RESUMO
BACKGROUND: Papillomavirus infections in dogs have a variety of manifestations and involve multiple viral genera. Canine pedal papillomas have been infrequently studied and reported in the literature. OBJECTIVE: To report the signalment, history, treatment and outcome of biopsy-confirmed cases of canine pedal papillomatosis, collected from veterinarians across the United States and Canada ANIMALS: Medical records from 44 dogs were submitted by North American veterinarians. METHODS AND MATERIALS: Surveys were submitted through the Veterinary Information Network for biopsy-confirmed cases of canine pedal papillomatosis. Submissions included information on patient signalment, history, biopsy report, treatment and outcome. RESULTS: Forty-four cases were reviewed. The median age of presentation was four years old. Dogs most commonly presented with lameness and/or paw licking/chewing. Only one paw was affected in 35 cases, and front paws were more often affected than back paws. Twenty-eight dogs presented with one mass. Histopathological evaluation documented 33 cases of noninverted papillomas and 11 cases of inverted papillomas. Thirty-four papillomas resolved in total; 25 resolved within three weeks after biopsy collection. Twenty-one dogs received no additional treatment and 15 of those cases resolved. Azithromycin was the most commonly reported treatment initiated after biopsy was collected. CONCLUSIONS AND CLINICAL IMPORTANCE: The biological behaviour of canine pedal papillomas in this case series was similar to oral papillomas, and most lesions resolved with or without additional treatment. Further research is needed to better characterise the causative papillomavirus types and genera involved in the development of canine pedal papillomas.
Assuntos
Doenças do Cão , Papiloma , Infecções por Papillomavirus , Animais , Doenças do Cão/diagnóstico , Doenças do Cão/tratamento farmacológico , Doenças do Cão/epidemiologia , Cães , Papiloma/diagnóstico , Papiloma/tratamento farmacológico , Papiloma/veterinária , Papillomaviridae , Infecções por Papillomavirus/diagnóstico , Infecções por Papillomavirus/tratamento farmacológico , Infecções por Papillomavirus/veterinária , Estudos RetrospectivosRESUMO
BACKGROUND: Meticillin-resistant (MR) staphylococcal species have been cultured from veterinary hospital environments and veterinary instruments. Pet-grooming salon environments and grooming tools may pose a risk for dissemination of MR staphylococcal bacteria into the pet population. OBJECTIVE: The objectives of this study were to investigate the frequency of MR staphylococcal colonization of pet-grooming salons and to collect information regarding cleaning procedures in grooming salons. METHODS AND MATERIALS: A nonrandomized, observational study was performed in 2018. Locations inside 19 grooming salons near Tacoma, WA, USA, were sampled and selectively cultured for MR, coagulase-positive staphylococci. Sampled sites included clipper blades and handles, leashes, rims of bathtub drains, insides of shampoo caps, and bathtub spray hoses or faucet handles. Grooming salons were asked to complete surveys regarding their cleaning practices. RESULTS: Meticillin-resistant coagulase-positive staphylococci were isolated from 12 of 19 grooming salons and 25 of 112 total samples. Meticillin-resistant S. pseudintermedius, S. aureus and S. schleiferi were isolated from multiple salons, most commonly from electric clipper blades, clipper handles and grooming leashes. No statistically significant correlations were identified between cleaning practices and the isolation of MR coagulase-positive staphylococci. CONCLUSIONS AND CLINICAL IMPORTANCE: Clipper blades, clipper handles and leashes are potential fomites for MR staphylococci in a grooming salon; increased disinfection practices for these items are indicated. A prospective, controlled, large-scale study is warranted to examine the effect of grooming salon hygiene practices on the isolation of MR staphylococci in salons.
