Osteomyelitis
- Overview
- Theory
- Diagnosis
- Management
- Follow up
- Resources
Treatment algorithm
Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups: see disclaimer
Look out for this icon: for treatment options that are affected, or added, as a result of your patient's comorbidities.
suspected sepsis
follow local sepsis protocol
Practical tip
Think 'Could this be sepsis?
See our topics Sepsis in adults and Sepsis in children.
Refer to local guidelines for the recommended approach at your institution for assessment and management of the adult patient with suspected sepsis.
Refer to your local paediatric sepsis protocol.
Aim to take blood cultures before commencing antibiotic therapy.[2]Glaudemans AWJM, Jutte PC, Cataldo MA, et al. Consensus document for the diagnosis of peripheral bone infection in adults: a joint paper by the EANM, EBJIS, and ESR (with ESCMID endorsement). Eur J Nucl Med Mol Imaging. 2019 Apr;46(4):957-70. https://link.springer.com/article/10.1007/s00259-019-4262-x http://www.ncbi.nlm.nih.gov/pubmed/30675635?tool=bestpractice.com [6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
Start intravenous broad-spectrum antibiotic therapy within 1 hour if the patient is at high risk for sepsis.
suspected acute peripheral osteomyelitis
antibiotic therapy
Peripheral osteomyelitis usually occurs in the major long bones (e.g., femur, tibia, humerus), but can occur in small bones too. An acute presentation has a history of <2 weeks.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com For a patient with diabetes and suspected osteomyelitis in a foot, see the patient group suspected osteomyelitis in diabetic foot below.
Establish the aetiology of infection and classify the disease to plan individual treatment. Follow local antibiotic protocols.
Base initial antibiotic choice on the most likely causative organism, which depends on:
The patient’s age
Immunisation history
Local organism prevalence and their sensitivities
Comorbidities
Local protocols.
Select appropriate care setting
Admit any patient who is systemically unwell to hospital for intravenous antibiotic therapy.
If your patient is well, you can arrange for intravenous antibiotic therapy to be given through an ambulatory care pathway, depending on local resources.
Admit any child with acute osteomyelitis to hospital for intravenous antibiotic therapy, unless there are exceptional circumstances.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
Adults
If the patient is unwell, give intravenous flucloxacillin within 1 hour of reaching hospital. If the patient has a penicillin allergy, give intravenous vancomycin.
If the patient is systemically well, wait for results of the culture before giving targeted intravenous antibiotic therapy.
Take account of antibiotic susceptibilities demonstrated in organism cultures.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
Switch to appropriate oral antibiotic therapy when clinically indicated. Narrow the antibiotic regimen in line with microbiological culture and sensitivity results, or PCR results.
The optimal duration of antimicrobial therapy is not certain.[63]Li HK, Rombach I, Zambellas R, et al. Oral versus intravenous antibiotics for bone and joint infection. N Engl J Med. 2019 Jan 31;380(5):425-36. https://www.nejm.org/doi/full/10.1056/NEJMoa1710926 http://www.ncbi.nlm.nih.gov/pubmed/30699315?tool=bestpractice.com In practice, continue antibiotic treatment for about 6 weeks in total.
Antibiotics are usually sufficient to treat acute bone infection (i.e., surgical procedures are usually unnecessary) if all of the following exist for any particular patient:
The diagnosis is made within a few days of symptom onset
No dead bone or abscesses are present on imaging
Rapid response is seen to systemic antibiotic treatment
There is no associated septic arthritis.
If any diagnosis is delayed, dead bone or abscesses are present, response to antibiotics is slow, or a septic arthritis is associated with the osteomyelitis, additional treatment, such as drainage or surgery, will often be required.
Children
For children aged 3 months to 5 years, give an intravenous cephalosporin such as cefazolin or cefuroxime.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com In UK practice, ceftriaxone is considered a better option for methicillin-sensitive Staphylococcus aureus (MSSA) than cefuroxime.
First-generation cephalosporins (e.g., cefazolin) may be suboptimal if the osteomyelitis is caused by Streptococcus pneumoniae or Haemophilus influenzae type b in unvaccinated children.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
While second-generation cephalosporins (e.g., cefuroxime) and third-generation cephalosporins (e.g., ceftriaxone) demonstrate better coverage for S pneumoniae and H influenzae, they may be inferior to first-generation cephalosporins (or flucloxacillin) for osteomyelitis caused by S aureus.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com In the UK, it is generally accepted that ceftriaxone provides adequate cover against MSSA.
Alternative options include amoxicillin/clavulanate, ceftriaxone, an antistaphylococcal penicillin (e.g., flucloxacillin), or clindamycin (for non-Kingella species). An antistaphylococcal penicillin is not effective against Kingella kingae.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
For children aged ≥5 years, give an intravenous antistaphylococcal penicillin, or cefazolin.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
When risk factors for atypical organisms are present (e.g., sickle cell disease), consider ceftriaxone with or without an antistaphylococcal penicillin or clindamycin.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
Consider switching from intravenous to oral antibiotics after 2 to 4 days when the child:[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
Has been afebrile for 24 to 48 hours
Shows clinical improvement with reduced pain, inflammation, and improved mobility
Has a C-reactive protein (CRP) level that has decreased by at least 30% of the highest value.
See the European Society For Paediatric Infectious Diseases guideline on bone and joint infections for the antibiotics most appropriate for organisms that have been identified by PCR.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com However, if the organism has been identified by culture, and sensitivity to antibiotics has been determined, narrow antibiotics accordingly.
Treat uncomplicated acute osteomyelitis in children with antibiotics for at least 3 to 4 weeks.
In children who respond well, early transition from intravenous to oral therapy (after 3 days to 1 week) may be as effective as longer courses of intravenous treatment.[70]Howard-Jones AR, Isaacs D. Systematic review of duration and choice of systemic antibiotic therapy for acute haematogenous bacterial osteomyelitis in children. J Paediatr Child Health. 2013 Sep;49(9):760-8. http://www.ncbi.nlm.nih.gov/pubmed/23745943?tool=bestpractice.com [71]Bouchoucha S, Gafsi K, Trifa M, et al. Intravenous antibiotic therapy for acute hematogenous osteomyelitis in children: short versus long course [in French]. Arch Pediatr. 2013 May;20(5):464-9. http://www.ncbi.nlm.nih.gov/pubmed/23566577?tool=bestpractice.com Signs suggestive of clinical improvement include:[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
Apyrexia
Increased mobility
Decreased inflammation
Decreased pain
Decreasing CRP.
Complicated or high-risk infections may need longer intravenous and oral antibiotic therapy.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
These regimens are examples only; follow local antibiotic protocols.
Primary options
Adults
flucloxacillin: 1-2 g intravenously every 6-8 hours
OR
Children
cefazolin: 25-100 mg/kg/day intravenously given in 2-4 divided doses
OR
Children
cefuroxime: 20 mg/kg intravenously every 8 hours (maximum 750 mg/dose), may increase to 50-60 mg/kg every 6-8 hours in severe infections (maximum 1500 mg/dose)
OR
Children
flucloxacillin: 50 mg/kg intravenously every 6 hours, maximum 2000 mg/dose
Secondary options
Adults
vancomycin: 15-20 mg/kg intravenously every 8-12 hours, maximum 2000 mg/dose
More vancomycinAdjust dose according to serum vancomycin level.
OR
Children
ceftriaxone: 50-100 mg/kg intravenously every 24 hours, maximum 4000 mg/day
OR
Children
amoxicillin/clavulanate: 30 mg/kg intravenously every 8 hours, maximum 1200 mg/dose
OR
Children
clindamycin: 3.75 to 10 mg/kg intravenously every 6 hours, maximum 1200 mg/dose
OR
Children
ceftriaxone: 50-100 mg/kg intravenously every 24 hours, maximum 4000 mg/day
-- AND --
flucloxacillin: 50 mg/kg intravenously every 6 hours, maximum 2000 mg/dose
or
clindamycin: 3.75 to 10 mg/kg intravenously every 6 hours, maximum 1200 mg/dose
These drug options and doses relate to a patient with no comorbidities.
Primary options
Adults
flucloxacillin: 1-2 g intravenously every 6-8 hours
OR
Children
cefazolin: 25-100 mg/kg/day intravenously given in 2-4 divided doses
OR
Children
cefuroxime: 20 mg/kg intravenously every 8 hours (maximum 750 mg/dose), may increase to 50-60 mg/kg every 6-8 hours in severe infections (maximum 1500 mg/dose)
OR
Children
flucloxacillin: 50 mg/kg intravenously every 6 hours, maximum 2000 mg/dose
Secondary options
Adults
vancomycin: 15-20 mg/kg intravenously every 8-12 hours, maximum 2000 mg/dose
More vancomycinAdjust dose according to serum vancomycin level.
