Postpartum uterine infections results from uterine contamination with bacteria during parturition. The prevalence of uterine infections varies considerably among studies. Uterine infection implies adherence of pathogenic organisms to the mucosa, colonization or penetration of the epithelium, and/or release of bacterial toxins that lead to establishment of uterine disease. The development of uterine disease depends on the immune response of the cow, as well as the species and number (load or challenge) of bacteria. The postpartum uterus has a disrupted surface epithelium in contact with fluid and tissue debris that can support bacterial growth. A variety of species of bacteria, both Gram-positive and Gram-negative aerobes and anaerobes, can be isolated from the early postpartum uterus. Most of these are environmental contaminants that are gradually eliminated during the first 6 weeks postpartum. A normal postpartum cow resolves uterine infection by rapid involution of the uterus and cervix, discharge of uterine content, and mobilization of natural host defenses, including mucus, antibodies and phagocytic cells. Clinical signs of uterine infection vary with the virulence of the causative organisms and the presence of factors that predispose to the disease. The treatment of endometritis and metritis in bovine should be directed towards improving fertility. The antibiotic should be active against the main uterine pathogens and should maintain its activity in the environment of the uterus. Also, should not inhibit the normal defense mechanisms and should be well tolerated and not induce irritation in the endometrium. Effective use of hormones in uterine infection requires knowledge of both normal reproductive endocrinology and the therapeutic characteristics of available hormonal preparations. (c) 2008 Elsevier B.V. All rights reserved.
机构:
Swansea Univ, Med Sch, Inst Life Sci, Singleton Pk, Swansea SA2 8PP, W Glam, WalesSwansea Univ, Med Sch, Inst Life Sci, Singleton Pk, Swansea SA2 8PP, W Glam, Wales
Sheldon, I. Martin
Molinari, Paula C. C.
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Univ Florida, Dept Anim Sci, Gainesville, FL 32611 USASwansea Univ, Med Sch, Inst Life Sci, Singleton Pk, Swansea SA2 8PP, W Glam, Wales
Molinari, Paula C. C.
Ormsby, Thomas J. R.
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Swansea Univ, Med Sch, Inst Life Sci, Singleton Pk, Swansea SA2 8PP, W Glam, WalesSwansea Univ, Med Sch, Inst Life Sci, Singleton Pk, Swansea SA2 8PP, W Glam, Wales
Ormsby, Thomas J. R.
Bromfield, John J.
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Univ Florida, Dept Anim Sci, Gainesville, FL 32611 USASwansea Univ, Med Sch, Inst Life Sci, Singleton Pk, Swansea SA2 8PP, W Glam, Wales
机构:
Univ Georgia, Dept Large Anim Med, Coll Vet Med, Athens, GA 30602 USA
Univ Georgia, Dept Populat Hlth, Coll Vet Med, Athens, GA 30602 USAUniv Georgia, Dept Large Anim Med, Coll Vet Med, Athens, GA 30602 USA
Credille, B. C.
Giguere, S.
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Univ Georgia, Dept Large Anim Med, Coll Vet Med, Athens, GA 30602 USAUniv Georgia, Dept Large Anim Med, Coll Vet Med, Athens, GA 30602 USA
Giguere, S.
Vickroy, T. W.
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Univ Florida, Coll Vet Med, Dept Physiol Sci, Gainesville, FL 32610 USAUniv Georgia, Dept Large Anim Med, Coll Vet Med, Athens, GA 30602 USA
Vickroy, T. W.
Fishman, H. J.
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Univ Georgia, Dept Large Anim Med, Coll Vet Med, Athens, GA 30602 USAUniv Georgia, Dept Large Anim Med, Coll Vet Med, Athens, GA 30602 USA
Fishman, H. J.
Jones, A. L.
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Univ Georgia, Dept Populat Hlth, Coll Vet Med, Athens, GA 30602 USAUniv Georgia, Dept Large Anim Med, Coll Vet Med, Athens, GA 30602 USA
Jones, A. L.
Mason, M. E.
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Univ Georgia, Dept Large Anim Med, Coll Vet Med, Athens, GA 30602 USAUniv Georgia, Dept Large Anim Med, Coll Vet Med, Athens, GA 30602 USA
Mason, M. E.
DiPietro, R. O.
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Univ Georgia, Dept Large Anim Med, Coll Vet Med, Athens, GA 30602 USAUniv Georgia, Dept Large Anim Med, Coll Vet Med, Athens, GA 30602 USA
DiPietro, R. O.
Ensley, D. T.
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Boehringer Ingelheim Vetmedica Inc, St Joseph, MO USAUniv Georgia, Dept Large Anim Med, Coll Vet Med, Athens, GA 30602 USA