Analgesic Tools for the Small Animal Practitioner
World Small Animal Veterinary Association Congress Proceedings, 2016
Paulo V.M. Steagall, MV, MS, PhD, DACVAA
Department of Clinical Sciences, Faculty of Veterinary Medicine, University of Montréal, Saint-Hyacinthe, QC, Canada

Ferramentas Anestésicas na Clinica e Cirurgia de Pequenos Animais

Several analgesic drugs and techniques may be used in small animal anesthesia in order to reduce intra- and postoperative pain while minimizing side effects and analgesic requirements. These "tools" can be used solely or as part of a balanced anesthesia and multimodal analgesia protocol. The latter involves the use of two or more classes of analgesics that act by different modes of action within the pain pathways, leading to additive or, even synergistic analgesia. Analgesic tools can be used in a cost-efficient and practical manner in the clinical setting. Some of these techniques do not require extensive training skills.

Local anesthetics block transmission of nociceptive afferent input to the CNS by blocking sodium and potassium channels in a reversible manner. They are cost-effective and available worldwide (see lectures on "Basic Concepts on Local Anesthetics" and "Five Blocks Everyone Should Know").

Sustained-release systems include any drug-delivery system that achieves slow release of drug over an extended period of time (hours and/or days) in a controlled manner. Such systems provide "hands-off" analgesia, minimize systemic side effects and drug accumulation, reduce fluctuations in drug plasma concentrations and may not require infusion devices. Long sustained-release formulations of opioid drugs have been shown to provide longer release kinetics, fewer undesirable side effects, and in some cases superior efficacy compared with standard formulations of the same opioid. There has been some evidence that these formulations may be a promising technique to relieve long-term acute pain.1 A topical eutectic mixture of lidocaine and prilocaine or a liposome-encapsulated formulation of lidocaine can be applied to the skin after shaving, and prior to catheterization and/or venous puncture in dogs, cats and small mammals, in order to provide analgesia.2 Absorption of local anesthetic occurs but they are usually below the toxic doses. In this lecture, the application of intraperitoneal analgesia, incisional and intratesticular blocks are discussed as potential "analgesic tools."

Transdermal patches (fentanyl, lidocaine and buprenorphine) are adhesive patches that are placed on the skin to deliver a specific dose of drug through the skin and into the plasma. The patch provides a controlled release of the drug through a rate-limiting porous membrane with a drug reservoir. These patches are usually available in different sizes based on the delivery rate to the systemic circulation across the skin. The recommended location for patch placement includes the dorsal or lateral thorax, or dorsal neck. The onset and duration of action vary according to the drug in use and species, but they can be up to 12–24 h and 72 h, respectively. There may be large individual variability in analgesic plasma concentrations and efficacy. Fentanyl patches have been extensively evaluated in the veterinary literature. This opioid has shown great potential for postoperative analgesia in dogs, but some limitations in the cat due to individual variability and erratic/unpredictable pharmacokinetics (PK).3 Further studies are warranted to identify the analgesic effects of lidocaine and buprenorphine patches in dogs and cats.4 The PK of lidocaine patches have been determined in dogs and cats.5

Dexmedetomidine is an agonist of alpha-2 adrenergic receptors that produces sedation, muscle relaxation and chemical restraint. Lower doses are used for premedication, especially in combination with opioid analgesics. Higher doses are used for sedation and chemical restraint, especially in fractious animals or when immobility is required for radiographs and lancing of abscesses. The drug has also been administered in the early postoperative period to control dysphoria. It smooths anesthetic recovery in healthy patients when administered at 0.5–1 mcg/kg IV. In cats, dexmedetomidine can be given by the buccal route of administration (oral transmucosal) for hands-off, off-label sedation.

Drugs such as fentanyl, morphine, remifentanil, lidocaine, ketamine and/or dexmedetomidine have been used in clinical anesthesia in order to provide better cardiovascular stability by reducing inhalant agent requirements.6 They are commonly administered as infusions. This lecture will present the advantages and disadvantages of the administration of morphine-lidocaine-ketamine infusions. In addition, the combination of these drugs with different pharmacologic mechanisms may provide profound analgesia and even greater inhalant-sparing effect in animals undergoing surgery.

Wound "soaker" catheters are flexible indwelling catheters that are imbedded near or in surgical sites that can be used to deliver continuous or intermittent infusions of local anesthetics for postoperative pain management. These catheters have been used in dogs and cats after major surgery. Although there are very few reports in veterinary medicine about the efficacy of pain management with these catheters, a recent retrospective study showed that the incidence of complications is low7 and the amount of rescue analgesics is considerably less in treated dogs versus non-treated dogs8. This technique is becoming more popular as a pain management adjuvant.

A sacrococcygeal epidural block has been recently described to facilitate catheterization in male cats with urethral obstruction. The technique is performed under aseptic conditions and produces anesthesia of the perineal area, penis, urethra, colon and anus. It is performed preferentially under sedation. This may not be required if the cat is obtunded. Under aseptic conditions, the space between the sacrum and first coccygeal vertebra is palpated. The nondominant index finger identifies the space. A 25-G 1-inch needle is used to penetrate the skin at midline at a 30–45° angle and advanced through the inter-acuate ligament/ligamentum flavum. As the needle is advanced, there should be minimal resistance after entering the epidural space. The needle is repositioned if bone is encountered, or if blood is aspirated. Preservative-free lidocaine 2% (0.1–0.2 mL/kg) is injected. Relaxation of tail and perineal region is normally observed.

This lecture discusses different, practical and cost-effective approaches to pain management in the clinical setting.

References

1.  Krugner-Higby L, Smith L, Schmidt B, et al. Experimental pharmacodynamics and analgesic efficacy of liposome-encapsulated hydromorphone in dogs. J Am Anim Hosp Assoc. 2011;47:185–195.

2.  Wagner KA, Gibbon KJ, Strom TL, et al. Adverse effects of EMLA (lidocaine/prilocaine) cream and efficacy for the placement of jugular catheters in hospitalized cats. J Feline Med Surg. 2006;8:141–144.

3.  Hofmeister EH, Egger CM. Transdermal fentanyl patches in small animals. J Am Anim Hosp Assoc. 2004;40:468–478.

4.  Murrell JC, Robertson SA, Taylor PM, et al. Use of a transdermal matrix patch of buprenorphine in cats: preliminary pharmacokinetic and pharmacodynamic data. Vet Rec. 2007;28:578–583.

5.  Weiland L, Croubels S, Baert K, et al. Pharmacokinetics of a lidocaine patch 5% in dogs. J Vet Med A Physiol Pathol Clin Med. 2006;53:34–39.

6.  Steagall PV, Teixeira Neto FJ, Minto BW, et al. Evaluation of the isoflurane-sparing effects of lidocaine and fentanyl during surgery in dogs. J Am Vet Med Assoc. 2006;229:522–527.

7.  Abelson AL, McCobb EC, Shaw S, et al. Use of wound soaker catheters for the administration of local anesthetic for post-operative analgesia: 56 cases. Vet Anaesth Analg. 2009;36:597–602.

8.  Hardie EM, Lascelles BD, Meuten T, et al. Evaluation of intermittent infusion of bupivacaine into surgical wounds of dogs postoperatively. Vet J. 2011;190:287–289.

  

Speaker Information
(click the speaker's name to view other papers and abstracts submitted by this speaker)

Paulo V.M. Steagall, MV, MS, PhD, DACVAA
Department of Clinical Sciences
Faculty of Veterinary Medicine
University of Montréal
Saint-Hyacinthe, QC, Canada


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