Klinické zhodnocení kombinace medetomidinu-opioidního agonisty, -parciálního agonisty a agonisty/antagonisty pro premedikaci celkové anestezie u psů
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62157124%3A16170%2F03%3A00000382" target="_blank" >RIV/62157124:16170/03:00000382 - isvavai.cz</a>
Výsledek na webu
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DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Clinical evaluation of medetomidine-opioid agonists, -partial agonists and -mixed agonist/antagonists combination for anesthesia premedication in the dog
Popis výsledku v původním jazyce
The goal of the study is to emphasise clinically significant properties of medetomidine - opioids combinations. Total of 90 dogs were included to the study, in which various painful procedures had been performed. Dogs were divided into three groups. In the FEN group medetomidine 0.01 mg/kg (n=30) had been given with fentanyl 0.01 mg/kg bolus following by 0.01 mg/kg/hr infusion. The BUT group (n=30) presented combination of medetomidin 0.01 mg/kg with butorphanol 0.2 mg/kg bolus only. The BUP group (n=30) had been given medetomidine 0.01 mg/kg with buprenorphine 0.01 mg/kg. All combinations were used as a bolus mixed in one syringe. Anesthesia induction had been facilitate by propofol administration and then maintained by O<sub>2<sub>/N<sub>2<sub>O/halothane inhalation. Insufficient depth of anesthesia was solved by propofol readministration. As main criteria, the level of sedation, initiative dose of propofol, as well as the need of its readministration had been observed. Furth
Název v anglickém jazyce
Clinical evaluation of medetomidine-opioid agonists, -partial agonists and -mixed agonist/antagonists combination for anesthesia premedication in the dog
Popis výsledku anglicky
The goal of the study is to emphasise clinically significant properties of medetomidine - opioids combinations. Total of 90 dogs were included to the study, in which various painful procedures had been performed. Dogs were divided into three groups. In the FEN group medetomidine 0.01 mg/kg (n=30) had been given with fentanyl 0.01 mg/kg bolus following by 0.01 mg/kg/hr infusion. The BUT group (n=30) presented combination of medetomidin 0.01 mg/kg with butorphanol 0.2 mg/kg bolus only. The BUP group (n=30) had been given medetomidine 0.01 mg/kg with buprenorphine 0.01 mg/kg. All combinations were used as a bolus mixed in one syringe. Anesthesia induction had been facilitate by propofol administration and then maintained by O<sub>2<sub>/N<sub>2<sub>O/halothane inhalation. Insufficient depth of anesthesia was solved by propofol readministration. As main criteria, the level of sedation, initiative dose of propofol, as well as the need of its readministration had been observed. Furth
Klasifikace
Druh
D - Stať ve sborníku
CEP obor
FP - Ostatní lékařské obory
OECD FORD obor
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Návaznosti výsledku
Projekt
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Návaznosti
Z - Vyzkumny zamer (s odkazem do CEZ)
Ostatní
Rok uplatnění
2003
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název statě ve sborníku
8th World Congress of Veterinary Anesthesia
ISBN
5400-5166
ISSN
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e-ISSN
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Počet stran výsledku
1
Strana od-do
138
Název nakladatele
University of Tennessee
Místo vydání
Knoxville, Tennessee, USA
Místo konání akce
Knoxville, Tennessee, USA
Datum konání akce
16. 9. 2003
Typ akce podle státní příslušnosti
WRD - Celosvětová akce
Kód UT WoS článku
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