Effect of medetomidine-butorphanol and dexmedetomidine-butorphanol combinations on intraocular pressure in healthy dogs
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62157124%3A16170%2F12%3A43871417" target="_blank" >RIV/62157124:16170/12:43871417 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1111/j.1467-2995.2011.00703.x" target="_blank" >http://dx.doi.org/10.1111/j.1467-2995.2011.00703.x</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1111/j.1467-2995.2011.00703.x" target="_blank" >10.1111/j.1467-2995.2011.00703.x</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Effect of medetomidine-butorphanol and dexmedetomidine-butorphanol combinations on intraocular pressure in healthy dogs
Popis výsledku v původním jazyce
Objective To assess the effects of intravenous (IV) medetomidine-butorphanol and IV dexmedetomidine-butorphanol on intraocular pressure (IOP). Study design Prospective, randomized, blinded clinical study. Animals Forty healthy dogs. Mean +/- SD body mass37.6 +/- 6.6 kg and age 1.9 +/- 1.3 years. Methods Dogs were allocated randomly to receive an IV combination of dexmedetomidine, 0.3 mg m-2, combined with butorphanol, 6 mg m-2, (group DEX) or medetomidine 0.3 mg m-2, combined with butorphanol 6 mg m-2,(group MED). IOP and pulse (PR) and respiratory (fR) rates were measured prior to (baseline) and at 10 (T10), 20 (T20), 30 (T30) and 40 (T40) minutes after drug administration. Oxygen saturation of hemoglobin (SpO2) was monitored following sedation. Data were analyzed by anova followed by Dunnetts tests for multiple comparisons. Changes were considered significant when p { 0.05. Results Following drug administration, PR and fR were decreased significantly at all time points but did not
Název v anglickém jazyce
Effect of medetomidine-butorphanol and dexmedetomidine-butorphanol combinations on intraocular pressure in healthy dogs
Popis výsledku anglicky
Objective To assess the effects of intravenous (IV) medetomidine-butorphanol and IV dexmedetomidine-butorphanol on intraocular pressure (IOP). Study design Prospective, randomized, blinded clinical study. Animals Forty healthy dogs. Mean +/- SD body mass37.6 +/- 6.6 kg and age 1.9 +/- 1.3 years. Methods Dogs were allocated randomly to receive an IV combination of dexmedetomidine, 0.3 mg m-2, combined with butorphanol, 6 mg m-2, (group DEX) or medetomidine 0.3 mg m-2, combined with butorphanol 6 mg m-2,(group MED). IOP and pulse (PR) and respiratory (fR) rates were measured prior to (baseline) and at 10 (T10), 20 (T20), 30 (T30) and 40 (T40) minutes after drug administration. Oxygen saturation of hemoglobin (SpO2) was monitored following sedation. Data were analyzed by anova followed by Dunnetts tests for multiple comparisons. Changes were considered significant when p { 0.05. Results Following drug administration, PR and fR were decreased significantly at all time points but did not
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
FP - Ostatní lékařské obory
OECD FORD obor
—
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2012
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Veterinary anaesthesia and analgesia
ISSN
1467-2987
e-ISSN
—
Svazek periodika
39
Číslo periodika v rámci svazku
3
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
5
Strana od-do
301-305
Kód UT WoS článku
000303158700011
EID výsledku v databázi Scopus
—