Bupivacaine

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Bupivacaine: Uses, Dosage and Side Effects

Bupivacaine: Uses, Dosage and Side Effects

Overview

  • Reversible blockade of the sodium channel in nerve fibers produces local anesthesia.

Uses of Bupivacaine

Provision of analgesia by perineural nerve blocks, regional and epidural techniques.

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Dose of Bupivacaine in Dogs and Cats

Dogs:

• Perineural: volume of injection depends on the site of placement and size of the animal.

  • 0.1 ml/kg per injection site for femoral and sciatic nerve blocks.
  • 0.1 ml/kg for each of the three injection sites for the combined radial, ulnar, musculocutaneous, and median nerve blocks.
  • 0.3 ml/kg for brachial plexus nerve block.
  • 0.25–1 ml total volume for blockade of the infraorbital, mental, maxillary and mandibular nerves.

Choose an appropriate concentration of bupivacaine to achieve a 1–2 mg/kg dose within these volume guidelines.

• Epidural:

  • 1.6 mg/kg (analgesia to the level of L4).
  • 2.3 mg/kg (analgesia to the level of T11–T13).
  • 1 mg/kg bupivacaine combined with preservative-free morphine 0.1–0.2 mg/kg.

Limit the total volume of solution injected into the epidural space to 1 ml/4.5 kg up to a maximum volume of 6 ml in order to limit the cranial distribution of drugs in the epidural space and prevent adverse pressure effects.

• Interpleural:

1 mg/kg diluted with normal saline to a total volume of 5–20 ml depending on the size of the animal. The solution can be instilled via a thoracotomy tube. Dilution reduces pain on injection due to the acidity of bupivacaine.

Cats:

Doses as for dogs. Accurate dosing in cats is essential to prevent overdose.

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Side Effects of Bupivacaine in Dogs and Cats

The inadvertent intravascular injection may precipitate severe cardiac arrhythmias that are refractory to treatment.

Contraindications of Bupivacaine in Dogs and Cats

  • Do not give i.v. or use for i.v. regional anesthesia.
  • Use of bupivacaine with adrenaline is not recommended when local vasoconstriction is undesirable (e.g. end arterial sites) or when a significant degree of systemic absorption is likely.

Some Notes:

  • Onset of action is significantly slower than lidocaine (20–30 minutes for epidural analgesia) but duration of action is relatively prolonged (6–8 hours).
  • Lower doses should be used when systemic absorption is likely to be high (e.g. intrapleural analgesia).
  • Small volumes of bupivacaine can be diluted with normal saline to enable wider distribution of the drug for perineural blockade.
  • Doses of bupivacaine up to 2 mg/kg q8h are unlikely to be associated with systemic side effects if injected perineurally, epidurally or intrapleurally.
  • Combining bupivacaine with lidocaine can prolong the duration of the sensory block while limiting the duration of the motor block compared with the administration of bupivacaine alone.
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