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Book cover for Oxford Textbook of Trauma and Orthopaedics (2 edn) Oxford Textbook of Trauma and Orthopaedics (2 edn)

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Book cover for Oxford Textbook of Trauma and Orthopaedics (2 edn) Oxford Textbook of Trauma and Orthopaedics (2 edn)
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Oxford University Press makes no representation, express or implied, that the drug dosages in this book are correct. Readers must therefore always … More Oxford University Press makes no representation, express or implied, that the drug dosages in this book are correct. Readers must therefore always check the product information and clinical procedures with the most up to date published product information and data sheets provided by the manufacturers and the most recent codes of conduct and safety regulations. The authors and the publishers do not accept responsibility or legal liability for any errors in the text or for the misuse or misapplication of material in this work. Except where otherwise stated, drug dosages and recommendations are for the non-pregnant adult who is not breastfeeding.

Bacteraemia resulting in bone deposition of bacteria

Local bony tenderness, fever, and malaise may not be present initially

WCC may be normal, ESR and CRP normally raised

Plain radiographs normally take 10–12 days to occur

Staphylococcus aureus remains the commonest organism

Immediate antibiotics with surgical drainage of abscess formation.

Osteomyelitis is inflammation of the bone caused by an infecting organism. It may be classified as acute, subacute, or chronic, determined by duration of symptoms.

Most commonly seen in children (see Chapter 13.1) it has a low incidence in adults following closure of the physis where capillary loops result in a predominance of metaphyseal childhood infection. In adults the immunocompromised host is most susceptible with infection seen most frequently in the elderly or adults with immune deficiency. The spine is the most common site (see Chapter 3.18) but any bone at any site may be involved. Bacteraemia results in deposition of bacteria at the sight of bone involvement but factors such as malnutrition or localized trauma may contribute to the resulting infection.

Pain with local bony tenderness but fever and malaise may not be present initially. Local swelling is associated with periosteal or soft tissue abscess formation. Associated erythema and warmth are cardinal signs of infection. There may be loss of local joint function and with extreme pain on swollen joint move-ment septic arthritis must be excluded, the infection ext-ending through the bone to directly involve the joint. In long-standing cases, cortical bone destruction can lead to pathological fracture.

Blood tests: the white cell count may be normal. The erythrocyte sedimentation rate and C-reactive protein are usually raised

Radiological: plain radiographs in the acute phase show no changes, Periosteal changes or cortical destruction normally take 10–12 days to occur

Technetium-99m bone scans will demonstrate increased uptake

Magnetic resonance imaging will show perisoteal reaction, soft tissue involvement, and bone marrow inflammation.

The causative organism can be identified by blood cultures in approximately 50% of patients. Bone aspiration or pus specimens may be taken at surgical drainage

Staphylococcus aureus remains the commonest causative organism in adult osteomyelitis

Pseudomonas is often seen in intravenous drug abusers

Salmonella osteomyelitis is reported in patients with sickle cell disease, most often affecting the diaphysis. This, however, is still less common than Staphylococcus aureus.

Systemic treatment should include limb splintage, analgesia, and fluid resuscitation

Antibiotics: intravenous administration of broad spectrum antibiotics are commenced immediately after culture specimens taken (blood and/or direct bone aspiration). Change is then directed by sensitivity and specificity after culture. Continuation is generally for 6 weeks although this is controversial. Debate also is undecided over timing of change from intravenous to oral route

Surgical drainage is indicated when significant subperiosteal or soft tissue abscesses are present. Drainage is usually via an incision centered over point of maximum tenderness. Bone drilling may be required both proximal and distal to the involved area to ensure complete drainage

Surgical exploration may also be indicated if a patient fails to improve symptomatically after 24–48h of antibiotic treatment

Packing of the wound with a planned second look, further debridement, and wound closure may be considered. The use of antibiotic beads or collagen sponge is not usually required.

Box 11.4.1
Treatment of acute haematogenous osteomyelitis

An appropriate antibiotic, effective prior to pus formation

Avascular tissues and abscesses require surgical removal

After successful removal, antibiotics should prevent recurrence and primary wound closure can be undertaken

Surgery should not damage further already ischaemic bone and soft tissue

Antibiotics should be continued after surgery.

Infection can recur several years following apparent successful primary treatment; most occur within 1 year, however. Therefore patients should be consented for recurrence and possible need for further treatment.

This has a more insidious onset with few symptoms. Pain may be present for some weeks with minimal systemic symptoms or signs. Often no temperature or malaise is present.

Blood tests are usually normal; the erythrocyte sedimentation rate may be slightly raised in 50% of cases. Radiographs and bone scans are positive and a classification based on radiographic changes was proposed by Gledhill and modified further by Roberts and colleagues (Box 11.4.2).

Box 11.4.2
Classification of subacute osteomyelitis

Gledhill (1973):

I: solitary localized zone of radiolucency surrounded by reactive new bone formation

II: metaphyseal radiolucencies with cortical erosion

III: cortical hyperostosis in diaphysis; no onion skinning

IV: subperiosteal new bone and onion skin layering

Roberts et al. (1982):

V: central radiolucency in epiphysis

VI: destructive process involving vertebral body.

The lack of symptoms is thought to be due to increased host resistance. The differential diagnosis must include exclusion of a primary bone tumour and biopsy and curettage are advised. An organism is identified in only 60% of cases and those negative cases with a high index of diagnostic suspicion should be treated empirically with antibiotics for 6 weeks.

Nade,
S. (
1983
).
Acute haematogenous osteomyelitis in infancy and childhood.
 
Journal of Bone and Joint Surgery
, 65B, 109–19.

Peltola,
H., Unkila-Kallio, L., and Kallio, M.J. (
1997
).
Simplified treatment of acute staphylococcal osteomyelitis of childhood.
 
Pediatrics
, 99, 846–50.

Gillespie,
W.J., and Mayo, K.M., (
1981
).
The management of acute haematogenous osteomyelitis in the antibiotic era.
A study of the outcome. Journal of Bone and Joint Surgery, 63B, 126–31.

Gledhill,
R.B. (
1973
).
Subacute osteomyelitis in children.
 
Clinical Orthopaedics and Related Research
, 96, 57–69.

Roberts
J.M., Drummond D.S., Breed A.L., et al. (
1982
).
Subacute haematogenous osteomyelitis in children: a retrospective study.
 
Journal of Pediatric Orthopaedics
, 2, 249–54.

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