A nurse is preparing to administer a lipophilic medication to a client with a high body fat percentage. What should the nurse consider?
The client may require a higher dose of the medication.
The client may require a lower dose of the medication.
The client may require more frequent dosing of the medication.
The client’s body fat percentage does not affect pharmacokinetics.
The Correct Answer is A
Lipophilic medications are soluble in fat and can accumulate in adipose tissue, reducing their concentration in plasma and potentially reducing their therapeutic effect. A client with a high body fat percentage may require a higher dose of a lipophilic medication to achieve therapeutic levels.
b. The client may require a higher, not lower, dose of the medication due to accumulation in adipose tissue.
c. More frequent dosing may not be necessary if an appropriate dose is administered.
d. The client’s body fat percentage can affect pharmacokinetics by altering distribution of lipophilic medications.
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Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is B
Explanation
Medications that are primarily excreted by the kidneys can accumulate in clients with renal impairment, potentially leading to toxicity.A client with renal impairment may require a lower dose of a medication that is primarily excreted by the kidneys to avoid accumulation and toxicity.
a.The client may require a lower, not higher, dose of the medication due to reduced renal excretion.
c.More frequent dosing may not be necessary if an appropriate dose is administered.
d.The client’s renal function can affect pharmacokinetics by altering excretion of medications that are primarily eliminated by the kidneys.
Correct Answer is A
Explanation
P-glycoprotein is a membrane protein that pumps certain drugs out of cells and can affect their absorption, distribution, and elimination. Inhibition of P-glycoprotein can increase the concentration of other medications that are substrates for this protein, potentially increasing their therapeutic effect and the risk of drug interactions.
b. There is an increased, not decreased, risk of drug interactions due to increased concentration of other medications that are substrates for P-glycoprotein.
c. There is an increased risk of drug interactions due to increased concentration of other medications that are substrates for P-glycoprotein.
d. P-glycoprotein inhibition can affect pharmacokinetics by altering absorption, distribution, and elimination of other medications that are substrates for this protein.
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