Pharmacokinetics in Patients with Hepatic Dysfunction
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Questions and Answers

How does liver dysfunction impact drug pharmacokinetics?

  • Increases blood/plasma clearance
  • Reduces the extent of drug absorption
  • Decreases plasma protein binding
  • Affects presystemic elimination of high extraction drugs (correct)

In advanced liver cirrhosis, what effect can portal-systemic shunting have on drug pharmacokinetics?

  • Enhances drug metabolism
  • Decreases CYP450 enzyme activity
  • Reduces presystemic elimination of high extraction drugs (correct)
  • Increases plasma protein binding

How are drug-metabolizing activities affected in chronic liver diseases?

  • Uniform increase in all CYP450 enzyme activities
  • Enhancement of all drug metabolism processes
  • Improved presystemic elimination
  • Greater reduction in glucuronidation than in CYP450 metabolism (correct)

Why is it important to consider hepatic dysfunction when adjusting drug dosages?

<p>To account for variable reductions in drug-metabolizing activities (D)</p> Signup and view all the answers

What is the main purpose of the recommendations from the FDA and EMEA discussed in the text?

<p>To generate specific dosage recommendations for patients with hepatic dysfunction (D)</p> Signup and view all the answers

Why is further research needed, according to the text?

<p>To develop more sensitive liver function tests for drug dosage adjustment (A)</p> Signup and view all the answers

Which parameter is highlighted as not only the most important biotransformation site but also crucial for drug pharmacokinetics?

<p>The liver (C)</p> Signup and view all the answers

What does the text suggest as a key area for future development in drug dosage adjustment?

<p>More sensitive liver function tests (B)</p> Signup and view all the answers

Why is it necessary to adjust drug dosages in patients with advanced cirrhosis?

<p>Because impaired renal function affects drug elimination in these patients (D)</p> Signup and view all the answers

What is a limitation of the Child-Pugh score in adjusting drug dosages for patients with liver dysfunction?

<p>It lacks sensitivity to quantitate the liver's specific ability to metabolize individual drugs (B)</p> Signup and view all the answers

Which statement is true regarding liver tests to predict drug elimination capacity in cirrhotic patients?

<p>They use marker substrates like galactose and sorbitol to evaluate liver function (B)</p> Signup and view all the answers

Why are cirrhotic patients more sensitive to the adverse effects of certain drugs?

<p>As a result of impaired liver function impacting drug pharmacokinetics (C)</p> Signup and view all the answers

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