Pansteatitis in a free-ranging red-tailed hawk (Buteo jamaicensis).

A free-ranging juvenile female red-tailed hawk (Buteo jamaicensis) that was unable to fly was admitted to a rehabilitation center and died 1 day later. Hematology and serum chemistry abnormalities included moderate regenerative anemia, elevated creatine kinase, and hyperphosphatemia. Necropsy revealed a generalized steatitis, and histology showed a necrotizing and granulomatous pansteatitis with intralesional pigment compatible with ceroid. There was also moderate diffuse myodegeneration, mild multifocal cardiomyopathy, and mild multifocal hepatic necrosis. These changes and lesions resemble those caused by vitamin E deficiency in mammals and fish-eating birds.     

Knemidokoptes in a Swainson's hawk, Buteo swainsoni.

A male Swainson's hawk (Buteo swainsoni) at a rehabilitation facility in Colorado was presented with severe crusting of the skin on the medial thighs and caudal ventral body. Male and female Knemidokoptes mites were found on a cellophane tape preparation of the affected area. The hawk's clinical signs resolved with treatment with ivermectin administered at 200 microg/kg, i.m., every 10 days for three treatments.     

Valvular endocarditis and septic thrombosis associated with a radial fracture in a red-tailed hawk (Buteo jamaicensis)

A free-ranging adult female red-tailed hawk died suddenly after 3 weeks in rehabilitation for a radial fracture. Cause of death was septic thrombosis from a chronic bacterial valvular endocarditis, probably associated with injury at the fracture site. The challenge of clinical diagnosis of sepsis in wild birds is emphasized.     

Gizzard nematodiasis in Japanese mountain hawk eagle (Spizaetus nipalensis)

In this paper, we report spontaneous gizzard nematodiasis in an adult Japanese mountain hawk eagle (Spizaetus nipalensis). Grossly, the gizzard had a black mucoid substance attached to the surface mucous membrane, and the heart was dilated. Histologically, immature larvae with yellow pigments invaded crypts of the mucous membrane. More developed larvae invaded the lamina propria and muscular layers and serosa of the gizzard, with pressure atrophy and cellular reaction (infiltration of heterophils and macrophages and proliferation of fibrous connective tissue). Moderate bronchopneumonia due to larvae invasion was also seen in the lung. The morphology suggests that the parasites may be nematodes, but the species of nematode could not be confirmed. The bird may have died from malabsorption and respiratory damage as a result of the gizzard and lung lesions.     

Retinal Photoreceptor Fine Structure in the Red-Tailed Hawk (Buteo jamaicensis)

The retinal photoreceptors of the red-tailed hawk (Buteo jamaicensis) consist of rods, single cones and double (unequal) cones present in a ratio of about 2: 11 5. In the light-adapted state, the rods are slender elongated cells with outer segments that reach to the retinal epithelial (RPE) cells. The inner segment displays an ellipsoid of mitochondria, plentiful polysomes, some rough ER and Golgi zones. The rod nucleus is located deep within the outer nuclear layer and the synaptic spherule displays both invaginated (ribbon) and superficial (conventional) synaptic sites. Single cones show a thin tapering outer segment, a large electron lucent oil droplet at the apex of the inner segment and an ellipsoid of mitochondria. Double cones consist of a larger chief member which displays a thin tapering outer segment and an electron dense oil droplet as well as a smaller accessory cone which shows no oil droplet, an ellipsoid and a paraboloid of glycogen. As in the single cone, polysomes, RER and Golgi zones are also noted in the inner segments of both members of the double cone. Near the external limiting membrane the chief and accessory cones show membrane specializations indicative of junctions on their contiguous surfaces. All cone photoreceptors are of a smaller diameter than is normally reported for avian species. Both single and double cones display several invaginated synapses as well as numerous superficial synaptic sites.     

Pharmacokinetics of butorphanol tartrate in red-tailed hawks (Buteo jamaicensis) and great horned owls (Bubo virginianus)

OBJECTIVE: To determine the pharmacokinetics of butorphanol tartrate after IV and IM single-dose administration in red-tailed hawks (RTHs) and great horned owls (GHOs). ANIMALS: 6 adult RTHs and 6 adult GHOs. PROCEDURES: Each bird received an injection of butorphanol (0.5 mg/kg) into either the right jugular vein (IVj) or the pectoral muscles in a crossover study (1-week interval between treatments). The GHOs also later received butorphanol (0.5 mg/kg) via injection into a medial metatarsal vein (IVm). During each 24-hour postinjection period, blood samples were collected from each bird; plasma butorphanol concentrations were determined via liquid chromatography-mass spectrometry. RESULTS: 2- and 1-compartment models best fit the IV and IM pharmacokinetic data, respectively, in both species. Terminal half-lives of butorphanol were 0.94 +/- 0.30 hours (IVj) and 0.94 +/- 0.26 hours (IM) for RTHs and 1.79 +/- 1.36 hours (IVj), 1.84 +/- 1.56 hours (IM), and 1.19 +/- 0.34 hours (IVm) for GHOs. In GHOs, area under the curve (0 to infinity) for butorphanol after IVj or IM administration exceeded values in RTHs; GHO values after IM and IVm administration were less than those after IVj administration. Plasma butorphanol clearance was significantly more rapid in the RTHs. Bioavailability of butorphanol administered IM was 97.6 +/- 33.2% (RTHs) and 88.8 +/- 4.8% (GHOs). CONCLUSIONS AND CLINICAL RELEVANCE: In RTHs and GHOs, butorphanol was rapidly absorbed and distributed via all routes of administration; the drug's rapid terminal half-life indicated that published dosing intervals for birds may be inadequate in RTHs and GHOs.     

