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53 Cards in this Set

  • Front
  • Back

What is "PT"? What does it measure?

Prothrombin Time:


- Tests extrinsic coagulation pathway

What is "PTT"? What does it measure?

Partial Thromboplastin Time:


- Tests intrinsic coagulation pathway

What is "INR"? What does it measure?

International Normalized Ratio


- Reports PT results

What is in PRBCs? Amount?

1U = ~300 mL (+/- 50 mL)



No platelets or clotting factors, can be mixed with NS to infuse faster

What do "platelets" replace?

Replaces platelets with units of platelets (6-10 units from single donor or random donors)

What does FFP replace?

Replaces clotting factors (no RBCs/WBCs/platelets)

What does cryoprecipitate (cryo) replace?

Replaces fibrinogen, von Willebrand factor, and some clotting factors

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

Ionized calcium; the citrate preservative used for storage of blood binds serum calcium

What changes occur in the storage of PRBCs?

- Decreases Ca2+


- Increases K+


- Decreases 2,3-DPG


- Increases H+ (decreases pH)


- Decreases PMNs

What are general guidelines/indications for blood transfusions?

- Acute blood loss, Hgb <10, and history of CAD/COPD


OR


- Healthy symptomatic pt with Hgb <7

What is the rough formula for convering Hgb to Hct?

Hgb x 3 = Hct

One unit of PRBC increases HCT by how much?

~3-4%

Which blood type is the "universal" donor for PRBCs?

O negative

What blood type is the universal donor for FFP?

AB

What is a type and screen?

Pt's blood type is determined and the blood is screened for antibodies; a type and cross from that sample can then be ordered if needed later

What is a type and cross?

Pt's blood is sent to the blood bank and cross-matched for specific donor units for possible blood transfusion

Define thrombocytopenia?

Low platelet count <100,000

What are the common causes of thrombocytopenia in the surgical patient?

- Sepsis


- H2 blockers


- Heparin


- Massive transfusion


- DIC


- Antibiotics


- Spurious lab value


- Swann-Ganz catheter

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

DDAVP (desmopressin)

What common med causes platelets to irreversibly malfunction?

Aspirin (inhibits cyclooxygenase)

What is Plavix

Clopidogrel - irreversibly inhibits platelet P2Y(12)-ADP receptor (blocks fibrin cross-linking of platelets)

What platelet count is associated with spontaneous bleeding?

<20,000

What should the platelet count be before surgery?

>50,000

When should "prophylactic" platelet transfusions be given?

With platelets <10,000 (old recommendation was 20,000)

What is microcytic anemia "until proven otherwise" in a man or post-menopausal woman?

Colon cancer

Why not infuse PRBCs with lactated ringers?

Calcium in LR may result in coagulation within the IV line (use NS)

For how long can PRBCs be stored?

About 6 weeks (42 days)

What is the most common cause of transfusion hemolysis?

ABO incompatibility as a result of clerical error

What is the risk of receiving a unit of blood infected with HIV?

~1 in 1,000,000

What are the symptoms of a transfusion reaction?

Fever, chills, nausea, hypotension, lumbar pain, chest pain, abnormal bleeding

What is the treatment for transfusion hemolysis?

Stop transfusion, provide fluids, perform diuresis (Lasix) to protect kidneys, alkalinize urine (bicarb), and give pressors as needed

What component of the blood transfusion can cause a fever?

WBCs

What is the transfusion "trigger" Hct in young healthy patients?

21%

What is the widely considered "optimal" Hct in a patient with a history of heart disease or stroke?

~30%

When should aspirin administration be discontinued pre-op?

At 1 week, because platelets live 7 to 10 days (must use judgment if pt is at risk for stroke or MI; it may be better to continue and use excellent surgical hemostasis in these patients)

What can move the oxyhemoglobin dissociation curve to the right? Implications?

- Acidosis


- 2,3-DPG


- Fever


- Elevated PCO2


(to the right means greater ability to release O2 to tissues)

What is the normal life of RBCs?

120 days

What is the normal life of platelets?

7-10 days

What factor is deficient in hemophilia A?

Factor VIII (8 sounds like A)

What is the pre-op treatment of hemophilia A?

Factor VIII infusion to >100% normal preop levels

What coag study is elevated in hemophilia A?

PTT


(there are two major hemophilias and two t's in PTT)

What factor is deficient in hemophilia B?

Factor IX

How do you remember which factors are deficient in hemophilia A and B?

Alphabetically and chronologically:


- Hemophilia A = Factor VIII


- Hemophilia B = Factor IX

How are hemophilias A and B inherited?

X-linked recessive

What is von Willebrand's disease?

Deficiency of von Willebrand factor (vWF) and factor VIII:C

How is von Willebrand's disease inherited?

Autosomal dominant

What is used to correct von Willebrand's disease?

DDAVP (desmopressin) or cryoprecipitate (fibrinogen, vWF, some clotting factors)

What coagulation test is abnormal in Hemophilia A, B, and vWF?

- Hemophilia A: PTT (elevated)


- Hemophilia B: PTT (elevated)


- von Willebrand's disease: bleeding time

What is the effect on the coagulation system if the patient has a deficiency in protein C, protein S, or anti-thrombin III?

Hypercoagulable state

What is a "left shift" on a CBC?

Juvenile polymorphonuclear leukocytes (bands)



(Legend has it that the old counters for all the blood cells had the lever for bands on the LEFT of the counter)

What is the usual "therapeutic" INR?

With coumadin, usually shoot for INR of 2-3

What is the most common inherited hypercoagulable state?

Factor V Leiden


(think LEiden = LEader)

What is Xigris? Indication?

Activated protein C, which is used in severe sepsis