Physiology Flashcards

(37 cards)

1
Q

Prolonged APTT is a problem with the

A

Intrinsic pathway

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2
Q

Conditions associated with prolonged APTT

A

Haemophilias

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3
Q

Prolonged PT is a problem with the

A

Extrinsic pathway

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4
Q

Prolonged APTT and Prolonged PT

A

Common Pathway

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5
Q

Describe the steps of the intrinsic pathway and the resulting product

A
XII to XIIa 
XI to XIa
IX to IXa
IXa with the help of VIII allows the conversion of X to Xa 
Final product = Xa
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6
Q

Describe the steps of the extrinsic pathway and the resulting product

A

VII to VIIa with the assistance of TF
Conversion of X to Xa with the help of VII
Final product = Xa

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7
Q

Clotting factors that are part of the intrinsic pathway

A

12, 11, 9 and 8

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8
Q

Clotting factors that are part of the extrinsic pathway

A

Tissue Factor

7

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9
Q

Describe the steps of the common pathway and the resulting product

A

Xa (plus Va) allow the conversion of prothrombin to thrombin
Thrombin allows the conversion of fibrinogen to fibrin
Fibrin and XIIIa produce a fibrin clot
Final product = fibrin clot

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10
Q

Clotting factors that are part of the common pathway

A
10, 5 
Prothrombin (2) 
Thrombin (2a) 
Fibrinogen (1)
Fibrin (1a)
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11
Q

Factor II is also known as

A

Prothrombin

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12
Q

Factor IIa is also known as

A

Thrombin

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13
Q

Factor I is also known as

A

Fibrinogen

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14
Q

Factor Ia is also known as

A

Fibrin

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15
Q

Prothrombin is also known as

A

Factor II

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16
Q

Thrombin is also known as

17
Q

Fibrinogen is also known as

18
Q

Fibrin is also known as

19
Q

Describe the events of fibrinolysis

A

Fibrin is degraded to FDPs which requires plasmin

Plasmin is converted from plasminogen which requires tPA

20
Q

What are involved in fibrinolysis?

What is the final product?

A

Plasmin
Plasminogen
tPA
Final Product = FDPs

21
Q

What are direct Xa inhibitors (2)?

A

Rivoroxiban

Apixaban

22
Q

Anti-thrombin III inhibits…

A

IIa (thrombin)
IXa
Xa

23
Q

General problem in microcytic anaemia

A

Cytoplasmic/haemoglobinisation defects

24
Q

Causes of microcytic anaemia

A

Iron deficiency
Thalassaemia
Congenital Sideroblastic Anaemia

25
Iron deficiency anaemia is a
Microcytic hypochromic anaemia
26
General problem in macrocytic anaemia
Nuclear defects
27
Causes of macrocytic anaemia
``` Megaloblastic = folate deficiency, B12 deficiency Normoblastic = alcohol, liver disease, hypothyroidism ```
28
Difference between megaloblastic and normoblastic macrocytic anaemia
Normoblastic = no problem with DNA synthesis, large size is due to other factors e.g. increased deposition of cholesterol
29
B12 deficiency anaemia is a
Macrocytic megaloblastic normochromic anaemia
30
Anaemia in liver disease is a
Macrocytic normoblastic normochromic anaemia
31
What form is iron absorbed into enterocytes in?
Fe2+
32
What transporter moves iron into enterocytes?
DMT-1
33
Where in the digestive tract is iron absorbed?
Duodenum
34
What transporter exports iron out of the enterocytes into the blood?
Ferroportin
35
What regulates ferroportin expression?
Hepicidin
36
What binds iron in blood?
Transferrin
37
What stores iron?
Ferritin