Assuntos
Equipamentos e Provisões/veterinária , Fômites/microbiologia , Abrigo para Animais , Staphylococcus aureus Resistente à Meticilina/isolamento & purificação , Infecções Cutâneas Estafilocócicas/veterinária , Animais , Desinfecção , Doenças do Cão/microbiologia , Cães , Equipamentos e Provisões/microbiologia , Staphylococcus aureus Resistente à Meticilina/genética , Estudos Prospectivos , Infecções Cutâneas Estafilocócicas/microbiologiaRESUMO
Objectives This study was designed to evaluate the efficacy and safety of reducing ciclosporin (CsA) dosing frequency from daily to every other day (EOD) or twice a week (TW) according to clinical response in cats with hypersensitivity dermatitis (HD) and treated with CsA. Methods One hundred and ninety-one cats with HD were given 7 mg/kg CsA daily for at least 4 weeks. Depending on clinical response, the dosing frequency was tapered from daily to EOD over the next 4 weeks and further to TW for an additional 4 weeks. Safety was evaluated through physical examinations, clinical pathology and the monitoring of adverse events (AEs). Results The majority of cats were able to have their dose of CsA tapered to either EOD (15.5%) or TW (62.9%) according to the clinical response. Observed AEs were most frequently mild and self-limiting vomiting and diarrhea. A higher percentage of AEs occurred with daily administration (73%) compared with other dosing regimens (27%). Conclusions and relevance Following 4 weeks of daily dosing at 7 mg/kg, CsA may be tapered to EOD or TW while maintaining the desired therapeutic response in cats with HD. Additionally, CsA appears to be well tolerated with fewer AEs at EOD or TW dosing. Establishing the lowest effective dosing frequency of CsA improves the drug's safety profile.
Assuntos
Doenças do Gato/tratamento farmacológico , Ciclosporina/administração & dosagem , Dermatite Atópica/veterinária , Imunossupressores/administração & dosagem , Administração Oral , Animais , Doenças do Gato/patologia , Gatos , Dermatite Atópica/tratamento farmacológico , Relação Dose-Resposta a Droga , Esquema de Medicação/veterinária , Feminino , Masculino , Índice de Gravidade de Doença , Resultado do TratamentoRESUMO
Endemic Microsporum canis dermatophytosis was identified in a large, open admission, private, no-kill shelter that admitted >1200 cats per year. Fungal culture (FC) screening revealed that 166/210 (79%) and 38/99 (38%) cats in the non-public and public area were culture positive, respectively. However, pending screening FC results, the 99 cats in the public area were treated with once-weekly lime sulfur rinses and monitored with once-weekly FC. Cats in the non-public area were not treated. When FC results were available, cats were separated into low-risk (n = 61) and high-risk (n = 38) groups based upon the presence or absence of skin lesions. Low-risk cats continued to receive once-weekly topical lime sulfur and rapidly achieved culture-negative status. High-risk cats were divided into two groups based upon the number of colony-forming units/plate (low or high). All 38 cats were treated with twice-weekly lime sulfur and oral terbinafine and within 6-7 weeks only 5/38 cats were still FC-positive. These cats were moved to a separate room. Dermatophytosis was eradicated within 5 months; eradication was prolonged owing to reintroduction of disease into the remaining room of cats under treatment from three kittens returning from foster care. Continued admissions and adoptions were possible by the institution of intake procedures that specifically included careful Wood's lamp examination to identify high-risk cats and use of a 'clean break strategy'.
