Coagulation A Surgical Perspective (Exam III) Flashcards

1
Q

What events occur in primary hemostasis (3)

A

1- vasoconstriction
2- platelet activation
3- platelet plug formation

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2
Q

What events occur in secondary hemostasis (2)

A

1- coagulation cascade
2- formation of fibrin clot

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3
Q

What molecule degrades the blood clot after it has done its job

A

Plasmin

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4
Q

What event initiates hemostasis

A

Vascular injury

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5
Q

What are three phases of hemostasis (normal)

A

1- vascular phase
2- platelet phase
3- coagulation phase

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6
Q

What causes the vasoconstriction following injury to a blow vessel

A

Vascular spasm

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7
Q

First step of the platelet phase

A

Exposed collagen bind and activates platelets

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8
Q

What is the second step of the platelet phase

A

Release of platelet factors

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9
Q

In the third step of the platelet phase after the release of platelet factors

A

Attracts more platelets

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10
Q

In the final step of the platelet phase

A

Platelet plug forms

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11
Q

The plug formed in the platelet phase is:

A

Loose and temporary

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12
Q

What molecule do platelets bind during the platelet phase

A

Collagen

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13
Q

What pathways make up the coagulation phase

A

Intrinsic and extrinsic and common

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14
Q

The common pathway ultimately leads to

A

Cross-linking of fibrin

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15
Q

Name the pathway that involves the conversion to fibrinogen to fibrin

A

Intrinsic and extrinsic

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16
Q

Drug that affects clotting

A

Warfarin

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17
Q

Drug that affects platelets

A

Aspirin

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18
Q

When someone has issues with ____ this results in a bleeding issue

A

Platelets

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19
Q

Partial or complete dissolution of the hemostatic plug by plasmin

A

Fibrinolysis

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20
Q

What activates plasmin

A

Thrombin

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21
Q

List factors affecting a normal hemostasis mechanism (5)

A

1- vessel wall integrity
2- adequate numbers of platelets
3- proper functioning of platelets
4- adequate levels of clotting factors
5- proper function of fibrinolytic pathway

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22
Q

You cannot perform oral surgery if the platelet count is:

