|  | 
      
      
        
          | Table of Major Systems, and
            Signs 
              
              
                
                  
                    | Disease | Species
                      affected | Systems
                      affected | Signs
                      noted | Transfer
                      to humans? |  
                    | Actinomycosis | Dogs | Skin,
                      bones, joints | Abscesses,
                      pain, fever, lameness | No |  
                    | Bartonellosis
                      (Cat Scratch Disease) | Cats | Lymph
                      nodes | Usually
                      none in cats | Yes |  
                    | Bordetella | Dogs,
                      cats, pigs | Upper
                      respiratory | Harsh,
                      moist, honking cough ('kennel cough") | No |  
                    | Brucellosis | Dogs | Reproductive,
                      whole body | Failure
                      to conceive, abortion, swollen testicles, swollen lymph
                      nodes. | Yes |  
                    | Campylobacter | Dogs,
                      cats, all mammals | Gastrointestinal | diarrhoea
                      (often bloody), vomiting, reluctance to eat | Yes |  
                    | Chlamydia | Cats | Respiratory | Weepy
                      eyes, nasal discharge, sneezing | Yes |  
                    | Clostridium | Dogs,
                      cats | Diarrhoea, | acute
                      or intermittent | unknown |  
                    | Colibacillosis | Dogs,
                      cats, dairy animals | Intestinal,
                      whole body | Sudden
                      death in newborns, diarrhoea, mastitis. | Transmission
                      potential low but possible |  
                    | Ehrlichiosis | Dogs,
                      cats | Blood
                      cells, whole body Anaemia, | bruising
                      of gums, fever, lethargy, haemorrhage | Not
                      passed directly from pet to person |  
                    | Helicobacter | Dogs,
                      cats, ferret, people, | other
                      Gastrointestinal | vomiting
                      primarily; ulcers, inflammatory bowel disease | Possible |  
                    | Hemobartonella | Dogs,
                      cats | Red
                      blood cells | Anaemia;
                      weakness and pale mucous membranes | No |  
                    | Leptospirosis | Dogs,
                      cats, farm animals, people | Kidney,
                      liver, whole body | Signs
                      variable: fever, lethargy, increased thirst, vomiting | Yes |  
                    | Lyme | Dogs,
                      rarely cats, people | Whole
                      body, joints, heart | Fever,
                      lethargy, lameness that shifts from leg to leg | No
                      direct spread from pets to people |  
                    | Mycobacteria | Dogs,
                      cats, people | Any
                      system may be infected; lungs, skin | common
                      Wasting, emaciation, coughing, skin wounds | Yes |  
                    | Mycoplasma | Dogs,
                      cats | Respiratory,
                      reproductive | Sneezing,
                      coughing; failure to conceive and abortion | No |  
                    | Nocardiosis | Dog,
                      cat | Skin,
                      respiratory, whole body | Non-healing,
                      draining wounds, difficulty breathing | No |  
                    | Plague | Cats,
                      dogs, wildlife (esp. prairie dogs), humans | Lymph
                      nodes, respiratory, whole body | Draining
                      lymph nodes, high fever, cough, weight loss | Yes |  
                    | Rocky
                      Mountain Spotted Fever | Dog,
                      people, rarely cat | Blood
                      vessels, whole body | Fever,
                      bruising, bleeding from nose, lameness, | Not
                      directly transmitted to people from pets |  
                    | Salmon
                      Poisoning | Dog | Gastrointestinal | Diarrhoea,
                      vomiting, fever | No |  
                    | Salmonellosis | Dog,
                      cat, reptiles, people | Gastrointestinal,
                      whole body | Diarrhoea,
                      vomiting, dehydration | Yes |  
                    | Streptococcosis | Dog,
                      Cat, Human | Various:
                      abscesses, | early
                      puppy and kitten death Group A is rarely passed from human
                      to pet |  |  |  |  |  
                    | Staphylococcosis | Dog,
                      Cat, Human, other | Skin,
                      ears, reproductive, whole body | Various;
                      scabs, abscesses of skin; odour in ears | No |  
                    | Tularemia | Cat,
                      rarely dog, human | Lymph
                      nodes, liver, whole body | Fever,
                      swollen lymph nodes, lethargy, icterus | Yes |  
                    | Tyzzer's
                      Disease | Cat,
                      dog, rodent | Whole
                      body, liver | Lethargy,
                      stomach pain, depression, rapid death | No |  Joanne Howl, DVM EditorWalt Ingwersen, DVM, DVSc, Diplomate ACVIM
 Web
            Site
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          |  |  
          | BACTERIAL SKIN INFECTIONS IN SMALL ANIMALS |  
          |  |  
          |  Introduction Bacterial skin infections are common in small animal veterinary
            practice. These vary in severity from a transient involvement of the
            skin surface only to deep discharging infections which are
            non-responsive to therapy and which commonly relapse. The most
            frequent causal organism in bacterial skin infections in pets is
            Staphylococcus intermedius. S. aureus is the species usually
            isolated in man. Escherichia coli and Proteus species may also play
            a role in pyoderma's. S. intermedius is a normal resident in the pet
            - nasal cavity, oropharynx, and the perianal region. It can be a
            transient resident in other sites especially if there is trauma to
            the area. The organism is probably transferred to these sites from
            the oral and anal mucosae during grooming. A dense hair coat has a
            protective effect, preventing the pathogenic bacteria from having
            access to the skin. This may explain why certain pyoderma's are
            common in glabrous areas (e.g. impetigo in abdominal skin). Normally
            skin is highly resistant to colonisation by bacteria. Inflammation
            of the skin results in temperature changes and increased skin
            permeability. Colonisation is thus favoured which in turn results in
            the production of toxins and irritants and a cycle of further
            inflammation, infection, etc. In subcutaneous abscesses in cats
            which are usually from fighting, Pasteurella multocida is the
            principle bacterium found.
 
