Cardiopulmonary Effects and Pharmacokinetics of Dexmedetomidine Used as an Adjunctive Analgesic to Regional Anesthesia of the Oral Cavity with Levobupivacaine in Dogs

• Published in: Animals (Basel) Vol. 12; no. 9; p. 1217
• Main Authors: Pavlica, Matic, Kržan, Mojca, Nemec, Ana, Kosjek, Tina, Baš, Anže, Seliškar, Alenka
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 09.05.2022; MDPI
• Subjects: Absorption; adjuvant; Analgesia; Analgesics; Anesthesia; Anesthetics; Bioavailability; Blood pressure; Bradycardia; Cardiac arrhythmia; dog; Dogs; Drug dosages; Heart rate; Hemodynamics; Hypertension; Intravenous administration; Local anesthetics; Mandible; Maxilla; nerve blocks; Oral cavity; Pain perception; Parameters; Pharmacokinetics; Pharmacology; Regional anesthesia; Veterinary medicine; United States > US; nerve blocks; local anesthetics; adjuvant; dog; regional anesthesia
• ISSN: 2076-2615; 2076-2615
• DOI: 10.3390/ani12091217

This study investigated the cardiopulmonary effects and pharmacokinetics of dexmedetomidine (DEX) used as an adjunctive analgesic for regional anesthesia of the oral cavity with levobupivacaine in anesthetized dogs. Forty dogs were randomly assigned to four groups of 10 dogs. All dogs received levobupivacaine (4 blocks) with DEX IO (infraorbital block, = 10) or IA (inferior alveolar block, = 10) or placebo (PLC; = 10) or DEX ( = 10) was injected intravenously (IV) after administration of levobupivacaine. The dose of DEX was always 0.5 µg/kg. Cardiopulmonary parameters were recorded, and blood was drawn for the quantification of DEX in plasma using LC-MS/MS. Heart rate was lower in all LB + DEX groups, while mean arterial pressure (MAP) was higher in the LB + DEX IV and LB + DEX IA groups compared to the LB + PLC IV group. Compared to DEX IV, IO and IA administration resulted in lower MAP up to 2 min after application. Absorption of DEX was faster at IO administration (C and T were 0.47 ± 0.08 ng/mL and 7.22 ± 1.28 min and 0.76 ± 0.09 ng/mL and 7.50 ± 1.63 min for the IO and IA block, respectively). The IA administration resulted in better bioavailability and faster elimination (t was 63.44 ± 24.15 min and 23.78 ± 3.78 min for the IO and IA block, respectively). Perineural administration of DEX may be preferable because of the less pronounced cardiovascular response compared to IV administration.