Technical Note No. CD 0338
Introduction
In an effort to decrease morbidity of bovine respiratory
disease (BRD) in feedlot cattle, it has become popular to
mass medicate calves on arrival with antibiotics, usually
injectables. After evaluation by the Food and Drug
Administration's Drug Efficacy Study Implementation
(DESI) program, Aureomycin was approved for the treatment
of bacterial pneumonia caused by
Pasteurella multocida organisms susceptible to chlortetracycline when fed at the rate
of 10 mg/lb body weight for not more than 5 days.
Aureomycin fed at 10 mg/lb body weight results in
concentrations of Aureomycin in blood and lung not
achievable with previous indications for use. This
technical bulletin describes a study which compares
the effects of
feeding Aureomycin at 10 mg/lb BW, and administering
Liquamycin® LA-200® (oxytetracycline HCI injection) to
newly arrived feedlot calves on health and performance
parameters.
Materials and Methods
Four-hundred seventy-five male Holstein calves from
California calf ranches were assembled at a southern
California feedlot. Average weight on arrival was 280.5 lb.
Calves were processed on arrival according to standard
feedyard procedures, individually weighed, and randomized
to two treatment groups: (1) two-hundred thirty-seven
head received 4.5 mL/cwt (9 mg/lb) of long-acting
oxytetracycline (LA-200) IM; and (2) two-hundred
thirty-eight head were fed Aureomycin at 10 mg/lb BW for 5
days starting on day of arrival. Aureomycin crumbles (4 g
chlortetracycline/lb) were administered once daily as a top
dress on the morning feeding. The injectable antibiotics
used in treatment of BRD were Nuflor® (florfenicol) on
days 1 and 3, followed by Naxcel® (ceftiofur) for 3 days, if
needed. The study was conducted for an average of 55
days.
Results
While BRD morbidity was low in both treatment groups,
the Aureomycin group experienced less morbidity (5% vs
8.4%) than the LA-200 group (Table 1). Day to first pull
was 0 for Aureomycin calves and 1 for the LA-200 treatment.
Average days to first pull was 19 and 16 for the
Aureomycin and LA-200 groups, respectively. Average
rectal temperature for all Aureomycin pulls was 105.5°F,
and 83% responded to first therapy; average rectal
temperature was 105.7°F for the LA-200 group and response
to first therapy was 95%. Neither group experienced death
loss.
Average daily gain was similar in both treatment groups
(2.52 lb for Aureomycin vs 2.51 lb for LA-200). Dry matter
feed efficiency was also similar (3.63 for Aureomycin and
3.69 for LA-200). Cost of gain (feed, medicine and processing)
was $0.452 for calves fed Aureomycin and
$0.466 for calves receiving LA-200.
Conclusions
Numerically, calves medicated with Aureomycin experienced
less sickness due to BRD, performed as well as
those calves receiving LA-200, and experienced a lower
cost of gain for the duration of the study.
The use of Aureomycin offers advantages over injectable
antibiotics beyond performance and health. When administered
on arrival, or at any point in the feeding period,
Aureomycin does not present negative quality assurance
aspects, such as injection site soreness or carcass blemishes,
which may occur with injectable antibiotics.
When considering mass medication of cattle for BRD with
either Aureomycin or LA-200, Aureomycin fed at 10 mg/lb
body weight for 5 days can be an effective option.
Aureomycin® is a registered trademark of Alpharma Inc.
Liquamycin® LA-200® is a registered trademark of Pfizer Inc.
Nuflor® is a registered trademark of Schering-Plough Corp.
Naxcel® is a registered trademark of Pharmacia & Upjohn Co.
Rumensin® and Tylan® are registered trademarks of Elanco Animal Health.
Data in Alpharma research file.
Copyright © 2002 Alpharma Inc.
Alpharma Inc.
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Additional technical information is available at
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