OR
Children
ceftriaxone: 50-100 mg/kg intravenously every 24 hours, maximum 4000 mg/day
OR
Children
amoxicillin/clavulanate: 30 mg/kg intravenously every 8 hours, maximum 1200 mg/dose
OR
Children
clindamycin: 3.75 to 10 mg/kg intravenously every 6 hours, maximum 1200 mg/dose
OR
Children
ceftriaxone: 50-100 mg/kg intravenously every 24 hours, maximum 4000 mg/day
-- AND --
flucloxacillin: 50 mg/kg intravenously every 6 hours, maximum 2000 mg/dose
or
clindamycin: 3.75 to 10 mg/kg intravenously every 6 hours, maximum 1200 mg/dose
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
Adults
flucloxacillin
OR
Children
cefazolin
OR
Children
cefuroxime
OR
Children
flucloxacillin
Secondary options
Adults
vancomycin
OR
Children
ceftriaxone
OR
Children
amoxicillin/clavulanate
OR
Children
clindamycin
OR
Children
ceftriaxone
-- AND --
flucloxacillin
or
clindamycin
Pseudomonas antibiotic cover
Additional treatment recommended for SOME patients in selected patient group
Walking barefoot may predispose children, particularly, but not exclusively, to osteomyelitis from penetrating injury. Pseudomonas can also be waterborne.
In UK practice, use piperacillin/tazobactam in the first instance if you suspect infection with Pseudomonas.
If the patient is allergic to penicillin, use a fluoroquinolone such as ciprofloxacin (consider safety issues - see Drug safety alert below).[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
These regimens are examples only; follow local antibiotic protocols.
Drug safety alert: Restrictions on the use of fluoroquinolone antibiotics
In November 2018, the European Medicines Agency (EMA) completed a review of serious, disabling, and potentially irreversible adverse effects associated with systemic and inhaled fluoroquinolone antibiotics. These adverse effects include tendonitis, tendon rupture, arthralgia, neuropathies, and other musculoskeletal or nervous system effects.
As a consequence of this review, the EMA now recommends that fluoroquinolone antibiotics be restricted for use in serious, life-threatening bacterial infections only. Furthermore, it recommends that fluoroquinolones should not be used for mild to moderate infections unless other appropriate antibiotics for the specific infection cannot be used, and should not be used in non-severe, non-bacterial, or self-limiting infections. Patients who are older, have renal impairment, or have had a solid organ transplant, and those being treated with a corticosteroid are at a higher risk of tendon damage. Coadministration of a fluoroquinolone and a corticosteroid should be avoided.[67]European Medicines Agency. Quinolone- and fluoroquinolone-containing medicinal products. Mar 2019 [internet publication]. https://www.ema.europa.eu/en/medicines/human/referrals/quinolone-fluoroquinolone-containing-medicinal-products The UK-based Medicines and Healthcare products Regulatory Agency (MHRA) supports these recommendations.[68]Medicines and Healthcare products Regulatory Agency. Fluoroquinolone antibiotics: new restrictions and precautions for use due to very rare reports of disabling and potentially long-lasting or irreversible side effects. Mar 2019 [internet publication]. https://www.gov.uk/drug-safety-update/fluoroquinolone-antibiotics-new-restrictions-and-precautions-for-use-due-to-very-rare-reports-of-disabling-and-potentially-long-lasting-or-irreversible-side-effects
Primary options
piperacillin/tazobactam: children: 90 mg/kg intravenously every 6-8 hours, maximum 4.5 g/dose; adults: 4.5 g intravenously every 8 hours, may increase to 4.5 g every 6 hours in severe infections
More piperacillin/tazobactamAdult dose consists of 4 g of piperacillin plus 0.5 g of tazobactam.
Secondary options
ciprofloxacin: children: 10 mg/kg intravenously every 8 hours, maximum 400 mg/dose; adults: 400 mg intravenously every 8-12 hours
These drug options and doses relate to a patient with no comorbidities.
Primary options
piperacillin/tazobactam: children: 90 mg/kg intravenously every 6-8 hours, maximum 4.5 g/dose; adults: 4.5 g intravenously every 8 hours, may increase to 4.5 g every 6 hours in severe infections
More piperacillin/tazobactamAdult dose consists of 4 g of piperacillin plus 0.5 g of tazobactam.
Secondary options
ciprofloxacin: children: 10 mg/kg intravenously every 8 hours, maximum 400 mg/dose; adults: 400 mg intravenously every 8-12 hours
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
piperacillin/tazobactam
Secondary options
ciprofloxacin
supportive care
Treatment recommended for ALL patients in selected patient group
Offer pain relief to all patients as required. Start with paracetamol or a non-steroidal anti-inflammatory drug (NSAID) such as ibuprofen, with an opioid such as morphine for breakthrough pain relief. If regular use of morphine is required, switch to a slow-release oral formulation. In practice, severe pain usually suggests there is a collection (abscess) that needs to be drained.
Elevate and immobilise the limb for comfort if necessary.
Look out for deep vein thrombosis particularly with S aureus osteomyelitis.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com [66]Mejer N, Westh H, Schønheyder HC, et al. Increased risk of venous thromboembolism within the first year after Staphylococcus aureus bacteraemia: a nationwide observational matched cohort study. J Intern Med. 2014 Apr;275(4):387-97. https://onlinelibrary.wiley.com/doi/full/10.1111/joim.12147 http://www.ncbi.nlm.nih.gov/pubmed/24118528?tool=bestpractice.com Refer to a haematologist and follow local protocols. See our topic Deep vein thrombosis.
Address any comorbidities. It is particularly important to maintain strict blood glucose control in any patient with diabetes and a major infection such as osteomyelitis.
Consider referral to other specialist teams, such as:
The haematology team for a patient with sickle cell disease
The diabetes inpatient specialist team for a patient with diabetes mellitus but who does not have a diabetic foot problem.
Primary options
paracetamol: children: consult specialist for guidance on dose; adults: 500-1000 mg orally every 4-6 hours when required, maximum 4000 mg/day; adults: 15 mg/kg (maximum 1000 mg/dose) intravenously every 4-6 hours when required, maximum 4000 mg/day
OR
ibuprofen: children: consult specialist for guidance on dose; adults: 300-600 mg orally (immediate-release) every 6-8 hours when required, maximum 2400 mg/day
Secondary options
morphine sulfate: children: consult specialist for guidance on dose; adults: 5-10 mg orally (immediate-release)/subcutaneously/intravenously/intramuscularly every 4 hours initially, adjust dose according to response
These drug options and doses relate to a patient with no comorbidities.
Primary options
paracetamol: children: consult specialist for guidance on dose; adults: 500-1000 mg orally every 4-6 hours when required, maximum 4000 mg/day; adults: 15 mg/kg (maximum 1000 mg/dose) intravenously every 4-6 hours when required, maximum 4000 mg/day
OR
ibuprofen: children: consult specialist for guidance on dose; adults: 300-600 mg orally (immediate-release) every 6-8 hours when required, maximum 2400 mg/day
Secondary options
morphine sulfate: children: consult specialist for guidance on dose; adults: 5-10 mg orally (immediate-release)/subcutaneously/intravenously/intramuscularly every 4 hours initially, adjust dose according to response
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
paracetamol
OR
ibuprofen
Secondary options
morphine sulfate
surgery
Additional treatment recommended for SOME patients in selected patient group
A rapid response to antibiotic therapy is usually expected, but if the limb deteriorates or imaging suggests progressive bone destruction, discuss choice of antibiotics with microbiology and consider surgery to prevent progression to chronic osteomyelitis.
Although acute osteomyelitis often responds to antibiotics alone if it can be treated promptly and aggressively, once dead bone or a biofilm has become established, antibiotics alone cannot cure the infection and thorough surgical debridement is required. See chronic osteomyelitis section below.
If you are considering surgery, seek advice from orthopaedics.
Practical tip
Note that tuberculous osteomyelitis usually does not require surgical intervention.
Ensure drainage of fluid collections, if present, by radiological guidance or surgery.
For adults who may require surgery, consult a specialist orthopaedic surgeon.
For children with osteomyelitis, consider surgery in the following situations:[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
Persistent or recurring fever after 3 to 4 days
Periosteal abscess with persistent fever and raised CRP
Sequestration
MRSA or Panton-Valentine leukocidin (PVL)-positive S aureus
Chronic osteomyelitis
Prosthetic material.
Seek paediatric orthopaedic advice.