 Pyoderma's can be frustrating to deal with. They can be
            non-responsive to therapy and relapse repeatedly. Pursuing the
            underlying predisposing factors and using general principles of
            therapy, including antibacterials is necessary to successfully
            manage pyoderma's. Gram negative bacteria are generally secondary
            invaders which are controlled by therapy effective against
            Staphylococcus. Pseudomonas, however, is a Gram negative bacterium
            which is difficult to eliminate and requires specific therapy.
 Classification
            of bacterial skin diseasePyoderma can be classified as localised or generalised, primary or
            secondary, and also according to the depth of the affected tissue.
            Surface pyoderma's include acute moist dermatitis ('hotspot'), and
            intertrigo (fold dermatitis). Superficial pyoderma involves the
            epidermis and often the hair follicles. Included here are impetigo
            and superficial folliculitis. It is important to treat these cases
            adequately to prevent recurrence and progression to deep pyoderma.
            Deep pyoderma may be an extension of a surface or superficial
            pyoderma, or may occur after a primary insult. Deep pyoderma's
            include muzzle folliculitis, pyotraumatic folliculitis, bacterial
            pododermatitis, German Shepherd Dog pyoderma, and subcutaneous
            abscessation.
 
 Surface pyoderma
 This involves colonisation of the epidermis only. Clinical signs
            include erythema, papules, pustules, and alopecia. Self-excoriation
            may result in larger alopecic areas. The hallmark finding,
            especially early in the disease process, is intact pustules (Figure
            1). These may enlarge in the epidermis and rupture, resulting in a
            circular alopecia with scale at the periphery - 'epidermal
            collarette'. Gently removing the roof of an intact pustule gives an
            uncontaminated sample. An impression smear can be made from the
            pustule contents. A stain such as Kyro-Quick stain (Kyron) enables
            cell cytology to be performed. To achieve a pure growth of the
            causative organism, samples for culture are taken from intact
            pustules.
 
 
 | 
 |  
          | Acute moist dermatitisAcute moist dermatitis is commonly encountered in practice. There is
            usually a single erythematous lesion, starting in the haired areas,
            which may rapidly enlarge. Erythema, folliculitis and crusting may
            be evident under the hair coat beyond the edge of the alopecic area
            (Figure 2). The ability to spread rapidly like a veld fire has lead
            to the term 'hotspot'. The rump, dorsum, tail base, and flanks are
            the most common sites involved. Fleas are usually incriminated.
            Erythema of the skin indicates enlarged dermal blood vessels which
            probably further attract fleas to an easy blood meal. For this
            reason, corticosteroids at anti-inflammatory levels are often
            sufficient on their own. In early hotspots topical glucocorticoids
            may be sufficient. Where systemic glucocorticoids are required, a
            covering antibiotic effective against skin pathogens should be
            considered. Self-excoriation and the resultant hair loss may make it
            difficult to find evidence of flea involvement, but strict flea
            control is necessary. Deeper pyoderma's involving usually the
            peri-auricular and facial areas (known as 'pyotraumatic dermatitis')
            require more intensive investigation and therapy.
 
