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Meloxicam is a nonsteroidal anti-inflammatory drug commonly used in avian species. In this study, the pharmacokinetic parameters for meloxicam were determined following single intravenous (i.v.), intramuscular (i.m.) and oral (p.o.) administrations of the drug (1 mg/kg·b.w.) in adult African grey parrots ( Psittacus erithacus; n = 6). Serial plasma samples were collected and meloxicam concentrations were determined using a validated high-performance liquid chromatography assay. A noncompartmental pharmacokinetic analysis was performed. No undesirable side effects were observed during the study. After i.v. administration, the volume of distribution, clearance and elimination half-life were 90.6 ± 4.1 mL/kg, 2.18 ± 0.25 mL/h/kg and 31.4 ± 4.6 h, respectively. The peak mean ± SD plasma concentration was 8.32 ± 0.95 μg/ mL at 30 min after i.m. administration. Oral administration resulted in a slower absorption ( tmax = 13.2 ± 3.5 h; Cmax = 4.69 ± 0.75 μg/ mL) and a lower bioavailability (38.1 ± 3.6%) than for i.m. (78.4 ± 5.5%) route. At 24 h, concentrations were 5.90 ± 0.28 μg/ mL for i.v., 4.59 ± 0.36 μg/ mL for i.m. and 3.21 ± 0.34 μg/ mL for p.o. administrations and were higher than those published for Hispaniolan Amazon parrots at 12 h with predicted analgesic effects. [ABSTRACT FROM AUTHOR]

The article discusses a research study on African grey parrots or Psittacus e erithacus with a diagnosis of congestive heart failure and cardiomyopathy. Study subjects were 6 parrots aged 15 days to 8 years and clinical signs include rales, bradyarrhythmia and crop stasis while gross findings include coelemic effusion, atrophy of the liver and left-sided cardiomyopathy. Conclusions indicated that development of cardiac disease could be due to hypoxia-induced pulmonary hypertension or genetic endocrine disease as suggested by thyroidal lesions.

The objective of the present study was to evaluate whether gender determination in two amphibian species ( Kaloula pulchra and Xenopus laevis ) can be reliably carried out by means of magnetic resonance imaging (benchtop magnetic resonance imaging; BT-MRI) or ultrasound (high-resolution ultrasound; HR-US) techniques. Two species of healthy, sexually mature anurans have been used in the present study. Eight Kaloula (blind study) and six Xenopus were used as controls. Magnetic resonance imaging experiments were carried out on a low-field (1 Tesla) benchtop-MRI (BT-MRI) system. HR-US examination was performed with high-resolution equipment. Low-field BT-MRI images provided a clear and quantifiable identification of all the sexual organs present in both genders and species. The HR-US also allowed the identification of testes and ovaries in both species. Results indicate that BT-MRI allowed a very precise sex identification in both anuran species, although its use is limited by the cost of the equipment and the need for anesthesia. HR-US allowed an accurate identification of ovaries of both species whereas a precise identification of testes is limited by the ultrasonographer experience. The main advantages of this technique are the possibility of performing it without anesthesia and the higher availability of equipment in veterinary and zoo institutions.

Early diagnosis of kidney diseases in avian species is limited. Endogenous markers currently used in avian practice are not sensitive enough to identify early kidney failure. Consequently, alternative markers should be evaluated. To be able to evaluate these alternative markers, an accurate marker to estimate the GFR should be validated. This study determined the GFR, measured as clearance of exogenous creatinine and exo-iohexol, in six different bird species, i.e. broiler chickens, laying chickens, turkeys, Muscovy ducks, pigeons and African grey parrots (4♀/4♂). To be able to compare the six bird species, normalization to bodyweight (BW) of the GFR was performed, after a good correlation between BW and kidney weight was demonstrated (R² = 0.9836). Clearance of exo-iohexol normalized to BW (mL/min/kg) was determined in all bird species, i.e. 3.09 in broiler chickens; 2.57 in laying chickens; 1.94 in turkeys; 1.29 in pigeons; 2.60 in ducks and 1.11 in parrots. However, these results differed significantly with the clearance of exogenous creatinine: 8.41 in broiler chickens; 9.33 in laying chickens; 5.62 in turkeys; 14.97 in pigeons; 17.59 in ducks and 25.56 in parrots 25.56. Iohexol is preferred to measure the GFR, since it is not prone to tubular reabsorption nor secretion.