Practical tip
Note that necrotising features, multifocal osteomyelitis, and recurrence may be caused by PVL-producing S aureus and is associated with serious risk. The British Society for Antimicrobial Chemotherapy (BSAC) makes antibiotic recommendations for this rare aetiology.[56]Nathwani D, Morgan M, Masterton RG, et al. Guidelines for UK practice for the diagnosis and management of methicillin-resistant Staphylococcus aureus (MRSA) infections presenting in the community. J Antimicrob Chemother. 2008 May;61(5):976-94. https://academic.oup.com/jac/article/61/5/976/849478 http://www.ncbi.nlm.nih.gov/pubmed/18339633?tool=bestpractice.com [69]Health Protection Agency. Guidance on the diagnosis and management of PVL-associated Staphylococcus aureus infections (PVL-SA) in England: report prepared by the PVL sub-group of the Steering Group on Healthcare Associated Infection. 2008 [internet publication]. https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/322857/Guidance_on_the_diagnosis_and_management_of_PVL_associated_SA_infections_in_England_2_Ed.pdf
antibiotic therapy
Peripheral osteomyelitis usually occurs in the major long bones (e.g., femur, tibia, humerus), but can occur in small bones too. An acute presentation has a history of <2 weeks.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com For a patient with diabetes and suspected osteomyelitis in a foot, see the patient group suspected osteomyelitis in diabetic foot below.
Establish the aetiology of infection and classify the disease to plan individual treatment. If the prevalence of MRSA in the community is high, or your patient is known to have had MRSA in the past, ensure that the initial empirical antibiotics cover for MRSA. Follow local antibiotic protocols.
When deciding on the empirical regimen, also take into account:
The patient’s age
Immunisation history
Local organism prevalence and their sensitivities
Comorbidities
Local protocols.
Select appropriate care setting
Admit any patient who is systemically unwell to hospital for intravenous antibiotic therapy.
If your patient is well, you can arrange for intravenous antibiotic therapy to be given through an ambulatory care pathway, depending on local resources.
Admit any child with acute osteomyelitis to hospital for intravenous antibiotic therapy, unless there are exceptional circumstances.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
Adults
If the patient is unwell, give intravenous vancomycin within 1 hour of reaching hospital.
Teicoplanin and linezolid are reasonable alternatives if the patient cannot tolerate vancomycin, or if vancomycin is contraindicated.
If the patient is systemically well, wait for results of the culture before giving targeted intravenous antibiotic therapy.
Take account of antibiotic susceptibilities demonstrated in organism cultures.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
Switch to appropriate oral antibiotic therapy when clinically indicated. Narrow the antibiotic regimen in line with microbiological culture and sensitivity results, or PCR results.
The optimal duration of antimicrobial therapy is not certain.[63]Li HK, Rombach I, Zambellas R, et al. Oral versus intravenous antibiotics for bone and joint infection. N Engl J Med. 2019 Jan 31;380(5):425-36. https://www.nejm.org/doi/full/10.1056/NEJMoa1710926 http://www.ncbi.nlm.nih.gov/pubmed/30699315?tool=bestpractice.com In practice, continue antibiotic treatment for about 6 weeks in total.
Antibiotics are usually sufficient to treat acute bone infection (i.e., surgical procedures are usually unnecessary) if all of the following exist for any particular patient:
The diagnosis is made within a few days of symptom onset
No dead bone or abscesses are present on imaging
Rapid response is seen to systemic antibiotic treatment
There is no associated septic arthritis.
If any diagnosis is delayed, dead bone or abscesses are present, response to antibiotics is slow, or a septic arthritis is associated with the osteomyelitis, additional treatment, such as drainage or surgery, will often be required.
Children
For children aged <2 years, if the prevalence of MRSA is >10% to 15% in the community, add clindamycin to the empirical regimen as indicated for low MRSA prevalence in the patient group above.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com If, however, the prevalence of clindamycin resistance in MRSA is ≥10%, prescribe vancomycin or linezolid.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
For children aged ≥2 years, if the prevalence of MRSA is >10% to 15% in the community, give clindamycin alone, as long as the prevalence of clindamycin resistance in MRSA is <10%.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
Rifampicin or an antistaphylococcal beta-lactam (e.g., amoxicillin/clavulanate) may be added depending on patient and prevalence factors.
If there is a high rate of MRSA and there is severe infection, a high rate of clindamycin resistance (≥10%), or initial treatment failure, give vancomycin or teicoplanin. Rifampicin may be added; however, there is little evidence to support this.
Always consider adding a beta-lactam until MRSA is confirmed to be the causative organism.
When risk factors for atypical organisms are present (e.g., sickle cell disease), consider ceftriaxone with or without an antistaphylococcal penicillin or clindamycin.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
Consider switching from intravenous to oral antibiotics after 2 to 4 days when the child:[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
Has been afebrile for 24 to 48 hours
Shows clinical improvement with reduced pain, inflammation, and improved mobility
Has a C-reactive protein (CRP) level that has decreased by at least 30% of the highest value.
See the European Society For Paediatric Infectious Diseases guideline on bone and joint infections for the antibiotics most appropriate for organisms that have been identified by PCR.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com However if the organism has been identified by culture, and sensitivity to antibiotics has been determined, narrow antibiotics accordingly.
Treat uncomplicated acute osteomyelitis in children with antibiotics for at least 3 to 4 weeks.
In children who respond well, early transition from intravenous to oral therapy (after 3 days to 1 week) may be as effective as longer courses of intravenous treatment.[70]Howard-Jones AR, Isaacs D. Systematic review of duration and choice of systemic antibiotic therapy for acute haematogenous bacterial osteomyelitis in children. J Paediatr Child Health. 2013 Sep;49(9):760-8. http://www.ncbi.nlm.nih.gov/pubmed/23745943?tool=bestpractice.com [71]Bouchoucha S, Gafsi K, Trifa M, et al. Intravenous antibiotic therapy for acute hematogenous osteomyelitis in children: short versus long course [in French]. Arch Pediatr. 2013 May;20(5):464-9. http://www.ncbi.nlm.nih.gov/pubmed/23566577?tool=bestpractice.com Signs suggestive of clinical improvement include:[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
Apyrexia
Increased mobility
Decreased inflammation
Decreased pain
Decreasing CRP.
Complicated or high-risk infections may need longer intravenous and oral antibiotic therapy.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
Practical tip
Note that necrotising features, multifocal osteomyelitis, and recurrence may be caused by Panton-Valentine leukocidin (PVL)- producing Staphylococcus aureus and is associated with serious risk. The British Society for Antimicrobial Chemotherapy (BSAC) makes antibiotic recommendations for this rare aetiology.[56]Nathwani D, Morgan M, Masterton RG, et al. Guidelines for UK practice for the diagnosis and management of methicillin-resistant Staphylococcus aureus (MRSA) infections presenting in the community. J Antimicrob Chemother. 2008 May;61(5):976-94. https://academic.oup.com/jac/article/61/5/976/849478 http://www.ncbi.nlm.nih.gov/pubmed/18339633?tool=bestpractice.com [69]Health Protection Agency. Guidance on the diagnosis and management of PVL-associated Staphylococcus aureus infections (PVL-SA) in England: report prepared by the PVL sub-group of the Steering Group on Healthcare Associated Infection. 2008 [internet publication]. https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/322857/Guidance_on_the_diagnosis_and_management_of_PVL_associated_SA_infections_in_England_2_Ed.pdf
These regimens are examples only; follow local antibiotic protocols.
Primary options
Adults
vancomycin: 15-20 mg/kg intravenously every 8-12 hours, maximum 2000 mg/dose
More vancomycinAdjust dose according to serum vancomycin level.
OR
Children
clindamycin: 3.75 to 10 mg/kg intravenously every 6 hours, maximum 1200 mg/dose
OR
Children
clindamycin: 3.75 to 10 mg/kg intravenously every 6 hours, maximum 1200 mg/dose
-- AND --
rifampicin: 10 mg/kg intravenously every 12 hours, maximum 600 mg/dose
or
amoxicillin/clavulanate: 30 mg/kg intravenously every 8 hours, maximum 1200 mg/dose
Secondary options
Adults
teicoplanin: 6 mg/kg intravenously every 12 hours for 3 doses, followed by 6 mg/kg every 24 hours
OR
Adults
linezolid: 600 mg intravenously every 12 hours
OR
Children
vancomycin: 10-15 mg/kg intravenously every 6 hours, maximum 2000 mg/dose
More vancomycinAdjust dose according to serum vancomycin level.
