Hematology and fetal circulation Flashcards

1
Q

What is hematocrit and what percentage of blood is this

A

Hematocrit are red blood cells (erythrocytes)
47% in males, 42% in females

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2
Q

Describe reasons that a patient might present with high or low hematocrit

A

High: High iron, blood doping
Low: Anemia, blood loss

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3
Q

What is 55% of the blood made of

A

Plasma- whole blood

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4
Q

What is 1% of whole blood made of

A

buffy coat- leukocytes, platelets

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5
Q

Which cells make all of the blood cells

A

HSC’s- hematopoietic stem cells

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6
Q

What are the 2 pools of progenitor cells

A

Myeloid- RBC’s, megakaryocytes (make platelets), eosinophils, basophils, neutrophils, monocytes
Lymphoid- make lymphocytes

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7
Q

What is the makeup (in percent) of RBC to WBC in the bone marrow

A

75% WBC (progenitor or maturing)
25% maturing RBCs (Progenitors or maturing)

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8
Q

What is the makeup of RBCs vs WBCs in circulation

A

500x as many RBCs in circulation vs WBCs

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9
Q

Where does extramedullary hematopoiesis occur

A

liver and spleen

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10
Q

Where do we find bone marrow in bones in kids vs adults

A

kids- all through cavities of bones
adults- only ends of long bones and in flat bones

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11
Q

What are platelets

A

fragments of megakaryocytes

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12
Q

What cell is the most abundant in the blood

A

RBC’s

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13
Q

What leukocyte is the most abundent in the blood

A

neutrophils

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14
Q

How much of plasma is made of plasma proteins

A

8%

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15
Q

Life span of RBCs/erythryocyes

A

120 days

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16
Q

How do RBCs make ATP

A

anaerobically

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17
Q

Function of erythryocytes bi-concave shape

A

Allow for swelling, flexibility to push through capilaries, increased surface area

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18
Q

structure of adult hemoglobin

A

2 alpha, 2 beta polypeptide chains (4 total)
an iron (heme) group on each chain (4 total)

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19
Q

What is the test that measures the terminal valine on each beta chain of hemoglobin to measure the 1-2 month average glucose level?

A

Hemoglobin A1c

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20
Q

What is the biggest factor to determine how much oxygen binds to hemoglobin

A

the amount of oxygen present that is creating the diffusion gradient

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21
Q

What are the 2 factors that make it harder for oxygen to bind to hemoglobin

A

high levels of 2,3, BPG or Hydrogen ions
- These both compete w oxygen

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22
Q

What is the significance of carbon monoxide and hemoglobin

A

Carbon monoxide competes with oxygen to bind on hemoglobin, and binds 200x stronger than oxygen(greater affinity)

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23
Q

Structure of fetal hemoglobin

A

Hemoglobin F: 2 alpha chains, 2 gamma hemoglobin chans
Stronger affinity for oxygen than hemoglobin A

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24
Q

Does hemoglobin A or hemoglobin F have a stronger affinity?

A

Hemoglobin F has a stronger affinity for oxygen

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25
What are RBCs produced in response to
Blood loss, high altitude, aerobic exercise training, low o2 levels
26
List the pathway for RBC production
Chemoreceptors in kidneys sense low 02 levels--> release EPO--> stimulate production
27
Where is iron stored after RBC distruction
Liver
28
What is the heme group used to make after RBC destruction
Bilirubin which is stored in the gallbladder for digestion use
29
What is jaundice pathologically
buildup of biliruben in the blood
30
What is the treatment for jaundice
phototherapy- convert biliruben to lumiruben to get rid of it from the blood
31
If you have stem cell damage, what is the resulting anemia
aplastic anemia
32
What anemia is common after chemotherapy
aplastic anemia
33
If you have the distruction of RBCs or loss from bleeding, what type of anemia is this
hemolytic anemia (can be an autoimmune disorder
34
What occurs when a glutamine is exchanged for a valine in terms of anemia?
sickle cell anemia- changes shape of hemoglobin
35
What occurs in hemoglobin with sickle cell anemia
hemoglobin clumps more, higher prevalence in black and hispanic people
36
If you have a lack of hemoglibin due to an inherited blood disorder, what is this
thalassemias
37
What is on the tail of an A antigen
N-acetylgalactososomine
38
What is on the tail of the B antigen
glactose
39
What is on the tail of the antigen on O blood
It does not have anything in addition to the H antigen (every type has H antigen, but nothing extra)
40
What antigen is Rh factor
Antigen D
41
What is universal recipient
AB+ (no antibodies)
42
What is universal donor
O- (no antigens)
43
What do endothelial cells release when they are injured
5-HT
44
What causes the vascular spasm?
Direct injury to smooth muscle, disrupted endothelial cells, local pain receptors stimulated
45
What activates platelets
When platelets contact collagen they activate (swell and become sticky)
46
What do platelets release when activated
ADP, Serotonin, Thromboxane A2
47
End goal of phase 1 of coagulation
Prothrombin activator (Xa) (10a)
48
End goal of phase 2 of coagulation
Thrombin
49
End goal of phase 3 of coagulation
Fibrin
50
End goal of stabilization of coagulation
13a
51
What are the 2 pathways in phase 1, and what do both lead to the formation of?
intrinsic and extrinsic (both lead to the formation of factor X, which forms Xa)
52
What occurs in phase 2 of coagulation
Factor Xa (prothrombin activator) converts prothrombin into thrombin
53
What occurs in phase 3 of coagulation
thrombin converts fibrinogin ( soluble) into fibrin (insoluble)
54
Which phase of coagulation requires Ca
stabilization
55
What is the clot buster, and what activates it?
Plasmin is clot buster (remove clot), activated form of plasminogen, activated by Tissue Plasminogin Activator (TPA)
56
Describe DIC
Uncontrolled clotting in all vessels, followed by bleeding due to the rest of the blood not being able to clot
57
What causes DIC
sepsis, incompatable blood transfusions, pregnancy
58
What does DIC lead to
multiple organ failure, death
59
Describe thrombocytopenia
low platelet count leads to bleeding in small vessels all over the body (petechiae) Platelet count under 50,000/ul blood
60
Treatment of thrombocytopenia
platelet infusion
61
Causes of imparied liver function related to blood disorders
Vitamin K deficiency (common in newborns) Hepatitis or cirrhosis --> reduction of bile to absorb vitamin K, reduction in plasma proteins
62
Hemophilias description and treatment
Hereditary bleeding disorder, missing one or more clotting factor Treated with clotting factor transfusion ( most are x-linked recessive)
63
Describe blood volume restoration when not in a hospital
Severe bleeding causes a low blood volume and in an emergency no time for blood typing or matching. Need to replace immediately, so use normal saline or electrolytes
64
Describe the uterine blood flow in pregnancy
No pregnancy- arteries connect to capillaries and veins, no shuts Preegnant- trophoblast invasion- bore holes in endometrium into maternal sinuses post-partum- return to non-pregnant state
65
Describe the fetal circulation of oxygenated blood
Placenta-->umbilical vein-->through the liver-->IVC-->R atrium-->Foramen ovale-->L atrium-->L ventrical-->Aorta-->Head
66
Describe the fetal circulation of deoxygenated blood
Upper body/head-->SVC-->R atrium-->R ventricle-->Pulm artery-->Ductaus arteriosus-->Aorta-->feet and umbilical arteries
67