 Skin fold pyoderma (intertrigo)
 Any of the body folds (e.g. lip, facial, tail, and vulva fold) can
            be involved, but also the interdigital spaces of the paws. Irritant
            substances and lack of ventilation combine with sweating,
            self-excoriation, and eventually swelling of the folds. Where these
            folds rub together, as in the paws, intense inflammation results.
            Colonisation by bacteria and the yeast organism, Malassezia
            pachydermatis causes further inflammation. Where swollen folds rub
            together, as in the paws, a cycle of inflammation, pruritus,
            swelling, and infection is perpetuated.
 
 Mucocutaneous pyoderma
 This has recently been recognised as a distinct entity which
            involves the oral mucocutaneous junction. There can also be
            concurrent mucocutaneous involvement of the anus. Superficial
            pustules and crusts involve the full extent of the lips as opposed
            to lip fold pyoderma which is less extensive, involving the dimple
            (fold) in the lip only. Ulceration leading to deeper infection may
            occur. Histopathologically, the dermis contains a dense,
            predominantly plasmacytic, interface dermatitis. Pigmentary
            incontinence may also be present.
 
 Superficial pyoderma
 Superficial pyoderma is a deeper invasion of bacteria with
            involvement of all layers of the epidermis. The hair follicle is
            invaded and the hair shaft may fracture resulting in alopecia. In
            both cat and dog pyoderma's, Staphylococcus is the most frequently
            isolated bacterium. Cytology and culture may fail to reveal a
            causative organism. This is indicative of non-Staphylococcal, or
            aseptic pyoderma's which can mimic a bacterial pyoderma. Pemphigus,
            juvenile cellulitis, sterile nodular panniculitis, subcorneal
            pustular dermatosis, eosinophilic folliculitis and furunculosis,
            sterile nodular pododermatitis, linear immunoglobulin A pustular
            dermatosis and sterile eosinophilic pustulosis have all been
            described as aseptic pyoderma's or 'pyoderma impersonators' occurring
            in dogs.
 
 Impetigo
 The term 'impetigo' is used to denote a superficial pyoderma
            affecting dogs which have not yet reached puberty. Puppies from 6
            weeks to 7 months old are affected. The clinical finding in impetigo
            is the presence of pustules on the ventrum which are not centred on
            the hair follicle. Verminosis, systemic disease, and nutrition may
            all play a role. However, often no inciting cause can be found. The
            problem may self-cure, however, antibacterial shampoos and
            antibiotics are sometimes necessary. Impetigo may occur in older
            pets that are immuno-incompetent. In these patients, an
            immunosuppressive condition should be searched for.
 
 Superficial folliculitis
 In folliculitis, the infection is limited to the hair follicle. The
            hallmark finding, a pustule with a hair in the centre, may only be
            found early in the disease process. Superficial folliculitis occurs
            in young and older pets, and is generally secondary to other
            conditions. Allergic skin disease, demodicosis, hypothyroidism and
            lack of adequate hygiene should be investigated. Control or
            eradication of the underlying causes can be combined with systemic
            antibiotics, antibacterial shampoos and/or antiseborrheic shampoos.
 
 Superficial spreading pyoderma
 Expanding papular and macular areas indicate a spreading S.
              intermedius pyoderma (Figure 3). Differentials include other common
              dermatoses such as dermatophytosis, demodicosis, and scabies. In the
              early stages pustules and epidermal collarettes are seen, sometimes
              with hyperpigmentation of the centre. These may coalesce to form an
              alopecic area which may be pruritic. Intense erythema indicates a
              hypersensitivity to Staphylococci present within the pustule (Figure
              1). The pruritus associated with this hypersensitivity is so intense
              that the condition is only seen in a pet that has had adequate
              restraint (e.g. with an  Elizabethan
                collar). Self-excoriation often
              results in a penetration of the infection into the dermis. The
              circular lesions of superficial pyoderma (Figure 3) have a close
              resemblance to ringworm lesions and hence this pyoderma is commonly
              misdiagnosed as a dermatophytosis. Features which assist in
              distinguishing between these two are listed in Table 1.
 
