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█ _ 0 حصريا كتاب ❞ Bovine mastitis therapy and why it fails ❝ 2024 fails: من كتب طب بيطرى Continuing education — Voortgesette opleiding Bovine fails J H du Preez a INTRODUCTION Mastitis can occur at any stage of a cow’s productive life Microbiological investiga tions clinical bovine reveal a causative agent in 75–95% cases There is good evidence that microorganisms are involved almost all cases 36,40,49 At least 137 infectious causes mastitis are known, but the majority are caused by only few common bacterial pathogens, namely staphylococci, strep tococci, coliforms and Arcanobacterium pyogenes For antibacterial to be successful, active drug must attain and maintain concentrations exceeding the minimum inhibitory concentration (MIC) focus infection for long enough break production and toxin producing cycle causative pathogen 3 This may be prevented a number factors include udder pa thology poor selection anti microbials, is also influenced the route administration Therapy may have results owing tissue damage and introduction new infections dur ing treatment, or failure eliminate the management predispose to Although there an underly assumption primary goal of antibacterial kill bac teria normal sterile, usually best achieved is temporary reduction suppression of the bacterial population allow host to overcome The mecha nisms cleanse are evidently poorly developed some cows, as re lapses re commonly follow antimicrobial Udder infections tend dynamic, stress con tribute becoming clin ically apparent 48,49 The purpose this article provide an update on and reasons its PRINCIPLES OF MASTITIS THERAPY The success depends on correct diagnosis, appropriateness route drug selected, which treatment initi ated, severity pathology, sup portive elimination of predisposing There no standard treatment mastitis, advocated that forms should treated according in flammation 12 Bovine most commonly treated intramammary infusion of drugs 29,64 choice in subclinical, mild moderately severe mastitis, used adjunct to parenteral severe mas titis Some clinicians prefer intra mammary administration, without systemic even severe disease 40 For effective intramammary treatment, drugs distribute throughout rapidly ab sorbed into general blood circulation (Table 1) Significantly better can be obtained when adminis tered intracisternally 1 of 5 % glu cose solution, rather than 50 m saline 23 disadvantage local application of antimicrobials slow uneven dis tribution certain infected udder (Table In acute, disease, distribution through be impaired inflammation blockage of milk ducts debris Parenteral tration these problems, al though usual administer agents concurrently intramammary route 17 Severely inflamed udders should be milked out frequently, with aid of oxytocin if necessary peracute acute clinical systemic signs, combined intramammary treatment compatible antibiotics, supplemented supportive therapy, is recommended 64 It always desirable treat infectious mastitis according antimicrobial drug sensitivity pattern pathogens and experience 40 basic rule in selecting opt one as narrow spectrum possible, focus treatment specific pathogen and minimise side effects Because takes time do determinations, broad antibiotics given initially practical reasons, based on knowledge pharmacokinetic prop erties formula tion 9,29,32,65,66,67 general, narrow spec trum bacteriocidal and those broad bacterio static 58 Response increases with persistence antibiotic concentration must at least exceed MIC value the pathogen, preferably MBC value (minimum concentra tion) If bacteriostatic drugs are used, need high con centrations target organ creased Successful intravenous intramuscu lar depends effective passage from milk to reach foci infection, largely governed lipid solubility, degree of ionisation (dependent dissocia tion constant (pKa)), extent of protein binding with plasma 44,45,53 , since cross the blood–milk barrier passive diffusion 30 Only unbound free dif fuse blood–milk and exert pharmacological antimicrobial 0038 2809 Jl S Afr vet Ass (2000) 71(3): 201–208 201 a Technology Transfer Division, ARC Onderstepoort Veterinary Institute, Private Bag X05, Onderstepoort, 0110 South Africa Treatment cause, manifestation susceptibility Mastitis unsuccessful pathological changes parenchyma result inflammatory reaction mastitogenic bacteria, properties antimicrobial drugs, related factors, animal husbandry veterinary interventions مجاناً PDF اونلاين الطب البيطري (بالإنجليزية: Veterinary medicine) أو البيطرة هو تطبيق المبادئ الطبية والتشخيصية والعلاجية الحيوانات الإنتاجية والمنزلية والبرية يحتوي هذا القسم علي العديد الكتب المتميزة حول المجال يمارس عادة عيادة بيطرية مستشفى بيطري المزرعة للطب دور كبير حماية البشر الأمراض التي تنتقل عن طريق الأكل أصبح التخصص شائعاً السنوات الأخيرة ومن تلك التخصصات: التخدير علم السلوك الجلدية الحالات الطارئة والعناية الحثيثة الباطني امراض القلب السرطان العيون الأعصاب المشتركة المعدية التناسليات والولادة التصوير الشعاعي والجراحة

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Bovine mastitis therapy and why it fails
كتاب

Bovine mastitis therapy and why it fails

Bovine mastitis therapy and why it fails
كتاب

Bovine mastitis therapy and why it fails

عن كتاب Bovine mastitis therapy and why it fails:
Bovine mastitis therapy and why it fails من كتب طب بيطرى

Continuing education — Voortgesette opleiding
Bovine mastitis therapy and why it fails
J H du Preez
a
INTRODUCTION
Mastitis can occur at any stage of a cow’s
productive life. Microbiological investiga

