presents with an international normalized ratio (INR) of 4.2. His examination shows
no evidence of bleeding. Which action taken by the APN is most appropriate?
correct
1.Hold one or more doses, recheck the INR and adjust the dose accordingly.
2.Treat with 2 mg of vitamin K and adjust the dose accordingly.
3.Treat with protamine sulfate and adjust the dose accordingly.
4.Stop the warfarin and begin treatment with a direct factor Xa inhibitor.
Rationales
Option 1:Toxicity and overdose are usually treated by withholding one or two doses of warfarin.
Option 2:Vitamin K is not needed in this situation.
Option 3:Protamine sulfate is the antidote for heparin toxicity or overdose.
Option 4:This situation is most often remedied by dose adjustment.
Question 2. The anticoagulation effects of warfarin (Coumadin) often do not occur
for 3 to 4 days after initiating treatment. Which of these is the reason for this
phenomenon?
correct
1.The effects of warfarin are dependent on depletion of clotting factors.
2.Warfarin is not well absorbed from the gastrointestinal (GI) tract.
3.Metabolism of warfarin may be delayed in the presence of kidney disease.
4.Foods containing vitamin K interfere with absorption of warfarin from the gastrointestinal (GI)
tract.
Rationales
Option 1:The half-life of clotting factors influenced by warfarin, including factor IIa, may be up to
72 hours.
Option 2:Warfarin is rapidly and completely absorbed when taken orally.
Option 3:Warfarin is metabolized by hepatic micro enzymes and excreted by the kidneys.
Option 4:Vitamin K has an antagonistic effect on warfarin, decreasing the drug's effectiveness,
but this is not the reason for this phenomenon.
Question 3. The APN is reviewing labs for a patient with suspected iron deficiency
anemia (IDA). Which finding would the APN document in the chart after reviewing a
complete blood count with differential?
correct
1.Microcytic hypochromic
2.Macrocytic normochromic
3.Normocytic normochromic
4.Macrocytic
Rationales
, Option 1:Anemias are categorized by size, shape, and color. IDA is typically identified as a
microcytic hypochromic anemia.
Option 2:Macrocytic normochromic is seen in patients who have folic acid deficiency or
pernicious anemia.
Option 3:Normocytic normochromic is seen in 75% of the patients identified with anemia of
chronic disease (ACD) or those who have sickle cell disease (SCD).
Option 4:Macrocytic anemia is seen in patients with folic acid deficiency or pernicious anemia
and is associated with large cell size.
Question 4. Which recommendation should the APN provide to a parent of a child
diagnosed with sickle cell disease (SCD) being treated with hydroxyurea?
correct
1.Inspect oral mucosa daily
2.If you miss a dose, then double up on the next dose
3.Limit fluid intake to 1,000 mL per day
4.Do not take the medication if nausea or vomiting occurs
Rationales
Option 1:Inspect oral mucosa for erythema and ulceration
Option 2:If a dose is missed, do not take it at all; do not double the dose.
Option 3:Hydration is critical in managing SCD. Encourage intake of 2 to 3 L of noncaffeinated
fluid daily.
Option 4:Take the drug exactly as prescribed, even if nausea, vomiting, or diarrhea occurs.
Question 5. Interference of the effectiveness of factor Xa inhibitors such as
rivaroxaban (Xarelto) can occur when given with some drugs. Which drug should
be avoided when rivaroxaban is in use?
correct
1.Phenytoin
2.Penicillin
3.Acetaminophen
4.Digitalis
Rationales
Option 1:Phenytoin and carbamazepine are strong inducers of CYP3A4 and should be avoided
when rivaroxaban is prescribed.
Option 2:Penicillin can alter platelet aggregation, causing increased risk for bleeding when used
in combination with heparin, not rivaroxaban.
Option 3:Concomitant use of acetaminophen with warfarin may potentiate its action causing
increased risk for bleeding, but it has no effect when taken with rivaroxaban.
Option 4:Digitalis may interfere with the anticoagulation effects of heparin, but it has no effect
when taken with rivaroxaban.
, Question 6. There is little risk associated with administration of epoetin alpha;
however, monitoring is necessary to prevent complications. Which of these is a
major adverse effect of epoetin alpha?
correct
1.Hypertension
2.Fatigue
3.Dyspnea
4.Rash
Rationales
Option 1:The major adverse reaction associated with epoetin alpha and darbepoetin alpha is
hypertension.
Option 2:Fatigue is often reduced with administration epoetin alpha and darbepoetin alpha when
anemia is successfully treated.
Option 3:Anemia with associate dyspnea is improved with treatment of these agents. Adult
respiratory distress syndrome (ARDS) may occur in patients with sepsis receiving filgrastim.
Option 4:Although it is a reported adverse reaction to filgrastim, rash is uncommon with use of
epoetin alpha or darbepoetin alpha.
Question 7. An adult male patient has been receiving ongoing therapy for
treatment of pernicious anemia (PA). Which lab value would indicate a potential
complication?
correct
1.Potassium level 2.0 mEq/L
2.Hemoglobin 15.8 g/dL
3.Hematocrit 48%
4.Sodium 138 mEq/L
Rationales
Option 1:The APN should be alert for the potential for hypokalemia as this can occur with
replacement therapies. This value indicates significant hypokalemia which can also
predispose the patient towards cardiac manifestations.
Option 2:This finding indicates a normal range for hemoglobin.
Option 3:This finding indicates a normal range for hematocrit.
Option 4:This finding indicates a normal range for serum sodium level.
Question 8. The APN is evaluating a patient diagnosed with deficiency anemia
(IDA), who has been on iron therapy for 3 months. Which finding requires
intervention?