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Drug library

Bupivacaine

Local anesthetic

Bupivacaine

Bupivacaine is a long-acting amide local anesthetic used to interrupt sensation at a surgical site or along a regional nerve distribution. It supports local infiltration, peripheral nerve blocks and selected epidural techniques, reducing nociceptive input and the need for systemic analgesics within a multimodal plan. It generally has a slower onset and longer action than lidocaine.

Conventional bupivacaine hydrochloride and liposomal bupivacaine are distinct formulations. Slow release from liposomes can prolong local exposure, but dosing, permitted sites and expected duration cannot be transferred indiscriminately between products.

Group

Local anesthetic

Mechanism of Action

The uncharged fraction of bupivacaine crosses the nerve-cell membrane. Within the cell, drug interacts with voltage-gated sodium channels and limits the sodium influx required to initiate and propagate action potentials. Blocking conduction prevents sensory signals from reaching the central nervous system from the anesthetized region.

The extent of block depends on concentration, dose, tissue environment and the nerve structures exposed. Sensory, motor and autonomic fibers can all be affected, so the result may include muscle weakness or sympathetic blockade as well as analgesia. Regional analgesia therefore differs from simply sedating the animal.

In liposomal products, gradual release from lipid vesicles maintains drug near the administration site for longer. The sodium-channel target remains the same. Excess systemic exposure can also block cardiac sodium channels and affect central neurons, explaining potentially severe cardiovascular and neurologic toxicity.

Dose Rates

Dogs

Use / stageDoseRouteScheduleInstructions
Epidural anesthesiaReference onlyEPIDURALConventional bupivacaine 1–1.5 mg/kg epidurally. Maintain approximately 0.2 mL/kg total volume and no more than 6 mL in large dogs; the volume cap is formulation- and procedure-dependent.

Cats

Use / stageDoseRouteScheduleInstructions
Epidural anesthesiaReference onlyEPIDURALConventional bupivacaine 1–1.5 mg/kg epidurally. Maintain approximately 0.2 mL/kg total volume and no more than 6 mL in large dogs; the volume cap is formulation- and procedure-dependent.

Indications

Contraindications

Interactions

Adverse effects

Toxicity

Systemic toxicity may cause severe cardiac arrhythmias or seizures. The reported feline toxic dose for conventional bupivacaine is 5 mg/kg; this must not be applied to liposomal products.

Preparations

PreparationFormStrengthRoute
Bupivacaine 2.5 mg/mL injection
Conventional hydrochloride solution. Local and peripheral uses are described under Monitoring and Administration.
Injection2.5 mg / mLEPIDURAL
Bupivacaine 5 mg/mL injection
Conventional hydrochloride solution. Local and peripheral uses are described under Monitoring and Administration.
Injection5 mg / mLEPIDURAL
Bupivacaine 7.5 mg/mL injection
Conventional hydrochloride solution. Local and peripheral uses are described under Monitoring and Administration.
Injection7.5 mg / mLEPIDURAL

Monitoring and Administration

Have respiratory support available for epidural procedures. Conventional epidural volume is approximately 0.2 mL/kg and should not exceed 6 mL in large dogs.

A conventional peripheral block commonly uses 0.2 mL/kg of 0.5% solution (1 mg/kg).

Liposomal bupivacaine 13.3 mg/mL: canine tissue infiltration uses 5.3 mg/kg (0.4 mL/kg) once. Feline onychectomy uses 5.3 mg/kg per forelimb, total 10.6 mg/kg per cat, by four-point nerve block; individual nerve-site volumes are 0.02–0.16 mL/kg according to the procedure. Local infiltration and peripheral blocks are outside the calculator route set.

The human multivesicular formulation has also been described at 100–200 mg per site with effect up to 96 hours. Do not substitute this for veterinary liposomal regimens.

For veterinary liposomal infiltration, use a 25-gauge needle and inject slowly. Saline or lactated Ringer’s may be added up to an equal volume; do not use water or incompatible solutions.

Do not use discolored conventional solutions. Liposomal vials are refrigerated and must not be frozen. After drawing up, discard after 4 hours. Unopened liposomal vials may remain at room temperature for up to 30 days and must not be re-refrigerated.

Liposomal bupivacaine is procedure-specific and must not be interchanged with conventional bupivacaine hydrochloride. For the veterinary liposome product, do not administer concurrently with conventional bupivacaine, lidocaine or other amide local anesthetics; a safe separation interval has not been established. Avoid intravascular injection. Use incremental injection with repeated aspiration to reduce inadvertent vascular delivery.

Veterinary use

For veterinary reference. Confirm the indication, dose, route, interval, product strength and any applicable withdrawal period before administration.