Lecture 21- Immunocompromised Host Flashcards

1
Q

Why is immunodeficiency a problem?

A

Many different diseases and hard to diagnose. Most patients diagnosed 8-12 years from onset of symptoms. Organ damage has already occurred in a lot of cases

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is an immunocompromised host?

A

State in which the immune system is unable to respond appropriately and effectively to infectious microorganisms due to a defect in one or more components of immune system

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are the main reasons for secondary or acquired immunodeficiency?

A

Malnutrition
Malignancy
Infection (HIV)
Chemotherapy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What components of immune system or defective in most immunodeficiency disease?

A

Neutrophils, B cells and T cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

When should immunodeficiency be suspected?

A

SPUR

Severe
persistent
Unusual
Recurrent

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

10 warning signs?

A

10 signs for children and adults that you may have immunodeficiency such as repeated ear infections in one year etc

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Immunodeficiency and cancer?

A

Prone to certain cancers eg lymphoma, leukaemia, Hodgkin’s disease and adenocarcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Percentage of immunodeficiencies caused by antibody defects?

A

65%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Main antibody defect PID?

A

Defect in B cell development such as Brutons

Defect in antibody production such as common variable immunodeficiency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Immunodeficiency caused by T cell defects?

A

Combined B and T cell defects like SCID

T cell defects like Di George syndrome

15%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Phagocytes defects immunodeficiency?

A

10% of PIDs

Defects in respiratory burst- chronic granulomatous disease (CGD)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Presentation of PID?

A

If under 6 months suggests T-cell or phagocyte defect as antibodies have been passed on from mother and should last 6 months

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Between 6 months and 5 years?

A

B- cell antibody or phagocyte defect

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Onset over 5 years?

A

B cell antibody or complement or secondary immunodeficiency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Identifyingcause of immunodeficiency disease?

A

Certainpathogens are associated with specific components of immune system. Recurrent type of infection can pin point component that is defective

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Clinical cases?

A

Practice in lecture

17
Q

How to manage PIDs?

A

Supportively through giving treatment promptly and aggressively. Preventing infection from occurring and grieving nutritional support as well as avoiding attenuated live vaccines

Manage specifically through immunoglobulin therapy and haematopoietic stem cell therapy

18
Q

Immunoglobulin replacement therapy?

A

Goal to get serum IgG over 8g/L

Life long treatment

Indicated for CVID
Burtons disease
Hyper IgM syndrome

19
Q

Secondary immune deficiency p?

A

Decreased production of immune components through malnutrition, HIV infection, liver disease, splenectomy etc

Increas3d loss of immune components

20
Q

Lab investigations of IDs?

A

Antibody or B cell- IgG, IgA etc

T cell- lymphocyte count

Phagocyte- neutrophil count

Complement- individual complements