OR
Children
linezolid: 10 mg/kg intravenously every 8 hours, maximum 600 mg/dose
OR
Children
teicoplanin: 12 mg/kg intravenously every 12 hours for 3-5 doses, followed by 12 mg/kg every 24 hours
OR
Children
vancomycin: 10-15 mg/kg intravenously every 6 hours, maximum 2000 mg/dose
More vancomycinAdjust dose according to serum vancomycin level.
or
teicoplanin: 12 mg/kg intravenously every 12 hours for 3-5 doses, followed by 12 mg/kg every 24 hours
-- AND --
rifampicin: 10 mg/kg intravenously every 12 hours, maximum 600 mg/dose
These drug options and doses relate to a patient with no comorbidities.
Primary options
Adults
vancomycin: 15-20 mg/kg intravenously every 8-12 hours, maximum 2000 mg/dose
More vancomycinAdjust dose according to serum vancomycin level.
OR
Children
clindamycin: 3.75 to 10 mg/kg intravenously every 6 hours, maximum 1200 mg/dose
OR
Children
clindamycin: 3.75 to 10 mg/kg intravenously every 6 hours, maximum 1200 mg/dose
-- AND --
rifampicin: 10 mg/kg intravenously every 12 hours, maximum 600 mg/dose
or
amoxicillin/clavulanate: 30 mg/kg intravenously every 8 hours, maximum 1200 mg/dose
Secondary options
Adults
teicoplanin: 6 mg/kg intravenously every 12 hours for 3 doses, followed by 6 mg/kg every 24 hours
OR
Adults
linezolid: 600 mg intravenously every 12 hours
OR
Children
vancomycin: 10-15 mg/kg intravenously every 6 hours, maximum 2000 mg/dose
More vancomycinAdjust dose according to serum vancomycin level.
OR
Children
linezolid: 10 mg/kg intravenously every 8 hours, maximum 600 mg/dose
OR
Children
teicoplanin: 12 mg/kg intravenously every 12 hours for 3-5 doses, followed by 12 mg/kg every 24 hours
OR
Children
vancomycin: 10-15 mg/kg intravenously every 6 hours, maximum 2000 mg/dose
More vancomycinAdjust dose according to serum vancomycin level.
or
teicoplanin: 12 mg/kg intravenously every 12 hours for 3-5 doses, followed by 12 mg/kg every 24 hours
-- AND --
rifampicin: 10 mg/kg intravenously every 12 hours, maximum 600 mg/dose
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
Adults
vancomycin
OR
Children
clindamycin
OR
Children
clindamycin
-- AND --
rifampicin
or
amoxicillin/clavulanate
Secondary options
Adults
teicoplanin
OR
Adults
linezolid
OR
Children
vancomycin
OR
Children
linezolid
OR
Children
teicoplanin
OR
Children
vancomycin
or
teicoplanin
-- AND --
rifampicin
Pseudomonas antibiotic cover
Additional treatment recommended for SOME patients in selected patient group
Walking barefoot may predispose children, particularly, but not exclusively, to osteomyelitis from penetrating injury. Pseudomonas can also be waterborne.
In UK practice, use piperacillin/tazobactam in the first instance if you suspect infection with Pseudomonas.
If the patient is allergic to penicillin, use a fluoroquinolone such as ciprofloxacin (consider safety issues - see Drug safety alert below).[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
These regimens are examples only; follow local antibiotic protocols.
Drug safety alert: Restrictions on the use of fluoroquinolone antibiotics
In November 2018, the European Medicines Agency (EMA) completed a review of serious, disabling, and potentially irreversible adverse effects associated with systemic and inhaled fluoroquinolone antibiotics. These adverse effects include tendonitis, tendon rupture, arthralgia, neuropathies, and other musculoskeletal or nervous system effects.
As a consequence of this review, the EMA now recommends that fluoroquinolone antibiotics be restricted for use in serious, life-threatening bacterial infections only. Furthermore, it recommends that fluoroquinolones should not be used for mild to moderate infections unless other appropriate antibiotics for the specific infection cannot be used, and should not be used in non-severe, non-bacterial, or self-limiting infections. Patients who are older, have renal impairment, or have had a solid organ transplant, and those being treated with a corticosteroid are at a higher risk of tendon damage. Coadministration of a fluoroquinolone and a corticosteroid should be avoided.[67]European Medicines Agency. Quinolone- and fluoroquinolone-containing medicinal products. Mar 2019 [internet publication]. https://www.ema.europa.eu/en/medicines/human/referrals/quinolone-fluoroquinolone-containing-medicinal-products The UK-based Medicines and Healthcare products Regulatory Agency (MHRA) supports these recommendations.[68]Medicines and Healthcare products Regulatory Agency. Fluoroquinolone antibiotics: new restrictions and precautions for use due to very rare reports of disabling and potentially long-lasting or irreversible side effects. Mar 2019 [internet publication]. https://www.gov.uk/drug-safety-update/fluoroquinolone-antibiotics-new-restrictions-and-precautions-for-use-due-to-very-rare-reports-of-disabling-and-potentially-long-lasting-or-irreversible-side-effects
Primary options
piperacillin/tazobactam: children: 90 mg/kg intravenously every 6-8 hours, maximum 4.5 g/dose; adults: 4.5 g intravenously every 8 hours, may increase to 4.5 g every 6 hours in severe infections
More piperacillin/tazobactamAdult dose consists of 4 g of piperacillin plus 0.5 g of tazobactam.
Secondary options
ciprofloxacin: children: 10 mg/kg intravenously every 8 hours, maximum 400 mg/dose; adults: 400 mg intravenously every 8-12 hours
These drug options and doses relate to a patient with no comorbidities.
Primary options
piperacillin/tazobactam: children: 90 mg/kg intravenously every 6-8 hours, maximum 4.5 g/dose; adults: 4.5 g intravenously every 8 hours, may increase to 4.5 g every 6 hours in severe infections
More piperacillin/tazobactamAdult dose consists of 4 g of piperacillin plus 0.5 g of tazobactam.
Secondary options
ciprofloxacin: children: 10 mg/kg intravenously every 8 hours, maximum 400 mg/dose; adults: 400 mg intravenously every 8-12 hours
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
piperacillin/tazobactam
Secondary options
ciprofloxacin
supportive care
Treatment recommended for ALL patients in selected patient group
Offer pain relief to all patients as required. Start with paracetamol or a non-steroidal anti-inflammatory drug (NSAID) such as ibuprofen, with an opioid such as morphine for breakthrough pain relief. If regular use of morphine is required, switch to a slow-release oral formulation. In practice, severe pain usually suggests there is a collection (abscess) that needs to be drained.
Elevate and immobilise the limb for comfort if necessary.
Look out for deep vein thrombosis particularly with S aureus osteomyelitis.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com [66]Mejer N, Westh H, Schønheyder HC, et al. Increased risk of venous thromboembolism within the first year after Staphylococcus aureus bacteraemia: a nationwide observational matched cohort study. J Intern Med. 2014 Apr;275(4):387-97. https://onlinelibrary.wiley.com/doi/full/10.1111/joim.12147 http://www.ncbi.nlm.nih.gov/pubmed/24118528?tool=bestpractice.com Refer to a haematologist and follow local protocols. See our topic Deep vein thrombosis.
Address any comorbidities. It is particularly important to maintain strict blood glucose control in any patient with diabetes and a major infection such as osteomyelitis.
Consider referral to other specialist teams, such as:
The haematology team for a patient with sickle cell disease
The diabetes inpatient specialist team for a patient with diabetes mellitus but who does not have a diabetic foot problem.
Primary options
paracetamol: children: consult specialist for guidance on dose; adults: 500-1000 mg orally every 4-6 hours when required, maximum 4000 mg/day; adults: 15 mg/kg (maximum 1000 mg/dose) intravenously every 4-6 hours when required, maximum 4000 mg/day
OR
ibuprofen: children: consult specialist for guidance on dose; adults: 300-600 mg orally (immediate-release) every 6-8 hours when required, maximum 2400 mg/day
Secondary options
morphine sulfate: children: consult specialist for guidance on dose; adults: 5-10 mg orally (immediate-release)/subcutaneously/intravenously/intramuscularly every 4 hours initially, adjust dose according to response
These drug options and doses relate to a patient with no comorbidities.
Primary options
paracetamol: children: consult specialist for guidance on dose; adults: 500-1000 mg orally every 4-6 hours when required, maximum 4000 mg/day; adults: 15 mg/kg (maximum 1000 mg/dose) intravenously every 4-6 hours when required, maximum 4000 mg/day
OR
ibuprofen: children: consult specialist for guidance on dose; adults: 300-600 mg orally (immediate-release) every 6-8 hours when required, maximum 2400 mg/day
Secondary options
morphine sulfate: children: consult specialist for guidance on dose; adults: 5-10 mg orally (immediate-release)/subcutaneously/intravenously/intramuscularly every 4 hours initially, adjust dose according to response
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
paracetamol
OR
ibuprofen
Secondary options
morphine sulfate
surgery
Additional treatment recommended for SOME patients in selected patient group
A rapid response to antibiotic therapy is usually expected, but if the limb deteriorates or imaging suggests progressive bone destruction, discuss choice of antibiotics with microbiology and consider surgery to prevent progression to chronic osteomyelitis.
