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1.
Am J Vet Res ; 83(4): 317-323, 2022 Jan 21.
Article de Anglais | MEDLINE | ID: mdl-35066488

RÉSUMÉ

OBJECTIVE: To determine whether delivery of compounded liquid sildenafil directly to the stomach of dogs with megaesophagus (ME) would affect esophageal clearance, regurgitation frequency, body weight, or quality of life. ANIMALS: 10 client-owned otherwise healthy dogs with stable ME. PROCEDURES: A randomized crossover study was performed. Dogs received either sildenafil (1 mg/kg, PO, q 12 h) or a placebo for 14 days, followed by a 7-day washout period, then the opposite treatment for 14 days. Esophageal clearance time was assessed by means of videofluoroscopy prior to treatment and on day 1 of each treatment period. Owners maintained logs of regurgitation episodes and quality of life. RESULTS: Compounded liquid sildenafil moved into the stomach during 21 of 30 (70%) videofluoroscopy sessions. Sildenafil resulted in a significant reduction in the number of regurgitation episodes (median, 3.5 episodes/wk; range, 0 to 14.5 episodes/wk), compared with baseline (median, 6.5 episodes/wk; range, 1.5 to 19.5 episodes/wk) and the placebo (median, 4 episodes/wk; range, 0 to 28 episodes/wk), and a significant increase in body weight (median, 22.05 kg; range, 6 to 26.3 kg), compared with baseline (median, 21.55 kg; range, 5.1 to 26.2 kg) and the placebo (median, 22.9 kg; range, 5.8 to 25.9 kg). There were no differences in esophageal clearance times or quality-of life-scores between sildenafil and placebo. CLINICAL RELEVANCE: Although significant differences with placebo administration were identified, clinically relevant improvements were not seen with the use of compounded liquid sildenafil in dogs with ME.


Sujet(s)
Maladies des chiens , Achalasie oesophagienne , Animaux , Études croisées , Maladies des chiens/traitement médicamenteux , Chiens , Méthode en double aveugle , Achalasie oesophagienne/traitement médicamenteux , Achalasie oesophagienne/médecine vétérinaire , Qualité de vie , Citrate de sildénafil/usage thérapeutique
2.
Vet Pathol ; 57(2): 286-289, 2020 03.
Article de Anglais | MEDLINE | ID: mdl-32081095

RÉSUMÉ

The genus Neorickettsia includes obligate, intracellular bacteria responsible for diseases including Potomac horse fever caused by Neorickettsia risticii and salmon poisoning disease (SPD) caused by Neorickettsia helminthoeca. The Stellanchasmus falcatus (SF) agent is a member of this genus previously associated only with mild clinical signs in dogs. Between 2013 and 2016, 3 dogs in Washington State (USA) presented with disease suggestive of SPD, but N. helminthoeca was not detected by molecular techniques. Clinical signs included depression, anorexia, and diarrhea. Cytologic examination of aspirates supported a diagnosis of granulomatous lymphadenitis with organisms suggestive of Neorickettsia. Dogs either died or were humanely euthanized due to poor response to therapy. Necropsy findings included lymphadenomegaly and hepatomegaly. Histopathology identified granulomatous and lymphoplasmacytic splenitis, lymphadenitis, enteritis, and hepatitis with extensive necrosis. Neorickettsia DNA was detected using genus-specific primers and direct sequencing showed 100% sequence identity to the SF agent in all 3 dogs. This is the first clinicopathologic description of severe disease in dogs attributed to the SF agent. These findings may suggest the emergence of a novel neorickettsial disease in the Pacific Northwest.


Sujet(s)
Infections à Anaplasmataceae/médecine vétérinaire , Maladies transmissibles émergentes/médecine vétérinaire , Maladies des chiens/microbiologie , Neorickettsia/classification , Infections à Anaplasmataceae/diagnostic , Infections à Anaplasmataceae/microbiologie , Infections à Anaplasmataceae/anatomopathologie , Animaux , Cytoponction/médecine vétérinaire , Maladies transmissibles émergentes/diagnostic , Maladies transmissibles émergentes/microbiologie , Maladies transmissibles émergentes/anatomopathologie , Maladies des chiens/diagnostic , Maladies des chiens/anatomopathologie , Chiens , Femelle , Mâle , Neorickettsia/génétique , Neorickettsia/isolement et purification , États du Nord-Ouest des États-Unis
3.
BMC Vet Res ; 13(1): 85, 2017 Apr 04.
Article de Anglais | MEDLINE | ID: mdl-28376869

