Buprenorphine Dosing for Feline Pain Management
For an adult cat (2-8 kg) with moderate to severe pain when NSAIDs are contraindicated, administer buprenorphine 0.02-0.04 mg/kg intravenously or intramuscularly every 6-8 hours for optimal analgesia. 1
Route-Specific Dosing Recommendations
Preferred Routes for Acute Pain
- Intravenous or intramuscular administration at 0.02-0.04 mg/kg is the gold standard for acute pain management in cats, providing reliable onset and duration of analgesia 1
- The subcutaneous route at standard clinical dosages does not provide adequate antinociception and should be avoided 1
- Buccal (oral transmucosal) administration has produced inconsistent results and is not recommended as a primary route 1
High-Dose Formulations for Extended Analgesia
- Doses up to 0.12-0.24 mg/kg subcutaneously using high-concentration formulations can provide prolonged antinociception lasting 24-30 hours in a single injection 2
- These higher doses have demonstrated no ceiling effect for analgesia and no adverse effects in clinical studies 2
- The traditional 0.01-0.02 mg/kg dosing range commonly cited is likely suboptimal for many cats with moderate to severe pain 3, 1
Pharmacokinetic Considerations Critical to Dosing
Delayed Onset Phenomenon
- Do not expect immediate pain relief after administration—buprenorphine exhibits negative hysteresis, meaning plasma concentrations are not correlated with immediate analgesic effect 1
- The pharmacokinetic-pharmacodynamic relationship is best described by a receptor association-dissociation model with delayed equilibration to the effect compartment 1
- Clinical analgesia typically begins 15-30 minutes after IV/IM administration, with peak effects at 1-2 hours 2
Duration of Action
- Standard doses (0.02 mg/kg) provide analgesia for approximately 6-8 hours 3, 1
- Higher doses (0.12-0.24 mg/kg) extend duration to 24-30 hours 2
- Elimination half-life varies dramatically with dose: 1.4-5.3 hours at 0.02 mg/kg versus 10-34 hours at higher doses (0.12-0.24 mg/kg) 2
Novel Transdermal Formulations
Extended-Duration Transdermal Solution
- A transdermal buprenorphine solution (TBS) provides 4 days of analgesia from a single preoperative dose 4, 5
- Approved dosing: 8 mg for cats 1.2-3 kg; 20 mg for cats >3-7.5 kg (equivalent to 2.7-6.7 mg/kg) 5
- Applied topically to unclipped dorsal cervical skin with peak plasma concentrations occurring at 2-12 hours post-application 4
- Absolute bioavailability is 16% with terminal half-life of approximately 65 hours due to flip-flop kinetics 4
- Safety demonstrated at 3X the approved dose with minimal adverse effects 5
Important Clinical Caveats
Individual Variability
- Significant individual variability in response to buprenorphine has been documented—some cats may not achieve sufficient analgesia even at appropriate doses 1
- Pain assessment using validated feline pain scales is essential to determine if additional or alternative analgesia is needed 1
Expected Physiological Effects
- Transient sedation, mydriasis, and euphoria are normal within 4 hours of administration 4, 5
- Body temperature may increase 0.6-0.9°C above baseline (normal 37.4-37.8°C) and persist through the duration of effect 4, 5
- These effects diminish with repeated dosing due to accommodation 5
Safety Profile
- No ceiling effect for analgesia has been demonstrated at clinical doses in cats, contrary to concerns extrapolated from human medicine 1, 2
- Respiratory depression is minimal even at doses up to 0.24 mg/kg 2
- Constipation occurs transiently but at similar rates to placebo-treated cats 5
Dosing Algorithm for Clinical Practice
For acute moderate-to-severe pain:
- Administer 0.02-0.04 mg/kg IV or IM initially
- Reassess pain at 1-2 hours (peak effect window)
- Redose every 6-8 hours as needed based on pain scores
For postoperative pain requiring extended coverage:
- Consider high-dose formulation (0.12-0.24 mg/kg SC) for 24-30 hour duration
- Or apply transdermal solution (8-20 mg based on weight) preoperatively for 4-day coverage
For chronic pain:
- Standard dosing every 8 hours is appropriate (0.02 mg/kg IV/IM)
- Transdermal formulation may improve compliance for home management