The present study involved seven horses in a randomized crossover clinical trial to evaluate the effect of lidocaine on horses with induced endotoxemia. Horses received intravenous lidocaine (1.5 mg/kg bolus, followed by 0.05 mg/kg bwt/min) or placebo (0.9% sodium chloride at the same manner) one hour before LPS administration (0.03 μg/kg, IV infusion over 30 min). We monitored clinic and hematologic parameters, abdominal auscultation, ultrasound, and pain over time. No relevant clinical differences existed between treatments regarding peristalsis, abdominal pain, or any other parameters before and after endotoxemia induction. These findings do not support the clinical use of lidocaine to mitigate abdominal pain and intestinal hypomotility promoted by endotoxemia in horses.

The present study involved seven horses in a randomized crossover clinical trial to evaluate the effect of lidocaine on horses with induced endotoxemia. Horses received intravenous lidocaine (1.5 mg/kg bolus, followed by 0.05 mg/kg bwt/min) or placebo (0.9% sodium chloride at the same manner) one hour before LPS administration (0.03 mu g/kg, IV infusion over 30 min). We monitored clinic and hematologic parameters, abdominal auscultation, ultrasound, and pain over time. No relevant clinical differences existed between treatments regarding peristalsis, abdominal pain, or any other parameters before and after endotoxemia induction. These findings do not support the clinical use of lidocaine to mitigate abdominal pain and intestinal hypomotility promoted by endotoxemia in horses.

A standing oral examination under sedation in horses is essential to facilitate the handling and ensure an excellent examination. This study aimed to determine if the use of diazepam associated with detomidine would increase the action of the α2 agonist (detomidine), mainly by tongue motion and chewing reduction without excessive destabilization. Twelve adult horses of different age, breed and gender underwent dental correction. The animals were randomly assigned to two treatments: detomidine (20 µg.kg -1 , IV) and diazepam (20 µg.kg -1 , IV) (DD; n=6) or detomidine (20 µg.kg -1 , IV) and 0.9% NaCl (DS; n=6). Tongue relaxation and exposure, heart rate, PR interval, respiratory rate, systolic blood pressure, rectal temperature, second-degree atrioventricular blocks, degree of ataxia and head movement were assessed at nine separated time points. Height of head above ground (HHAG) was

A sedação para o exame odontológico, em estação, nos equinos é essencial para facilitar o manejo e garantir um exame de excelência. O presente estudo objetivou avaliar se o diazepam associado à detomidina potencializaria a sedação do agonista α2 (detomidina), principalmente pela redução do movimento da língua e mastigação sem excessiva desestabilização. Foram examinados 12 equinos adultos de diferentes idades, raças e sexos submetidos a correção dos arcos dentários e distribuídos aleatoriamente entre dois tratamentos: detomidina (20 µg.kg-1, IV) e diazepam (20 µg.kg-1, IV) (DD; n=6) ou detomidina (20 µg.kg-1, IV) e solução salina de NaCl 0,9% (DS; n=6). Foram avaliados o relaxamento e a exposição da língua, frequência cardíaca, intervalo PR, frequência respiratória, pressão arterial sistólica, temperatura retal, bloqueios atrioventriculares de segundo grau, grau de ataxia, movimento da cabeça, em nove momentos. E a distância da cabeça ao solo (HHAG) foram avaliadas em três momentos. Sempre que houve necessidade de aumentar a sedação, foi administrado um bolus de detomidina adicional (5µg.kg-1, IV). Todos os tratamentos proporcionaram sedação e relaxamento muscular. Foram observadas diferenças entre os momentos para o relaxamento da língua (língua VAS mm) e isto foi melhor observado em T7 para o tratamento DD e T5 para o tratamento DS e manteve-se significativamente inferior à linha de base durante todo o tempo avaliado. O presente estudo sugere que a detomidina forneceu sedação adequada em cavalos submetidos ao exame odontológico mas não há necessidade de utilizar o diazepam da forma proposta porque não foi encontrada qualquer diferença entre tratamentos para qualquer variável estudada. A adição de diazepam não melhorou a sedação e nem diminuiu o movimento da língua.