OBJECTIVE To determine the pharmacokinetics of meloxicam in African grey parrots (Psittacus erithacus) during administration of multiple doses. ANIMALS 6 healthy African grey parrots. PROCEDURES Meloxicam was administered at each of 3 dosages (1 mg/kg, IM, q 24 h, for 7 days; 1 mg/kg, PO, q 24 h, for 12 days; and 1.6 mg/kg, PO, q 24 h, for 7 days) with an 8-week washout period between treatments. Blood samples were collected 12 and 24 hours after each drug administration (times of presumptive peak and trough drug concentrations) for pharmacokinetic analysis. Birds were visually assessed during all experiments and monitored for changes in selected plasma and urine biochemical variables after administration of the drug at 1.6 mg/kg. RESULTS Mean trough plasma concentrations at steady state were 10.7 and 9.16 μg/mL after meloxicam administration at 1 mg/kg, IM, and 1 mg/kg, PO, respectively. Plasma drug accumulation was evident (accumulation ratios of 2.04 ± 0.30 [IM treatment] and 2.45 ± 0.26 [PO treatment]). Plasma and urine N-acetyl-β-d-glucosaminidase activities were significantly increased at the end of meloxicam treatment at 1.6 mg/kg. CONCLUSIONS AND CLINICAL RELEVANCE Plasma concentrations of meloxicam were maintained at values greater than effective analgesic concentrations described for other avian species. Although administration of meloxicam at a dosage of 1 mg/kg IM and PO daily for 1 week and 12 days, respectively, was not associated with adverse clinical effects in this population, further studies are needed to assess the efficacy and safety of the drug during prolonged treatment and the clinical relevance of its accumulation.

To date, descriptions of pathologic conditions of the seminal vesicle in rabbits are scarce and limited to the laboratory animals in experimental conditions. The present article describes three cases of strangury, abdominal pain, and anorexia associated with seminal vesiculitis in pet rabbits. Three non-neutered male pet rabbits aged 3.6, 1.5, and 2.1 yrs were presented with strangury, abdominal pain, and anorexia. Seminal vesiculitis was diagnosed based on clinical signs and ultrasonography findings. Vesiculectomy was performed in two cases that presented strangury refractory to medical treatment, and diagnosis was confirmed by histopathology. In the third case, the patient received medical treatment, and a sequela in the form of lithiasis of the seminal vesicle was detected 3 yrs later. Plain radiographs were nearly unremarkable, and results from complete blood analysis and urinalysis were not specific in all three cases. Contrast radiography was performed in one case, showing a dilated seminal vesicle. Ultrasound and surgical biopsy seem to be the most sensitive techniques in the diagnosis of this pathology. Seminal vesiculitis must be included in the differential diagnosis of acute or chronic strangury in male pet rabbits.

Two cases of renal klossiellosis were diagnosed by histopathology in pet sugar gliders (Petaurus breviceps). In both cases, parasites were associated with tubular dilation and mild interstitial nephritis. Rare schizonts were seen in the proximal convoluted renal tubular epithelium, whereas all other life cycle stages were found within distal convoluted tubule cells or the urinary space of the structures distal to the loop of Henle. Conventional optical and transmission electron microscopies were used to assess the life stages of the parasite. The morphologic characteristics and measurements observed differ from those of previously described species of Klossiella infecting marsupial hosts, and the name Klossiella dulcis n. sp. is hereby proposed. This is the first report of a Klossiella sp. infection in Petaurus breviceps .

