Allergy and Immunology 🤧 Flashcards

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1
Q

Tacrolimus side effects

A

Hyperkalemia, glucose intol, HTN, glucose intol, irate high, neurotoxicity (tremor), lil N/V,

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2
Q

Do you need to do allergy testing in the first episode of urticaria. When would we do testing

A

No, just give anti H. Only if severe or if sus specific trigger or if fails anti H

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3
Q

Is it significant that lymph nodes or adenoids are undeveloped in in SCID/x linked agammaglob, less than 2 yo

A

No. They are underdeveloped in all less than 2 yo

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4
Q

How to clinch the Dx of x linked agammaglob

A

BTK gene mutation

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5
Q

How to Tx x linked agammaglob

A

Treatment is immunoglobulin replacement therapy (eg, intravenous immunoglobulin) with or without
prophylactic antibiotics.

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6
Q

Transient hypogammaglobulinemia of infancy. Which Ig go up and which go down. When does it normalise? Which infx do they get

A

Transient hypogammaglobulinemia of infancy is characterized by decreased IgG, variable IgM, and
normal IgA and B-cell concentrations. Affected patients develop mild, recurrent sinopulmonary and gastrointestinal infections. Immunoglobulin levels generally normalize by age 9-15 months.

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7
Q

Wisdom aldrich Ig levels (clue = vowels)

A

immunoglobulin profile shows low to normal lG and IgM with elevated IgA and IgE.

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8
Q

Less than one month post transplant…. Infx cause?

A

<1 month: Bacterial causes from operative complications (eg, hepatic abscess, biliary leak, wound infection) or hospitalization (eg, intravascular catheter, external drain)

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9
Q

Months 1-6 post transplant. Cause of infx

A

Months 1-6: Opportunistic pathogens (g, Cytomegalovirus, Aspergillus, Mycobacterium tuberculosis) in the setting of high-dose immunosuppressive medication

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10
Q

More than 6 mo post transplant, cause of infx

A

> 6 months: Immunosuppressants usually at maintenance levels. Patients primarily at risk for typical
community-acquired pathogens (at a higher rate than the general population)

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11
Q

Most transplant fever and pain etc. how to really tel if bac infx or acute rejection

A

Look at hemodynamic,,,, shock would be seen in infx, not acute rejection

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12
Q

Chronic complications of CVID

A
  • Autoimmune (eg, RA, thyroid disease)
    • Pulmonary (eg, bronchiectasis, fibrosis)
    • Gl (eg, chronic diarrhea, IBD-like
    conditions)
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13
Q

How to Dx CVID

A

Diagnosis is made by quantitative measurement of immunoglobulin levels

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14
Q

XLA, CVID. Do quant Ig and flow cytom for which ones

A

Flow cytom for XLA

Quant Ig for CVID

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15
Q

Serum sickness like syndrome signs and symptoms. Any Tx needed? Main difference between serum sickness

A

Athralgia, urticaria, following a medication usually. Penicillin, ceph, TMP SMX. Compared to serum sickness, the fever, compliment activation and complex titre are more mild

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16
Q

CGD prphlx and cure

A

Prophylaxis: TMP-SMX, itraconazole, interferon gamma
• Active infection: culture-based, antimicrobial therapy
Hematopoietic cell transplant is curative

17
Q

Two ways to prevent IgA def associated tranfusion anaphylaxis

A

wear medical alert bracelets and receive blood products that are washed of residual plasma or from an IgA-deficient donor.

18
Q

Tx of transient hypo gamma glob of infancy

A

Observation; self-resolution in early childhood. Abx if severe infx

19
Q

In transient hypogammaglob of infancy, what is the response to vx

A

Normal response to Vx, unlike XLA and SCID

20
Q

Do we see atopic features in transient hypogamaglob of infancy

A

Yes

21
Q

Early compliment disorders are marked by what type of infx? And what other disorders

A

Early complement disorders (eg, C1 complex) are marked by recurrent sinopulmonary bacterial
infection and childhood systemic lupus erythematosus.

22
Q

HIV cd4/cd8 ratio

A

CD4/CD8 ratio would be low.

23
Q

how do we screen for SCID

A

Therefore, SCID is included in routine newborn screening in the United States and is detected by the absence of T cell receptor excision circles (circular DNA excreted by developing T cells in the thymus) in dried blood.

24
Q

HiB infx in fully vx person… should raise suspicion for what

A

Hum oral immunodeficiency

25
Q

Vaccine responses…. XLA vs asplenic Patients

A

Vaccine antibody response is normal with anatomic or functional asplenia. Whereas in XLA they will have low Vx titres. Both have encapsulated bac infx, so this can help differentiate

26
Q

CVID and XLA are usually easy to tell apart… but if they have overlap, what’s the main way to decide the dx

A

XLA will occur around 3-6 mo old

27
Q

How to Dx hereditary angioedema

A

• 1 C4 level
• | C1 inhibitor protein or function

28
Q

Mx for hereditary angioedema (3 components)

A

C1 inhibitor concentrate
• Bradykinin antagonist (eg, icatibant)
• Kallikrein inhibitor (eg, ecallantide)

29
Q

Do patients with HIV have LN swell, and why?

A

HIV infection causes generalized lymphadenopathy in infants because B cells are produced normally.

30
Q

Hereditary angioedema… is the edema itchy?

A

No, it’s angioedema, not mast cell stuff

31
Q

Main bacteria seen in LAD

A

Staph A

32
Q

High high neutrophil is in the face of recurrent mucocut infx

A

LAD

33
Q

Weight requirement for infant to have hep B vx

A

The first hepatitis B vaccine is administered when the patient weighs 22 kg

34
Q

Chronic enteroviral infx common in which immunodef

A

XLA

35
Q

IFN receptor deficiency results in what

A

IFN-y receptor deficiency results in disseminated mycobacterial disease beginning in infancy.

36
Q

CI for DTaP Vx

A

Previous enceph, or anaphylaxis after vx, or uncontrollled epilepsy

37
Q

Abscesses difference in CGD and hyper IgE

A

Cold in hyper IgE

38
Q

Normal caloric intake

A

(up to 32
ounces a day)

39
Q

Tx of renal vein thrombosis. Consider if AKI present

A

Anticoag, or thrombolysis is AKI present