Module 2.8 Disorders of RBC's Flashcards

1
Q

Until age 5 erythropoiesis occurs where?

A

In almost every bone

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2
Q

After age 20 erythropoiesis occurs where?

A

Vertebra, sternum, ribs, pelvis

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3
Q

Erythropoietin is releases by kidneys in response to

A

low tissue oxygen

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4
Q

Normal reticulocyte count

A

1-2% tells you rate of RBC production

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5
Q

reticulorcyte count in someone being treated for anemia

A

much higher

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6
Q

RBC family tree

A

Pluripotent Stem cell > Normoblast > Reticulocyte > RBC

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7
Q

Transferrin

A

transports iron in blood

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8
Q

Ferritin

A

protein-iron complex for iron storage in liver

Can measure serum ferritin levels.

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9
Q

RBC life span

A

120 days

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10
Q

What happens to heme molecule after RBC degredation

A

converted to bilirubin and transported to liver.

Then is conjugated and made water soluble for elimination via bile

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11
Q

RBC metabolism

A

Glucose dependant

Glucose-6-phosphate dehydrogenase (G6PD) helps release O2.

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12
Q

Methemoglobin

A

Produced in response to exposure to chems like nitrate. Does not release O2 molecule > hypoxia

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13
Q

Hematocrit

A

Volume of RBC’s in 100uL of blood.

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14
Q

RBC count x 3 =

A

Hgb

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15
Q

Hgb x 3 =

A

Hct

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16
Q

Pt with Type A blood has which antibodies

A

B

17
Q

Blood type decribes

A

the antigens on your RBC’s

18
Q

Acute Anemia (trauma) lab results

A

Very low HCT but normal MCV (>80)

19
Q

MCV

A

mean cell volume - normally >80

20
Q

Chronic Anemia (GI bleed compensated by increased RBC production) Lab Results

A

Normal to Low Hct with low MCV (<80)

21
Q

Inherited Hemolytic Anemias

A

Hereditary Spherocytosis (misshapen RBC’s)
Sickle Cell
Thalassemia: a or ß
G6PD deficiency

22
Q

Acquired Hemolytic Anemia

A
Detected with Coombs test
Drugs
toxins
malaria
venoms
23
Q

Hemolytic disease of the newborn

A

ABO incompatibility

Less severe than Rh Incompatibility

24
Q

Meds that can be devastating to people with G6PD deficiency

A

Nitrofunrantoin (Macrobid)
(sulfa) Bactrim
Cipro

25
Q

Extravascular Hemolysis

A

less deformable RBC’s cant travers splenic sinusoids

26
Q

Intravascular hemolysis

A

result of complement fixation

27
Q

Sickle Cell disease heritability

A

Autosomal Recessive

28
Q

Megaloblastic anemia causes

A
Vitamin B12 (cobalamin) deficiency. 
Folic Acid deficiency
29
Q

Vitamin B12 (cobalamin) deficiency causes

A

low meat consumption

Low intrinsic factor from parietal cells in stomach.

30
Q

Neuro changes associated with Vitamin B12 deficiency

A

Parasthesias
Loss of vibratory sensation
Dementia
Psych issues

31
Q

Difference in megaloblastic anemia caused by folic acid deficiency vs B12 deficiency

A

Same but NO NEURO CHANGES

32
Q

Methotrexate

A

chemo med that blocks conversion of inactive to active folic acid.

33
Q

Aplastic Anemia

A

total suppression of bone marrow. hematologic emergency.

34
Q

Types of polycythemia

A

Relative - due to fluid loss

Primary - proliferative disease of bone marrow. Excess production.

Secondary - increased erythropoietin. Caused by hypoxia

35
Q

Causes of hyperbilirubinemia in newborns

A

immature liver
breast feeding - FA’s inhibit bilirubin conjugation
Hemolytic Disease of NB
Hypoxia