2014
DOI: 10.1111/vaa.12076
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Sedative and antinociceptive effects of dexmedetomidine and buprenorphine after oral transmucosal or intramuscular administration in cats

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Cited by 42 publications
(28 citation statements)
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References 26 publications
(49 reference statements)
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“…The taste of OTM administered drugs will also influence the degree of absorption. Adverse effects (resentment to administration and salivation) observed in the PD study (Porters et al ., ) and the present study are likely to be caused by the preservative 0.135% chlorocresol in Vetergesic Multidose ® . Hence, preservative‐free buprenorphine is preferable for OTM administration to prevent adverse reactions (Bortolami et al ., ).…”
Section: Pharmacokinetic Parameters Of Dexmedetomidine After Otm (Oramentioning
confidence: 49%
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“…The taste of OTM administered drugs will also influence the degree of absorption. Adverse effects (resentment to administration and salivation) observed in the PD study (Porters et al ., ) and the present study are likely to be caused by the preservative 0.135% chlorocresol in Vetergesic Multidose ® . Hence, preservative‐free buprenorphine is preferable for OTM administration to prevent adverse reactions (Bortolami et al ., ).…”
Section: Pharmacokinetic Parameters Of Dexmedetomidine After Otm (Oramentioning
confidence: 49%
“…Vomiting and salivation were also observed, but not recorded in this study. Observed adverse reactions were comparable to the ones reported in the PD study on the identical drug combination (Porters et al ., ).…”
Section: Pharmacokinetic Parameters Of Dexmedetomidine After Otm (Oramentioning
confidence: 97%
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“…13 Dexmedetomidine, an enantiomer of medetomidine, has been reported to cause vomiting in cats that received the medication at various doses for anesthesia and sedation. [14][15][16][17][18][19] Additionally, dexmedetomidine has been found to be approximately twice as potent as medetomidine. 14 The use of dexmedetomidine hydrochloride as an emetic agent in cats in clinical and research settings has been infrequently reported.…”
mentioning
confidence: 99%
“…Antinociception with dexmedetomidine is mediated primarily through α-2a receptors in the spinal cord (Yaksh, 1985;Takano and Yaksh, 1991;Guo et al, 1996;Zhao et al, 2013), but an effect within the locus coeruleus also produces antinociception (Guo et al, 1996;Funai et al, 2013). The antinociceptive effect of dexmedetomidine has been reported in dogs (Valtolina et al, 2009;van Oostrom et al, 2011) and cats (Slingsby et al, 2009(Slingsby et al, , 2010Porters et al, 2014) but not in conscious horses.…”
Section: Introductionmentioning
confidence: 94%