Although acute osteomyelitis often responds to antibiotics alone if it can be treated promptly and aggressively, once dead bone or a biofilm has become established, antibiotics alone cannot cure the infection and thorough surgical debridement is required. See chronic osteomyelitis section below.
For adults, who may require surgery, consult a specialist orthopaedic surgeon.
Practical tip
Note that tuberculous osteomyelitis usually does not require surgical intervention.
Ensure drainage of fluid collections, if present, by radiological guidance or surgery.
For children with osteomyelitis, consider surgery in the following situations:[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
Persistent or recurring fever after 3 to 4 days
Periosteal abscess with persistent fever and raised CRP
Sequestration
MRSA or PVL-positive S aureus
Chronic osteomyelitis
Prosthetic material.
Seek paediatric orthopaedic advice.
suspected acute native vertebral osteomyelitis
1st line – referral to infectious disease specialist and spine surgeon
referral to infectious disease specialist and spine surgeon
As this is a difficult diagnosis, referral to an infectious disease specialist and a spine surgeon is prudent.[7]Berbari EF, Kanj SS, Kowalski TJ, et al. 2015 Infectious Diseases Society of America (IDSA) clinical practice guidelines for the diagnosis and treatment of native vertebral osteomyelitis in adults. Clin Infect Dis. 2015 Sep 15;61(6):e26-46. https://academic.oup.com/cid/article/61/6/e26/452579 http://www.ncbi.nlm.nih.gov/pubmed/26229122?tool=bestpractice.com
If neurological signs deteriorate, seek urgent surgical review.
In practice, if you suspect spondylodiscitis or vertebral osteomyelitis in a child, then in addition to the above, seek advice from paediatrics and/or paediatric orthopaedics, depending on local resources.
supportive care
Treatment recommended for ALL patients in selected patient group
Offer pain relief to all patients as required. Start with paracetamol or a non-steroidal anti-inflammatory drug (NSAID) such as ibuprofen, with an opioid such as morphine for breakthrough pain relief. If regular use of morphine is required, switch to a slow-release oral formulation. In practice, severe pain usually suggests there is a collection (abscess) that needs to be drained.
Address any comorbidities. It is particularly important to maintain strict blood glucose control in any patient with diabetes and a major infection such as osteomyelitis.
Consider referral to other specialist teams, such as:
The haematology team for a patient with sickle cell disease
The diabetes inpatient specialist team for a patient with diabetes mellitus but who does not have a diabetic foot problem.
Primary options
paracetamol: children: consult specialist for guidance on dose; adults: 500-1000 mg orally every 4-6 hours when required, maximum 4000 mg/day; adults: 15 mg/kg (maximum 1000 mg/dose) intravenously every 4-6 hours when required, maximum 4000 mg/day
OR
ibuprofen: children: consult specialist for guidance on dose; adults: 300-600 mg orally (immediate-release) every 6-8 hours when required, maximum 2400 mg/day
Secondary options
morphine sulfate: children: consult specialist for guidance on dose; adults: 5-10 mg orally (immediate-release)/subcutaneously/intravenously/intramuscularly every 4 hours initially, adjust dose according to response
These drug options and doses relate to a patient with no comorbidities.
Primary options
paracetamol: children: consult specialist for guidance on dose; adults: 500-1000 mg orally every 4-6 hours when required, maximum 4000 mg/day; adults: 15 mg/kg (maximum 1000 mg/dose) intravenously every 4-6 hours when required, maximum 4000 mg/day
OR
ibuprofen: children: consult specialist for guidance on dose; adults: 300-600 mg orally (immediate-release) every 6-8 hours when required, maximum 2400 mg/day
Secondary options
morphine sulfate: children: consult specialist for guidance on dose; adults: 5-10 mg orally (immediate-release)/subcutaneously/intravenously/intramuscularly every 4 hours initially, adjust dose according to response
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
paracetamol
OR
ibuprofen
Secondary options
morphine sulfate
antibiotic therapy
Treatment recommended for ALL patients in selected patient group
After taking blood for culture, immediately give empirical antibiotic therapy to a patient with progressive or severe neurological symptoms.[7]Berbari EF, Kanj SS, Kowalski TJ, et al. 2015 Infectious Diseases Society of America (IDSA) clinical practice guidelines for the diagnosis and treatment of native vertebral osteomyelitis in adults. Clin Infect Dis. 2015 Sep 15;61(6):e26-46. https://academic.oup.com/cid/article/61/6/e26/452579 http://www.ncbi.nlm.nih.gov/pubmed/26229122?tool=bestpractice.com
If your patient does not have progressive neurological symptoms, delay starting antibiotics until microbiology cultures and sensitivity results are available to guide pathogen-targeted antibiotic therapy.[7]Berbari EF, Kanj SS, Kowalski TJ, et al. 2015 Infectious Diseases Society of America (IDSA) clinical practice guidelines for the diagnosis and treatment of native vertebral osteomyelitis in adults. Clin Infect Dis. 2015 Sep 15;61(6):e26-46. https://academic.oup.com/cid/article/61/6/e26/452579 http://www.ncbi.nlm.nih.gov/pubmed/26229122?tool=bestpractice.com
Select appropriate care setting
Admit any patient who is systemically unwell to hospital for intravenous antibiotic therapy.
If your patient is well, you can arrange for intravenous antibiotic therapy to be given through an ambulatory care pathway, depending on local resources.
Admit any child with acute osteomyelitis to hospital for intravenous antibiotic therapy, unless there are exceptional circumstances.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
Adults
Give an empirical antibiotic regimen that covers staphylococci (including MRSA), streptococci, and gram-negative bacilli.[7]Berbari EF, Kanj SS, Kowalski TJ, et al. 2015 Infectious Diseases Society of America (IDSA) clinical practice guidelines for the diagnosis and treatment of native vertebral osteomyelitis in adults. Clin Infect Dis. 2015 Sep 15;61(6):e26-46. https://academic.oup.com/cid/article/61/6/e26/452579 http://www.ncbi.nlm.nih.gov/pubmed/26229122?tool=bestpractice.com
Vancomycin plus a third- or fourth-generation cephalosporin (e.g., ceftriaxone) is an example of a suitable regimen.[7]Berbari EF, Kanj SS, Kowalski TJ, et al. 2015 Infectious Diseases Society of America (IDSA) clinical practice guidelines for the diagnosis and treatment of native vertebral osteomyelitis in adults. Clin Infect Dis. 2015 Sep 15;61(6):e26-46. https://academic.oup.com/cid/article/61/6/e26/452579 http://www.ncbi.nlm.nih.gov/pubmed/26229122?tool=bestpractice.com
For patients with an allergy or intolerance, give daptomycin plus a fluoroquinolone such as ciprofloxacin (consider safety issues - see Drug safety alert below).[7]Berbari EF, Kanj SS, Kowalski TJ, et al. 2015 Infectious Diseases Society of America (IDSA) clinical practice guidelines for the diagnosis and treatment of native vertebral osteomyelitis in adults. Clin Infect Dis. 2015 Sep 15;61(6):e26-46. https://academic.oup.com/cid/article/61/6/e26/452579 http://www.ncbi.nlm.nih.gov/pubmed/26229122?tool=bestpractice.com
These regimens are based on Infectious Diseases Society of America (IDSA) guidance.[7]Berbari EF, Kanj SS, Kowalski TJ, et al. 2015 Infectious Diseases Society of America (IDSA) clinical practice guidelines for the diagnosis and treatment of native vertebral osteomyelitis in adults. Clin Infect Dis. 2015 Sep 15;61(6):e26-46. https://academic.oup.com/cid/article/61/6/e26/452579 http://www.ncbi.nlm.nih.gov/pubmed/26229122?tool=bestpractice.com Note that UK regimens may be narrower spectrum due to less resistance; consult local protocols because no national guidance for native vertebral osteomyelitis has been published.
Drug safety alert: Restrictions on the use of fluoroquinolone antibiotics
In November 2018, the European Medicines Agency (EMA) completed a review of serious, disabling, and potentially irreversible adverse effects associated with systemic and inhaled fluoroquinolone antibiotics. These adverse effects include tendonitis, tendon rupture, arthralgia, neuropathies, and other musculoskeletal or nervous system effects.
