t4 U10 - hematology/oncology Flashcards

1
Q

normal RBC level for 1-6 yr?

A

4.5-5

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2
Q

normal RBC level for 6-18Y?

A

4.5-5

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3
Q

normal Hmg for 1-6?

A

9.5-14

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4
Q

normal Hmg for 6-18?

A

10-15.5

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5
Q

normal Hmt for 1-6?

A

30-40%

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6
Q

normal Hmt for 6-18?

A

32-44%

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7
Q

s/sx of Anemia?

A

Fatigue/Lethargy
SOB
Tachycardia
Pale skin
Dizzy

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8
Q

what would a CBC show for a suspected anemic patient?

A

Low RBC
Low hmg
Low hmt
Low reticulocyte count

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9
Q

iron supplement considerations?

A

Give with Vit C rich foods
Brush teeth after (can stain)
DONT give with milk

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10
Q

common age for children to develop anemia & why?

A

2-3Y
Food lags

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11
Q

who is at highest risk for iron deficient anemia?

A

pre mature infants & btwn 6-12mth

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12
Q

what would be good to include in a childs diet to increase Iron?

A

Beans
Red meat
Fortified cereal
Eggs
Green leafy veggies

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13
Q

what should be monitored with taking iron?

A

constipation – increase the fiber

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14
Q

what is a common finding when taking iron supplements?

A

black tarry stools

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15
Q

sickle cell can present with _____?

A

Pallor
Fatigue Jaundice
Tissue hypoxia

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16
Q

ensuring what for sickle cell patients can increase the good outlook?

A

being up to date on vaccines

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17
Q

primary to focus on for sickle cell?

A

Rest
Hydration
Pain control
Oxygenation

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18
Q

what organ can become damaged/overworked from sickle cell?

A

Spleen

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19
Q

what medication can be given at home for sickle cell pain?

A

Acetaminophen/Ibuprofen

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20
Q

if in a vaso-occlusive crisis, what medication is given?

A

Morphine (Duramorph)
Ketorolac (Toradol)

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21
Q

edu about Toradol?

A

No longer than 5 days due to GI bleeding

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22
Q

what can be observed with a vaso-occlusive crisis?

A

Tissue engorgement
Pain

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23
Q

with aplastic sickle cell, what should be closer monitored/why?

A

Fever (101.5+)
Body cant filter out bacteria = sepsis

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24
Q

what symptoms would be present in splenic sickle cell that = life threatening?

A

profound anemia
hypovolemia
shocl

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25
Q

lack of what factor causes hemophilia A & that does what?

A

factor 8
can’t form clots = prolonged bleeding

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26
Q

s/sx of hemophilia?

A

Bruising
Soft tissue bruising
Intracranial hemorrhage (infants)
Excessive bleeding

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27
Q

situations were hemophilia bleeding could be seen?

A

circumcision
tooth removal/loss

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28
Q

what is hemarthrosis?

A

Internal bleeding btwn joint spaces

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29
Q

most common sites for Hemarthrosis?

A

Knees
Elbows

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30
Q

presentation of hemarthosis?

A

Swelling
Warmth/redness
Loss of redness

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31
Q

what should a child with hemophilia avoid doing?

A

playing sports

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32
Q

does hemophilia always present immediately?

A

No
Can present at 6m

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33
Q

steps to take for bleeding with hemophilia?

A

Pressure for 15 min
Ice application
Factor 8 given at hospital

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34
Q

what medical related things should hemaphilia pt avoid?

A

Im injections
Aspirin

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35
Q

important education for adolscents with hemophilia?

A

how to self administer IV factor

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36
Q

level that classifies as Neutropenia in infants?

A

<1,000/uL

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37
Q

level that classifies as Neutropenia for 1y +?

A

<1,500u/L

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38
Q

bruising, pale and petechiae can present with Neutropenia, why/what is the cause?

A

Neutropenia effects RBC & platelets

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39
Q

s/sx of Neutropenia?

A

Lymphadenopathy
Pallor
Fever
Bruising
Fever

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40
Q

what is important to assess with Neutropenia?

A

underlying infection
especially around mouth, skin, ears & perianal area

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41
Q

how would a Neutropenia be placed in a hospital?

A

reverse isolation

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42
Q

how would be Neutropenia room be set up/have to do?

A

Nurse wear a gown
No roomie
No fresh fruit/flowers

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43
Q

when monitoring for infection with Neutropenia what is given?

A

broad spectrum ABX (Empiric therapy)

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44
Q

how can colony stimulating factors be given

A

@ home
SubQ injection once/day

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45
Q

considerations with Neutropenia?

A

No rectal temps
Avoid hot tubs
Use a soft toothbrush

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46
Q

what is not given to Neutropenia pt with low counts?

