Immunity 3- drug allergy Flashcards

1
Q

Drug hypersensitivity statistics

A

Direct cause for at least 50000 UK hospital admissions a year

10% UK population penicillin allergy

Anaphylaxis during 0.5-1/10000 anaesthetics

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2
Q

Type A drug reaction
(side effects/ toxicity)
NOT ALLERGY

A

Related to pharmacology of drug

Predictable

Usually dose dependent

High morbidity, low mortality

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3
Q

Examples of type A

A

Drowsiness with first generation anti-histamines

Liver failure in paracetamol overdose

Nausea and constipation with opiates

Dry mouth with tricyclic anti-depressants

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4
Q

Type B drug reaction

includes allergy

A

Not (directly) related to pharmacology

Unpredictable

(often) dose- independent

High mortality

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5
Q

Type B examples

A

Anything that clinically resembles and ‘allergic’ or immunological reaction belongs to this group known as drug hypersensitivity reaction

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6
Q

Immediate clinical classification of DHR

A

Within 1 hour

  • skin: urticaria, angiodema
  • resp: rhinitis, bronchospams, laryngeal oedema
  • gut: vomiting, diarrhoea
  • cardiovascular collapse

Generally result of mast cell activation

May be IgE mediated or form of non-allergic immediate DHR

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7
Q

Immediate DHR: non-IgE mediated

A

Non-specific mast cell activation
- opiates, myorelaxants, radiocontrast media

ACEi

  • also inhibit de-activator of bradykinin
  • angioedema
  • timing not related to symptoms

NSAIDs

  • urticaria/ angioedema
  • aspirin sensitive asthma/ rhinitis
  • true anaphylaxis
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8
Q

Events that follow mast cell IgE ligation

A

IgE binds to specific allergen

Cross linking of IgE antibodies by allergen leads to clustering of FcεR1 receptors

Intracellular portion of receptor becomes phosphorylated

Resulting intracellular cascade leads to cellular activation

Mast cell ‘degranulates’ releasing histamine, tryptase and other preformed mediators

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9
Q

Immediate DHR: key features

A

Within 1 hour of last dose

  • often much quicker, particularly iv treatment
  • NSAIDs may be little delayed

Soon after initiation, usually 1st dose

  • sensitisation typically during an earlier course
  • usually takes 14 days to class switch to IgE

Appropriate clinical features of mast cell degranulation

Recede rapidly after drug is stopped

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10
Q

Biggest drug groups of DHR

A

Myorelaxants

Taxene based chemo

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11
Q

Mast cell tryptase

A

Released from mast cells during anaphylaxis; easier to measure than histamine

Serum tryptase recommended to confirm acute anaphylaxis

Take blood 1-2 hours after onset of symptoms, again after 24 hours

Increase followed by normalisation in correct context confirms anaphylaxis

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12
Q

Allergic approach to immediate DHR

A

Often do diagnostic tests other than drug provocation (challenge test)- which is resource intensive and dangerous

All about the history

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13
Q

B lactam allergy

A

Reported by 10% of UK population

True prevalence 1-2%

Over reported because

  • sensitisation lost at a rate of 10% per year, label persists
  • rash may have been infection rather than drug related
  • different drug caused the rash
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14
Q

Pathophysiology of B lactam allergy

A

Includes multiple different antibiotic groups

  • penicillin
  • penicillinase resistant (fluclox)
  • aminopenicillins (amoxycillin)
  • extended spectrum (tazocin)
  • cephalosporin
  • carbopenems
  • monobactams

All have B lactam ring

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15
Q

Choosing alternative to penicillin

A

Must consider potential cross reactivity

No risk with non-B lactam

Cross reactivity with 2/3rd gen cephalalosporin very low

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16
Q

Non immediate

A

Delayed: delayed urticaria, maculo-papular eruptions, fixed drug eruptions

Systemic: TEN, SJS, DRESS, vasculitis

17
Q

Non-immediate DHR: key features

A

Not directly related to drug dose, although may appear to be so by chance

Typically during treatment course

  • 3-5 days if treated with drug before
  • 5-8 days if first sensitisation

Taken together, clinical features not in keeping with mast cell degranulation

Typically continue for some time after drug is stopped

18
Q

Biggest drug group for non-immediate DHR

A

Antimicrobials

19
Q

SJS

TENS

A

Steven johnson syndrome

Toxic epidermal necrolysis syndrome

20
Q

SJS/TENS: the dangerous non-immediate DHR

A

Fever, cough, conjunctivitis, mucositis

Men> women, mostly 30 years or under

Typically 3-8 days after dose

Very high mortality and gets worse with each exposure

21
Q

SJS/ TENS biggest drug groups

A

Antibiotics

Anticonvulsants

22
Q

Standard type IV hypersensitivity

A

Onset 3-8 days into course

Maculo-papular

Skin may be dry/ inflamed

Gradually fades over days/ weeks

No systemic upset

23
Q

Testing for B lactam allergy

A

Negative results have high negative predictive value- usually confirm tolerance with brief challenge test

When positive, perform challenge with alternative to demonstrate tolerance

24
Q

Local anaesthesia

A

Most reactions involve local swelling/ syncope/ sensitivity to adrenaline

Virtually never reproducible- presumably related to dental procedures/ anxiety

Drugs will generally not be given again without confirmation of tolerance

25
Q

NSAIDs

A

Wide spectrum of reactions

  • cutaneous only (usually urticaria/ angioedema often on background of spontaneous urticaria)
  • true anaphylaxis
  • aspirin sensitive asthma/ rhinitis

10% react to paracetamol as well