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1.
Am J Vet Res ; 83(6)2022 May 08.
Artigo em Inglês | MEDLINE | ID: mdl-35524961

RESUMO

OBJECTIVE: To compare ketamine-butorphanol-azaperone-medetomidine (KBAM) to detomidine-etorphine-acepromazine (DEA) for field anesthesia in captive Przewalski horses (Equus przewalskii). ANIMALS: 10 adult Przewalski horses. PROCEDURES: A prospective randomized crossover trial was conducted. Each horse was immobilized once with KBAM (200 mg ketamine, 109.2 mg butorphanol, 36.4 mg azaperone, and 43.6 mg medetomidine) and once with DEA (40 mg detomidine premedication, followed 20 minutes later by 3.9 to 4.4 mg etorphine and 16 to 18 mg acepromazine). Both protocols were administered by IM remote dart injection with a washout period of 6 months between treatments. Selected cardiorespiratory variables and quality of anesthesia were recorded. Antagonists were administered IM (KBAM, 215 mg atipamezole and 50 mg naltrexone; DEA, 4 mg RX821002 and 100 mg naltrexone). RESULTS: All horses were anesthetized and recovered uneventfully. Inductions (DEA, 6.8 min; KBAM, 11.6 min; P = 0.04) and recoveries (DEA, 3.2 min; KBAM, 19.6 min; P < 0.01) were faster with DEA compared with KBAM. Quality scores for induction and recovery did not differ between protocols, but maintenance quality was poorer for DEA (P < 0.01). Clinical concerns during DEA immobilizations included apnea, severe hypoxemia (arterial partial pressure of oxygen < 60 mm Hg), muscle rigidity, and tremors. Horses treated with KBAM were moderately hypoxemic, but arterial partial pressures of oxygen were higher compared with DEA (P < 0.01). CLINICAL RELEVANCE: Captive Przewalski horses are effectively immobilized with KBAM, and this protocol results in superior muscle relaxation and less marked hypoxemia during the maintenance phase, but slower inductions and recoveries, compared with DEA.


Assuntos
Anestesia , Ketamina , Acepromazina/farmacologia , Anestesia/veterinária , Animais , Azaperona/farmacologia , Butorfanol/farmacologia , Etorfina/farmacologia , Frequência Cardíaca , Cavalos , Hipnóticos e Sedativos/farmacologia , Hipóxia/tratamento farmacológico , Hipóxia/veterinária , Imidazóis , Imobilização/métodos , Imobilização/veterinária , Ketamina/farmacologia , Medetomidina/farmacologia , Naltrexona/farmacologia , Oxigênio/farmacologia , Estudos Prospectivos
2.
J Feline Med Surg ; 24(12): 1173-1180, 2022 12.
Artigo em Inglês | MEDLINE | ID: mdl-34904480

RESUMO

OBJECTIVES: The aim of this study was to evaluate the change in packed cell volume (PCV) and total protein following intramuscular preanesthetic sedation with one of three drug combinations in cats. METHODS: Thirty client-owned cats were enrolled in this prospective, randomized, blinded, clinical study. A venous blood sample was obtained prior to administration of any sedation and PCV, total protein, electrolytes (Na+, K+, Cl-, iCa2+), glucose and lactate were measured. Cats were randomly assigned to receive one of three intramuscular sedation protocols (n = 10 cats/protocol): methadone 0.2 mg/kg + acepromazine 0.02 mg/kg (MA), methadone 0.2 mg/kg + dexmedetomidine 5 µg/kg (MD) or methadone 0.2 mg/kg + midazolam 0.2 mg/kg + alfaxalone 2 mg/kg (MMA). Twenty-five minutes later, cats were assessed for level of sedation followed by another venous blood sampling to evaluate the same variables as above. RESULTS: There were no significant differences in demographics (age, weight, sex) between groups. Level of sedation was significantly higher in MMA cats. Within groups, after premedication, PCV and hemoglobin significantly decreased in all groups, total protein significantly decreased in the MA and MMA groups and glucose significantly increased in the MD group. For electrolytes, statistical changes were not clinically relevant; Cl- mean difference was significantly different between MA and MD; in the MD group Na+ and Cl- significantly decreased and in the MMA group Cl- significantly increased. CONCLUSIONS AND RELEVANCE: All three sedation protocols caused significant decreases in PCV and hemoglobin in healthy cats.


Assuntos
Células Sanguíneas , Proteínas Sanguíneas , Sedação Consciente , Animais , Gatos , Hemoglobinas , Estudos Prospectivos , Sedação Consciente/métodos , Proteínas Sanguíneas/análise , Injeções Intramusculares
3.
Vet Anaesth Analg ; 48(3): 407-414, 2021 May.
Artigo em Inglês | MEDLINE | ID: mdl-33736938

