Hematological & Immunological Dysfunction Flashcards

1
Q

History for child with suspected hemotological/
immunological issue

A

what’s normal for them vs new onset

child’s energy

family history

pale, fatigued, easily bruised (low platelets)

bleeding

diet (iron sources)

infections

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2
Q

Complete Blood Count components

A

WBCs

RBCs

Hemoglobin

Hematocrit

Platelets

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3
Q

WBCs indicate…

A

infection, leukaemia, immunodeficiency, viral illness

bone marrow or immune dysfunction

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4
Q

Hemoglobin indicates…

A

also in bone marrow

can be low in anemia?

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5
Q

Hematocrit

A

% of RBC in the blood

will be low with anemia

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6
Q

Most common RBC/hematological disorder for childhood

A

anemia

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7
Q

Anemia

A

decrease in the # of RBCs AND/OR hemoglobin concentration below normal

decreased oxygen-carrying capacity 
of blood

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8
Q

T or F: Anemia is usually a manifestation of something else.

A

TRUE

leukemia or lymphoma

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9
Q

T or F: It is normal for newborns to experience anemia.

A

TRUE

why - premature - not getting all the iron rich blood from mom

delayed cord clamping can help to increase iron

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10
Q

Sign of SEVERE anemia

A

murmur

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11
Q

Classification of anemias (2)

A

1) Etiology and physiology

2) Morphology

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12
Q

1) Etiology and physiology classification

A

RBC and/or Hgb depletion

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13
Q

2) Morphology classification

A

characteristic changes in RBC size, shape, and/or color

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14
Q

Management of anemia

A

physical exam & diagnostics

treat underlying cause
-transfusion
-nutrition

supportive care
-IV fluids
-O2
-bed rest - decrease the demand

prep for lab tests

prevent complications

support/educate family

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15
Q

Things you can do to help kids during lab tests

A

play with equipment beforehand

educate, explain

bring stuffed animal

distraction**

freezing cream or spray

sucrose in infants

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16
Q

Safety thing to look out for with anemia patients

A

dizziness

falls risk

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17
Q

Anemia signs and symptoms

A

tired

pallor

sometimes jaundice

splenomagoly

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18
Q

Iron deficiency anemia

A

inadequate supply of dietary iron

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19
Q

Who is at a higher risk of iron deficiency anemia?
a) bottled fed babies
b) breast fed babies

A

b) breast fed babies

supplementation in the formula

may need to supplement iron at 4 months

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20
Q

Populations at an increased risk of iron deficiency anemia

A

Indigenous populations

babies

adolescence

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21
Q

Ways to prevent iron deficiency anemia

A

iron-fortified cereals and formulas for infants

breastfed babies: supplement at 4 months

premature: supplement at 2 weeks

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22
Q

T or F: Cow’s milk contains iron.

A

FALSE

avoid until 12 months

limit to 600 mL daily

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23
Q

Amount of iron to give

A

3-6 mg per kg

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24
Q

Sickle cell anemia

A

normal adult hemoglovin is partly or completely replaced by abnormal sickle hemoglobin

most common in black population

doesn’t necessarily present in infants

changes over time - crisis starting in toddlerhood

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25
Q

Sickle cell anemia patho

A

obstruction of the sickled RBCs

vascular inflammation

increased RBC destruction

abnormal adhesion + inflammatory process = vasoconstriction

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26
Q

Sickle cell anemia can result in…

A

local hypoxia

tissue ischemia

infarction

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27
Q

Clinical manifestations of sickle cell anemia

A

vaso-occlusive crisis

stroke (cells block vessels)

Chest Syndrome

Acute Splenic Sequestration

Hyperhemolytic

Infection

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28
Q

vaso-occlusive crisis

A

pain crisis

episode characterized by ischemia

pain can be very very severe

minutes to days

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29
Q

Chest Syndrome

A

similar to pneumonia

fever, cough, hypoxia, wheezing

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30
Q

Acute Splenic Sequestration

A

pooling of blood, usually in the spleen

may have to have spleen removed

or not working properly

increased risk of infection

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31
Q

Hyperhemolytic

A

anemia

jaundice

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32
Q

Management of a sickle cell crisis

A

prevent and treat

rest

hydration

oxygen - above 95%

electrolyte replacement

pain management!**
-morphine or hydromorphone

blood tranfusions

antibiotics

education/support

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33
Q

What is an important focus of education for parents of a child with sickle cell?

A

education surrounding addiction

medication important for a child in pain

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34
Q

Leading cause of death from disease in children past infancy

A

neoplastic disorders

most common childhood cancer: leukemia

35
Q

T or F: Leukemia has a good prognosis.

A

TRUE

survival rate: 95%

36
Q

Between what ages does leukemia peak?

A

2 and 5 years

37
Q

Leukemia

A

broad group of malignant diseases of bone marrow and lymphatic system

38
Q

Types of leukemias (3)

A

1) Acute lymphoid leukemia (ALL)
-most common**

2) Acute nonlymphoid (myelogenous) leukemia (ANLL or AML)

3) Stem cell or blast cell leukemia

39
Q

Pathophysiology of leukemia

A

overproduction of WBC, but immature

can have high WBC count

acute - super low leukocytes

bone marrow

most affected organs: liver and spleen

cellular destruction takes place by infiltration and subsequent competition for metabolic elements

40
Q

Symptoms of leukemia

A

presents like a viral illness, then more frequent illnesses

fever, fatigue (anemic)

aching bones or joints (bone marrow full of cells)

headaches

rashes

swollen glands (lymph nodes)

frequent infections

unexplained weight loss

bleeding or swollen gums

enlarged spleen or liver, or a feeling of abdominal fullness

slow-healing cuts, nosebleeds, or frequent bruises

41
Q

Leukemia rashes (2)

