Using chitosan microparticles to treat metritis in lactating dairy cows.


Journal

Journal of dairy science
ISSN: 1525-3198
Titre abrégé: J Dairy Sci
Pays: United States
ID NLM: 2985126R

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 09 12 2019
accepted: 16 03 2020
pubmed: 9 6 2020
medline: 26 11 2020
entrez: 8 6 2020
Statut: ppublish

Résumé

The main objective of this study was to evaluate the efficacy of intrauterine administration of chitosan microparticles (CM) in curing metritis in dairy cows. A secondary objective was to evaluate the effects of metritis treatments on milk yield, survival, and reproductive performance. Cows with a fetid, watery, red-brownish vaginal discharge were diagnosed with metritis. Holstein cows (n = 826) with metritis from 3 dairies located in northern Florida were blocked by parity (primiparous or multiparous) and, within each block, randomly assigned to one of 3 treatments: CM (n = 276) = intrauterine infusion of 24 g of CM dissolved in 40 mL of sterile distilled water at the time of metritis diagnosis (d 0), 2 (d 2), and 4 (d 4) d later; ceftiofur (CEF; n = 275) = subcutaneous injection of 6.6 mg/kg ceftiofur crystalline-free acid in the base of the ear at d 0 and d 3; Control (CON; n = 275) = no treatment applied at metritis diagnosis. All groups could receive escape therapy if condition worsened. Cure was considered when vaginal discharge became mucoid and not fetid. A group of nonmetritic (NMET; n = 2,436) cows was used for comparison. Data were analyzed by generalized linear mixed and Cox's proportional hazard models. Cows in CM and CON had lesser risk of metritis cure on d 12 than cows in CEF (58.6 ± 5.0 vs. 61.9 ± 4.9% vs. 77.9 ± 3.9, respectively). The proportion of cows culled within 60 days in milk (DIM) was greater for cows in CM than for cows in CEF and CON (21.5 ± 2.7 vs. 9.7 ± 1.9 vs. 11.3 ± 2.0%, respectively). Treatment did not affect rectal temperature or plasma nonesterified fatty acids, β-hydroxybutyrate, and haptoglobin concentrations. Milk yield in the first 60 DIM differed for all treatments, and it was lowest for CM (35.8 ± 0.3 kg/d), followed by CON (36.8 ± 0.3 kg/d) and CEF (37.9 ± 0.3 kg/d). The hazard of pregnancy up to 300 DIM was lesser for CM than CEF (hazard ratio = 0.62; 95% CI: 0.50-0.76), for CM than CON (hazard ratio = 0.77; 95% CI: 0.62-0.95) and for CON than CEF (hazard ratio = 0.80; 95% CI: 0.65-0.99). Culling was greater, and milk yield and fertility were lesser for CEF than NMET. In summary, CM did not improve the cure of metritis, and was detrimental to milk yield, survival, and fertility compared with CON. In contrast, CEF increased the cure of metritis, milk yield, and fertility compared with CM and CON. Finally, the negative effects of metritis on milk yield culling and fertility could not be completely reversed by CEF.

Identifiants

pubmed: 32505402
pii: S0022-0302(20)30430-6
doi: 10.3168/jds.2019-18028
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Cephalosporins 0
Fatty Acids, Nonesterified 0
ceftiofur 83JL932I1C
Chitosan 9012-76-4
3-Hydroxybutyric Acid TZP1275679

Types de publication

Journal Article Randomized Controlled Trial, Veterinary

Langues

eng

Sous-ensembles de citation

IM

Pagination

7377-7391

Informations de copyright

Copyright © 2020 American Dairy Science Association. Published by Elsevier Inc. All rights reserved.

Auteurs

E B de Oliveira (EB)

Department of Large Animal Clinical Sciences, University of Florida, Gainesville 32610.

F Cunha (F)

Department of Large Animal Clinical Sciences, University of Florida, Gainesville 32610.

R Daetz (R)

Department of Large Animal Clinical Sciences, University of Florida, Gainesville 32610.

C C Figueiredo (CC)

Department of Large Animal Clinical Sciences, University of Florida, Gainesville 32610.

R C Chebel (RC)

Department of Large Animal Clinical Sciences, University of Florida, Gainesville 32610.

J E Santos (JE)

Department of Animal Sciences, University of Florida, Gainesville 32610; D. H. Barron Reproductive and Perinatal Biology Research Program, University of Florida, Gainesville 32610.

C A Risco (CA)

Department of Large Animal Clinical Sciences, University of Florida, Gainesville 32610.

K C Jeong (KC)

Department of Animal Sciences, University of Florida, Gainesville 32610; Emerging Pathogens Institute, University of Florida, Gainesville 32610.

V S Machado (VS)

Department of Veterinary Sciences, Texas Tech University, Lubbock 79409.

K N Galvão (KN)

Department of Large Animal Clinical Sciences, University of Florida, Gainesville 32610; D. H. Barron Reproductive and Perinatal Biology Research Program, University of Florida, Gainesville 32610. Electronic address: galvaok@ufl.edu.

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Classifications MeSH