Pediatrics- Hematologic Disorders Flashcards

(53 cards)

1
Q

What is Epistaxis

A

Blood nose

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2
Q

What is ridk factor for a bloody nose

A

Trauma(picking or rubbing the nose)
Low humidity
What injury?
Medication, side effect, clotting factors

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3
Q

What should the nurse do if a child has a bloody nose

A

Maintain, calm demeanor
Have child sit up with head, tilted slightly forward to prevent aspiration of blood
Apply pressure to the lower nose
If needed pet cotton into side of nose, that’s bleeding
Encourage breathing through their mouth
Apply ice

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4
Q

How should a patient be sitting if they have a bloody nose

A

Slightly forward sitting up

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5
Q

Why are adolescence at risk to iron deficiency anemia

A

Poor diet
Rapid growth
Menses
Obesity
Strenuous activity

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6
Q

What are risk factors for getting iron deficiency anemia

A

Premature birth
Excessive cow milk
Poor diet
Infants : Gerd, pyloric stenosis
Older children : G.I. polyps, colitis
Adolescence : menorrhagia

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7
Q

Findings in a patient with iron deficiency anemia

A

Pallor
Riddle, spoon shaped fingernails
Muscle weakness
Craving nonnutritive substances

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8
Q

How does milk affect iron deficiency anemia?

A

Milk is not a good source of iron
Milk takes the place of iron, rich, solid foods

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9
Q

By what age should you provide iron supplements for premature low, birthweight infant

A

By age of two months

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10
Q

Play what age should you supply iron supplements if full-term baby is anemic

A

4 to 6 months

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11
Q

What should the infants diet include if they are iron deficient, anemia to help absorb iron?

A

High iron in vitamin C

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12
Q

How do you give iron supplements?

A

One hour before or two hours after milk to prevent decreased absorption
G.I. upset is common
Give with meals
Give with vitamin C
You strong with liquid to prevent staining of teeth

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13
Q

What do you teach a patient who is taking iron supplements?

A

Expects stools to turn Tary Green
Brush teeth after oral dose to prevent staining

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14
Q

What should infants be taking as their dietary source of iron

A

Iron fortified cereals in formula

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15
Q

What is sickle cell disease?

A

A group of diseases in which abnormal sickle hemoglobulin replace his normal adult hemoglobulin

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16
Q

What is sickle cell anemia?

A

The most common form of sickle cell disease, results of RBC sickling, which leads to increased blood viscosity obstruction of blood flow in tissue hypoxia

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17
Q

What is the sickle cell trait

A

Child has genes but is asymptomatic

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18
Q

What is sickle cell crisis?

A

Is the acute exacerbation of sickle cell anemia

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19
Q

What does risk factors of sickle cell anemia?

A

Recessive genetic disorder
African-American
Children who have a tree, but do not manifest. The disease can pass to their offspring.

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20
Q

Expected findings in a child with sickle cell anemia

A

Family history
Reports of pain
SOB
Pallor
Hands and feet cool to touch
Dizziness

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21
Q

What is a vaso-occlusive crisis

A

A painful episode of sickle cell anemia

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22
Q

What is an acute crisis of sickle cell anemia?

A

Usually related to dehydration and decreased oxygen

Severe pain
Swollen joints
Abdominal pain
Hematuria
Visual disturbances

23
Q

What is a chronic crisis of sickle cell anemia?

A

Increased risk of respiratory infection and osteomyelitis
Retinal detachment in blindness
Systolic murmur
Renal failure
Liver cirrhosis