A

1) purpleish rash
-blood pooling caused by a lack of platelets

2) petichia
-broken capillaries from low platelets

42
Q

Term for low platelets

A

thrombocytopenia

43
Q

Term for low hemoglobin

44
Q

Term for low WBC/leukocytes

A

leukopenia

45
Q

Term for when everything is low

A

pancytopenia

46
Q

Diagnostic evaluation for leukemia (4)

A

1) history, physical manifestations**

2) Peripheral blood smear
-immature leukocytes
-frequently low blood counts

3) Bone marrow aspiration or biopsy
-taken at the iliac crest
-to see if there are blasts in the bone marrow

4) Lumbar puncture to evaluate CNS involvement/disease
-test for blasts or leukaemia cells as well

47
Q

What does chemo help prevent?

A

CNS involvement

48
Q

High risk WBC count

A

over 50,000

49
Q

High risk age of diagnosis

A

over 10
-high risk: ALL

want adolescents to have AML

under want, want to have ALL

50
Q

Low risk cell involvement

51
Q

High risk phenotype

A

Philadelphia chromosome

52
Q

Higher risk gender

A

boys

girls have more favourable outcome

53
Q

When should patients ideally be in remission?

A

end of induction therapy (1 month)

54
Q

Relapse after transplant prognosis

A

dismal

stem cell or bone marrow transplant

55
Q

Therapeutic management of leukemia

A

Chemotherapeutic agents

Cranial irradiaiton

Transfusion

56
Q

When are transfusions needed?

A

hemoglobin < 70, OR symptomatic e.g. fatigue, pallor

platelets < 10

57
Q

4 phases of leukemia therapy

A

1) Induction therapy: 4 to 6 weeks

2) CNS prophylactic therapy
-intrathecal chemotherapy

3) Intensification (consolidation/post remission) therapy
-to eradicate residual leukemic cells and prevent resistant leukemic clones

4) Maintenance therapy
-to preserve remission

58
Q

Mneumonic for 4 phases

A

I care, I monitor

59
Q

Length of leukemia treatment

60
Q

Febrile Neutropenia criteria (2)

A

1) absolute neutrophil count <0.5

2) fever

61
Q

T or F: Feb neut is a medical emergency.

A

TRUE

go to ER asap**

62
Q

Feb neut management

A

admitted to hospital

IV antibiotics
-Pip/Tazo

min. 48H in hospital

63
Q

When can a child with feb neut be discharged?

A

no fever within 48h –> can be discharged

once 48h period is up, must go 24h without a fever to be discharged

64
Q

What happens if cultural are positive?

A

10 - 14 days of IV antibiotics

65
Q

What happens if the child continues to have a fever?

A

will think fungal infection

kidneys, brain, lungs, heart

66
Q

Chemo precautions

A

nitrile gloves
-and while changing diapers

flush toilet 2x with lid down

beware of bodily fluids

letting others know cytotoxic status of child when transferring

67
Q

How long is a child cytotoxic for after chemo?

68
Q

What to do if you are exposed/contaminated to chemo meds?

A

spill kits

eye wash

69
Q

Main types of lymphomas (2)

A

1) Hodgkin’s disease

2) Non-Hodgkin’s lymphoma (NHL)

70
Q

Which lymphoma is more common?
a) Hodgkin’s
b) non-Hodgkin’s

A

b) non-Hodgkin’s

71
Q

Which lymphoma is worse?
a) Hodgkin’s
b) non-Hodgkin’s

A

b) non-Hodgkin’s

72
Q

Hodgkin’s disease most prevalent in…..

A

15 to 19 years

usually diagnosed at earlier stage of disease

73
Q

Non-Hodgkin’s lymphoma (NHL) most prevalent in….

A

<14 years of age

74
Q

Hodgkin’s lymphoma

A

cancer of lymph tissue found in the lymph nodes, spleen, liver, bone marrow, and other sites

RF: past EBV

75
Q

Hodgkin’s lymphoma - Classification A symptoms

A

PAINLESS swelling of the LYMPH NODES in the neck,armpits, or groin (swollen glands)

76
Q

Hodgkin’s lymphoma - Classification B symptoms

A

PAINLESS swelling of the LYMPH NODES in the neck,armpits, or groin (swollen glands)

fatigue

fever and chills that come and go

unexplained itching

soaking night sweat

unexplained weight loss

chest pain - depending on where tumour is

big spleen, liver, abdominal fullness

77
Q

What is one of the first signs of Hodgkin’s lymphoma type B

A

pruritis

itching

78
Q

Hodgkin’s lymphoma diagnostics (4)

A

1) lymph node biopsy

2) chest x-ray

3) bone marrow biopsy

4) Presence of Reed-Sternberg cells
-owl looking cells
-double nucleus

79
Q

Hodgkin’s lymphoma management

A

radiation and/or chemo

infection prevention

80
Q

Non-Hodgkin’s Lymphoma

A

cancer of the lymphoid tissue

81
Q

Non-Hodgkin’s Lymphoma symptoms

A

depend on area affecting, how fast its growing

new onset wheeze

facial swelling

respiratory distress

asymmetrical tonsils

acute abdominal pain

82
Q

Non-Hodgkin’s Lymphoma treatment

A

depends on age, stage, symptoms etc.

CHEMO**

radiation –> not often

surgery

Rituximab (Rituxan) (B-cell)

83
Q

Care priorities for the child with cancer

A

Family Centred Care
-health care team
-support
-education
-cultural considerations