A

NSAIDS/Aspirin

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47
Q

important teaching for Neutropenia?

A

proper handwashing technique

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48
Q

what is done before giving blood transfusions?

A

2 PT identifiers
CONSENT

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49
Q

steps for pretransfusion of blood?

A

V/S
Call for blood
Hang blood w/in 30min but NO LONGER than 4 hr

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50
Q

what do you do when starting a blood transfusion?

A

V/S Q 15min
CAN’T leave for first 15 min (monitor for reaction)

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51
Q

Post blood transfusion, what does the nurse do?

A

Keep bag for an hour
Paperwork

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52
Q

what should the nurse wear during blood transfusion?

A

Gloves & goggles

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53
Q

what to do in case of reaction to blood transfusion?

A

Stop infusion
Call PCP
Flush line w/saline
Monitor VS

54
Q

what is HSCT?

A

Bone marrow transplant

55
Q

what are the 3 types of HSCT?

A

Autologous: Own stem cells
Allogeneic: Compatiable donor (usually sibling)
Syngeneic: Twin

56
Q

indications for HSCT?

A

Sickle cells
Severe Aplastic anemia

57
Q

what is characterisitc sign of asplastic anemia?

A

Pancytopenia: Reduction in all cellular elements of blood

58
Q

possible hematological complication for PT with chronic illness?

A

Development of thrombosis
Most often in lung or extremity

59
Q

what is the goal with chemotherapy?

A

Decrease size of primary tumor
Good for “broad spread”

60
Q

what is the goal with radiation?

A

Break apart bonds within cell & cause to die
Delivers PRECISE targeting

61
Q

what is the priority nursing intervention for infection prevention in cancer patients?

A

Neutropenic precautions

62
Q

things to monitor/teach for infection prevention in cancer patients?

A

Meticulous skin care
S/sx of infection

63
Q

Cisplatin can cause what complication?

A

high tone hearing loss

64
Q

how can the kidney be affected by cancer treatment?

A

Bleeding
Protein wasting

65
Q

Lung consequences of cancer treatment?

A

reduced elasticity = SOB, reduced exercise ability

66
Q

if a cancer patient has open oral sores, what is the recommended diet?

A

bland foods

67
Q

cancer patients are on what type of precautions?

A

neutropenic
(no flowers/fruit)

68
Q

what/where does ALL focus on?

A

immature/undifferentiated cells
WBC

69
Q

children who have what are at higher risk for ALL?

A

downs syndrome

70
Q

what is a common “overview” of s/sx of ALL?

A

vague flu feelings

71
Q

specific s/sx of ALL?

A

blueberry muffin lesions on trunk
petechiae
limping/refusal to walk
abdominal distention

72
Q

where would the swelling be with ALL?

A

enlarged supraclavicular lymph nodes

73
Q

why would a pt with ALL have abdominal distention? & why does it happen

A

enlarged spleen
can’t filter

74
Q

what WBC counts would be best & worst to see in ALL?

A

Best: Under 5,000
Worst: 50,000

75
Q

in worst case WBC how do we treat ALL patients?

A

Doxorubicin (abx)

76
Q

what are the 3 phases of chemo?

A

remission-induction
consolidation
maintaince

77
Q

what is the primary goals in remission induction?

A

reduce tumor to undetectable size
protect brain

78
Q

consolidation stage consists of what?

A

destroy residual tumor

79
Q

where is neuroblastoma most common?

A

the ABDOMEN

80
Q

what s/sx would neuroblastoma present with?

A

palpation of mass
edema in LE
bruising/swelling around eyes

81
Q

what would a neuroblastoma mass feel like?

A

crossess midline
hard & painless

82
Q

what is a priority management in neuroblastoma

83
Q

most important thing to know about wilm’s tumor patients?

A

NO ABDOMINAL PALPATION

84
Q

s/sx of wilms tumor?

A

unilateral mass/abdominal swelling
Hematuria

85
Q

what/where does Wilm’s tumor affect?

86
Q

what will happen if Wilm’s tumor is palpated?

A

Spread over body

87
Q

important management for Wilm’s?

A

Monitor I&O’s & bowel output
Monitor BP

88
Q

what should a Wilm’s PT diet consist of?

A

foods high in protein & calories
(offer options to encourage eating)

89
Q

examples of medication used in Wilm’s

A

Actinomycin D (dactinomycin)
Vincristine (Oncovorin)

90
Q

what should be assess in a Wilms PT urine?

A

presence of clots
odor
color
amount
protein in urine

91
Q

s/sx of retinoblastoma?

A

strabismus: red painful eye
whitish glow in pupil (Leukocoria)
Inward/outward turning of eye

92
Q

nursing care/management for retinoblastoma?

