Allergology Flashcards

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1
Q

Diagnostic methods for allergic diseases

A
  1. Clinical history - age, symptoms, pattern, occupations, treatments…
  2. Physical examination - inspection + palpation of the lesions
  3. Confirmatory tests - Prick test, patch test, intradermal (imp. in Venom or drug hypersensitivities), allergen specific IgE serology
  4. Provocation tests
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2
Q

Prick test

  • indication
  • positive if…
  • things to remember
A
  • immediate type I hypersensitivity
  • wheal >3mm
  • antihistamines and antidepressants suppress skin tests for 3-7d
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3
Q

Patch test

  • indication
  • results
A

-delayed type IV hypersensitivity

+ –> weak positive (non vesicular)
++ –> strong positive (edematous or vesicular)
+++ –> extreme positive (ulcerative or bullous)
IR –> irritant reaction

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4
Q

Allergic rhinitis

  • definition
  • causes
A
  • inflammation of the nasal mucosa due to allergen exposure
  • atopic disease

-indoor allergens (most common = dust mites), outdoor allergens (main = pollen), chemical allergens

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5
Q

Allergic rhinitis

-classification

A

Intermittent
-<4 days per weeks or < 4 weeks

Persistent
-4 days per week and > 4 weeks

Mild - normal sleep

Moderate/severe
-abnormal sleep, impairment in daily activities, abnormal works and school, troublesome symptoms

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6
Q

Allergic rhinitis

-symptoms

A
  • rhinorrhea
  • sneezing
  • nasal obstruction and pruritus
  • with or without conjunctivitis

more than 2 or >1h on most days
-mouth breathing, recurrent sinusitis, long cough or asthma, atopic dermatitis, frequent acute otitis media

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7
Q

Allergic rhinitis

  • diagnosis
  • treatment
A
  • history, physical examination
  • lab - eosinophils, + prick test, + IgE
  • anterior rhinoscopy and nasal endoscopy
  • nasal provocative test for confirmation
  • 1st line: oral anti-histamines
  • 2nd line: intranasal anti-histamines +/- nasal decongestants
  • 3rd line: add intranasal GCS +/- intranasal cromone + or LTRA
  • 4th line: immunotherapy
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8
Q

Allergic bronchial asthma

-symptoms

A

mild signs

  • dry cough - worse at night with exercise or on exposure to triggers
  • end- expiratory wheezes
  • dyspnea
  • chest tightness
  • chronic allergic rhinitis with nasal congestions

severe signs

  • severe dyspnea
  • pulsus paradoxus
  • hypoxemia
  • accessory muscle use
  • increase risk of pulmonary infection
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9
Q

Allergic bronchial asthma

-diagnosis (6)

A
  • anamnesis, clinical examination
  • SPT - differentiate non-allergic and allergic
  • spirometry
  • bronchial reversibility test - one with SABA and another without SABA
  • blood tests: CBC, antibody testing, total IgE and allergen specific IgE
  • methacholine challenge test - + if FEV1 reduced >20%
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10
Q

Allergic bronchial asthma

-treatment

A
  • avoid triggers, allergen immunotherapy
  • mild symptoms –> short acting beta 2 agonist (salbutamol)
  • exercise induced asthma –> short acting beta 2 agonist prior to exercise
  • asthma exacerbations –> albuterol, steroids, theophylline, humidified O2, magnesium, anti-cholinergics
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11
Q

Allergic bronchial asthma

-medications for symptomatic treatment (6)

A
  1. Beta - 2 - agonists - bronchodilators
  2. Inhaled corticosteroids (inhibit transcription factors) decrease expression of pro-inflammatory genes)
  3. Leukotriene receptor antagonists (decrease bronchoconstriction and inflammation)
  4. Muscarinic antagonists (bronchodilation)
  5. Methyxanthines (phosphodiesterase inhibitor –> anti-inflammatory and mild bronchodilatory effect)
  6. Biologic agents
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12
Q

Urticaria

-definition

A

-wheal and flare reaction initiated at level of small venules of skin

  • pruritic, erythematous transient superficial swelling - wheal +/- angioedema
  • mast cell degranulation and histamine liberation = local vasodilation (erythema) + vascular permeability (edema) + fibrin deposition + inflammatory cells infiltration + pruritus
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13
Q

Urticaria

-classification

A

Acute (< 6 weeks)

  • all ages, abrupt onset, pruritic and widespread, angioedema
  • fever, malaise (depend on the cause)
  • causes: viral infection, drugs, foods, vaccines
  • treatment: adrenaline, anti H1, short oral GCS

Chronic (daily urticaria eruptions >6 weeks)
Vascular urticaria
-causes: idiopathic, CT diseases, hepatitis
-labs: complement scree, ESR, CRP, XR, ECG
-treatment: anti H1 are not effective!

