Ch. 21: Hematologic Disorders-Sickle Cell Anemia & Hemophilia Flashcards

1
Q

Sickle cell disease (SCD) is a group of diseases in which abnormal sickle _____ replaces normal adult hemoglobin (Hgb A)

A

Hemoglobin S (HbS)

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2
Q

What is the most common form of SCD?

A

Sickle cell anemia is the homozygous and most common form of SCD

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3
Q

Manifestations and complications of SCA are the result of _____, which leads to increased ______, obstruction of ____, and tissue ____.

A

Result of RBC sickling which lead to

  • increased blood viscosity
  • obstruction of blood flow
  • tissue hypoxia
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4
Q

Why are manifestations of SCA not usually apparent until later in infnancy?

A

Due to the presence of fetal Hgb

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5
Q

What causes the pain from SCA?

A

Tissue hypoxia, which causes ischemia, which results in pain

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6
Q

What is sickle cell crisis?

A

The exacerbation of SCA

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7
Q

SCD is what kind of disorder?

A

An autosomal recessive genetic disorder

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8
Q

Who does SCA primarily affect? Can it affect others?

A

Primarily African American, other forms of SCD are individuals of Mediterranean, Indian, or Middle Eastern descent

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9
Q

T/F: Children with sickle cell trait do not manifest the disease.

A

True…but they can pass the trait to their offspring

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10
Q

What are S&S of SCA?

A
SOB
Fatigue
Pallor/pale mucous membranes
Jaundice
Hands and feet cool to touch
Dizziness
Headache
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11
Q

SCA: What is a vaso-occulsive crisis and how long does it last?

A

A painful episode and it lasts 4-6 days

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12
Q

SCA: What are the acute signs of vaso-occulsive crisis?

A
  • Severe pain (bones, joints, abdomen)
  • Swollen joints, hands, and feet
  • Anorexia, Vomiting, fever
  • Hematuria
  • Obstructive jaundice
  • Visual disturbances
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13
Q

SCA: What are the chronic signs of vaso-occulsive crisis?

A
  • Increased resp. infections and osteomyelitis
  • Retinal detachment and blindness
  • Systolic murmur
  • Renal failure and enuresis
  • Liver cirrhosis; hepatomegaly
  • Seizures
  • Skeleteal deformities; shoulder or hip avascular necrosis
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14
Q

SCA: What is sequestration?

A

Excessive pooling of blood primarily in the spleen (splenomegaly) and sometimes in the liver (hepatomegaly)

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15
Q

SCA: Sequestration–reducing circulating blood volume results in ____ and can progress to ___

A

Hypovolemia..progress to shock

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16
Q

SCA: Sequestration–What are the signs of hypovolemic shock?

A
Irritability
Tachycardia
Pallor
Decreased urinary output
Tachypnea
Cool extremities
Thready pulse
Hypotension
17
Q

SCA: Aplastic crisis..What is it and what is it usually triggered by?

A

Extreme anemia as a result of decreased RBC production

Triggered by infection

18
Q

SCA: What is hyper hemolytic crisis?

A

Increased rate of RBC destruction leading to anemia, jaundice, and/or reticulocytosis

19
Q

Is screening for SCA a mandatory thing for newborns?

A

Yes, in most states

20
Q

What lab test detects anemia?

A

CBC

21
Q

What lab test is a screening tool that detects the presence of HbS. What does this test NOT do?

A

Detects the presence of HbS= Sickledex (sickle-turbidity)…This test DOES NOT differentiate the trait from the disease!

22
Q

What is the definitive diagnosis of sickle cell anemia? What does this test do?

A

Hemoglobin electrophoresis–separates the various forms of Hgb

23
Q

What happens in lab findings during a sickle cell crisis?

A
  • Hgb= decreased
  • WBC, biliruben, reticulocyte levels= elevated
  • Peripheral blood smear reveals sickled cells
24
Q

What is the transcranial dropper (TCD) test and how often is this done?

A

Assesses intracranial vascular flow and detects the risk for CVA–done annually on children ages 2-16 who have SCD

25
Q

SCA: Should we promote rest or exercise?

A

Rest–to decrease oxygen consumption