MTB - Allergology/Immunology Flashcards

1
Q

initial therapy - anaphylaxis

A
  1. subcutaneous Epi. 1:1000 conc
  2. corticosteroids
  3. H1-antagonist antihistamines (diphenhydramine or hydroxyzine)
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2
Q

sudden swelling of the face, palate, tongue and airway in assoc. w/ minor trauma to the face or hands OR ingestion of ACE inhibitors

A

angioedema

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3
Q

hereditary angioedema

A

C1 esterase inhibitor deficiency

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4
Q

assoc. symptoms with angioedema

A

stridor
abdominal pain
lack of response to steroids

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5
Q

diagnosis of angioedema

A

low levels of C2 and C4 complement

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6
Q

Tx. of acute episodes of angioedema

A

infusion of FFP

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7
Q

DOC for hereditary angioedema

A

ecallantide

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8
Q

Ecallantide

A

inhibitor of kallikrein; blocks bradykinin production

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9
Q

what drug class may be used for chronic therapy of angioedema

A

androgens - danazol, stanazol

- raise levels of C1 esterase inhibitor

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10
Q

CCS - patient comes in with signs of anaphylaxis after insect bite w/ no improvement after Epi injection, steroids or H1 blockers - > what do you do?

A

admit patient to ICU

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11
Q

when desensitizing a patient to a drug what other drugs should be stopped?

A

propranolol and all B-Blockers should be stopped prior to attempting desensitization (in case Epi needs to be used)

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12
Q

Symptoms of Allergic Rhinitis

A
recurrent episodes of nasal itching
nasal stuffiness
rhinorrhea
paroxysms of sneezing
eye itching
dermatitis
wheezing
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13
Q

DOC allergic rhinitis

A

intranasal steroids

- single most effective tx

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14
Q

Aside from intranasal steroids, what other therapies may be used for allergic rhinitis?

A
antihistamines (oral, intranasal)
cromolyn
ipratroprium bromide
LT inhibitors
nasal saline spray and wash
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15
Q

older man presents with recurrent episodes of sinopulmonary infections and a sprue-like abdominal disorder; he has enlarged LN and splenomegaly - dx?

A

Common variable immune deficiency

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16
Q

diagnostic testing - CVID

A

low levels of total IgG

B and T cells are present but do not make enough antibody

17
Q

Tx. CVID

A

infusion of IV immunoglobulins

18
Q

young male child presents with recurrent sinopulmonary infections - dx?

A

X-linked agammaglobulinemia

  • no B cells = no Ig
  • LN, adenoids and spleen are diminished or absent
19
Q

MC primary immunodeficiency

A

IgA deficiency

20
Q

CF: IgA deficiency

A
mostly asx
recurrent sinopulmonary infections
sprue-like malabsorption
increased incidence of atopic conditions
anaphylaxis w/ blood products
21
Q

Tx. IgA deficiency

A

tx. infections as they arise

IVIG will not work as there is little IgA in it

22
Q

patient comes in w/ recurrent skin infections caused by Staphylococcus

A

hyper IgE syndrome

23
Q

Tx. hyper IgE syndrome

A

tx. infections as they arise