Infections in Immunocompromised Flashcards

1
Q

Opportunistic infections

A

An infection caused by a microorganism that generally does not cause disease, but does so when lowered resistance is caused by impairment of the body’s immune system.

Pneumocystis
Cryptococcus
Fungal infections

KNOW THESE THREE Pneumoc, cryptoc, fungo

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2
Q

Characteristics of primary immunodeficiencies *

A
  • Often begin in the first days to weeks of life
  • Therapeutic response often slow
  • Therapy often leads to suppression and not eradication
  • Common organisms cause severe manifestation or recurrent infection
  • Unusual opportunistic organisms cause infection
  • Growth delayed
  • multiple infections simultaneously
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3
Q

Within the phagocyte abnormalities category, what is the syndrome which is defined by an absence of neutrophils

A

Kostmann’s syndrome

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4
Q

What is cyclic neutropenia

A

phagocyte populations wax and wane

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5
Q

Phagocyte abnormalities such as Kostmann’s syndrome and/or cyclic neutropenia are characterized by what

A

Recurrent bacterial infections and aspergillus infections.

Makes sense

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6
Q

Defects in phagocyte function

A
  • Defective intracellular bacterial killing

- Defective trafficking and adhesion

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7
Q

Complement deficiency C1-C4 leads to

A

recurrent bacterial infections and autoimmune

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8
Q

Terminal complement deficiency leads to

A

Neisseria Sp infection

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9
Q

Management of complement deficiencies

A

immunizations and prophylactic antibiotics

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10
Q

x linked agammaglobulinemia due to deficiency in

A

bruton tyrosine kinase

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11
Q

common variable immunodeficiency presents when

A

age 2-20, typically in early teens, due to variable genetic defects

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12
Q

Most common imunodeficiency

A

IgA

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13
Q

clinical manifestations of immunoglobulin deficiencies

A
  • recurrent bacterial and viral infections (especially encapsulated organisms like strep pneumo and H flu)
  • recurrent sinopulmonary infections or otitis
  • Giardiasis
  • Some may be associated with autoimmune disorders or increased risk of malignancy
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14
Q

Management of IgG deficiency

A

replace it

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15
Q

Lymphocytic disorders can represent

A

Abnormal antigen processing or presentation to T cells
Defects in T cells
Defects in cytokine production or responsiveness

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16
Q

Lymphocytic disorders are generally inherited as autosomal recessive or x-linked

A

ok…know

17
Q

Severe combined immunodeficiency

A

No T cells and Poor B cell function

18
Q

Di George syndrome

A

Thymic hypoplasia, hypoparathyroidism, hypocalcemia, heart disease

May develop autoimmune later in life

19
Q

Wiscott- Aldrich

A

thrombocytopenia, severe eczema, treateed with stem cell

High risk of malignancy

20
Q

Categories of Primary Immunodeficiencies

A
  • Innate immunity
    includes phagocyte number and function as well as complement
  • B cell leading to dysfunction in Ig production
  • T cell
21
Q

Phagocyte deficiencies leave pts susceptible to

A

Catalase positive bacteria/fungi

22
Q

Complement deficiencies leave pts susceptible to

A

Neisseria

23
Q

Antibody deficiency leaves pts susceptoble to

A

organisms with polysaccharide capsules

24
Q

Cellular and combined immunodefiiency leaves ppl at risk for

A

opportunistics, fungi, viruses

25
Q

splenectomy and sickle cell watch out for

A

Sepsis with encapsulated bacteria like strep pneumo and H flu

26
Q

Pregnancy

A

UTI, Hep E, H1N1 assoc with increased morbidity and mortality

27
Q

Chemo

A
  • Risk of infection proportional to degree and duration of chemo
  • Watch for bacterial and candidal sepsis
  • Aspergillosis
  • pneumocystis pneumonia
  • Disseminated Varicella