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| December 2004 |
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| Effects of Exercise on Urinary Albumin Excretion in Dogs |
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Persistent microalbuminuria has been shown to be an indicator of glomerular damage associated
with early progressive renal disease in people and dogs. In people, transient or reversible
microalbuminuria has been shown to occur with exercise. A semi-quantitative test to measure
microalbuminuria in the dog (ERD®, Heska Corp, Ft. Collins, CO) recently has become available.
This study was aimed at determining if microalbuminuria could be induced by mild to moderate exercise
in the dog. Twenty-six dogs were studied after undergoing tests to rule out hyperglycemia, urinary tract
infection, azotemia, and a urine protein:creatinine ratio > 1. Exercise consisted of 20 min of flat
treadmill running. Urine samples were collected on 2 separate days before exercise, the morning of exercise,
3 h post-exercise, 7-9 h post-exercise, and each of 2 mornings after exercise. For 24 of 26 dogs, this
procedure was repeated after a minimum 7-d interval between exercise sessions. The canine ERD (early
renal disease)-Screen Urine Test was used to determine semiquantitative urine albumin concentrations.
Microalbuminuria-positive samples were further analyzed to determine quantitative albumin concentrations.
Four (15%) dogs were microalbuminuria positive. In each of them, microalbuminuria was present both before
and after exercise with no quantitative increase in urine albumin concentration post-exercise. Twenty-two
(85%) dogs were microalbuminuria-negative throughout the study and did not develop microalbuminuria at any
time after exercise. On a 95% confidence interval, the proportion of dogs that might be expected to develop
microalbuminuria after exercise is between 0 and 15%.
Reference: Gary, Cohn, Kerl, Jensen. J Vet Intern Med 18: 52-55, 2004
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| Persistent Urinary Tract Infections and Reinfections in 100 Dogs (1989-1999) |
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Retrospective study of 100 dogs with persistent urinary tract infections (UTIs) or reinfections was performed.
Criteria for selection included > or = 2 positive urine cultures within a 6-mo period. Signalment, presence of
predisposing disorders, urinalysis and urine culture results, and treatment strategies were extracted from the
medical records. Dogs had median age of 7 y when 1st diagnosed. Dogs younger than 3 and > 10 y were at increased
and decreased risks, respectively, for reinfections or persistent UTIs. Spayed females were more common in the UTI
population. More than 50% of the dogs were asymptomatic for UTI at 1st presentation. Urine sediment examinations
identified hematuria, pyuria, and bacteriuria in 47, 72, and 85% of the samples, respectively. The most commonly
isolated organisms were E.coli and Strep/Enterococcus spp.; multiple isolates also were common. Of the isolates,
29.5% were resistant to achievable serum concentrations of all antibiotics commonly prescribed for PO administration.
Dogs with abnormal micturition were more likely to have infections by organisms resistant to commonly prescribed
antibiotics. Potentially predisposing disorders were identified in 71 dogs. A correction of these disorders was
accomplished in 35% of them. Dogs given standard antibiotic therapy without addressing predisposing disorders
experienced poor control of UTIs; 74.5% of these dogs had an apparent disease-free interval of > 8 weeks. By
comparison, dogs in which predisposing disorders were corrected or those that were treated with low-dose,
long-term antibiotic regimens subjectively had better control.
References: Seguin, Vaden, Altier, et al. J Vet Intern Med Volume 17: 622-31, 2003.
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| Utility of Plasma D-Dimer to Identify Thromboembolic Disease in Dogs |
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This prospective study investigated D-dimer concentrations in clinically healthy dogs, clinically ill dogs
without thromboembolic disease (TE), and dogs with TE. The goals were to determine whether the coagulation cascade
is activated in nonembolic metabolic and inflammatory conditions and whether differentiation from TE is possible.
Group 1 consisted of 30 clinically healthy dogs presented for routine care. Group 2 consisted of 67 clinically ill
dogs without TE. This group was subdivided into the following categories: postoperative surgical procedures, congestive
heart failure, renal failure, hepatic disease, and neoplastic disease. Group 3 consisted of 20 dogs diagnosed with TE.
CBC and measurement of prothrombin time (PT), activated partial thromboplastin time (PTT), fibrinogen degradation product
(FDP) concentration, and plasma D-dimer concentration was performed on dogs in all groups. D-dimer concentrations were
highest in dogs with TE; and next highest was the hepatic disease group. Only these 2 groups had median D-dimer concentrations
markedly different from clinically healthy dogs. The frequency of platelet abnormalities was markedly greater for the TE and
neoplastic disease groups. The sensitivity of D-dimer concentrations > 500 ng/mL for predicting TE was 100%; however,
the specificity of D-dimer for TE at that concentration was only 70%. The specificity of D-dimer concentrations > 1,000
ng/mL to predict TE was 94% (sensitivity, 80%), and the specificity of D-dimer concentrations > 2,000 ng/mL was 98.5%
(sensitivity, 36%). FDPs were not high in any TE patient; and thus, the FDP test may be an insensitive indicator of
thromboembolism, with or without overt disseminated intravascular coagulation (DIC).
Reference: Nelson, Andreasen. J Vet Intern Med Volume 17: 830-4, 2003.
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