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. 2006 Jun;72(6):3872–3878. doi: 10.1128/AEM.02239-05

TABLE 1.

Criteria for clinical diagnosis and therapeutic decisions used in the clinical triala

Health condition Clinical sign(s) Score Therapeutic choice(s)
Nonantimicrobial Antimicrobialb
Diarrhea Formed 0
Semiformed 1
Watery 2 Bismuth, Kaolin-Pectin Ceftiofurc
Watery with mucus 3 Kaolin-Pectin Ceftiofurc
Blood in feces 4 Kaolin-Pectin, UAA Ceftiofurc
Respiratory signs Normal 0
Rhinitis 1
Coughing 2 Ceftiofurc
Heavy thoracic breathing 3 Ceftiofur
Abdominal breathing 4 Ceftiofur
Dehydration Normal appearance 0
Sunken eyes 1 Electrolytesb
Skin tented 5-10 s 2 Electrolytes
Skin tented >10 s 3 Electrolytes
Attitude Alert 0
Depressed 1 Flunixine meglumine
Nonresponsive 2 Flunixine meglumine
Appetite Normal 0
Consuming <3/4 bottle 1
Eye appearance Normal 0
Swelling/redness/discharge 1 Penicillin G, subconjunctival
Umbilicus/joints Normal 0
Swelling/heat/pain/lameness 1 Iodine, topical Penicillin G
Normal 0
Otitis Head tilt, hanging head 1 Tilmicosin
a

The clinical trial assessed the influence of antimicrobial use in milk replacer and as disease therapy in 120 preweaned calves on antimicrobial susceptibility in fecal commensal Escherichia coli.

b

Treatment was initiated if clinical sign was combined with appetite loss, depressed attitude, or multiple diagnosis.

c

Ceftiofur dose, 2.2 mg/kg/day for 3 to 5 days; penicillin G, 300,000 IU/ml, 2.2 ml/100 kg/day for 1 to 3 days; tilmicosin, 10 mg/kg/day for 3 days.