As a consequence of this review, the EMA now recommends that fluoroquinolone antibiotics be restricted for use in serious, life-threatening bacterial infections only. Furthermore, it recommends that fluoroquinolones should not be used for mild to moderate infections unless other appropriate antibiotics for the specific infection cannot be used, and should not be used in non-severe, non-bacterial, or self-limiting infections. Patients who are older, have renal impairment, or have had a solid organ transplant, and those being treated with a corticosteroid are at a higher risk of tendon damage. Coadministration of a fluoroquinolone and a corticosteroid should be avoided.[67]European Medicines Agency. Quinolone- and fluoroquinolone-containing medicinal products. Mar 2019 [internet publication]. https://www.ema.europa.eu/en/medicines/human/referrals/quinolone-fluoroquinolone-containing-medicinal-products The UK-based Medicines and Healthcare products Regulatory Agency (MHRA) supports these recommendations.[68]Medicines and Healthcare products Regulatory Agency. Fluoroquinolone antibiotics: new restrictions and precautions for use due to very rare reports of disabling and potentially long-lasting or irreversible side effects. Mar 2019 [internet publication]. https://www.gov.uk/drug-safety-update/fluoroquinolone-antibiotics-new-restrictions-and-precautions-for-use-due-to-very-rare-reports-of-disabling-and-potentially-long-lasting-or-irreversible-side-effects
Do not prescribe empirical antifungal and antimycobacterial therapy in most situations.[7]Berbari EF, Kanj SS, Kowalski TJ, et al. 2015 Infectious Diseases Society of America (IDSA) clinical practice guidelines for the diagnosis and treatment of native vertebral osteomyelitis in adults. Clin Infect Dis. 2015 Sep 15;61(6):e26-46. https://academic.oup.com/cid/article/61/6/e26/452579 http://www.ncbi.nlm.nih.gov/pubmed/26229122?tool=bestpractice.com
Children
For children with spondylodiscitis or vertebral osteomyelitis, seek advice from microbiology on empirical antibiotic regimens and doses.
Pathogen-targeted therapy
Narrow the antibiotic regimen according to culture and sensitivity results when they become available. Detailed guidance on regimens is available from the IDSA.[7]Berbari EF, Kanj SS, Kowalski TJ, et al. 2015 Infectious Diseases Society of America (IDSA) clinical practice guidelines for the diagnosis and treatment of native vertebral osteomyelitis in adults. Clin Infect Dis. 2015 Sep 15;61(6):e26-46. https://academic.oup.com/cid/article/61/6/e26/452579 http://www.ncbi.nlm.nih.gov/pubmed/26229122?tool=bestpractice.com
Give a total duration of 6 weeks of parenteral or highly bioavailable oral antimicrobial therapy.[7]Berbari EF, Kanj SS, Kowalski TJ, et al. 2015 Infectious Diseases Society of America (IDSA) clinical practice guidelines for the diagnosis and treatment of native vertebral osteomyelitis in adults. Clin Infect Dis. 2015 Sep 15;61(6):e26-46. https://academic.oup.com/cid/article/61/6/e26/452579 http://www.ncbi.nlm.nih.gov/pubmed/26229122?tool=bestpractice.com
When the aetiological agent is Brucella, culture may be difficult and results slow to obtain, as the organism is intracellular and the number of circulating bacteria is usually low.[105]Mangalgi S, Sajjan A. Comparison of three blood culture techniques in the diagnosis of human brucellosis. J Lab Physicians. 2014 Jan;6(1):14-7. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3969635 http://www.ncbi.nlm.nih.gov/pubmed/24696554?tool=bestpractice.com Therefore, targeted antibiotic therapy may need to be started when PCR results are available and infection has been confirmed, regardless of whether culture and sensitivity results are available. Follow local antibiotic protocols or seek advice from microbiology on choice of antibiotic regimen in endemic areas. Give antibiotics for Brucella infection for 3 months.[7]Berbari EF, Kanj SS, Kowalski TJ, et al. 2015 Infectious Diseases Society of America (IDSA) clinical practice guidelines for the diagnosis and treatment of native vertebral osteomyelitis in adults. Clin Infect Dis. 2015 Sep 15;61(6):e26-46. https://academic.oup.com/cid/article/61/6/e26/452579 http://www.ncbi.nlm.nih.gov/pubmed/26229122?tool=bestpractice.com See our Brucellosis topic for more information. Seek evaluation by a spine surgeon and an infectious disease specialist in nonendemic areas.[7]Berbari EF, Kanj SS, Kowalski TJ, et al. 2015 Infectious Diseases Society of America (IDSA) clinical practice guidelines for the diagnosis and treatment of native vertebral osteomyelitis in adults. Clin Infect Dis. 2015 Sep 15;61(6):e26-46. https://academic.oup.com/cid/article/61/6/e26/452579 http://www.ncbi.nlm.nih.gov/pubmed/26229122?tool=bestpractice.com
These regimens are examples only; follow local antibiotic protocols.
Primary options
vancomycin: adults: 15-20 mg/kg intravenously every 8-12 hours, maximum 2000 mg/dose
More vancomycinAdjust dose according to serum vancomycin level.
and
ceftriaxone: adults: 2 g intravenously every 24 hours
Secondary options
daptomycin: adults: 4-6 mg/kg intravenously every 24 hours
and
ciprofloxacin: adults: 400 mg intravenously every 8-12 hours
These drug options and doses relate to a patient with no comorbidities.
Primary options
vancomycin: adults: 15-20 mg/kg intravenously every 8-12 hours, maximum 2000 mg/dose
More vancomycinAdjust dose according to serum vancomycin level.
and
ceftriaxone: adults: 2 g intravenously every 24 hours
Secondary options
daptomycin: adults: 4-6 mg/kg intravenously every 24 hours
and
ciprofloxacin: adults: 400 mg intravenously every 8-12 hours
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
vancomycin
and
ceftriaxone
Secondary options
daptomycin
and
ciprofloxacin
surgery
Additional treatment recommended for SOME patients in selected patient group
Surgical intervention is required for progressive neurological deficits, progressive deformity, and spinal instability with or without pain despite adequate antimicrobial therapy.[7]Berbari EF, Kanj SS, Kowalski TJ, et al. 2015 Infectious Diseases Society of America (IDSA) clinical practice guidelines for the diagnosis and treatment of native vertebral osteomyelitis in adults. Clin Infect Dis. 2015 Sep 15;61(6):e26-46. https://academic.oup.com/cid/article/61/6/e26/452579 http://www.ncbi.nlm.nih.gov/pubmed/26229122?tool=bestpractice.com
Surgical debridement with or without stabilisation is needed for persistent or recurrent bloodstream infection (without alternative source) or worsening pain despite appropriate medical therapy.[7]Berbari EF, Kanj SS, Kowalski TJ, et al. 2015 Infectious Diseases Society of America (IDSA) clinical practice guidelines for the diagnosis and treatment of native vertebral osteomyelitis in adults. Clin Infect Dis. 2015 Sep 15;61(6):e26-46. https://academic.oup.com/cid/article/61/6/e26/452579 http://www.ncbi.nlm.nih.gov/pubmed/26229122?tool=bestpractice.com
Practical tip
Note that vertebral osteomyelitis without cord compression usually does not require surgical intervention.
In practice, if you suspect spondylodiscitis or vertebral osteomyelitis in a child, seek advice from paediatrics and/or paediatric orthopaedics, depending on local resources.
suspected acute osteomyelitis in diabetic foot
referral to multidisciplinary foot care team
If you have a clinical concern about bone infection particularly in the patient's feet, inform the multidisciplinary foot care service immediately so that the patient can be assessed and an individualised treatment plan can be put in place.[26]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19
This is a limb-threatening or life-threatening diabetic foot problem.[26]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19
The specialist from the multidisciplinary foot care service should take responsibility for managing a patient with a diabetic foot and suspected osteomyelitis.[26]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19
antibiotic therapy
Treatment recommended for ALL patients in selected patient group
Start empirical antibiotic therapy for a patient with a suspected diabetic foot infection as soon as possible.[26]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19
When choosing an empirical antibiotic regimen for suspected osteomyelitis in a patient with a diabetic foot problem, take into account:[26]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19
The risk of developing complications
Previous microbiological results
Previous antibiotic use
Patient preferences.
Practical tip
In practice, see your local treatment protocol and discuss the patient with the multidisciplinary foot care service and/or microbiology in order to start an appropriate antibiotic regimen.
Select appropriate care setting
Admit any patient who is systemically unwell to hospital for intravenous antibiotic therapy.