24
Q

What is this Sequestration

A

Excessive pooling of blood primarily in the spleen, and sometimes in the liver

25
What can happen when sequestration occurs?
Where do circulating blood volume results in hypervolemia and can progress to shock
26
What is hypovolemic, shock signs and symptoms
Irritability Tachycardia Pallor Decrease urinary output Tachypnea Cool extremities Thready pulse
27
What is in aplastic crisis in sickle cell anemia?
 Extreme anemia, as a result of temporary decrease RBC production Typically triggered by an infection
28
What does hyper hemolytic crisis?
Increase rate of RBC destruction, leading to anemia, jaundice, or reticulosytosis
29
How do you detect, sickle cell anemia?
CBC
30
What is a transcranial Doppler test
Assess intracranial vascular flow and detect the risk for cerebrovascular accident CVA Annually performed on children ages 2 to 16 who have sickle cell disease
31
What should the nurse do for a patient who has sickle cell anemia?
Promote rest to decrease oxygen consumption Administer oxygen, if hypoxia is President Administer IV fluids with electrolyte Caution, potassium replacement Administer packed red blood cells
32
Medication’s for sickle cell anemia
Opioids and HydroXyurea Increases oxygenation to the cells
33
How can sickle cell anemia cause stroke?
Sickle cells can occlude blood vessels
34
What are signs and symptoms of stroke?
Seizures Abnormal behavior Weakness, or an ability to move extremity Slurred speech Visual changes
35
What is a life-threatening complication of sickle cell anemia?
Acute chest syndrome Common in adolescence Look for pain Fever of, 101.3 or higher. Wheezing Retractions Decrease oxygen saturation
36
What should the nurse do if a patient is in acute chest syndrome
May need a blood transfusion
37
What is hemophilia?
 Bleeding disorders characterized by difficulty, controlling, bleeding, and deficiencies in clotting factors
38
When is bleeding tendencies recognized in infancy
During circumcision
39
What is hemophilia a
Deficiency of factor VIII REFERRED TO AS CLASSIC HEMOPHILIA Most common
40
What is hemophilia B
Deficiency of factor IX Referred to as Christmas disease
41
What is von Willebrand hemophilia?
Inherited lack of the von Willebrand factor proteins, characterized by the inability of platelets to aggregate
42
Expected, finding in patient with hemophilia
Episodes of bleeding Excessive bleeding Impaired mobility Easy bruising Activity intolerance Bleeding gums Tarry stools
43
How do you diagnose hemophilia
DNA testing detects classic hemophilia trait in females
44
What are you do for a patient who has hemophilia?
Administer injections subcutaneous instead of IM Venipunctures our preferred Monitor for blood in urine and stool Do not administer aspirin
45
What is DDAVP
Form of vasopressin that increases plasma factor VIII to treat hemophilia a
46
What should you teach the patient about Hemophilia
Environment should be as safe as possible to prevent injury Set activity restrictions to avoid injury Low contact sports Soft, bristle, toothbrush Up-to-date identification Where medical identification
47
How to control bleeding in hemophilia
Use Acreman, RICE Rest Ice Compression Elevation
48
What can happen if there’s uncontrolled bleeding and hemophilia
Impending shock
49
A nurse is providing teaching about the management of epistaxis to an adolescent, which of the following position should the nurse instruct the adolescent to take when experiencing a nosebleed Set up an lean forward Set up until the head up Lying supine position Lie in a prone position
Sit up and lean forward
50
A nurse is providing teaching about Epistaxis to the parent of a school age child which of the following should the nurse include as an action to take when managing an episode of epistaxis (select) Press the nares together for at least 10 minutes Breathe through the nose until bleeding stops Pekka in or tissue into the nearis that is bleeding Apply warm cloth across the bridge of the nose Insert petroleum into the Nare after the bleeding stops
Press, the nares together for at least 10 minutes Pet, cotton or tissue into the nares that is bleeding
51
A nurse is providing teaching to the parent of a child, who has a new prescription for liquid, oral iron supplements, which of the following statements by the parent indicates an understanding of the teaching “ I should take my child to the emergency department if his stools become dark” “ my child should avoid eating citrus fruits while taking the supplements” “ I should give the iron with milk to help prevent an upset stomach” “ my child to take supplement through the straw”
My child should take the supplement through a straw
52
A nurse is preparing to administer iron dextran IM to a school age child who has iron deficiency anemia, which of the following actions by the nurse is appropriate Administer the dose in the deltoid muscle Use the Z track method when administering the dose Avoid injection more than 2 mL with each dose Massage the injection site for one minute after administering the dose
 Use the Z track method when administering the dose
53
A nurse is caring for an infant who is screening test reveals a potential diagnosis of sickle cell disease, which of the following test should be performed to distinguish is the infant has a tree or the disease Sickle cell solubility test Hemoglobin electrophoresis Complete blood count Transcranial Doppler
Hemoglobin electrophoresis