children
Asthma suspected - consider very low dose→low dose ICS 1) Infrequent, short-lived wheeze. Asthma diagnosed Regular preventer - very low (paediatric) dose ICS or LTRA <5 years ↓ 2) continue v.low dose ICS plus -children > or equal to 5yrs - add inhaled LABA -children<5yrs- add LTRA ↓ 3) Additional add-on therapies: -no response to LABA→stop LABA and increase dose of ICS to low dose -if benefit from LABA but still inadequate control, continue LABA and ↑ICS to low dose -If benefit from LABA but control still inadequate, continue LABA and consider trial of a LTRA ↓ 4) High dose therapies -refer patient to specialist care consider trials of: -↑ICS to medium dose -Addition of a 4th drug - SR theophylline ↓ 5) Continuous or frequent use of inhaled steroids -refer to specialist care -use daily steroid tablet in the lowest dose providing adequate control -maintain medium dose ICS -consider use of other treatments to minimise use of steroid tablets
48
General advice for acute asthma in adults
- do not underestimate risk of death - emergency admissions are avoidable - patients who die have well-recognised risk factors which can be modified - PEF<50% - severe - PEF <33% - life-threatening - RR>25/min - HR>110/min - O2 saturation <92%
49
Severe/life threatening exacerbations present with what symptoms?
- cyanosis - difficulty speaking - unconciousness - tachycardia - severe dysponea
50
If an asthma patient requires hospitalisation due to an asthma attack, what do you do?
immediate prescription - oxygen at highest possible concentration 40-60% aiming for arterial oxygen saturation of 94-98% - B2-agonist nebulised - 5mg QDS or multiple doses (2-10 puffs of sabutamol 100mcg at 10-20 minute intervals via spacer, depending on severity) - corticosteroid: prednisolone 40-50mg oral at least 5 days OR IV hydrocortisone every 6 hours (hold ICS) - Consider: - Ipratropium nebules 500mcg 4-6 hourly - single dose IV magnesium sulphate if PEF<50% - IV theophylline/IV salbutamol
51
Magnesium sulphate
smooth muscle relaxant, T cell and mast cell stabiliser
52
Monitoring requirements if you've just admitted someone having an asthma attack
- PEF - O2 saturation (aim 94-98%) - arterial blood gases - HR/RR - tachycardia/ponea - CRP - WCC if infection is suspected - Theophylline levels (if continued >24h) - serum K+ (nebulised SABA) - glucose - hydration - Blood pH~7.4 (check for risk of acidosis)
53
When do you refer an asthma patient who is having an asthma attack to ITU?
- deteriorating PEF - persistent hypoxia - exhaustion, drowsiness - coma, respiratory arrest
54
During hospitalisation, after attack is dealt with
- IV→nebuliser→inhaler - oral steroid 40mg/50mg for 5 days at least, depending on severity - restart steroid inhaler - write and meet discharge criteria - make action plan - inhaler technique education