Objective—To determine the effect of semen in urine specimens on urine protein concentration measured by means of dipstick analysis.
Sample Population—14 urine samples from 3 adult castrated male dogs and 14 semen samples from 7 adult sexually intact male dogs.
Procedures—Serial dilutions of the whole ejaculate or spermatozoa-free seminal fluid in urine were created, and unaltered and diluted urine samples were analyzed by means of a commercially available dipstick; pH and specific gravity of the samples were also measured. Spermatozoa and WBC counts of the semen samples and protein concentration of the seminal fluid were determined.
Results—Protein concentrations determined by means of dipstick analysis of urine samples to which whole ejaculate (dilutions of 1:1, 1:2, 1:16, 1:64, and 1:256) or seminal fluid (dilutions of 1:1, 1:2, 1:16, and 1:64) had been added were significantly higher than concentrations in unaltered urine samples. All 13 samples to which whole ejaculate was added at a dilution of 1:2 and 10 of 12 samples to which seminal fluid was added at a dilution of 1:2 were positive for blood on dipstick analysis. There was no significant linear correlation between spermatozoa or WBC count of the semen sample and protein concentration of the spermatozoa-free seminal fluid.
Conclusions and Clinical Relevance—Results suggested that regardless of whether spermatozoa were present, semen contamination could result in false-positive results for protein and blood during dipstick analysis of urine samples from sexually intact male dogs.
Objective—To compare accuracy of estimates of cystolith size obtained by means of plain radiography, double-contrast cystography, ultrasonography, and computed tomography.
Sample Population—30 canine cystoliths ranging from 1 to 11 mm in diameter with various mineral compositions.
Procedures—A bladder phantom model was created by filling a rubber balloon with saline (1% NaCl) solution and positioning it on top of a 2% gelatin cushion at the bottom of a water-filled 4-quart container. Cystoliths were individually placed in the bladder phantom and imaged by each of the 4 techniques. For each image, cystolith size was measured by 2 radiologists with computerized calipers, and size estimates were compared with actual cystolith size.
Results—Mean cystolith size estimates obtained by means of radiography, cystography, and computed tomography did not differ significantly from each other. However, for ultrasonographic images, mean ± SD difference between actual and estimated cystolith size (2.95 ± 0.73 mm) was significantly higher than mean difference for radiographic, cystographic, and computed tomographic images. For ultrasonography, mean ± SD percentage overestimation in cystolith size was 68.4 ± 51.5%.
Conclusions and Clinical Relevance—Results indicated that measurements of cystolith size obtained by means of ultrasonography may overestimate the true size. This suggests that cystolith size estimates obtained by means of ultrasonography should be interpreted with caution whenever cystolith size may influence patient management.
OBJECTIVE To estimate Brucella canis seropositivity rates for purebred dogs being bred by noncommercial breeders, describe epidemiological findings in infected commercial dog-production facilities, and characterize B canis infection in pet dogs and the risk to human health.
DESIGN Retrospective descriptive study.
SAMPLE 2,799 canine specimens submitted to the Michigan State University Veterinary Diagnostic Laboratory for B canis testing and records of B canis reports provided to the Michigan Department of Agriculture and Rural Development from 2007 through 2016.
PROCEDURES Results of B canis laboratory tests and epidemiological findings for reported cases of B canis were reviewed and summarized. Federal and state public health officials were interviewed regarding human B canis infection. State veterinarians were interviewed regarding canine brucellosis reporting and control procedures.
RESULTS Estimated B canis seropositivity was 0.4% among purebred Michigan dogs owned by noncommercial breeders. Infection was confirmed in dogs from 17 commercial dog-production facilities, 3 shelters, and 1 rescue agency. Estimated infection prevalence in production facilities ranged from 2 of 22 (9%) to 5 of 6 (83%). Transfer of infected dogs involved 22 Michigan counties and 11 states. Seven of 20 privately owned infected dogs had diskospondylitis; I also had uveitis. Fifty-three veterinary hospital or diagnostic laboratory personnel had inadvertent exposure to the pathogen. Brucella canis was isolated from 1 commercial production facility owner.
CONCLUSIONS AND CLINICAL RELEVANCEB canis was uncommon in purebred dogs being bred by noncommercial breeders but endemic in Michigan commercial facilities producing dogs destined to become household pets. Infected pet dogs caused human B canis exposure, and several pet dogs had debilitating disease not associated with the reproductive system.
Objective—To investigate the duration of dark-adaptation
time required for recovery of electroretinographic
responses after fundus photography or indirect
ophthalmoscopy in dogs.
Procedure—Initially, scotopic-intensity series of electroretinograms
(ERGs) were recorded after 20 minutes
of dark adaptation. The fundus of the left eye of
each dog was photographed (n = 10) or examined via
indirect ophthalmoscopy for 5 minutes with moderate-
(117 candela [cd]/m2) or bright-intensity (1,693
cd/m2) light; ERGs were repeated after a further 20 or
60 minutes of dark adaptation (6 procedures/dog).
Results—Following 20 minutes of dark adaptation
after fundus photography, the b- and a-wave amplitudes
were reduced in response to brighter stimuli,
compared with pretest ERGs; after 60 minutes of
dark adaptation, ERG amplitudes had recovered.
Following 20 minutes of dark adaptation after indirect
ophthalmoscopy (moderate-intensity light), significantly
lower b-wave amplitudes were recorded in
response to 2 of the brighter flash stimuli, compared
with pretest ERGs; after 60 minutes of dark adaptation,
ERG amplitudes had recovered. Following 20
minutes of dark adaptation after indirect ophthalmoscopy
(bright-intensity light), all ERG amplitudes
were significantly decreased and implicit times were
significantly decreased at several flash intensities,
compared with pretest ERGs; after 60 minutes of
dark adaptation, ERG amplitudes and implicit times
had returned to initial values, except for b-wave amplitudes
recorded in response to dimmer stimuli.
Conclusions and Clinical Relevance—Results suggest
that at least 60 minutes of dark adaptation
should be allowed before ERGs are performed in
dogs after fundus photography or indirect ophthalmoscopy.
(Am J Vet Res 2005;66:1798–1804)