              
                
                  
                    
                      | Table 1.   
                        Features which assist to distinguish between superficial
                        pyoderma and dermatophytosis |  
                      |  | Superficial pyoderma | Dermatophytosis |  
                      | Distribution | trunk, ventrum mostly | head and limbs mostly |  
                      | Lesions | more in number | less in number |  
                      | Lesion size | smaller | larger |  
                      | Pruritus | more likely | less likely |  
                      | Responds to cephalexin | yes | no |  
                      | Course | relapses common | usually a single
                        infection |  
                      | Differentials | allergic skin disease,
                        demodicosis insect bites, dermatophytosis | demodicosis, pyoderma |  Deep pyodermaDeep pyoderma occurs when the infection extends through the
              epidermis or hair follicle and involves pyogenic inflammation of the
              dermis or subcutis (Figure 4). The hair follicle ruptures and the
              infection spreads into surrounding dermal structures (furunculosis),
              or becomes disseminated through the deeper dermal tissues into the
              subcutis (cellulitis). Since demodicosis may be an underlying cause
              in all deep pyoderma's, repeated skin scrapings are necessary.
              Although deep pyoderma is the rarest form of pyoderma, it is also
              the most severe form, requiring intensive systemic therapy.
 
 Muzzle folliculitis and furunculosis
 In dogs, muzzle folliculitis and furunculosis is more prevalent in
              puppies approaching maturity (Figure 5). However, in cats, this
              condition known as 'feline acne', may occur at any age. In dogs,
              mild cases self-cure, but furunculosis and cellulitis require both
              topical and systemic therapy. Since this condition is found in short
              coated dogs, it is usually not necessary to shave the area. Benzoyl
              peroxide in a shampoo or gel is effective. Malassezia dermatitis
              should be treated with topical products containing an antifungal
              agent such as miconasole (Daktarin, Janssen-Cilag), systemic
              antibiotics effective against S. intermedius are required and short
              courses of corticosteroids (anti-inflammatory doses) may be
              necessary. In dogs, this condition will usually resolve after
              puberty and adequate therapy but may, as in cats with feline acne,
              be a lifelong problem.
 
 Feline acne
 Feline acne (Figure 6) is considered a defective primary
              keratinization in areas rich in sebaceous glands. The presence of
              comedones and follicular casts in the skin of the chin of cats
              confirms the condition. Invading organisms include Pasteurella,
              Streptococcus, Malassezia, Demodex and dermatophytes. Feline acne
              can be distinguished from eosinophilic granuloma by the fact that
              comedones are not present in the latter disease. Cleansing and
              flushing with benzoyl peroxide and chlorhexidine are beneficial.
              Topical treatments include the antibiotic, mupirocin, and the
              antifungals, cotrimazole and miconazole. An ointment containing
              benzoyl peroxide combined with miconazole (Acnidazil, Jannsen-Cilag)
              is useful. The systemic antibiotic clindamycin (Antirobe, Pharmacia
              & Upjohn) can be administered for a four to six week course.
              Synthetic retinoids have been recommended for stubborn cases.
              However, as in man, a cautious approach to this last group of drugs
              is advised.
 
 Pyotraumatic folliculitis and furunculosis
 As the term denotes, this involves trauma (abrasion,
              self-excoriation) and a purulent discharge. It is often secondary to
              otitis externa, foreign body, atopy, and dietary allergy. Initially,
              there may be an acute moist dermatitis which extends deeper,
              especially in the facial and subauricular areas (Figure 7). Golden
              retrievers, bull mastiffs, and Rottweilers are at risk.
              Self-excoriation, wound soiling and contamination, inadequate
              therapy, and demodicosis can all result in pyotraumatic
              folliculitis. E coli, Proteus, and S. intermedius are often present.
              Shaving must extend beyond the border of involved skin. After
              careful scraping for mites, both topical and systemic therapy is
              administered. Ear canals and surrounding areas must be thoroughly
              evaluated. Sedation, bandaging up the paws and other forms of
              restraint are necessary to minimise self-excoriation.
 
 Pressure point pyoderma
 Localised infection of the elbows and hind limbs may be precipitated
              by lying on hard surfaces. A blanket on hard surfaces does not
              provide sufficient protection for the pressure points in large and
              giant breeds. A foam rubber mattress (covered in an impervious
              material) provides an insulating bedding.
 
