2002
DOI: 10.1016/s0749-0739(02)00011-1
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Use of opioids for pain and anesthetic management in horses

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Cited by 104 publications
(97 citation statements)
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“…Mu opioid agonists have been shown either to increase the MAC of volatile anaesthetics (Pascoe and others 1993, Steffey and others 2003) or to reduce anaesthetic requirement much less than in other species (Thomasy and others 2006). Although not entirely rational, the apparent MAC-increasing effect of some opioids has led a sustained opinion that opioids are not the best of perioperative analgesics to use in horses (Bennett and Steffey 2002). Two studies which failed to demonstrate antinociception after fentanyl or morphine (Sanchez and others 2007, Figueiredo and others 2012) probably add weight to this viewpoint.…”
Section: Discussionmentioning
confidence: 99%
“…Mu opioid agonists have been shown either to increase the MAC of volatile anaesthetics (Pascoe and others 1993, Steffey and others 2003) or to reduce anaesthetic requirement much less than in other species (Thomasy and others 2006). Although not entirely rational, the apparent MAC-increasing effect of some opioids has led a sustained opinion that opioids are not the best of perioperative analgesics to use in horses (Bennett and Steffey 2002). Two studies which failed to demonstrate antinociception after fentanyl or morphine (Sanchez and others 2007, Figueiredo and others 2012) probably add weight to this viewpoint.…”
Section: Discussionmentioning
confidence: 99%
“…75,76 OPIOIDS Opioids (Table 4) are generally indicated in moderate to severe pain, however, their analgesic efficacy in horses compared to other species is less well defined, especially when used in clinically common doses. 60,77,78 At higher doses known to produce significant analgesia or antinociception (e.g., butorphanol, methadone, or morphine ≥ 0.1 mg/kg) opioids commonly provoke central excitatory responses, requiring combination with sedatives such as acepromazine or α 2 agonists (Table 4). 60,77,78 In, addition, they decrease gastrointestinal motility and cause colon impaction, thus limiting their long--term use in animals with chronic laminitis.…”
Section: Nsaidsmentioning
confidence: 99%
“…60,77,78 At higher doses known to produce significant analgesia or antinociception (e.g., butorphanol, methadone, or morphine ≥ 0.1 mg/kg) opioids commonly provoke central excitatory responses, requiring combination with sedatives such as acepromazine or α 2 agonists (Table 4). 60,77,78 In, addition, they decrease gastrointestinal motility and cause colon impaction, thus limiting their long--term use in animals with chronic laminitis. Combining lower doses of µ--opioids with low doses of α 2 agonists (preferably in the form of a constant rate infusion [CRI]) may help achieve a desired level of analgesia by making use of the well known analgesic synergism between the two drug classes, while avoiding the profound CNS stimulatory effects of the opioids and hemodynamic effects of the α 2 agonists (Table 4).…”
Section: Nsaidsmentioning
confidence: 99%
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“…Horses may exhibit mild-to-profound sedation, but excitation and increased locomotion can also occur. 17 Morphine remains an option for providing analgesia to horses undergoing potentially painful procedures 18 ; however, the degree of analgesia can vary from profound to none, and increased excitation may occur.…”
mentioning
confidence: 99%