BL Garrington lecture review Flashcards

(42 cards)

1
Q

Characteristicsof RBCs?

A

Annucleate, biconcave disc, no mitochondria, deformable

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2
Q

Types of Hb?

A

Hb A (alpha and beta), Hb A2 (alpha and delta), Hb F (alpha and Ggamma, A gamma), Hb Gower 1 (lambda and epsilon), Hb Gower 2 (alpha and epsilon), Hb Portland (lambda and gamma)

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3
Q

Does embryonic hemoglobin have higher or lower oxygen affinity than adult hemoglobin?

A

Higher (left shifted curve)

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4
Q

Does fetal hemoglobin have higher or lower oxygen affinity than adult hemoglobin?

A

Higher (left shifted curve)

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5
Q

Does Hb A2 have higher or lower oxygen affinity than adult hemoglobin?

A

Higher (left shifted curve)

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6
Q

In which conditions is Hb A2 elevated?

A

Beta-thalassemia, sickle cell disease, hyperthyroidism, megaloblastic anemia

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7
Q

Numbers of Hb genes?

A

4 alphas on Ch 16, 2 betas on Ch 11

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8
Q

RBC membrane proteins involved in deformability?

A

Ankyrin, spectrin, and actin

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9
Q

RBC metabolism?

A

Anaerobic, depends on G6PD and PDH (for making NADPH and GSH)

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10
Q

Define anemia.

A

RBC deficiency leading to lack of oxygenation to tissues.

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11
Q

General causes of anemia?

A

Lack of RBC production, improper production, hemolysis, bleeding.

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12
Q

Non-neoplastic causes of decreased RBC production?

A

EPO deficiency, Iron deficiency, B12 deficiency, folate deficiency, aplastic anemia

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13
Q

Causes of Iron deficiency?

A

Chronic disease

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14
Q

Neoplastic causes?

A

Leukemia taking up the marrow space

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15
Q

Hemolytic anemias?

A

G6PD deficiency, PDH deficiency, autoimmune hemolytic anemia (cold and warm), transfusion reaction

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16
Q

Hemoglobin disorders?

A

Sickle cell disease, thalassemias (a and b), Hb C, Hb E

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17
Q

WBCs?

A

Neutrophils, Lymphocytes, Monocytes, Eosinophils, Basophils

18
Q

What is the difference between leukemia and lymphoma?

A

Leukemia occurs in the bone marrow. Lymphoma occurs in the lymph organs

19
Q

What is the difference between thrombosis and embolus?

A

Thrombosis is a block that builds up on a blood vessel wall. Embolus is a thrombus that breaks off and travels up to another blood vessels.

20
Q

What valence state must iron be in for proper hemoglobin function?

21
Q

What is Fe+3 hemoglobin called?

A

Methemoglobin

22
Q

When is hemoglobin taut and when is it relaxed?

A

Taut = deoxygenated; Relaxed = oxygenated

23
Q

Define allostery and positive coopertivity.

A

Allostery - a conformation change in other binding sites that occurs when an different binding site is occupied. Positive coopertivity - when the binding of one substrate increases the affinity for another substrate

24
Q

Which value is used to compare oxygen affinities of different hemoglobin?

25
What is P50?
The partial pressure of oxygen at which hemoglobin is 50% saturated
26
What environmental conditions alter the shape of the hemoglobin oxygen dissociation curve?
pH, CO2, temperature, 2,3-BPG
27
When hemoglobin oxygen dissociation increases (affinity decreases), is oxygen more or less likely to go into tissues?
More likely
28
What happens to hemoglobin oxygen affinity when the pH goes down? Up?
Shifts to the right (decreased affinity). Shifts to the left (increased affinity)
29
How does CO2 concentration affect the O2 binding curve?
When CO2 in the blood stream increases, it decreases pH
30
How does temperature affect hemoglobin oxygen affinity?
As temperature increases, oxygen affinity decreases (inverse relationship)
31
How does 2,3-BPG affect hemoglobin oxygen affinity?
As 2,3-BPG increases due to RBC anaerobic metabolism, oxygen affinity decreases (inverse relationship)
32
What are Heinz bodies and what causes them?
Precipitated hemoglobin and unstable hemoglobin mutations can cause them
33
What are the possible lab findings of a low affinity hemoglobin variant?
P50 left shifted, may lead to hemolytic anemia, physical signs of tissue hypoxia
34
What are the possible lab findings of a right affinity hemoglobin variant?
P50 right shifted, tissue hypoxia causes increased EPO but no physical signs of hypoxia
35
What is the differential diagnosis of cyanosis?
Unstable hemoglobin, methemoglobin, sulfhemoglobinemia, inadequate oxygenation of hemoglobin, drugs/toxins
36
What does blood with too much methemoglobin look like?
Chocolate brown color
37
What can cause methemoglobinemia?
Cytochrome b5 reductase deficiency (autosomal dominant mutation), drugs/toxins
38
Describe the binding of CO to hemoglobin?
Competitive with O2, higher affinity, long half-life
39
What are signs of CO poisoning?
Cherry red skin, headache, nausea
40
How does a pulse oximeter work?
Uses a photodetector and two emitters to detect levels of deoxy and oxyhemoglobin (660 nm and 940 nm, respectively)
41
Describe ways that a pulse ox can give a false reading.
Improper placement, nail polish, deeply pigmented skin, misinterpretation of presense of CO and methemoglobin
42
What conditions are the pulse ox not helpful in detecting?
Shock, anemia, CO2 poisoning