Allergy/Immunology Flashcards

1
Q

Anaphylaxis Presentation

A

hemodynamic instability (w/ hypotension & tachycardia) and difficulty breathing

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2
Q

Anaphylaxis Treatment

A

IM epi 1:1000 concentration
corticosteroids
H1-blocking antihistamine (diphenhydramine, hydroxyzine)

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3
Q

Angioedema etiologies

A

minor trauma to face or hands
ACE-I
C1 esterase inhibitor deficiency (hereditary)

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4
Q

How to dx hereditary angioedema

A

Look for low levels of C2 & C4 in the complement pathway

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5
Q

Angioedema treatment modalities

A
  • C1 inhibitor concentrate (best initial therapy w/ laryngeal involvement)
  • Icatibant
  • Androgens for chronic therapy (danazol & stanozolol)
  • FFP (acute episodes)
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6
Q

Efficacy of antihistamines, glucocorticoids, and epi in hereditary angioedema

A

Ineffective.

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7
Q

PPX for angioedema - treatment

A
  • antifibrinolytic (tranexamic acid)
  • androgens
  • C1 esterase inhibitor infusion
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8
Q

Most effective treatment for allergic rhinitis

A

intranasal corticosteroids

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9
Q

Allergic rhinitis Presentation

A

recurrent episodes of nasal itching, stuffiness, rhinorhea, paroxysms of sneezing. Eye itching and dermatitis may also be present.

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10
Q

Mainstay of treatment of allergic rhinitis

A

Avoidance of allergen.

If not possible, desensitization may work (can’t be on beta-blockers tho)

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11
Q

Common Variable Immunodeficiency - Presentation

A

recurrent sinopulmonary infections. more common in adults.
spruelike abdominal disorder (malabsorption, steatorrhea)
Enlargement of lymph nodes, adenoids, spleen.

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12
Q

Common Variable Immunodeficiency - Diagnosis

A

Total IgG levels are low.

Able to make Ig, but immune cells don’t make enough.

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13
Q

Common Variable Immunodeficiency - Treatment

A

Continuous Infusion of IVIG.

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14
Q

Bruton Agammaglobulinemia - Inheritance & Presentation

A

X-linked

recurrent sinopulmonary infx in male children

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15
Q

Bruton Agammaglobulinemia - Dx & Treatment

A
  • Diminished or absent lymph nodes, adenoids, and spleen. Missing B cells and Ig.
  • IVIG infusion.
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16
Q

IgA Deficiency - Presentation

A

recurrent sinopulmonary infx, spruelike malabsorption syndrome, increase in atopic conditions, anaphylaxis w/ blood transfusion.

17
Q

IgA Deficiency - Treatment

A

Treat the infections as they arise.

18
Q

Hyper IgE Syndrome - Presentation & Treatment

A

Recurrent skin infx caused by Staphylococcus.

Treat infx as they arise.