Which local anesthetics are amide-type and metabolized in the liver?

Study for the NPLEX II Minor Surgery Test. Prepare with flashcards and multiple-choice questions, offering hints and explanations for each task. Master your exam confidently!

Multiple Choice

Which local anesthetics are amide-type and metabolized in the liver?

Explanation:
Amide-type local anesthetics are cleared primarily by the liver using enzymatic breakdown of the amide bond, rather than by plasma cholinesterases. This makes hepatic metabolism a key factor for their duration and toxicity risk. Among the common agents, lidocaine and bupivacaine are classic amide-type drugs and both are metabolized in the liver. Procaine, on the other hand, is an ester-type local anesthetic that is rapidly hydrolyzed in the blood by plasma cholinesterases, so its clearance relies less on hepatic metabolism. That combination—lidocaine and bupivacaine—fits both criteria: amide-type and liver-metabolized.

Amide-type local anesthetics are cleared primarily by the liver using enzymatic breakdown of the amide bond, rather than by plasma cholinesterases. This makes hepatic metabolism a key factor for their duration and toxicity risk. Among the common agents, lidocaine and bupivacaine are classic amide-type drugs and both are metabolized in the liver. Procaine, on the other hand, is an ester-type local anesthetic that is rapidly hydrolyzed in the blood by plasma cholinesterases, so its clearance relies less on hepatic metabolism. That combination—lidocaine and bupivacaine—fits both criteria: amide-type and liver-metabolized.

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