Fine Structure of the Pecten Oculi of the Red-Tailed Hawk (Buteo jamaicensis)

The pecten oculi of the red-tailed hawk (Buteo jamaicensis) has been examined by light and electron microscopy. In this species the pecten is very large and of the pleated type. It consists of 17-18 accordion folds which are joined apically by a heavily pigmented bridge of tissue which holds the pecten in a fan-like shape, widest at its base. It is situated over the optic nerve head and extends into the vitreous. Within each fold are numerous capillaries, larger supply and drainage vessels and melanocytes. The capillaries are specialized and display extensive microfolds on both the luminal and abluminal borders. The endothelial cell bodies are thin with most organelles present in a paranuclear location. The capillaries are surrounded by thick fibrillar basal laminae which are probably structurally important and which often enclose pericytes. The melanocytes which are most plentiful in the bridge region and peripherally in the pecten, form an incomplete sheath around the capillaries and other blood vessels. These melanocytes are also felt to be fulfilling a structural role within the pecten. The morphology of the pecten of the red-tailed hawk is indicative of a heavy involvement in the transport of materials to the avascular avian retina.     

Pharmacokinetics and anesthetic and cardiopulmonary effects of propofol in red-tailed hawks (Buteo jamaicensis) and great horned owls (Bubo virginianus)

OBJECTIVE: To determine induction doses, anesthetic constant rate infusions (CRI), and cardiopulmonary effects of propofol in red-tailed hawks and great horned owls and propofol pharmacokinetics in the owls during CRI. ANIMALS: 6 red-tailed hawks and 6 great horned owls. PROCEDURE: The CRI dose necessary for a loss of withdrawal reflex was determined via specific stimuli. Anesthesia was induced by IV administration of propofol (1 mg/kg/min) and maintained by CRI at the predetermined dose for 30 minutes. Heart and respiratory rates, arterial blood pressures, and blood gas tensions were obtained in awake birds and at various times after induction. End-tidal CO2 (ETCO2) concentration and esophageal temperature were obtained after induction. Propofol plasma concentrations were obtained after induction and after completion of the CRI in the owls. Recovery times were recorded. RESULTS: Mean +/- SD doses for induction and CRI were 4.48 +/- 1.09 mg/kg and 0.48 +/- 0.06 mg/kg/min, respectively, for hawks and 3.36 +/- 0.71 mg/kg and 0.56 +/- 0.15 mg/kg/min, respectively, for owls. Significant increases in PaCO2, HCO3, and ETCO2 in hawks and owls and significant decreases in arterial pH in hawks were detected. A 2-compartment model best described the owl pharmacodynamic data. Recovery times after infusion were prolonged and varied widely. Central nervous system excitatory signs were observed during recovery. CONCLUSIONS AND CLINICAL RELEVANCE: Effects on blood pressure were minimal, but effective ventilation was reduced, suggesting the need for careful monitoring during anesthesia. Prolonged recovery periods with moderate-to-severe excitatory CNS signs may occur in these species at these doses.     

Pharmacokinetics of piperacillan after intramuscular injection in red-tailed hawks (Buteo jamaicensis) and great horned owls (Bubo virginianus).

This study characterized and compared the pharmacokinetics of piperacillin after single 100 mg/kg i.m. injections in nine red-tailed hawks (Buteo jamaicensis) and five great horned owls (Bubo virginianus) over 48 hr by a modified agar well diffusion microbial inhibition assay. The mean maximum plasma piperacillin concentrations were 204 microg/ml and 221 microg/ml for the hawks and owls, respectively, and times of maximum concentrations were 15 min and 30 min, respectively. The calculated mean terminal elimination half-lives were 77 min in the hawks and 118 min in the owls. Area-under-the-curve values were 218 +/- 52 microg x hr/ml in the hawks and 444 +/- 104 microg x hr/ml in the owls. On the basis of the most common minimal inhibitory concentration (90%) for various bacterial isolates from clinical samples of 8 microg/ml, analysis of the data suggests that the maximum dosing interval for piperacillin at 100 mg/kg in medium sized raptors should be 4-6 hr.     

The effects of isoflurane anaesthesia on some Doppler-derived cardiac parameters in the common buzzard (Buteo buteo)

In order to gain an initial overview of the influence of anaesthesia on the results of Doppler-derived blood flow measurements in raptors, the heart rate as well as three different sample volumes of pulsed-wave spectral Doppler-derived flow velocity (diastolic flow across the left and right atrioventricular valve, systolic flow across the aortic valve) were determined in 10 common buzzards (Buteo buteo). Measurements were taken once in conscious and once in anaesthetized birds. Anaesthesia was shown to produce significant changes in cardiac parameters recorded in the same birds whilst conscious. When comparing conscious birds with each other (with one exception for right sided ventricular inflow velocity) no correlation between the heart frequency and measured blood flow velocities was evident. This was also the case under anaesthesia. However, significant differences in these parameters were evident when comparing the results obtained before and under anaesthesia. The results suggest that the influence of anaesthesia in raptors is more than a simple reduction of heart rate and that there is also reduction in blood flow velocity.