Veterinarski Glasnik (Jan 2009)

Dairy calf pneumonia: Effective treatment depends on early and accurate diagnosis

  • Panousis Nikolaos

DOI
https://doi.org/10.2298/VETGL0904177P
Journal volume & issue
Vol. 63, no. 3-4
pp. 177 – 187

Abstract

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Dairy calf pneumonia is one of the most economically important diseases of calves. A delayed diagnosis could result endemic herd problem, prolonged use of antibiotics, high recurrence rate, pulmonary abscessation and ear infections. The key for effective control is the early detection of pneumonia and the accurate diagnosis of the etiologic factor. For the early detection, a respiratory disease score was assigned based on rectal temperature, character of nasal discharge, eye discharge or ear appearance, and presence of a cough. Each clinical sign has a point scale from 0 (normal) to 4 (severe). The respiratory disease score is the sum of points from the 4 categories of clinical signs, with increasing values representing progressive severity. The scoring system results in a minimum score of 0 and a maximum score of 12. Calves with score 5 or higher, having at least 2 clinical signs of respiratory disease, are considered sick and have to be treated. For the accurate diagnosis of the etiological agent the best tool in a live calf is bronchoalveolar lavage (BAL) fluid collection. Sampling of severely affected animals should be avoided. New acute cases are ideal. BAL is performed in sedated calves using a sterilized, flexible catheter with a 5-cc balloon cuff. The fresh BAL fluid sample is processed within 2 hours of collection or refrigerated until analysis. Part of the sample is used for microbiology and the remaining is submitted for cytology. BAL fluid that yields homogenous (>106 CFU/ml) bacterial or positive Mycoplasma bovis culture is considered abnormal. A disproportionate lowering of macrophages (39%) provides evidence of an inflammatory response with or without a positive culture. The ideal antibiotic selection would be based on the antibiotic susceptibility pattern of lung pathogens after BAL fluid culture.

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