A

Less than 50,000

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23
Q

Normal platelet range

A

150,000-400,000

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24
Q

People with a normal number of platelets (150-400k) can still have

A

Issues with platelet function

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25
What medications can affect platelet function
Aspirin Plavix
26
When someone has a platelet deficiency what can be an effective treatment
Platelet diffusion
27
Clotting disorders to be aware of as a clinician
Hemophilia A or B
28
Hemophilia A involves clotting factor
VIII
29
Hemophilia B involves clotting factor
IX
30
Platelet count is measured in a
CBC
31
Common laboratory tests to evaluate hemostasis
Platelet count Bleeding time Coagulation profile
32
What tests make up the coagulation profile (3)
1. Prothrombin time (PT) 2. Activated partial thromboplastin time (APTT) 3. Internationalized normal ration (INR)
33
Advanced tests used to evaluate hemostasis (2)
1. Platelet function tests 2. Clotting factor assays (II-XII)
34
A test that may be recommended for those who bruise easily, have excessive bleeding or taking medications following stroke or heart attack that can alter platelet function
Platelet function test
35
Test that measures the levels of functional activity of one or more coagulation factors
Clotting factor assays (II-XII)
36
Standard range for WBCs
4.5-11.0
37
Standard range for RBCs
3.5-5.5
38
Standard range for Hgb
12-15
39
Standard platelet range
150,000-400,000
40
A platelet count of 100,000-140,000 indicatives
Thrombocytopenia
41
An individual with a platelet count of 100,000-140,000 diagnosed with thrombocytopenia will have a bleeding time that is
Normal
42
What type of procedures can you perform on an individual with mild thrombocytopenia (Platelets 50,000-100,000)
Simple extractions, no major surgeries
43
An individual with a platelet count of 50,000-100,000 is considered to have
Mild thrombocytopenia
44
An individual with mild thrombocytopenia (platelet count 50,000-100,000) will have what kind of bleeding time
Mildly prolonged
45
An individual with a platelet count of less than 50,000 is considered to have
Severe thrombocytopenia
46
What type of oral surgery procedures can you perform on a patient with severe thrombocytopenia
You cannot
47
Individuals with a platelet count of less than 20,000 will have
Spontaneous bleeding
48
How long should it take a precise nick to stop bleeding
2-9 minutes
49
Normal bleeding time
2-9 minutes
50
Bleeding time provides an assessment of
Platelet function
51
A bleeding tie mom 9-15 minutes is indicative of
Platelet dysfunction
52
What test measures the effectiveness of the extrinsic pathway
Prothrombin time (PT)
53
The prothrombin time test measures the rate of conversion of
Factor VII-VIIa
54
Normal prothrombin time
12-13 seconds
55
What are common causes for prolonged prothrombin time (3)
1- warfarin use 2- vitamin K deficiency 3- liver disease
56
Test that measures the effectiveness of the intrinsic and common pathway
Activated partial thromboplastin time (aPTT)
57
Test that measures the intrinsic clotting of blood and congenital clotting disorders
Activated Partial Thromboplastin Time (aPTT)
58
Considered a more sensitive version of the PTT and is used to monitor the patients response to heparin therapy
APTT
59
Normal time frame for APTT
30-40 seconds
60
If a patient has an aPTT of more than 70 seconds that signifies
Spontaneous bleeding
61
Congenital deficiencies of intrinsic system clotting factors such as factors VII, IX, XI, XII including hemophilia A, and hemophilia B can cause a prolonged
APTT
62
Most commonly inherited bleeding disorder affecting patient function
Von Willebrand disease
63
What makes most of the clotting factors, including the vitamin K-dependent ones
Liver
64
Liver cirrhosis can cause a prolonged
APTT
65
The synthesis of some clotting factors requires vitamin K so vitamin K deficiency results in an inadequate quantity of intrinsic system and common pathway clotting factors resulting in a prolonged
APTT
66
Inhibits the intrinsic pathway at several points
Heparin therapy
67
Heparin therapy results in a prolonged
APTT
68
Inhibits the function of factors I, IX, and X, prolonging the APTT
Coumadin therapy
69
Congenital deficiencies of intrinsic clotting factors (8,9,11,12) Von Willebrand disease Liver Cirrhosis Vitamin K deficiency Heparin therapy Coumadin therapy People affected by any of these will have a:
Prolonged aPTT
70
INR stands for
International normalized ratio
71
INR equation is
Patient PT / mean normal PT and raised to the ISI
72
ISI stands for
International sensitivity index
73
The ISI value is normally between
1-2
74
Normal INR level
0.8-1.2
75
Therapeutic INR level
2-3.5
76
An INR range of 2.5 (2-3) is the goal for all of the following circumstances (7)
Atrial fibrillation (AF) Transient ischemic attack (TIA) Ischemic stroke Systemic embolism Mitral stenosis Planned cardio version After open heart surgery
77
We want a slightly higher INR of around 2.5 for patients with conditions that could make them
More prone to a blood clot
78
1. Bleeding time 2. Prothrombin time 3. APTT 4. INR 5. Therapeutic INR
1: 2-9 minutes 2: 12-13 seconds 3: 30-40 seconds 4: 0.8-1.2 5: 2-3.5
79
What bleeding disorders are more common (congenital or acquired)
Acquired
80
Someone taking Ibuprofen, Aspirin or NSAIDs can be at risk for
Compromised platelet numbers
81
What three congenital bleeding disorders constitute over 90% of all bleeding congenital bleeding disorders
Hemophilia A Hemophilia B Von Willebrands disease
82
What has a higher prevalence - hemophilia A or B
A (1 in 10,000)
83
Both hemophilia A and B are inherited in a
Sex-linked recessive manner
84
What sec does hemophilia affect more frequently
Males
85
Bleeding in between joints
Hemoarthrosis
86
The biggest concern is when people have ____ case of hemophilia
Mild
87
Why is mild hemophilia of great concern
Because typically patients are unaware
88
What is prepared from plasma and contains fibrinogen, fibronectin, Von Willebrand factor, Factor 8 and Factor 9 and is given to patients through IV
Cryoprecipitate
89
Desmopressin could be given to a patient with
Hemophilia A
90
What part of hemostasis does Von Willebrands disease effect
Primary
91
There are three types of Von Willebrands Disease: Type I involves: Type II invovles: Types III involves:
Type I - shortage of VWF Type II - flawed VWF Type III- absent VWF
92
Most common form of VWD
Type I
93
The two causes of thrombocytopenia
1- decreased platelet production 2- increased platelet destruction
94
If a patient is on oral anticoagulant/antiplatelet treatment are they recommended to stop use prior to a minor oral surgery procedure?
No
95
The decision to hold an anticoagulant/antiplatelet therapeutic drug can only be made by
Physician (NOT dentist)