 Pododermatitis
 Deep bacterial infections in the paws may be an extension of
              intertriginous pyoderma of the interdigital spaces. Malassezia
              dermatitis may be involved, either alone, or as a mixed infection.
              Other inciting factors include trauma, foreign bodies, atopy,
              contact allergy/irritant dermatitis, neoplasia and migrating
              nematodes. Deep draining fistulas and painful pododermatitis may
              require sedation or even general anaesthesia to allow for deep
              scrapings to rule out demodicosis. Bacterial paronychia is common in
              cats as a nail bed infection. Chronic nail bed infections may be
              secondary to underlying immune modulated disease and the
              immunosuppressive viruses should be screened for. Furunculosis of
              the paws indicates deep pyoderma with/without demodicosis. However,
              dermatophytoses, particularly those caused by Trichophyton species,
              should always be considered - especially in Jack Russell terriers,
              hunting dogs, digging and rooting dogs and where one paw only is
              involved.
 
 Nasal pyoderma
 This is encountered in rooting/digging dogs and outdoor/hunting
              dogs. Factors to be investigated include trauma, geophilic fungi,
              insect/arthropod hypersensitivity, auto-immune and allergic skin
              disease.
 
 German Shepherd Dog (GSD) pyoderma
 GSD pyoderma is the term given to frequent episodes of deep
              folliculitis and furunculosis in the German Shepherd Dog and its
              crosses. Hallmarks of this disease are middle aged and older GSDs
              and their crosses of either sex with a furunculosis, discharge and
              pain (Figure 8). It may be an extension of a surface pyoderma and
              begin as a mild infection, often unnoticed in the thick coat. Later,
              serous and bloody discharges cause matting of the coat, which
              becomes 'glued' to the lesions. Scarring can result in permanent
              deep draining fistulas. GSD pyoderma has been described as a
              syndrome of disproportionate severity and with frequent relapses.
              The familial nature and severity should be made clear to owners.
              Recent studies have shown that affected dogs have unusual lymphocyte
              characteristics indicating an immunodeficiency. Other inciting
              factors must be searched for. Ectoparasites, especially fleas, but
              also scabies and demodicosis are the most common predisposing causes
              in the author's experience.
 
 Abscessation
 Abscesses are common in cats, and are usually from fight wounds.
              Pasteurella multocida is the most common bacterium isolated.
              Subcutaneous abscesses must be lanced, drained and flushed. P.
              multocida is usually well controlled with penicillins. However, deep
              abscesses e.g. tail root abscesses, and those involving anaerobic
              bacteria require extended courses of clindamycin.
 
 Rare bacterial infections
 Atypical mycobacteria which are present in the soil may invade the
              subcutaneous skin. Feline leprosy is caused by rat bites. Nocardia
              is a filamentous bacteria which may affect cats and dogs.
   |  
          |  |  
          | Topical Therapy |  
          | Creams, ointments and gels
 Localised pyoderma's such as fold dermatitis, feline acne, otitis
                externa and impetigo may respond well to topical creams, ointments
                and gels. Kanamycin, neomycin, bacitracin, polymixin B,
                nitrofurazone and mupirocin are examples of topical antibiotics.
                Mupirocin (Bactroban, SmithKline Beecham) is especially useful in
                certain stubborn surface pyoderma's. Cat fight abscesses should be
                lanced, drained and flushed with a 2 % hydrogen peroxide and/or a
                0.5% chlorhexidine solution. Dilute povidone iodine solution may
                also be used.
 
 Baths, soaks and shampoos
 Clipping and shaving the coat and cleansing with antibacterial
                shampoos will be beneficial. Antibacterial shampoos are particularly
                beneficial in surface and superficial infections. Chlorhexidine is
                both anti-bacterial and anti-fungal and is available in a shampoo (Pyoderm,
                Virbac). In deep pyoderma's, pyodemodicosis, and stubborn cases of
                furunculosis, the follicular flushing effect of benzoyl peroxide may
                assist. In severe furunculosis, such as GSD pyoderma, it is
                essential to shave the effected areas (even if this is the whole
                body!). The lesions can be painful and this may have to be done
                under deep sedation or even general anaesthesia. Shaving exposes
                areas of infection previously hidden under a dense coat (Figure 8).
                It may be necessary to warn the patients owners as fragile skin may
                peal away leaving unsightly deep draining fistulas. Exposure of the
                deeper lesions is necessary, however, to allow for adequate
                cleansing and access for topical therapy. Washing helps to remove
                crusts, thereby improving ventilation and drainage and it can also
                have a soothing effect. Chlorhexidine is particularly effective and
                often less irritant. Avoid corticosteroids because of the
                possibility of underlying immuno-incompetence and/or demodicosis.
                The systemic antibiotics that have been advised are the
                fluoroquinolones and cephalexin.
 