Background: The clinical relevance of plasmatic L-lactate concentration (PLLC) is unknown in rabbits. Due to an entirely different metabolism of lactic acid, PLLC in rabbits can reach much higher concentrations than in other species., Objectives: The aim of this study was to establish a reference interval (95% RI) for venous PLLC in pet rabbits and to assess its diagnostic and prognostic significance in ill pet rabbits., Methods: Plasmatic L-lactate concentration was determined by an enzymatic colorimetric method. In the first study, healthy rabbits (n = 140) were the control group. The ill rabbits group (n = 405) included the deceased (n = 108) and the survivors (n = 266), depending on the outcome at day 14. In a second study, variation in the PLLC was determined in 25 boarding (control-serial), 99 hospitalized (deceased-serial [n = 27], and survivors-serial [n = 72]) rabbits sampled at 0, 12, 24 and 48 hours., Results: The 95% RI for PLLC in controls was 2.1-15.2 mmol/L. On-arrival PLLC in ill rabbits was not statistically different from those in the control group, but was significantly lower in deceased compared to survivors or controls. The range of PLLC variation differed significantly between control-serial, deceased-serial, and survivors-serial groups. A better prognosis was associated with an increase of 3.3 mmol/L PLLC within 48 hours after arrival., Conclusions: Contrary to the available information in other species, morbidity and mortality is associated with sustained low PLLC in pet rabbits, while a good prognosis is associated with an increase in PLLC. Monitoring PLLC in hospitalized rabbits is advisable., (© 2016 American Society for Veterinary Clinical Pathology.)

In this study we evaluated the effects of meloxicam administered at 0.5 mg/kg IM q12h for 14 days on hematologic and plasma biochemical values and on kidney tissue in 11 healthy African grey parrots (Psittacus erithacus). Before treatment with meloxicam, blood samples were collected and renal biopsy samples were obtained from the cranial portion of the left kidney from each of the birds. On day 14 of treatment, a second blood sample and biopsy from the middle portion of the left kidney were obtained from each bird. All birds remained clinically normal throughout the study period. No significant differences were found between hematologic and plasma biochemical values before and after 14 days of treatment with meloxicam, except for a slight increase in median beta globulin and corresponding total globulin concentrations, and a slight decrease in median phosphorus concentration. Renal lesions were absent in 9 of 10 representative posttreatment biopsy samples. On the basis of these results, meloxicam administered at the dosage used in this study protocol does not appear to cause renal disease in African grey parrots.

The i-STAT PCA can be used as a blood analyzer in critical avian patients, although single values must be interpreted carefully. The study of the acid-base status in companion birds is still in its infancy. Further research is needed to establish normal reference values in arterial blood gases, compare them with venous blood gas, and to determine if the formulas that deviate from small animal medicine are or are not applicable., (Copyright © 2013 Elsevier Inc. All rights reserved.)

This article outlines a practical approach for the use of blood-gas analysis in pet rabbits using the I-STAT analyzer. Sampling techniques and a theoretic approach to diagnosis are described. The following 95% RI were obtained from venous samples of 45 healthy rabbits: pH (7.245-7.533), PCO(2) (28.9-52.9 mm Hg), HCO(3) (17.0-32.5 mmol/L), total CO(2) (18-34 mmol/L), BE(ecf) (-10-8 mmol/L), AnGap (11-26 mmol/L), Na (136-147 mmol/L), K (3.4-5.7 mmol/L), Cl (93-113 mmol/L), Glu (93-245 mg/dL), BUN (9-33 mg/dL). Results from 20 arterial samples were pH (7.358-7.502), PCO(2) (29.1-36.8 mm Hg), HCO(3) (17.5-27.6 mmol/L), BE(ecf) (-7-5 mmol/L), PO(2) (75-101 mm Hg), iCa (1.67-1.85). The article also includes some conclusions obtained comparing results from healthy and ill rabbits over an 18-month period., (Copyright © 2013 Elsevier Inc. All rights reserved.)

A 52-year old woman developed severe cholestasis seven days after the administration of trimethoprim-sulfamethoxazole (RMP-SMZ) The clinical and pathologic features are discussed as well as the various mechanisms of liver injury following TMP-SMZ use.