Most patients need admission to ensure strict glucose control.
Admit any child with acute osteomyelitis to hospital for intravenous antibiotic therapy, unless there are exceptional circumstances.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com
Adults
The UK National Institute for Health and Care Excellence (NICE) recommends giving one of the following intravenous antibiotic regimens for 48 hours in an adult aged ≥18 years with suspected osteomyelitis (moderate to severe diabetic foot problem):[26]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19
Flucloxacillin with or without gentamicin and/or metronidazole
Amoxicillin/clavulanate with or without gentamicin
Ceftriaxone plus metronidazole.
In patients with a penicillin allergy, prescribe trimethoprim/sulfamethoxazole with or without gentamicin and/or metronidazole.[26]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19
Review intravenous antibiotics at 48 hours and consider switching to oral antibiotics if possible.
Children
Diabetic foot infections are uncommon in children. Seek specialist advice when prescribing antibiotics for a suspected diabetic foot infection in children and young people aged <18 years.[26]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19
Pathogen-targeted therapy
When microbiological results are available, review and change the antibiotic accordingly, using a narrow-spectrum antibiotic, if appropriate.[26]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19
Treat osteomyelitis in a patient with a diabetic foot problem for 6 weeks.[26]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19
Review the need for continued antibiotics regularly.[26]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19
These regimens are examples only; follow local antibiotic protocols.
Primary options
flucloxacillin: adults: 1-2 g intravenously every 6 hours; 1 g orally four times daily
More flucloxacillinThe oral dose may be off-label in some countries.
OR
flucloxacillin: adults: 1-2 g intravenously every 6 hours; 1 g orally four times daily
More flucloxacillinThe oral dose may be off-label in some countries.
-- AND --
gentamicin: adults: 5-7 mg/kg intravenously every 24 hours
More gentamicinAdjust dose according to serum gentamicin level.
and/or
metronidazole: adults: 500 mg intravenously every 8 hours; 400 mg orally three times daily
OR
amoxicillin/clavulanate: adults: 1.2 g intravenously every 8 hours; 500/125 mg orally three times daily
More amoxicillin/clavulanateIntravenous dose consists of 1 g of amoxicillin plus 0.2 g of clavulanate.
and
gentamicin: adults: 5-7 mg/kg intravenously every 24 hours
More gentamicinAdjust dose according to serum gentamicin level.
OR
ceftriaxone: adults: 2 g intravenously every 24 hours
and
metronidazole: adults: 500 mg intravenously every 8 hours; 400 mg orally three times daily
Secondary options
trimethoprim/sulfamethoxazole: adults: 160/800 mg intravenously every 12 hours, may increase to 240/1200 mg every 12 hours in severe infections; 160/800 mg orally twice daily
OR
trimethoprim/sulfamethoxazole: adults: 160/800 mg intravenously every 12 hours, may increase to 240/1200 mg every 12 hours in severe infections; 160/800 mg orally twice daily
-- AND --
gentamicin: adults: 5-7 mg/kg intravenously every 24 hours
More gentamicinAdjust dose according to serum gentamicin level.
and/or
metronidazole: adults: 500 mg intravenously every 8 hours; 400 mg orally three times daily
These drug options and doses relate to a patient with no comorbidities.
Primary options
flucloxacillin: adults: 1-2 g intravenously every 6 hours; 1 g orally four times daily
More flucloxacillinThe oral dose may be off-label in some countries.
OR
flucloxacillin: adults: 1-2 g intravenously every 6 hours; 1 g orally four times daily
More flucloxacillinThe oral dose may be off-label in some countries.
-- AND --
gentamicin: adults: 5-7 mg/kg intravenously every 24 hours
More gentamicinAdjust dose according to serum gentamicin level.
and/or
metronidazole: adults: 500 mg intravenously every 8 hours; 400 mg orally three times daily
OR
amoxicillin/clavulanate: adults: 1.2 g intravenously every 8 hours; 500/125 mg orally three times daily
More amoxicillin/clavulanateIntravenous dose consists of 1 g of amoxicillin plus 0.2 g of clavulanate.
and
gentamicin: adults: 5-7 mg/kg intravenously every 24 hours
More gentamicinAdjust dose according to serum gentamicin level.
OR
ceftriaxone: adults: 2 g intravenously every 24 hours
and
metronidazole: adults: 500 mg intravenously every 8 hours; 400 mg orally three times daily
Secondary options
trimethoprim/sulfamethoxazole: adults: 160/800 mg intravenously every 12 hours, may increase to 240/1200 mg every 12 hours in severe infections; 160/800 mg orally twice daily
OR
trimethoprim/sulfamethoxazole: adults: 160/800 mg intravenously every 12 hours, may increase to 240/1200 mg every 12 hours in severe infections; 160/800 mg orally twice daily
-- AND --
gentamicin: adults: 5-7 mg/kg intravenously every 24 hours
More gentamicinAdjust dose according to serum gentamicin level.
and/or
metronidazole: adults: 500 mg intravenously every 8 hours; 400 mg orally three times daily
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
flucloxacillin
OR
flucloxacillin
-- AND --
gentamicin
and/or
metronidazole
OR
amoxicillin/clavulanate
and
gentamicin
OR
ceftriaxone
and
metronidazole
Secondary options
trimethoprim/sulfamethoxazole
OR
trimethoprim/sulfamethoxazole
-- AND --
gentamicin
and/or
metronidazole
MRSA antibiotic cover
Additional treatment recommended for SOME patients in selected patient group
If you suspect MRSA infection, give one of the following:[26]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19
Vancomycin
Teicoplanin
Linezolid (if vancomycin or teicoplanin cannot be used; specialist use only).
Treat confirmed MRSA with antibiotics identified by culture and sensitivities.
Seek specialist advice when prescribing antibiotics for a suspected diabetic foot infection in children and young people aged <18 years.
These regimens are examples only; follow local antibiotic protocols.
Primary options
vancomycin: adults: 15-20 mg/kg intravenously every 8-12 hours, maximum 2000 mg/dose
More vancomycinAdjust dose according to serum vancomycin level.
OR
teicoplanin: adults: 6 mg/kg intravenously every 12 hours for 3 doses, followed by 6 mg/kg every 24 hours
Secondary options
linezolid: adults: 600 mg intravenously/orally every 12 hours
These drug options and doses relate to a patient with no comorbidities.
Primary options
vancomycin: adults: 15-20 mg/kg intravenously every 8-12 hours, maximum 2000 mg/dose
More vancomycinAdjust dose according to serum vancomycin level.
OR
teicoplanin: adults: 6 mg/kg intravenously every 12 hours for 3 doses, followed by 6 mg/kg every 24 hours
Secondary options
linezolid: adults: 600 mg intravenously/orally every 12 hours
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
vancomycin
OR
teicoplanin
Secondary options
linezolid
Pseudomonas antibiotic cover
Additional treatment recommended for SOME patients in selected patient group
If you suspect Pseudomonas infection, add in:[26]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19
Piperacillin/tazobactam
Clindamycin plus ciprofloxacin (consider safety issues - see Drug safety alert below) and/or gentamicin, if the patient has a penicillin allergy.
Drug safety alert: Restrictions on the use of fluoroquinolone antibiotics
In November 2018, the European Medicines Agency (EMA) completed a review of serious, disabling, and potentially irreversible adverse effects associated with systemic and inhaled fluoroquinolone antibiotics. These adverse effects include tendonitis, tendon rupture, arthralgia, neuropathies, and other musculoskeletal or nervous system effects.
As a consequence of this review, the EMA now recommends that fluoroquinolone antibiotics be restricted for use in serious, life-threatening bacterial infections only. Furthermore, it recommends that fluoroquinolones should not be used for mild to moderate infections unless other appropriate antibiotics for the specific infection cannot be used, and should not be used in non-severe, non-bacterial, or self-limiting infections. Patients who are older, have renal impairment, or have had a solid organ transplant, and those being treated with a corticosteroid are at a higher risk of tendon damage. Coadministration of a fluoroquinolone and a corticosteroid should be avoided.[67]European Medicines Agency. Quinolone- and fluoroquinolone-containing medicinal products. Mar 2019 [internet publication]. https://www.ema.europa.eu/en/medicines/human/referrals/quinolone-fluoroquinolone-containing-medicinal-products The UK-based Medicines and Healthcare products Regulatory Agency (MHRA) supports these recommendations.[68]Medicines and Healthcare products Regulatory Agency. Fluoroquinolone antibiotics: new restrictions and precautions for use due to very rare reports of disabling and potentially long-lasting or irreversible side effects. Mar 2019 [internet publication]. https://www.gov.uk/drug-safety-update/fluoroquinolone-antibiotics-new-restrictions-and-precautions-for-use-due-to-very-rare-reports-of-disabling-and-potentially-long-lasting-or-irreversible-side-effects
For confirmed Pseudomonas infection, be guided by culture and sensitivities results.
