Hemolytic Anemia Flashcards

1
Q

What are the lab markers for intravascular hemolytic anemia?

A

decrease in free haptoglobin

LDH increases

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2
Q

What are the lab markers for extravascular hemolytic anemia?

A

increase in indirect bilirubin

increase in LDH

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3
Q

What’s the deal with cold agglutinins?

A

IgM (cold weather is Miserable)
occurs w/ EBV or mycoplasma
occurs w/ malignancies, such as CLL
**problem comes when there is circulation to a cold extremity

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4
Q

What’s the deal with warm agglutinins?

A
IgG (warm weather is great)
react against RBC protein antigens at body temp
Seen iN:
EBV, HIV
Lupus
Malignancies: CLL, B cell lymphoma
Congenital Immune abnormalities
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5
Q

Describe a direct coombs test?

A

give patient antibodies that will bind their antibodies (already bound to RBCs) and cause agglutination

seen in hemolytic disease of newborn
drug-induced autoimmune hemolytic anemia
hemolytic transfusion reactions

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6
Q

Describe an indirect coombs test?

A

patient’s serum given normal RBCs. if agglutinate b/c patient has free floating antibodies–>+

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7
Q

What is the treatment for paroxysmal nocturnal hemoglobinuria?

A

terminal complement inhibitor

eculizumab

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8
Q

Crew cut skull on X-ray is indicative of what?

A

thalassemias

sickle cell anemia

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9
Q

What is the treatment for sickle cell anemia?

A

hydroxyurea, increases hbF

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10
Q

What are some complications of sickle cell disease?

A

aplastic crisis w/ parvovirus B19 infection
salmonella osteomyelitis
autosplenectomy–>then howell jolly bodies b/c spleen can’t get rid of them
w/o spleen–>increased risk for encapsulated organisms
splenic infarct/sequestration crisis
painful crises of vaso occlusion like dactylitis and avascular necrosis
renal papillary necrosis

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