 Systemic therapy
 S. intermedius, is the most commonly isolated bacterium in pyoderma's.
                Occasionally there will be mixed infections, and rarely, other
                bacteria will predominate. Antibiotic selection may be empirical
                (based on the clinicians preference and experience), or based on
                culture and sensitivity results. Therapy, however, should always
                include a beta-lactamase resistant antibiotic with known activity
                against Staphylococci. Antibiotics fulfilling these criteria are
                listed in Table 2. More specific antibiotics can be based on
                sensitivity results especially in recurrent infections, deep pyoderma's,
                non-responsive pyoderma's and immuno-incompetent patients. Cultures
                from draining sinuses may yield non-pathogenic contaminants.
                Cultures taken from intact pustules will give more accurate
                sensitivity results. Antibiotic sensitivity results generally give a
                good guide, but several strains of Staphylococcus may be present at
                any one time giving different results. The strain cultured may not
                be representative of the pathogen present. Furthermore, the
                correlation between in vitro and in vivo performance of antibiotics
                is not absolute. Sensitivity results must be interpreted in
                conjunction with clinical symptoms, and other factors such as drug
                costs, tolerance and availability. Furthermore, therapeutic failure
                may be due to insufficient penetration into affected tissue.
                Potentiated sulphonamides and ampicillin give mixed results and
                amoxycillin and tetracyclines have generally given poor results.
                Table 2 lists antibiotics which are useful in bacterial skin disease
                in small animals. Fluoroquinolones (enrofloxacin, marbofloxacin and
                orbifloxacin) are capable of good intracellular and intercellular
                penetration and also a high activity within phagocytes. Antibiotics
                can be divided into two groups, according to their pharmacodynamics;
                those that work in a concentration-dependant fashion (e.g.
                fluoroquinolones) and those which have a time dependant effect (e.g.
                cephalosporins). The significance of this is that for
                fluoroquinolones, efficacy is a function of peak plasma
                concentration rather than half-life whereas for cephalosporins, the
                duration of plasma and tissue concentration at high enough levels is
                more important. Fluoroquinolones are most effective if given once
                daily; and also, cephalosporins must be administered twice daily.
  
             |  
          | 
            
              
                
                  | Table 2.   
                    Dosages of systemic antibiotics useful in small animal
                    bacterial skin disease. |  
                  | Antibiotic | Dose (mg/kg) | Interval (hours) |  
                  | Amoxycillin with clavulanic acid | 12.5 | 12 |  
                  | Cephalexin | 22 - 33 | 12 |  
                  | Clindamycin | 5.5 - 11 | 12 |  
                  | Enrofloxacin | 5 | 24 |  
                  | Erythromycin | 15 | 8 |  
                  | Lincomycin | 22 | 12 |  
                  | Marbofloxacin | 4 | 24 |  
                  | Orbifloxacin | 5 | 24 |  
                  | Oxacillin | 22 | 8 |  
                  | Rifampicin | 5 - 10 | 24 |  
                  | Trimethoprim/sulfadiazine | 5/20 | 12 |  
                  | Trimethoprim/sulphamethoxasole | 5/20 | 12 |  
          
           Duration of
            therapyThis is at least as important as the choice of antibiotic to be
            used. The duration of therapy must be based on factors such as
            patient age and weight, depth of infection, concurrent therapy, type
            of infection (localised or generalised; superficial or deep) and
            immunosuppressive factors. Surface and superficial pyoderma's need
            10 days of therapy, whereas deep pyoderma's require 6 weeks or more.
            For pyodemodicosis, GSD pyoderma, and in immunocompromised patients
            treatment must be continued for a minimum of three weeks after what
            appears to be clinical cure. Glucocorticoids suppress the
            inflammation, reducing the blood supply at the site of infection and
            also the hosts immune response. The skin will appear normal, but
            will still be infected. Pet owners must be made aware that response
            to therapy may take weeks and premature drug withdrawal will only
            result in relapses, drug resistance, and extra costs. Some pet
            owners are reluctant to administer an adequate course of
            antibiotics. Re-assuring the pet owner of the safety of antibiotics,
            especially in relation to the risks posed by not treating, is
            central to successful control of bacterial skin disease.
 