RÉSUMÉ

BACKGROUND: Dyslipidemia, dysregulated adipokine secretion and alteration in glucagon and adropin concentrations are important obesity-related factors in the pathophysiology of human Type 2 diabetes; however, their roles in the pathophysiology of feline diabetes mellitus are relatively unknown. Here, we determined the concentrations of circulating leptin, adiponectin, pro-inflammatory cytokines, glucagon, adropin, triglycerides, and cholesterol, in non-diabetic lean and overweight cats and newly diagnosed diabetic cats. Client-owned cats were recruited and assigned into 3 study groups: lean, overweight and diabetic. Fasting blood samples were analyzed in lean, overweight and diabetic cats at baseline and 4 weeks after consumption of high protein/low carbohydrate standardized diet. RESULTS: Serum concentrations of triglycerides were greater in diabetics at baseline and were increased in both diabetic and overweight cats at 4 weeks. Plasma leptin concentrations were greater in diabetic and overweight at baseline and 4 weeks, whereas adiponectin was lower in diabetics compared to lean and overweight cats at baseline and 4 weeks. Diabetics had greater baseline plasma glucagon concentrations compared to lean, lower adropin than overweight at 4 weeks, and lower IL-12 concentrations at 4 weeks than baseline. CONCLUSIONS: Our results suggest that feline obesity and diabetes mellitus are characterized by hypertriglyceridemia and hyperleptinemia; however, diabetic cats have significantly lower adiponectin and adropin compared to overweight cats. Thus, despite having similar body condition, overweight and diabetic cats have differential circulating concentrations of adiponectin and adropin.


Sujet(s)
Adipokines/sang , Protéines du sang , Maladies des chats/sang , Diabète/médecine vétérinaire , Glucagon/sang , Surpoids/médecine vétérinaire , Animaux , Chats , Cholestérol/sang , Diabète/sang , Femelle , Mâle , Surpoids/sang , Triglycéride/sang
4.
Can Vet J ; 57(5): 514-8, 2016 May.
Article de Anglais | MEDLINE | ID: mdl-27152040

RÉSUMÉ

This study investigated the relationship between treatment protocol, survival to discharge, and relapse in 46 dogs diagnosed with primary immune-mediated thrombocytopenia (ITP) at the Western College of Veterinary Medicine between 2000 and 2013. Treatment was at the discretion of the attending clinician and consisted of either a corticosteroid alone or a corticosteroid plus a secondary therapy. There was no association between survival to discharge and treatment protocol (P = 0.23). Of the surviving in-patients, 39% experienced a relapse. Our study failed to show a significant difference in survival and relapse based on treatment protocol.


Résultat basé sur le protocole de traitement chez des patients atteints de thrombocytopénie canine primaire à médiation immunitaire : 46 cas (2000­2013). Cette étude a examiné la relation entre le protocole de traitement, la survie jusqu'au congé et la rechute chez 46 chiens diagnostiqués, entre 2000 et 2013, avec une thrombocytopénie primaire à médiation immunitaire (TPI) au Western College of Veterinary Medicine. Le traitement a été fait à la discrétion du clinicien traitant et se composait soit d'un corticostéroïde seul ou d'un corticostéroïde et d'une thérapie secondaire. Il n'y avait aucune association entre la survie jusqu'au congé et le protocole de traitement (P = 0,23). Parmi les patients hospitalisés survivants, 39 % ont eu une rechute. Notre étude n'a pas réussi à montrer une différence importante au niveau de la survie et de la rechute en fonction du protocole de traitement.(Traduit par Isabelle Vallières).


Sujet(s)
Maladies des chiens/thérapie , Thrombopénie/médecine vétérinaire , Animaux , Protocoles cliniques , Chiens , Femelle , Mâle , Évaluation des résultats et des processus en soins de santé , Récidive , Études rétrospectives , Analyse de survie , Thrombopénie/immunologie , Thrombopénie/thérapie
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