Platelets, coagulation and bleeding/thrombotic disorders Flashcards

(50 cards)

1
Q

What happens when primary hemostasis aggregates with other platelets?

A

Form a surface for coagulation cascade

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2
Q

In secondary hemostasis, what organ makes most coagulation factors?

A

The liver

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3
Q

3 features of a platelet?

A
  1. Anucleated
  2. Lifespan ~10 days
  3. Circulating platelets do not adhere-during stasis, adhesion occurs
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4
Q

What is primary hemostasis generally initiated by?

A

Injury

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5
Q

Primary hemostasis adheres to subendothelium by interacting with what?

A

von Willebrand factor

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6
Q

In secondary hemostasis, what two things combine to form a stable clot?

A

Fibrin and platelet aggregates

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7
Q

Secondary hemostasis involves a series of what?

A

activating enzymatic conversions

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8
Q

In secondary hemostasis, which factors are vitamin k dependant?

A

Factors II, VII, IX and X

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9
Q

What is an example of a natural anticoagulants and how does it work?

A

protein C

Prevent growth of clot

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10
Q

What is the purpose of fibrinolysis?

A

It breaks down clot

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11
Q

What are 3 ways to asses hemostasis?

A
  • Platelet count (part of CBC)
  • Coagulation cascade (Prothrombin time-PT and partial thromboplastin time-PTT)
  • Fibrinolysis
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12
Q

What might be a reason for prolonged coagulation tests?

A

deficiency or inhibitor of a coagulation factor

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13
Q

What is a pathological counterpart of hemostasis?

A

Thrombotic disorders

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14
Q

What 3 things make up “Virchow’s triad”?

A

Endothelial injury
Abnormal blood flow
Hypercoagulability

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15
Q

6 acquired hypercoagulable states

A
Surgery/trauma
Limb immobilization
Bedridden
Long-distance air travel
Pregnancy
Oral contraceptives
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16
Q

3 causes of blood disorders

A

Abnormal vessels
Decreased platelets/dysfunction
Abnormal factors

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17
Q

What are two causes of platelet-type bleeding?

A

thrombocytopenia, von Willebrand disease

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18
Q

3 causes of Thrombocytopenia

A

Decreased bone marrow production
Hemodilution due to multiple transfusions
Immune reaction due to platelet autoantibodies directed at platelet surface proteins

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19
Q

What platelet count might result in spontaneous bleeding?

A

<10-20,000

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20
Q

What platelet count might result in spontaneous bleeding?

A

<10-20,000

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21
Q

What kind of drugs can increase bleeding tendency?

A

Antiplatelet drugs, such as aspirin

22
Q

What are two inherited abnormalities in coagulation factors?

A

von Willebrand disease, Hemophilia A and B

23
Q

What factor is von Willebrand disease associated with?

24
Q

What are two acquired abnormalities in coagulation factors?

A

liver disease, vitamin K deficiency

25
What factors can alter CBC (complete blood count)?
``` Iron deficiency Medications Alcohol Infections Gender Pregnancy ```
26
What is included in your CBC?
red and white blood cells and platelets
27
What does the leukocyte count include?
all nucleated hematopoietic cells-except red blood cells
28
White blood count is important in evaluating:
infections, some drug effects, radiation therapy
29
What is a normal WBC
3500-10,000 cells/microliter
30
What percent (and total number) of the WBC are neutrophils?
1800-6700 (55%)
31
What percent (and total number) of the WBC are eosinophils?
0-570 (3%)
32
What percent (and total number) of the WBC are lymphocytes?
1400-3900 (35%)
33
Where would your WBC fall if you had leukocytosis?
> 10,000
34
What are 3 causes of leukocytosis?
Chronic infection or inflammation Exercise Some leukemias
35
(T/F) Microcytic anemia is when you have too many cells
False
36
Microcytic patients with an iron deficiency often also have what?
Glossitis
37
What are two causes of microcytic anemia?
Iron deficiency and lead poisoning
38
(T/F) Macrocytic anemia is when you have too many cells
True
39
3 causes of macrocytic anemia
Liver disease Drugs Vitamin B12 or folate deficiency
40
Macrocytic patients beacuse of vitamin B12 or folate deficiency often include what other types of symptoms?
neurological (paresthesia, weakness, dementia)
41
What is leukemia?
systemically distributed neoplasms of white cells
42
Acute myeloid or lymphatic leukemia shows no evidence of what?
maturation in blood or marrow
43
In acute myeloid or lymphatic leukemia, what percentage of cells are blast (immature)?
>20%
44
What type of leukemia can have skin and gum infiltration?
Acute myeloid or lymphatic
45
What are lymphomas, and what are the two specific types?
solid tumors of hematopoietic system/neoplasms of lymphoid tissue Non-hodgkin, and Hodgkin
46
Which type of lymphoma is curable in most patients?
Hodgkin
47
What are the characteristics of non-hodgkin lymphoma?
indolent to very aggressive: survival is years to weeks depending on type
48
Lymphomas usually have (enlarged/reduced), (painless/painful) lymphadenopathy
Enlarged, painless
49
Both hodgkins and non-hodgkins are __________ ____________ at various developmental stages.
Clonal expansions
50
Both hodgkins and non-hodgkins are __________ ____________ at various developmental stages.
Clonal expansions