Physical urticaria
-symptomatic dermographism: pruritus and red wheals aggravated by scratching, rubbing. No angioedema (mucus membrane is not affected), low dose antihistamines for treatment

-delayed pressure urticaria: swelling lasts for a long time, often tender and painful, anti-histamines are not effective, standardized 5kg test for diagnosis

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14
Q

Urticaria

-subtypes of chronic physical urticaria

A

-cholinergic urticaria: cause is unknown, treatment with antihistamines and anabolic steroids

  • ordinary chronic urticaria: autoimmune/ idiopathic, angioedema + physical urticaria + functional thyroid disease,
    labs: CBC + differential WBC + ESR + CRP + thyroid function + thyroid auto-ab
    treatment: antihistamines, GCS, cyclosporine, LTRA

-contact urticaria: substance causes local wheal and flare within minutes of skin contact

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15
Q

Atopic dermatitis

-symptoms

A

Infantile and childhood type

  • “wet forms” - vesicles, erosions
  • face, trunk, extensor surfaces of arms/legs

Childhood, adolescent and adult type

  • “dry forms” - papules, lichenification, excoriations
  • face, lateral aspects of neck, nuchal region, flexor surfaces of arms/legs

Atopic diathesis
Pruritus

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16
Q

Atopic dermatitis

-diagnosis (5)

A
  • anamnesis + inspection
  • prick and patch testing
  • blood tests - eosinophil count, overall IgE, allergen specific IgE
  • elimination diet
  • skin biopsy
17
Q

Allergic contact dermatitis

-symptoms

A

acute
-erythema, edema, vesiculations, papules, erosion, crusting scaling

chronic
-mild erythema, less vesicles, papules, scaling, fissures, lichenification

complains
-burning or itching

location
-sharp margination, stickly confined to exposure site, mostly hands and forearms

18
Q

Allergic contact dermatitis

-diagnosis (3)

A
  • anamnesis
  • inspection
  • patch test
19
Q

Drug hypersensitivity

-symptoms

A

IgE mediated type

  • rapidly appearing urticaria + angioedema
  • GI symptoms - cramps, vomiting, diarrhea
  • anaphylaxis and anaphylactic shock

T cell mediated type
-exanthema, acute generalized exanthematous pustulosis, patch test +

other symptoms: hepatomegaly, multi-organ failure, pruritus, diffuse lymphadenopathy

20
Q

Drug hypersensitivity

-diagnosis

A
  • skin tests - prick or intradermal
  • serology - IgE
  • lymphocyte transformation/ activation test
  • drug provocation tests - 6 weeks after acute stage
21
Q

Drug hypersensitivity

-lab findings

A

immediate
-serum tryptase, histamine, CAST-ELISA

delayed
-FBC, CRP, liver function tests, serum creatinine, urine microscopy

22
Q

Angioedema

  • definition
  • cause
A

-well demarcated non- pitting edema of the dermis, subcutaneous tissues and/or submucosal tissues

  • fluid leakage into the interstitial tissue
  • common in the face, tongue, lips, eyelids
23
Q

Angioedema

-classification (3)

A
  • mast-cell mediated angioedema
  • bradykinin- mediated angioedema
  • angioedema of unknown cause
24
Q

Angioedema

-mast-cell mediated angioedema

A

Direct mast cell activation

  • non- IgE mediated
  • triggers: NSAIDs, opiates, radiocontrast media

Allergic reaction

  • IgE mediated
  • triggers: food, insect bites/ stings, antibiotics, latex
25
Q

Angioedema

-bradykinin- mediated angioedema

A

hereditary angioedema - C1 inhibitory deficiency = build up of bradykinin

  • autosomal dominant
  • triggers: trauma, surgery, dental procedure, menstruation, infections, drugs

acquired angioedema - acquired C1 inhibitory deficiency

  • older age
  • associated with lymphoproliferative diseases and B-cell malignances

ACE inhibitor induced - impaired bradykinin breakdown

26
Q

Angioedema

-angioedema of unknown cause

A

idiopathic - histamine or non histamine mediated

  • recurrent episodes
  • triggers: cold, heat, stress, exercise

infections

  • more common in children
  • triggers: common cold, streptococcal pharyngitis, urinary tract infections

drug-induced
-calcium channel blockers, fibrinolytic, immunosuppressive drugs

27
Q

Angioedema

-symptoms

A
  • facial edema
  • dyspnea and inspiratory stridor

mast-cell mediated angioedema: urticaria and pruritus
bradykinin- mediated angioedema

-hereditary: angioedema of extremities or trunk, abdominal pain, nausea/vomiting, diarrhea

28
Q

Diagnostic criteria for anaphylaxis

A
  1. Acute onset of illness
    - respiratory compromise (dyspnea, wheezing, stridor…)
    - decrease BP, hypotonia, syncope, incontinence
  2. > or equal to 2 of the following that occur rapidly after exposure
    - skin-mucosal involvement: urticaria, itchiness, swollen lips…
    - respiratory compromise (dyspnea, wheezing, stridor…)
    - decrease BP, hypotonia, syncope, incontinence
    - persistent GI symptoms: abdominal pain, vomiting
  3. decreased BP after exposure to known allergen
    - infants and children: low systolic BP or >30% decrease in systolic BP
    - adults: systolic BP <90mmHg or >30% decrease from that person’s baseline
29
Q

Anaphylaxis

  • clinical feature that is almost always present
  • lab findings
A

-flushing and tachycardia

  • increase histamine –> earliest elevation
  • increase serum tryptase –> specific for mast cell degranulation - remain elevated for up to 6 hours
30
Q

Anaphylaxis

-emergency treatment

A

1st - adrenaline

  • adults and children (> or equal to 25kg) - 0.3mg
  • children (7,5-25kg) - 0.15mg

O2 - all patient with hypotension or SaO2 <95% or who required 2nd injection of adrenaline

I/V fluids - if hypotension or shock

other drugs: salbutamol, dopamine, glucagon (when beta blockers were used)