BL Garrington lecture review Flashcards

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?

A

Fe+2

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?

A

P50

25
Q

What is P50?

A

The partial pressure of oxygen at which hemoglobin is 50% saturated

26
Q

What environmental conditions alter the shape of the hemoglobin oxygen dissociation curve?

A

pH, CO2, temperature, 2,3-BPG

27
Q

When hemoglobin oxygen dissociation increases (affinity decreases), is oxygen more or less likely to go into tissues?

A

More likely

28
Q

What happens to hemoglobin oxygen affinity when the pH goes down? Up?

A

Shifts to the right (decreased affinity). Shifts to the left (increased affinity)

29
Q

How does CO2 concentration affect the O2 binding curve?

A

When CO2 in the blood stream increases, it decreases pH

30
Q

How does temperature affect hemoglobin oxygen affinity?

A

As temperature increases, oxygen affinity decreases (inverse relationship)

31
Q

How does 2,3-BPG affect hemoglobin oxygen affinity?

A

As 2,3-BPG increases due to RBC anaerobic metabolism, oxygen affinity decreases (inverse relationship)

32
Q

What are Heinz bodies and what causes them?

A

Precipitated hemoglobin and unstable hemoglobin mutations can cause them

33
Q

What are the possible lab findings of a low affinity hemoglobin variant?

A

P50 left shifted, may lead to hemolytic anemia, physical signs of tissue hypoxia

34
Q

What are the possible lab findings of a right affinity hemoglobin variant?

A

P50 right shifted, tissue hypoxia causes increased EPO but no physical signs of hypoxia

35
Q

What is the differential diagnosis of cyanosis?

A

Unstable hemoglobin, methemoglobin, sulfhemoglobinemia, inadequate oxygenation of hemoglobin, drugs/toxins

36
Q

What does blood with too much methemoglobin look like?

A

Chocolate brown color

37
Q

What can cause methemoglobinemia?

A

Cytochrome b5 reductase deficiency (autosomal dominant mutation), drugs/toxins

38
Q

Describe the binding of CO to hemoglobin?

A

Competitive with O2, higher affinity, long half-life

39
Q

What are signs of CO poisoning?

A

Cherry red skin, headache, nausea

40
Q

How does a pulse oximeter work?

A

Uses a photodetector and two emitters to detect levels of deoxy and oxyhemoglobin (660 nm and 940 nm, respectively)

41
Q

Describe ways that a pulse ox can give a false reading.

A

Improper placement, nail polish, deeply pigmented skin, misinterpretation of presense of CO and methemoglobin

42
Q

What conditions are the pulse ox not helpful in detecting?

A

Shock, anemia, CO2 poisoning