Bone and Joint Infection MD2009

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    Bone and joint infection

    Matthew Dryden

    RHCH

    WinchesterMatthew DrydenRoyal Hampshire County Hospital

    Winchester

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    Objectives

    1. Understand the causes of bone and

    joint infections

    2. Recognize the clinical presentation3. Develop an approach to the diagnosis

    of bone and joint infections

    4. Discuss antimicrobial management

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    Complications of an RTA

    Mr BA, retired barrister

    Serious RTA, 3/12 ago, head on collision

    Chest injury; 4 fractured ri

    bs

    Head; subdural haematoma, CSF leak

    Abdomen; lacerated liver/spleen

    Lower limbs; compound fracture of Rfemur

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    5 weeks in ITU

    Ventilated because of ARDS and hospitalacquired pneumonia

    3 weeks in orthopaedic ward:intramedullary nail

    Wound infection. Esch. coli isolated

    His wife died in the accident and he hastrouble coping since.

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    At orthopaedic clinic, Mr BA is apyrexial

    Discharge of pus from leg wound

    Dull acheWound swab Staph. aureus

    What should we do with him?

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    The issues

    Rehabilitation

    Bereavement

    SplenectomyLeg infection

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    Leg infection

    What is the significance of S.aureus in thewound

    It is reported as resistant to pen, flucloxacillin,erythromycin, ciprofloxacin. Is this unusual?

    X ray of femur; shows sclerosis of the bone &periosteum, soft tissue swelling

    BA taken to theatre, bone debrided, S.aureusgrown from bone

    Diagnosis?

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    Osteomyelitis and septic arthritis

    Primary

    acute,

    haematogenous,

    systemic illness

    Secondary

    Contiguous spread

    from ulcer, trauma Vascular problems of

    limb eg elderly,

    diabetic

    S.aureus 90%

    Hib, Strep pyogenes

    Rare -Brucella,salmonella, gram neg

    Polymicrobial,

    S.aureus, gram neg,

    Pseudomonas,anaerobes

    Coagulase negative

    staphylococci esp in

    prosthetic joint

    infection

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    Osteomyelitis

    Microbes invade bone

    Inflammation and pus tracksthrough Haversian andVolkmanns canals

    Ischaemia and necrosis

    Periosteal elevation Osteoblasts generate newbone

    Old dead bone calledsequestrum; surrounding livebone called involucrum

    No blood supply tosequestrum, therefore infectionmay persist

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    Source of infection

    1. Haematogenousspread

    2. Extension frombone to joint

    3. Spread from

    adjacent softtissue infection

    4. Diagnostic,surgicalinterventions

    5. Trauma

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    Clinical features native joint SA

    Monoarticular (90%)

    Mostly acute onset

    Fevermild (60 - 80% of cases)

    >39oC (third of cases)

    Movement limitation

    Swelling (effusion)

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    Chronic osteomyelitis

    Acute OM can progress to chronicAcute OM can progress to chronic

    OMOM

    Bone loss and persistent drainageBone loss and persistent drainagethrough sinus.through sinus.

    Squamous cell carcinoma andSquamous cell carcinoma and

    amyloidosis are rareamyloidosis are rarecomplicationscomplications

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    Tuberculous osteomyelitis

    Potts disease

    Potts disease: T and L spine bone destruction,

    deformity, and paraplegia.

    MRI of a 31-year-old man

    with tuberculosis of the

    spine. Images show the

    thoracic spine before and

    after an infusion ofintravenous gadolinium

    contrast. The abscess and

    subsequent destruction of

    the T11-T12 disc

    interspace is marked with

    arrowheads. Vertebralbody alignment is normal.

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    Osteomyelitis

    DiagnosisXray, CT, MRI

    Microbiology; bone, pus, blood

    ManagementAntibiotics; combination, prolonged

    Surgical washout; debridement, drainage

    Removal of metalwork, prosthetic jointMonitor inflammatory markers; ESR, CRP

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    Antibiotic treatment

    Be guided by microbiology

    Flucloxacillin 1-2gms qds IV plus oral fusidicacid 500 tds

    Penicillin allergic consider clindamycin orceftriaxone

    Child under5 consider ceftriaxone to cover Hib

    For MRSA: Vancomycin or teicoplanin plus

    fusidic acid (or Linezolid)

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    Antibiotic treatment

    Oral treatment can start after 10-14 days

    and needs to continue for 6-12 weeks.

    Monitor CRP + ESR

    Combinations include

    Flucloxacillin + fusidic acid

    Rifampicin plus doxycycline or fusidic acid

    Ciprofloxacin plus clindamycin

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    Septic arthritis

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    Septic arthritis

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    Joint pus

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    Osteomyelitis anddiabetes

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    Prosthetic-device septic arthritis or

    osteomyelitis

    Incidence should be under 1% of joint

    replacements

    Presents with swollen, hot joint, sinus,pain, loosening

    Prosthetic joint usually requires removal

    Culture of tissue and molecular diagnosis Bacterial 16s ribosomal DNA

    Two stage replacement

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    Treatment of PJI

    Antibiotic treatment

    with surgical

    debridement/ removal

    Monitor WBC andCRP

    Antibiotic cement

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    Vertebralosteomyelitis/discitis

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