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Effects of different rates of propofol with or without S-ketamine on ventricular function in healthy cats - a randomized study.
Marangoni, Sabrine; Ubiali, Matheus; Ambrosini, Francieli; Jahnel, Larissa; Vilani, Julia M; Steagall, Paulo V; Vilani, Ricardo Guilherme D'Otaviano de Castro.
Afiliação
  • Marangoni S; Department of Veterinary Medicine, Federal University of Paraná, Juvevê, Curitiba, PR, Brazil.
  • Ubiali M; Department of Veterinary Medicine, Federal University of Paraná, Juvevê, Curitiba, PR, Brazil.
  • Ambrosini F; Department of Veterinary Medicine, Federal University of Paraná, Juvevê, Curitiba, PR, Brazil.
  • Jahnel L; Department of Veterinary Medicine, Federal University of Paraná, Juvevê, Curitiba, PR, Brazil.
  • Vilani JM; Department of Veterinary Medicine, Federal University of Paraná, Juvevê, Curitiba, PR, Brazil.
  • Steagall PV; Department of Veterinary Clinical Sciences and Centre for Companion Animal Health and Welfare, Jockey Club College of Veterinary Medicine and Life Sciences, City University of Hong Kong, Kowloon, Hong Kong SAR, China.
  • Vilani RGDC; Department of Clinical Sciences, Faculty of Veterinary Medicine, Université de Montréal, Saint-Hyacinthe, QC, Canada.
Front Vet Sci ; 10: 1272949, 2023.
Article em En | MEDLINE | ID: mdl-38152595
ABSTRACT
Propofol is used for anesthetic induction in cats and procedural sedation in countries where alfaxalone is not available. Studies have reported propofol-related effects in echocardiography variables in dogs and humans. However, there is a lack of echocardiography studies investigating propofol-related effects on cats. This study aimed to use echocardiography to investigate echocardiographic changes in three protocols using propofol propofol-slow (2 mg/kg/min, PS); propofol-fast (8 mg/kg/min, PF); propofol-ketamine (S-ketamine 2 mg/kg bolus followed by propofol 2 mg/kg/min; PK) in healthy premedicated (gabapentin-buprenorphine-acepromazine; 200 mg/cat, 0.4, and 0.1 mg/kg, respectively), non-intubated cats. Echocardiographic measurements were obtained at three time points baseline (before the administration of propofol), end of propofol titration (end-point, T0), and 15 min after T0 (T15). Propofol at a lower rate continued from T0 to T15. Echocardiographic and physiological variables included fractional shortening (FS%), ejection fraction (EF%), HR, BP, and others. Propofol requirements at T0 for PF, PS, and PK groups were 5.0 ± 0.9, 3.8 ± 0.7, and 2.4 ± 0.5 mg/kg, respectively. EF% neither change over time nor between groups. PF and PK showed a reduction in FS% at T0 (47 ± 6 to 34 ± 6 and 42 ± 6 to 36 ± 5, respectively). BP reduced significantly in PF and PS groups (136 ± 26 to 105 ± 13 and 137 ± 22 to 115 ± 15 mmHg, respectively). It is unclear whether changes in echocardiography variables were of clinical relevance related to treatment groups or a result of within-group individual responses.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article