 Chronic recurrent pyoderma
 This is a common and frustrating problem (Figure 9). These cases
            require a review of the history, a thorough clinical examination and
            a repeat of the laboratory tests. Withdrawal of all therapy at this
            stage may be beneficial. There may be inappropriate concurrent
            therapy, or long-term antibiotic therapy may have resulted in
            antibiotic resistance. Searching for underlying causes (e.g. poor
            nutrition, demodicosis, atopy, flea, food and/or other allergy),
            while repeating culture and sensitivity regularly is necessary. Very
            old or very young animals may be immuno-incompetent, as are those
            with neoplastic disease or receiving immunosuppressive drug therapy.
            It has been proposed that an absolute neutrophilia as well as a
            lymphocyte count of at least 1000 cells/microlitre should be seen in
            dogs with a bacterial pyoderma. If these two criteria are not met,
            immuno-incompetence is suspected and underlying immunosuppressive
            disease processes should be searched for.
 
 Systemic antibiotics
 Antibiotic resistance of S. intermedius, the bacterium involved in
            small animal dermatology, is slow when compared to the rapid
            development of resistance which occurs in man with S aureus.
            However, high levels of resistance to penicillin G, ampicillin and
            amoxycillin, and to the tetracyclines are common (25 - 70% in a
            recent worldwide study). Resistance to trimethoprim and sulphonamide
            combinations is about 5%. Resistance to synthetic penicillins such
            as oxacillin, cloxacillin, and methicillin is uncommon.
            Marbofloxacin, enrofloxacin, cephalexin and amoxy-clav also have
            minimal resistance build-up. Where Gram-negative infections are
            encountered, a drug effective against Staphylococcus is usually
            sufficient except where Pseudomonas is involved.
 
 Deep granulomatous pyoderma's may respond to anti-mycobacterial
            therapy. Rifampicin is used for tuberculosis infections in man.
            Resistance to this drug builds up rapidly and it does have some
            hepatotoxicity. For these reasons short (two week) courses are used.
            Covering antibiotics (e.g. cephalexin) are administered concurrently
            to prevent the development of resistance.
 
 Pulse therapy
 Long term, low dose daily administration of antibiotics is not
            advised due to the development of antibiotic resistance. Pulse
            therapy, however, using the recommended dosage for one week a month
            (or week on, week off) has allowed many pets to live a relatively
            normal life. Cephalexin is advised in pulse therapy along with
            regular re-examinations and strict ectoparasite control.
 
 Immunomodulation
 Several drugs, such as levamisole and cimetidine have been used in
            an attempt to stimulate the immune system. These drugs are not
            licensed for this use and there is little support in the literature.
            The effect of autogenous vaccination is also not yet clear.
            Bacterial products derived from Staphylococcus aureus phage lysate
            and Propionibacterium acne are available commercially in some
            countries. These are administered as adjunctive therapy in an
            attempt to stimulate the immune system. Thorough treatment of acute
            and superficial cases of bacterial skin infections with appropriate
            products remains the most effective method of preventing development
            of deep pyoderma's.
 
 Successful therapy of pyoderma involves the identification and
            elimination of underlying inciting causes combined with appropriate
            antibacterial treatment. Systemic and topical antibacterial therapy
            may be necessary as well as immunostimulation. In those cases where
            the underlying causes cannot be identified and eliminated, prolonged
            and repeated therapy may be necessary.
 Bibliography 
            Briggs O.M. 2001 Skin disease of the extremities. Part I
              Vetmed 14: 5 - 10.
            Briggs O.M. 2001 Skin disease of the extremities. Part II
              Vetmed 15: 5 - 8.
            Lloyd D 2002 Feline infectious dermatoses. In: Proceedings of
              the 18th ESVD-ECVD Congress of Veterinary Dermatology pp 131 -
              134.
            Mason I. S. 2001 Antibiotic selection in practice. In:
              Proceedings of the 17th ESVD-ECVD Congress of Veterinary
              Dermatology pp 57 - 60. Dr O M Briggs BSc, BVSc, Msc(Med), FRCVS
 Royal College of Veterinary surgeons recognised specialist in veterinary dermatology
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