Lab Values & Bleeding Disorders Flashcards

1
Q

What is normal hemoglobin range?

A

12-18g/100mL

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2
Q

What is normal hematocrit?

A

35-50%

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3
Q

What is a normal RBC count?

A

4-6 million/mm3

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4
Q

What is a normal WBC count for an infant?

A

8,000-15,000/mm3

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5
Q

What is a normal WBC count for a 4-7 year old?

A

6,000-15,000/mm3

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6
Q

What is a normal WBC count for an 8-18 year old?

A

4,500-13,500/mm3

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7
Q

What is a normal ANC?

A

> 1500/uL

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8
Q

What defines neutrophilia?

A

ANC > 7,000/uL

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9
Q

What defines neutropenia?

A

ANC < 1,000/uL

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10
Q

At what ANC should elective dental care be deferred?

A

ANC < 1,000/uL

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11
Q

At what ANC should antibiotic prophylaxis be provided before dental care?

A

ANC < 2,000/uL

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12
Q

What is a normal platelet count?

A

150-450k/mL

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13
Q

What test evaluates the extrinsic clotting cascade?

A

prothrombin time (PT)

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14
Q

What test evaluates the intrinsic clotting cascade?

A

partial thromboplastin time (PTT)

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15
Q

What is the MOA of anticoagulation of warfarin?

A

Inhibition of Vitamin K reductase involved in synthesis of factors II, VII, IX, X

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16
Q

What is the MOA of anticoagulation of heparin?

A

Blocks inhibitory binding site on antithrombin III enzyme to keep it actively degrading thrombin

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17
Q

What is the MOA of anticoagulation of eliquis?

A

Direct inhibitor of factor Xa

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18
Q

What is the MOA of anti-platelet effects of aspirin?

A

Irreversible inhibition of COX-1, blocking thromboxane synthesis.

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19
Q

What type of hemoglobin is seen in sickle cell disease?

A

Hemoglobin S

20
Q

What is the life span of sickle cell red blood cell?

A

10-20 days

21
Q

What is the 10/30/50 rule for elective dental surgery?

A

Hemoglobin = 10+
Hematocrit = 30% +
Platelet count = 50k +

22
Q

What medication are sickle cell patients often taking?

A

folic acid - helps in proliferation of new RBCs

23
Q

To what age do children with sickle cell disease take daily penicillin to prevent infection?

24
Q

What occurs in sickle cell crisis?

A

sickle RBCs block blood flow to bones and results in intense pain that can last hours - days

25
What occurs in aplastic crisis?
a stop in the production of RBCs
26
Why do you have to be aware of ischemia in sickle cell patients?
can cause tooth pain without the presence of dental caries
27
T/F: nitrous oxide use is contraindicated in patients with sickle cell disease
False
28
What test is prolonged by vitamin K deficiency?
PT (extrinsic pathway)
29
What test is prolonged by hemophilia and von willebrands disease?
PTT (intrinsic pathway)
30
Why can't patients with bleeding disorders take NSAIDs or aspirin?
they both inhibit COX which decreases platelet aggregation and causes bleeding
31
What metabolizes NSAIDs?
kidney
32
What metabolizes acetaminophen?
liver
33
What occurs in von willebrands disease?
deficiency in von willebrand factor affecting platelet adhesion
34
What factor is deficient in hemophilia A?
Factor VIII
35
What factor is deficient in hemophilia B?
Factor IX
36
What factor is deficient in hemophilia C?
Factor XI
37
How is hemophilia inherited?
X-linked recessive
38
What is considered mild hemophilia A?
5-25% factor activity
39
What is considered moderate hemophilia A?
1-5% factor activity
40
What is considered severe hemophilia A?
<1% factor activity
41
What treatment is given to treat von willebrand?
humate P and desmopressin
42
What treatment is given for Hemophilia A?
Desmopressin and/or recombianant factor VIII
43
What treatment is given for hemophilia B?
Benefix
44
How is recombinant factor provided to patients undergoing surgical procedures?
1 infusion gives 60-80% recovery for minor surgeries, repeated every 8-24 hours for major surguries
45
What is Avitene?
topical agent that attracts platelets and triggers aggregation to produce fibrin
46
What is the MOA of aminocaproic acid (Amicar) and Tranexamic acid (Cyclokapron)?
inhibit fibrinolysis mechanism by blocking the binding site of plasminogen
47
What cannot be given to a hemophilia patient for pain control?
NSAIDs or Aspirin