  • tions of clinical bovine mastitis reveal a
    causative agent in 75–95% of cases. There
    is good evidence that microorganisms are
    involved in almost all cases
    36,40,49
    . At least
    137 infectious causes of bovine mastitis
    are known, but the majority of cases are
    caused by only a few common bacterial
    pathogens, namely staphylococci, strep-
    tococci, coliforms and
    Arcanobacterium
    pyogenes.
    For antibacterial mastitis therapy to be
    successful, the active drug must attain
    and maintain concentrations exceeding
    the minimum inhibitory concentration
    (MIC) at the focus of infection for long
    enough to break the production and
    toxin-producing cycle of the causative
    pathogen
    3
    . This may be prevented by a
    number of factors that include udder pa

  • thology and poor selection of anti

  • microbials, and is also influenced by the
    route of administration. Therapy may
    have poor results owing to tissue damage
    and introduction of new infections dur

  • ing treatment, and/or failure to eliminate
    the management factors that predispose
    to mastitis. Although there is an underly

  • ing assumption that the primary goal of
    antibacterial mastitis therapy is to kill bac

  • teria and that the normal udder is sterile,
    usually the best that can be achieved is
    temporary reduction or suppression of
    the bacterial population to allow the host
    to overcome the infection. The mecha

  • nisms to cleanse the udder are evidently
    poorly developed in some cows, as re

  • lapses and re-infections commonly follow
    antimicrobial therapy. Udder infections
    tend to be dynamic, and stress may con-
    tribute to udder infections becoming clin-
    ically apparent
    48,49
    .
    The purpose of this article is to provide
    an update on bovine mastitis therapy and
    reasons for its failure.
    PRINCIPLES OF MASTITIS THERAPY
    The success of mastitis therapy depends
    on correct diagnosis, appropriateness of
    the route of administration and the drug
    selected, stage at which treatment is initi

  • ated, severity of udder pathology, sup

  • portive treatment, and elimination of
    predisposing factors. There is no standard
    treatment for mastitis, but it is advocated
    that the clinical forms should be treated
    according to the severity of the udder in

  • flammation
    12
    .
    Bovine mastitis is most commonly
    treated by intramammary infusion of
    drugs
    29,64
    . This is the route of choice in
    subclinical, mild or moderately severe
    mastitis, and is used as an adjunct to
    parenteral administration in severe mas

  • titis. Some clinicians prefer intra

  • mammary administration, without
    systemic administration, even in severe
    disease
    40
    . For effective intramammary
    treatment, drugs should distribute
    throughout the udder and be rapidly ab

  • sorbed into the general blood circulation
    (Table 1). Significantly better results can
    be obtained when the drug is adminis

  • tered intracisternally in 1
    of 0.5 % glu

  • cose solution, rather than in 50 m
    saline
    23
    .
    The disadvantage of local application of
    antimicrobials is the slow and uneven dis

  • tribution of certain drugs in the infected
    udder (Table 1). In acute, severe disease,
    distribution through the udder may be
    impaired by inflammation or blockage of
    milk ducts by debris. Parenteral adminis

  • tration may overcome these problems, al

  • though it is usual to administer agents
    concurrently by the intramammary
    route
    17
    . Severely inflamed udders should
    be milked out frequently, with the aid of
    oxytocin if necessary. In peracute or acute
    clinical mastitis cases with systemic signs,
    combined systemic and intramammary
    treatment with compatible antibiotics,
    supplemented with supportive therapy,
    is recommended
    64
    .
    It is always desirable to treat infectious
    mastitis according to the antimicrobial
    drug sensitivity pattern of the pathogens
    and clinical experience
    40
    . The basic rule in
    selecting the drug is to opt for one with as
    narrow a spectrum as possible, to focus
    treatment on a specific pathogen and
    minimise side-effects. Because it takes
    time to do sensitivity determinations,
    broad-spectrum antibiotics must be given
    initially for practical reasons, based on
    knowledge of the pharmacokinetic prop-
    erties of the drugs and the formula-
    tion
    9,29,32,65,66,67
    . In general, narrow-spec-
    trum antibiotics are bacteriocidal and
    those with a broad spectrum are bacterio

  • static
    58
    .
    Response to treatment increases with
    persistence of the antibiotic in the udder.
    The concentration of the drug used must
    at least exceed the MIC-value for the
    pathogen, but preferably also the MBC-
    value (minimum bacteriocidal concentra

  • tion) in the udder. If bacteriostatic drugs
    are used, the need to maintain high con

  • centrations in the target organ is in

  • creased.
    Successful intravenous or intramuscu

  • lar mastitis therapy depends on effective
    passage of the drug from blood into milk
    to reach foci of infection, which is largely
    governed by lipid solubility, degree of
    ionisation (dependent on the dissocia

  • tion constant (pKa)), and the extent of
    protein-binding of the drug with
    plasma
    44,45,53
    , since drugs cross the
    blood–milk barrier by passive diffusion
    30
    .
    Only the unbound or free drug can dif

  • fuse through the blood–milk barrier and
    exert pharmacological or antimicrobial
    0038-2809 Jl S.Afr.vet.Ass. (2000) 71(3): 201–208
    201
    a
    Technology Transfer Division, ARC - Onderstepoort
    Veterinary Institute, Private Bag X05, Onderstepoort,
    0110 South Africa

    Treatment of bovine mastitis depends on the cause, the clinical manifestation and the antibiotic susceptibility of the agent. Mastitis therapy is commonly unsuccessful owing to pathological changes that occur in the udder parenchyma as a result of the inflammatory reaction to mastitogenic bacteria, pharmacokinetic properties of antimicrobial mastitis drugs, mastitogenic bacterial and related factors, and poor animal husbandry and veterinary interventions.
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