RESUMEN
OBJECTIVES: The purpose of this study was to assess serum concentrations of gabapentin in cats with chronic kidney disease (CKD) vs clinically healthy cats. METHODS: Five healthy cats were enrolled in a pharmacokinetic study. A single 20 mg/kg dose of gabapentin was administered orally and blood was obtained at 0, 0.25, 0.5, 1, 1.5, 2, 3, 4, 8, 12, 24 and 36 h via a jugular catheter. Serum gabapentin concentrations were measured using liquid chromatography coupled to tandem mass spectrometry. Non-compartmental pharmacokinetic analysis was performed. The same five healthy cats plus 25 cats with stable International Renal Interest Society stage 2 (n = 14) and 3 (n = 11) CKD were enrolled in a limited sampling study. Cats in both groups received a single 10 mg/kg dose of gabapentin, and serum gabapentin concentrations and compliance scores were obtained 3 and 8 h post-administration. RESULTS: Cats with CKD had significantly higher dose-normalized serum gabapentin concentrations than normal cats at 3 h (P = 0.0012 CKD vs normal 10 mg/kg; P = 0.008 CKD vs normal 20 mg/kg) and 8 h (P <0.0001 CKD vs normal 10 mg/kg; P <0.0001 CKD vs normal 20 mg/kg). Both 3 and 8 h dose-normalized serum gabapentin concentrations were significantly correlated with serum creatinine (3 h: P = 0.03, r = 0.39; 8 h: P = 0.001, r = 0.57) and symmetric dimethylarginine (3 h: P = 0.03, r = 0.41; 8 h: P = 0.007, r = 0.48). There was a significant correlation between 3 h serum gabapentin concentrations and compliance scores (P = 0.0002, r = 0.68). CONCLUSIONS AND RELEVANCE: Cats with CKD that received 10 mg/kg of gabapentin had significantly higher dose-normalized serum concentrations than normal cats that received 20 mg/kg, supporting the need to dose-reduce in this patient population.
Asunto(s)
Enfermedades de los Gatos , Gabapentina , Insuficiencia Renal Crónica , Animales , Gatos , Enfermedades de los Gatos/tratamiento farmacológico , Gabapentina/sangre , Gabapentina/farmacocinética , Estado de Salud , Insuficiencia Renal Crónica/tratamiento farmacológico , Insuficiencia Renal Crónica/veterinariaRESUMEN
Vitamin C is synthesized in the liver in most species, including dogs and cats, and is widely distributed through body tissues. Vitamin C has an important physiologic role in numerous metabolic functions including tissue growth and maintenance, amelioration of oxidative stress, and immune regulation. It is also a co-factor in the production of important substances such as catecholamines and vasopressin. Decreased vitamin C levels have been documented in a wide variety of diseases, and in critically ill human patients may be associated with increased severity of disease and decreased survival. Intravenous supplementation with vitamin C has been proposed as a potential life-saving treatment in conditions such as septic shock, and results of small some human trials are promising. Data in companion in animals is very limited, but the possible benefits and , seemingly low risk of adverse effects , and the low cost of this treatment make vitamin C therapy a promising area of future investigation in critically ill dogs and cats.
Asunto(s)
Ácido Ascórbico/uso terapéutico , Enfermedades de los Gatos/tratamiento farmacológico , Enfermedades de los Perros/tratamiento farmacológico , Animales , Ácido Ascórbico/administración & dosificación , Gatos , Enfermedad Crítica , Perros , MascotasRESUMEN
OBJECTIVE: To evaluate 2 point-of-care ethylene glycol (EG) tests in dogs. DESIGN: Prospective, randomized, blinded laboratory evaluation. SETTING: University teaching hospital. ANIMALS: Ten healthy adult dogs. INTERVENTIONS: Jugular venipuncture and in vitro evaluation for detection of EG in canine blood. MEASUREMENTS: Whole blood samples were centrifuged and separated, and the plasma was divided into 30 aliquots. The aliquots were mixed with EG to provide EG concentrations ranging from 0 to 100 mg/dL. The EG concentration of each sample was confirmed using gas chromatography. For the VetSpec EG Qualitative Reagent Test Kit, 100 µL of each sample was added to test vials and compared with 20 and 50 mg/dL reference vials. For the Kacey EG Test Strips, 20 µL of each sample was added to the test circle and compared with the color chart provided by the manufacturer. For each test, samples were prepared in groups of 5 and presented in randomized order to 2 readers who were blinded to the presumed EG concentration. Samples were scored as negative, 20-50 mg/dL, or greater than 50 mg/dL. For each test, the sensitivity and specificity for detecting EG was calculated. Cohen's unweighted kappa coefficient was calculated to determine the degree of agreement between readers. MAIN RESULTS: For detecting EG, the Kacey EG Test Strips had excellent sensitivity and specificity (both 100%) and good agreement between readers. The VetSpec EG Qualitative Reagent Test Kit was less sensitive and specific (65% and 70% for the first reader, 95% and 40% for the second) with less agreement. CONCLUSIONS: Of the 2 systems evaluated, the Kacey EG Test Strips displayed greater accuracy and ease of use.