Complications in Equine Surgery. Группа авторов

13 Complications of Systemic Analgesic Drugs

       Maria Amengual‐Vila DVM, DECVAA, MRCVS1 and Eva Rioja Garcia DVM, DVSc, PhD, DACVAA, DECVAA, MRCVS2

       1 Highcroft Veterinary Referrals, Wirchurch, Bristol, UK

       2 Optivet Referrals, Havant, Hampshire, UK

Overview

      Systemic analgesic medications are commonly used in the horse, and are encouraged for the majority of surgical conditions. There are many different agents available for use in the horse. While they are commonly prescribed, the consequences of extended use are not often considered. This chapter discusses the commonly‐used analgesic agents and the potential complications associated with their use.

List of Complications associated with systemic analgesic drugs

Intra‐Op Complications

      Bradyarrythmias

       Definition

      Bradycardia in horses is considered to be present when the heart rate is below 24 beats per minute. Atrio‐ventricular conduction blocks (AV blocks) occur when the conduction through the AV node is slower than normal and are classified as first‐, second‐ or third‐degree depending on the degree of conduction abnormality. Bradyarrhythmias are commonly associated to the administration of alpha‐2 adrenergic agonists.

       Risk factors

      The severity of bradycardia is dependent on the route of administration of the alpha‐2 adrenergic agonist, with a greater degree of bradycardia associated with an intravenous compared to an intramuscular route.

       Pathogenesis

      Alpha‐2 adrenergic agonists result in sedation, skeletal muscle relaxation and analgesia by activating alpha‐2 adrenergic receptors in the locus coeruleus and the spinal cord. They decrease the central nervous system sympathetic output and peripheral sympathetic tone. Bradycardia is observed within 2 minutes following an intravenous bolus and is initially caused by a baroreceptor reflex in response to vasoconstriction and systemic hypertension caused by alpha‐2b postsynaptic receptor activation in vascular smooth muscle. Bradycardia persists once the hypertension subsides due to the decrease in sympathetic tone. Severe bradycardia due to increased vagal tone and decrease sympathetic outflow predisposes to the development of first‐ and second‐degree AV block, and sometimes third‐degree AV block. Bradycardia contributes to the marked decrease in cardiac output observed following administration of these drugs.

      A retrospective evaluation of detomidine infusion for standing chemical restraint in 51 horses did not report any complications associated with cardiovascular compromise [3]. In the authors’ experience, the bradyarrhythmias associated with the use of alpha‐2 adrenergic agonists are not clinically concerning in most horses.

       Prevention

      The administration of a combination of drugs (i.e. alpha‐2 adrenergic agonist and opioid) reduces the dose required to achieve the same desired effect, sedation and analgesia, and therefore reduces the occurrence or degree of adverse effects. It was observed in horses that the administration of methadone, a pure mu opioid agonist, in combination with detomidine, reduced the duration of the bradycardia and increased and prolonged the hypertension induced by detomidine [4].

      The IV administration of an anticholinergic drug, such as atropine, glycopyrrolate or hyoscine‐N‐butylbromide, 5 minutes before the alpha‐2 adrenergic agonist drug, prevents the decrease in heart rate without affecting the degree of sedation/analgesia. However, these drugs induce a reduction in gastrointestinal motility through antimuscarinic effects on the intestinal M3 receptors and may cause impaction‐type colic. This effect is more pronounced and of longer duration with atropine, and therefore this drug is only used in emergency situations. Low dose of glycopyrrolate [4, 5] or hyoscine [6] administered before or after alpha‐2 adrenergic agonists prevent or reverse the bradycardia and cause shorter duration reduction in gastrointestinal motility compared with atropine. Hyoscine may be alternatively administered intramuscularly 10 minutes before the alpha‐2 adrenergic agonist to avoid the marked increase in heart rate and systemic blood pressure associated with the IV administration [7]. Slow injection of the drug while monitoring the horse for side effects (especially heart rate and blood pressure) should be performed, especially in cardiovascularly compromised horses (i.e. colic) [8].

       Diagnosis

      Bradycardia occurs within minutes of drug administration and it can be easily detected palpating a peripheral artery or with cardiac auscultation. The decrease in heart rate may be mild and short lasting or severe and long lasting, depending on the administered drug, dose and route. When second‐degree AV blocks occur, an intermittent irregular rhythm with missing beats is palpated or heard on auscultation. These blocks can be diagnosed with an electrocardiogram.

       Treatment

      Normally it is not necessary to treat these bradyarrhythmias unless the heart rate is dangerously low (i.e. life threatening).

      The bradycardia and AV conduction disturbances caused by alpha‐2 adrenergic agonists can be antagonized with alpha‐2 adrenergic antagonists such as yohimbine or atipamezole. These antagonists will also counteract the desired sedation and analgesic effect from these drugs and the cardiovascular effects may not be entirely reversed when sedation is withdrawn.

      The administration of anticholinergic drugs such as atropine, glycopyrrolate or hyoscine‐N‐butylbromide, can be used to increase the heart rate without affecting the sedation/analgesia. In cases of extreme bradycardia, the intravenous administration of an alpha‐2 adrenergic antagonist agent, atropine and/or epinephrine (adrenaline), may be necessary.

       Expected outcome

      Alpha‐2 adrenergic agonists are extensively used in horses for sedation/analgesia purposes with a very low incidence of complications. Healthy horses tolerate well their cardiovascular effects. Cardiovascularly