A

showing families photographs of children undergoing this procedure

93
Q

post op edu for rentinoblastoma

A

eyelid is closed & will wear a patch over eye
discharge 3-4 days
some clear drainage is ok
no straining/blowing nose
no rubbing eye for 2 wk

94
Q

how to clean/care for retinoblastoma post op

A

gentle irrigation w/ prescribed solution
thin coating of ABX

95
Q

where does osteosarcoma occur?

A

LONG BONES IN METAPHYSIS

96
Q

what can damage to the metaphysis cause?

A

stunted/delayed growth

97
Q

s/sx of osteosarcoma?

A

pain increased with activity/weight bearing
limp
dull ache several months prior

98
Q

what would palpation of osteosarcoma reveal?

A

tenderness
swelling
warmth!
redness!

99
Q

how/what would diagnose osteosarcoma/

A

Sunburst pattern on bone
XRAY

100
Q

primary management for osteosarcoma?

A

promote function & mobility post op

101
Q

what cancer treatment is used for osteosarcoma?

A

chemo before surgery to shrink tumor size

102
Q

what/where does Ewings Sarcoma effect?

A

Bones & soft tissue
Middle of bones
Most often femur/pelvis

103
Q

how can Ewings Sarcoma cause respiratory distress?

A

if in chest wall

104
Q

s/sx of Ewings Sarcoma

A

systemic (fever/weight loss)
pain/swelling at site

105
Q

primary nursing diagnosis for Ewings Sarcoma?

A

Impaired mobility

106
Q

how do you assess Ewings Sarcoma

A

palpate any firm or non tender enlargements

107
Q

when wouldnt surgery be an option of Ewings Sarcoma

A

if the lesions are in pelvic or sacral area

108
Q

why is chemo preferred over radiation for Ewings Sarcoma?

A

radiation could increase risk of induced secondary infection

109
Q

what/where does Hodgkins’s Lymphoma taken place?

A

Lymph system
SINGLE POINT

110
Q

presentation of Hodgkins’s Lymphoma?

A
  • Swollen, firm supraclavicular lymph nodes!
  • non-moveable !
  • anterior mediastinal mass
  • night sweats
111
Q

what would be seen on a biopsy that would confirm HODGKINS

A

Reed-Sternberg cells

112
Q

Important assessment for HODGKINS?

A
  • Resp assessment: Coughing/difficulty breathing
  • Chest pain
  • Chronic fatigue
113
Q

management for HODGKINS?

A

radiation & chemo

114
Q

what is NON-Hodgkins lymphoma?

A

NO single focal origin
Rapid onset with widespread involvement

115
Q

which tissues are most often affected with NON-Hodgkins lymphoma?

A

bowel
appendix
upper midsection of chest

116
Q

s/sx of NON-Hodgkins lymphoma?

A

pain/swelling @ abdomen, chest, head/neck
possible facial muscle weakness

117
Q

diagnosis for NON-Hodgkins lymphoma?

A

elevated serum lactic dehydrogenase (500+)

118
Q

management of NON-Hodgkins lymphoma?

A

aggressive multiagent chemo ASAP
(intrathecal chemo given for CNS prophlaxis)

119
Q

what are characteristic s/sx of ITP?

A

Thrombocytopenia (decrease in platelets)
Purpura (hemorrhage under skin)

120
Q

how is newly diagnosed ITP characterized?

A

normal platelet count w/in 6m of diagnosis with no evidence of relapse

121
Q

what child may present with ITP symptoms?

A

healthy child who recently had viral infection
measles/mumps/rubella/chkn pox

122
Q

s/sx that may present with ITP?

A

epistaxis: Nosebleeds
Intracranial hemorrhage
petechiae

123
Q

how is ITP diagnosed?

A

no definitive
often self limiting

124
Q

what would a CBC show for ITP?

A

platelet count less than 20,000

125
Q

usual platelet count?

A

150-400,000

126
Q

when is platelet transfusion recommended for ITP?

A

ONLY!! if severe life threatening bleeding

127
Q

medical care for ITP?

A

steroids
IVIG admin
anti-D antibody

128
Q

side effects of anti-D antibodies?

A

temporary anemia that resolved when IgD disperses
fever/chills
HA post infusion

129
Q

considerations for igD?

A

monitor VS

130
Q

what are the qualifications are a splenectomy in ITP?

A

episodes of life threatening bleeding
older than 5
low platelets affect ADL

131
Q

edu on how parents should handle nosebleeds?

A

child lean down and forward & pitch nose bridge

132
Q

what should ITP patients be instructed to avoid?

A

Aspirin
straight edge razors
tampons
rectal