Assuntos
Antifúngicos/uso terapêutico , Doenças do Gato/tratamento farmacológico , Dermatomicoses/tratamento farmacológico , Dermatomicoses/veterinária , Abrigo para Animais , Animais , Compostos de Cálcio/uso terapêutico , Doenças do Gato/microbiologia , Doenças do Gato/patologia , Gatos , Dermatomicoses/microbiologia , Gerenciamento Clínico , Quimioterapia Combinada , Microsporum/isolamento & purificação , Sulfetos/uso terapêutico , Tinha/tratamento farmacológico , Resultado do TratamentoRESUMO
BACKGROUND: Dermatophytosis is an important contagious and infectious skin disease in an animal shelter. Itraconazole is the commonly used systemic antifungal drug, but it is expensive in some countries and, at times, difficult to obtain. Terbinafine is a fungicidal allylamine with documented in vitro and in vivo efficacy against Microsporum canis in pet cats and in cats with experimental infections. HYPOTHESIS/OBJECTIVES: To describe the use of oral terbinafine for the treatment of M. canis dermatophytosis in shelter cats. METHODS: The response to treatment of 85 shelter cats with naturally occurring M. canis dermatophytosis was monitored by examination, weekly toothbrush fungal cultures and the number of colony-forming units on fungal culture plates. Cats were treated with either 14 (n = 21) or 21 days (n = 64) of terbinafine per os (p.o.) along with concurrent twice weekly lime sulphur rinses and daily environmental disinfection. RESULTS: Cats treated with 14 days of terbinafine p.o. showed an initial response to therapy but by week 6 had relapsed and required rescue therapy with a course of itraconazole (10 mg/kg p.o.) to obtain a cure. Cats treated with 21 days of terbinafine p.o. showed a response to treatment similar to published reports using itraconazole p.o. for 21 days. The mean and median number of days to mycological cure was 22.70 (range 13-39). Terbinafine was well tolerated. None of the cats developed oral lesions postgrooming of lime sulphur rinses. CLINICAL SIGNIFICANCE: Where itraconazole is not available, substitution with terbinafine in established protocols may allow shelters to treat cats that otherwise would go untreated.
Assuntos
Antifúngicos/uso terapêutico , Compostos de Cálcio/uso terapêutico , Doenças do Gato/tratamento farmacológico , Dermatomicoses/veterinária , Naftalenos/uso terapêutico , Sulfetos/uso terapêutico , Animais , Antifúngicos/administração & dosagem , Doenças do Gato/microbiologia , Gatos , Dermatomicoses/tratamento farmacológico , Dermatomicoses/microbiologia , Esquema de Medicação , Microsporum/efeitos dos fármacos , Naftalenos/administração & dosagem , TerbinafinaRESUMO
Feline allergen specific immunotherapy (ASIT) is considered to be a safe and effective treatment for feline atopy. ASIT is defined as the practice of administering gradually increasing quantities of an allergen extract to an allergic subject. The purpose of which is to reduce or eliminate the symptoms associated with subsequent exposures to the causative allergen. ASIT offers an effective and safe treatment option for cats. Reported success rates range for 60 to 78% in feline atopic patients. Additionally, the reported incidence of side effects in feline atopic patients undergoing ASIT is very low and mainly anecdotal.
Assuntos
Alérgenos/imunologia , Doenças do Gato/terapia , Dermatite Atópica/veterinária , Hipersensibilidade Imediata/veterinária , Imunoterapia/veterinária , Alopecia/etiologia , Alopecia/terapia , Alopecia/veterinária , Animais , Gatos , Dermatite Atópica/terapia , Hipersensibilidade Imediata/terapia , Imunoterapia/métodos , Segurança , Resultado do TratamentoRESUMO
Rush immunotherapy has been shown to be as safe as conventional immunotherapy in canine atopic patients. Rush immunotherapy has not been reported in the feline atopic patient. The purpose of this pilot study was to determine a safe protocol for rush immunotherapy in feline atopic patients. Four atopic cats diagnosed by history, physical examination and exclusion of appropriate differential diagnoses were included in the study. Allergens were identified via liquid phase immunoenzymatic testing (VARL: Veterinary Allergy Reference Labs, Pasadena, CA). Cats were premedicated with 1.5 mg triamcinolone orally 24 and 2 h prior to first injection and 10 mg hydroxyzine PO 24, 12 and 2 h prior to first injection. An intravenous catheter was placed prior to first injection. Allergen extracts (Greer Laboratories, Lenoir, North Carolina) were all administered subcutaneously at increasing protein nitrogen units (pnu) every 30 minutes for 5 h to maintenance dose of 15,000 pnus ml-1. Vital signs were assessed every 15 minutes. Two cats developed mild pruritus and the subsequent injection was delayed 30 minutes. No changes in either cat's vital signs were noted, nor was there any further pruritus. All four cats successfully completed rush immunotherapy. Two cats developed a dermal swelling on the dorsal neck one week later. In these four cats, this protocol appeared to be a safe regimen to reach maintenance therapy. A larger sample of feline patients is needed to determine the incidence of adverse reactions and to follow the success of ASIT based upon this method of induction.