SR 19 - Blood and Blood Products Flashcards

1
Q

Define - PT

A

Prothrombin time

Tests extrinsic coagulation pathway (Warfarin)

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2
Q

Define - PTT

A

Partial Thromboplastin Time

Tests intrinsic coagulation pathway (Heparin)

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3
Q

Define - INR

A

International normalized ratio (reports PT results)

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4
Q

Define - PRBC

A

Packed red blood cells
One unit - 300mL
No platelets or clotting factors
Can be mixed with NS to infuse faster
Remember - RBCs have the antigens - so O is the universal RBC donor (they have no antigens for plasma antibodies to react against)
-/+ only really matters for girls who still may get pregnant at some point

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5
Q

Define - FFP

A

Fresh frozen plasma
Replaces clotting factors
No RBCs, WBCs, platelets
Remember - plasma has the antibodies - so AB is the universal plasma donor (Since they both antigents, they cannot have AB antibodies swimming around in their blood)

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6
Q

Define - Cryoprecipitate

A

Replaces fibrinogen, von Willebrand factors, some clotting factors

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7
Q

Which electrolyte is most likel to fall with the infusion of stored blood? Why?

A

Ionized calcium

The citrate preservative used for the storage of blood binds serum calcium

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8
Q

What changes occur in the storage of PRBCs?

A
Decreased Calcium
Decreased 2,3-DPG
Decreased pH
Decreased PMNs
Increased potassium
Increased hydrogen
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9
Q

What are generaly guidlines for blood transfusions?

A

Acute blood loss, history of CAD/COPD - Hb

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10
Q

Which blood type is the universal donor for PRBCs?

A

O negative

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11
Q

Which blood type is the universal donor for FFP?

A

AB

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12
Q

What is type and screen?

A

Determine blood type and screen for antibodies

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13
Q

What is type and cross?

A

Cross-matched with specific donor units for possible transfusion

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14
Q

Define thombocytopenia

A

Low platelet count

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15
Q

Common causes of thrombocytopenia in the surigcal patient?

A
Sepsis
H2 blockers
Heparin
Massive transfusion
DIC
Antibiotics
Spurious lab value
Swan-Ganz catheter
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16
Q

What can be given to correct platelet dysfunction from uremia, ASA or bypass?

A

DDAVP (desmopressin)

Leads to increased levels of coagulation factor (F) VIII, von Willebrand factor (vWF), and tissue plasminogen activator

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17
Q

What common medication causes platelets to irreversibly malfunction?

A

ASA

Inhibits cyclooxygenase

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18
Q

What is Plavix?

A

Clopidogrel
Irreversibly inhibits platelet P2Y12 ADP receptor
Blocks fibrin crosslinking of platelets

19
Q

What platelet cout is associated with sponatneous bleeding?

20
Q

How high should the platelet count be before surgery?

21
Q

When should ‘prophylaxtic’ platelet transfusion be given?

22
Q

What is microcytic anemia ‘until proven otherwise’ in a man or postmenopausal woman?

A

Colon cancer

23
Q

Why not infuse PRBCs with LR?

A

Calcium in LR may result in coagulation within the IV line

Use NS

24
Q

How long can PRBCs be stored?

A

6 weeks (42 days)

25
What is the most common cause of transfusion hemolysis?
ABO incompatibility as a result of clerical error
26
What are the symptoms of a transfusion reaction?
``` Fever Chills Nausea Hypotension Lumbar pain Chest pain Abnormal beleding ```
27
What is the treatment for transfusion hemolysis?
``` Stop transfusion Profide fluids Perform diuresis (with lasix) to protect kidneys Alkalinize urine with bicarb Pressors as needed ```
28
What component of the blood transfusion can cause a fever?
WBCs
29
What is the transfusion 'trigger' Hct in young healthy patients?
21%
30
What is the 'optimal' Hct in a patient with a history of heart disease and stroke?
30%
31
When should ASA administration be discontinued preoperatively?
1 week Platelets live for 7-10 days (Use clinical judgement if patient is at risk for MI or stoke, may be better to continue the ASA and use excelelent surgical hemostasis instead)
32
What can move the oxyhemoglobin dissociation curve to the right?
Acidosis 2,3-DPG Fever Elvated Pco2 To the right means better unloading of O2 (Right = release)
33
What is the normal life of RBCs?
120 days
34
What is the normal life of platelets?
7-10 days
35
What factor is deficient in hemophilia A? What coagulation study is elevated?
Factor VIII | PTT
36
What is the preoperative treatment of hemophilia A?
Factor VIII infusion to 100%+ normal preoperative levels
37
What factor is deficient in hemophilia B? Elevated coagulation study?
Factor IX | PTT
38
What is von Willebrand's disease? Elevated coagulation study?
Deficiency of vWF and factor VIII-C Autosominal dominant Bleeding time
39
What is used to correct vWF deficiency?
DDAVP or cryoprecipitate
40
What is the effect on the coagulation system if the patient has a deficiency in protein C, protein S, or antithrombin III?
A hypercoagulable state
41
What is a 'left shift' on a CBC?
Juvenile polymorphonuclear leukocytes (bands)
42
What is the most common inherited hypercoagulable state?
Factor V leiden
43
What is Xigris?
Actived protein C | Which is used in severe sepsis