ABSTRACT The objective of this study was to determine pH and the concentrations of Calcium (Ca2+), Magnesium (Mg2+), Chloride (Cl-), Sodium (Na+), Potassium (K+) and Calcium (Ca2+) in the mammary gland secretion in pre-foaling Mangalarga Marchador (MM) mares to determine the best method to predict parturition in the breed. Forty-two pregnant MM mares were evaluated once daily from 310 days of gestation until parturition. Mammary gland secretion pH, measured by pH meter and pH paper strip, Mg2+, Ca2+ and Cl- levels significantly changed during the last 10 days prior to parturition (p<0.05). The lowest pH mean value (pH meter=6.67±0.42; pH strip=6.23±0.53) and significantly higher mean concentrations of Ca2+ (12.6±5.8mmol/L) and Mg2+ (10.93±3.66mmol/L) were obtained 24 hours prior to foaling (p<0.0001). Chloride levels reduced significantly 8 days prior to parturition (p<0.0001) but remained unchanged until the due date. Mammary gland pH secretion, measured by pH meter and pH paper strip, was effective to predict parturition. Quantitative pH values obtained with the pH meter had a greater accuracy in comparison to pH paper strips, but a strong correlation was found between both methods. Calcium and magnesium were the only electrolytes that changed in concentration immediately prior to parturition and are better indicators of when not to expect foaling.

EnglishClostridioides (Clostridium) difficile is the main causative agent of antimicrobial-related diarrhea in humans and a major pathogen-associated enteric disorder in foals and adult horses. Moreover, studies have suggested that animals are a possible reservoir of toxigenic C. difficile strains for humans. Despite this known importance, the epidemiology of C. difficile infection (CDI) in equine is still largely unknown. Therefore, this study described six cases of equine CDI occurring in Minas Gerais, Brazil, including the characterization of the isolates. All but one equine included in this research developed CDI after antimicrobial therapy, three of which occurred during hospitalization. Coinfection with Salmonella Heidelberg and S. Infantis was detected in three cases, making the antimicrobial treatment challenging. All animals recovered after metronidazole administration. All C. difficile isolates were susceptible to metronidazole and vancomycin, while three were resistant to moxifloxacin and two were resistant to clindamycin. The isolates were classified as RT126 (n = 4), RT078 (n = 1), and RT014/020 (n = 1), all previously reported infecting humans and animals worldwide portuguesClostridioides (Clostridium) difficile e o principal agente envolvido em diarreias associadas ao uso de antimicrobianos em seres humanos e um enteropatogeno de grande relevância em quadros de diarreia em potros e equinos adultos. Em adicao, estudos tem sugerido que animais sao possiveis reservatorios de estirpes toxigenicas de C. difficile para humanos. Apesar da importância na saude animal e humana, a epidemiologia da infeccao por C. difficile (ICD) e ainda pouco conhecida. Dessa forma, o presente estudo tem como objetivo caracterizar seis casos de diarreia por C. difficile ocorridos em Minas Gerais, Brasil. Com excecao de um animal, todos os equinos incluidos no presente estudo desenvolveram ICD apos antibioticoterapia, tres dos quais durante a hospitalizacao. Coinfeccao por Salmonella Heidelberg e S. Infantis foi detectada em tres casos, tornando o tratamento antimicrobiano desafiador. Todos os animais recuperaram apos administracao de metronidazol. Os isolados obtidos no presente estudo foram sensiveis a metronidazol e vancomicina, porem tres estirpes foram resistentes a moxifloxacina e duas a clindamicina. Os isolados foram classificados como ribotipos 126 (n=4), 078 (n=1) e 014/020 (n=1), todos previamente relatados em seres humanos com ICD no Brasil e em outros paises

ABSTRACT: Clostridioides (Clostridium) difficile is the main causative agent of antimicrobial-related diarrhea in humans and a major pathogen-associated enteric disorder in foals and adult horses. Moreover, studies have suggested that animals are a possible reservoir of toxigenic C. difficile strains for humans. Despite this known importance, the epidemiology of C. difficile infection (CDI) in equine is still largely unknown. Therefore, this study described six cases of equine CDI occurring in Minas Gerais, Brazil, including the characterization of the isolates. All but one equine included in this research developed CDI after antimicrobial therapy, three of which occurred during hospitalization. Coinfection with Salmonella Heidelberg and S. Infantis was detected in three cases, making the antimicrobial treatment challenging. All animals recovered after metronidazole administration. All C. difficile isolates were susceptible to metronidazole and vancomycin, while three were resistant to moxifloxacin and two were resistant to clindamycin. The isolates were classified as RT126 (n = 4), RT078 (n = 1), and RT014/020 (n = 1), all previously reported infecting humans and animals worldwide.