RESUMO

OBJECTIVE: To evaluate anesthetic conditions and postoperative analgesia with the use of intraoperative constant rate infusions (CRIs) of fentanyl-lidocaine or fentanyl-ketamine in dogs undergoing thoracolumbar hemilaminectomy. STUDY DESIGN: Prospective, randomized, blinded, clinical study. ANIMALS: A total of 32 client-owned dogs. METHODS: Dogs were premedicated with fentanyl (5 µg kg-1) administered intravenously (IV), anesthesia was induced with IV alfaxalone and maintained with isoflurane. Fentanyl (0.083 µg kg-1 minute-1) was infused IV with either ketamine (0.5 mg kg-1; then 40 µg kg-1 minute-1; group KF) or lidocaine (2 mg kg-1; then 200 µg kg-1 minute-1; group LF) assigned randomly. Heart rate, noninvasive arterial pressures, respiratory rate, esophageal temperature, end-tidal partial pressure of carbon dioxide and isoflurane concentration were recorded throughout anesthesia. Maintenance of anesthesia, recovery and postoperative pain (Glasgow Composite Pain Scale) were scored. Cardiopulmonary data were analyzed using a two-way anova with repeated measures, demographics of the two groups with a t test, and scores with Mann-Whitney U test, with p < 0.05. RESULTS: All dogs recovered from anesthesia without complications. No significant difference was found between groups for cardiopulmonary variables, total anesthesia time, sedation score and requirement for postoperative sedation or for rescue analgesia. Anesthetic maintenance score was of lower quality in KF than in LF [median (interquartile range): 0 (0-0.5) versus 0 (0-0); p = 0.032)], but still considered ideal. Recovery score was higher and indicative of less sedation in LF than in KF [1 (1-1.5) versus 0.5 (0-1); p < 0.0001]. Pain score was higher in KF than in LF [2 (1-3) versus 1 (1-2); p = 0.0009]. CONCLUSIONS AND CLINICAL RELEVANCE: Both CRIs of KF and LF provided adequate anesthetic conditions in dogs undergoing thoracolumbar hemilaminectomy. Based on requirement for rescue analgesia, postoperative analgesia was adequate in both groups.


Assuntos
Isoflurano , Ketamina , Analgésicos , Animais , Cães , Fentanila , Lidocaína , Estudos Prospectivos
4.
Vet J ; 258: 105455, 2020 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-32564865

RESUMO

Sympathomimetic drugs mimic the physiological action of the sympathetic nervous system through interaction with adrenergic receptors. These drugs are commonly used to provide cardiovascular support in many veterinary species. Despite their common use, the literature evaluating their effectiveness can be somewhat limited depending on the species. This review details the mechanism of action of various sympathomimetic drugs and summarizes the literature that is available describing the efficacy of these drugs and their use in anesthetized veterinary species.


Assuntos
Gatos/fisiologia , Cães/fisiologia , Cavalos/fisiologia , Sistema Nervoso Simpático/fisiologia , Anestesia/veterinária , Animais , Fenômenos Fisiológicos Cardiovasculares/efeitos dos fármacos , Dobutamina/farmacologia , Dopamina/farmacologia , Norepinefrina/farmacologia , Simpatomiméticos/farmacologia
5.
Vet Clin North Am Small Anim Pract ; 49(6): 1013-1027, 2019 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-31481257

RESUMO

Alpha-2 agonists have potent analgesic effects, in addition to their sedative actions. Alpha-2 agonists provide analgesia through any of several routes of administration, including parenteral, oral, epidural or intrathecal and intraarticular, because of spinal and supraspinal actions. Systemic doses are short acting, whereas local administration at the site of action result in longer analgesic effects. The potent cardiovascular and respiratory effects of alpha-2 agonists should be considered when used as analgesics.


Assuntos
Agonistas alfa-Adrenérgicos/uso terapêutico , Analgésicos Opioides/uso terapêutico , Dor/veterinária , Animais de Estimação , Analgesia/métodos , Analgesia/veterinária , Animais , Dor/tratamento farmacológico
7.
Mamm Genome ; 22(9-10): 583-8, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21597988

RESUMO

Mycobacterium avium ssp. paratuberculosis (MAP) infection causes a chronic granulomatous inflammatory condition of the bovine gut that is characterized by diarrhea, progressive weight loss, and emaciation, and ultimately leads to loss in productivity and profitability of dairy operations. The host cytokine machinery is known to play an important role in protecting against MAP infection. Therefore, the goal of the present study was to assess whether polymorphisms in candidate genes encoding important cytokines and cytokine receptors are associated with MAP infection status of dairy cattle. MAP infection status was evaluated based on serum and milk enzyme-linked immunosorbent assays (ELISAs) for MAP-specific antibodies. Twenty previously reported polymorphisms in genes encoding bovine interferon gamma (IFNG), IFNGR1, IFNGR2, IL22, IL22RA1, IL12RB1, IL12RB2, and IL23R were genotyped in a resource population of 446 dairy Holsteins with known MAP infection status, and logistic regression was used to assess the statistical association with a binomial MAP infection status phenotype. Four SNPs in IFNGR2, IL12RB1, IL12RB2, and IL23R were found to be associated with the MAP infection status of the resource population. These results underscore the importance of cytokines and their receptors in conferring protection against MAP infection and warrant further functional characterization of these associations.


Assuntos
Doenças dos Bovinos/genética , Mycobacterium avium subsp. paratuberculosis , Paratuberculose/genética , Polimorfismo de Nucleotídeo Único , Receptores de Citocinas/genética , Alelos , Animais , Bovinos , Doenças dos Bovinos/microbiologia , Frequência do Gene , Predisposição Genética para Doença , Genótipo , Paratuberculose/microbiologia , Receptores de Interferon/genética , Receptores de Interleucina/genética , Receptores de Interleucina-12/genética , Receptor de Interferon gama
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