Seek specialist advice when prescribing antibiotics for a suspected diabetic foot infection in children and young people aged <18 years.
These regimens are examples only; follow local antibiotic protocols.
Primary options
piperacillin/tazobactam: adults: 4.5 g intravenously every 8 hours, may increase to 4.5 g every 6 hours in severe infections
More piperacillin/tazobactamDose consists of 4 g of piperacillin plus 0.5 g of tazobactam.
Secondary options
clindamycin: adults: 600-2700 mg/day intravenously given in 2-4 divided doses, may increase to 1200 mg every 6 hours in life-threatening infections; 150-450 mg orally four times daily
-- AND --
ciprofloxacin: adults: 400 mg intravenously every 8-12 hours; 500 mg orally twice daily
and/or
gentamicin: adults: 5-7 mg/kg intravenously every 24 hours
More gentamicinAdjust dose according to serum gentamicin level.
These drug options and doses relate to a patient with no comorbidities.
Primary options
piperacillin/tazobactam: adults: 4.5 g intravenously every 8 hours, may increase to 4.5 g every 6 hours in severe infections
More piperacillin/tazobactamDose consists of 4 g of piperacillin plus 0.5 g of tazobactam.
Secondary options
clindamycin: adults: 600-2700 mg/day intravenously given in 2-4 divided doses, may increase to 1200 mg every 6 hours in life-threatening infections; 150-450 mg orally four times daily
-- AND --
ciprofloxacin: adults: 400 mg intravenously every 8-12 hours; 500 mg orally twice daily
and/or
gentamicin: adults: 5-7 mg/kg intravenously every 24 hours
More gentamicinAdjust dose according to serum gentamicin level.
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
piperacillin/tazobactam
Secondary options
clindamycin
-- AND --
ciprofloxacin
and/or
gentamicin
supportive care
Treatment recommended for ALL patients in selected patient group
Admit the patient for strict glucose control. It is particularly important to maintain strict blood glucose control in any patient with diabetes and a major infection such as osteomyelitis.
Offer pain relief to all patients as required. Start with paracetamol or a non-steroidal anti-inflammatory drug (NSAID) such as ibuprofen, with an opioid such as morphine for breakthrough pain relief. If regular use of morphine is required, switch to a slow-release oral formulation. In practice, severe pain usually suggests there is a collection (abscess) that needs to be drained.
Address any comorbidities.
Immobilise the limb for comfort if necessary.
Look out for deep vein thrombosis, particularly with Staphylococcus aureus osteomyelitis.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com [66]Mejer N, Westh H, Schønheyder HC, et al. Increased risk of venous thromboembolism within the first year after Staphylococcus aureus bacteraemia: a nationwide observational matched cohort study. J Intern Med. 2014 Apr;275(4):387-97. https://onlinelibrary.wiley.com/doi/full/10.1111/joim.12147 http://www.ncbi.nlm.nih.gov/pubmed/24118528?tool=bestpractice.com Follow local protocols. See our topic Deep vein thrombosis.
Primary options
paracetamol: children: consult specialist for guidance on dose; adults: 500-1000 mg orally every 4-6 hours when required, maximum 4000 mg/day; adults: 15 mg/kg (maximum 1000 mg/dose) intravenously every 4-6 hours when required, maximum 4000 mg/day
OR
ibuprofen: children: consult specialist for guidance on dose; adults: 300-600 mg orally (immediate-release) every 6-8 hours when required, maximum 2400 mg/day
Secondary options
morphine sulfate: children: consult specialist for guidance on dose; adults: 5-10 mg orally (immediate-release)/subcutaneously/intravenously/intramuscularly every 4 hours initially, adjust dose according to response
These drug options and doses relate to a patient with no comorbidities.
Primary options
paracetamol: children: consult specialist for guidance on dose; adults: 500-1000 mg orally every 4-6 hours when required, maximum 4000 mg/day; adults: 15 mg/kg (maximum 1000 mg/dose) intravenously every 4-6 hours when required, maximum 4000 mg/day
OR
ibuprofen: children: consult specialist for guidance on dose; adults: 300-600 mg orally (immediate-release) every 6-8 hours when required, maximum 2400 mg/day
Secondary options
morphine sulfate: children: consult specialist for guidance on dose; adults: 5-10 mg orally (immediate-release)/subcutaneously/intravenously/intramuscularly every 4 hours initially, adjust dose according to response
Drug choice, dose and interactions may be affected by the patient's comorbidities. Check your local drug formulary.
Show drug information for a patient with no comorbidities
Primary options
paracetamol
OR
ibuprofen
Secondary options
morphine sulfate
surgery
Additional treatment recommended for SOME patients in selected patient group
The NICE guideline on the prevention and management of diabetic foot problems does not address surgery for osteomyelitis in the foot of a patient with diabetes.[26]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19 Seek advice from the multidisciplinary foot care service.
chronic osteomyelitis
referral to specialist team
Once there is dead bone or a biofilm has become established, the osteomyelitis can be considered chronic. Chronic osteomyelitis usually has a history of >3 months.[6]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. European Society for Paediatric Infectious Diseases (ESPID) bone and joint infection guidelines. Pediatr Infect Dis J. 2017 Aug;36(8):788-99. https://journals.lww.com/pidj/Fulltext/2017/08000/Bone_and_Joint_Infections.18.aspx http://www.ncbi.nlm.nih.gov/pubmed/28708801?tool=bestpractice.com Antibiotics alone cannot cure the infection and thorough surgical debridement is required for full cure.
Consider where the patient should receive their treatment and discuss this with them.
In practice, treat a patient with an acute exacerbation of chronic osteomyelitis in the same way as you would treat a patient with a purely acute presentation, but refer them to the team that usually supervises their care.
Discuss admission of a patient with an acute exacerbation of chronic osteomyelitis with the team that usually provides their care.
Owing to the many and varied comorbidities present in class B patients under the Cierny-Mader classification (patients with comorbidities that directly reduce the likelihood of wound healing, reduce the efficacy of drug treatment, or increase the risks of surgery) and the particular surgical techniques required to tackle complex infections, these patients should be seen in a specialist bone infection centre.
In patients with type IV disease (where there is diffuse involvement of the entire circumference of the bone), in diffuse osteomyelitis, or when there are infected fractures, a multidisciplinary team specialising in bone infection should be involved.
The team should include orthopaedic surgeons, microbiologists, plastic surgeons, and clinical nurse specialists who assist with home intravenous therapy and wound care.
Involve a musculoskeletal radiologist to interpret imaging and perform percutaneous bone biopsies.
There is also a role for a vascular surgeon in a patient with peripheral vascular disease. For example, a patient with a non-union or a foot ulcer may require revascularisation prior to operative intervention to improve outcome.
For any patient with a limb-threatening or life-threatening diabetic foot problem, including a clinical concern that there is a bone infection, liaise with the multidisciplinary foot care service immediately.[26]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19 See the patient group suspected acute osteomyelitis in diabetic foot, above, and our topic Diabetic foot complications for more information.
In a patient with native vertebral osteomyelitis, consult a spine surgeon and an infectious disease physician.
Chronic osteomyelitis in children is rare. When it does occur, discuss the patient with a paediatric orthopaedic surgeon and infectious diseases consultant.
Arrange functional rehabilitation for all patients with chronic osteomyelitis.
clinical staging and assessment for surgery
Treatment recommended for ALL patients in selected patient group
Accurately stage the patient’s condition using the Cierny-Mader classification. See Classification (in the Aetiology section of this topic) for more details.
Perform diagnostic tests to assess general health and the condition of the limb or spine, including:
Guided biopsy to identify the causative organism
Blood tests
Scanning
Angiography.
Discuss treatment options and potential associated risks with the patient fully.
optimise patient’s condition
Treatment recommended for ALL patients in selected patient group
Manage any comorbidities, with hospitalisation if necessary. Consider the following:
Nutritional status
Smoking
Substance dependence
Anaemia
Coagulopathies
Glucose control
Vascular insufficiency
Sickle cell disease needing exchange transfusion.
antibiotic therapy ± limited surgery
Additional treatment recommended for SOME patients in selected patient group
For a patient with disease classified as class C in the Cierny-Mader classification (patients who are so severely compromised that treatment has an unacceptable risk-benefit ratio), or who can manage with few symptoms from their infection, it may be reasonable to withhold treatment or just to treat symptomatic flare-ups with short antibiotic courses.
Select an appropriate antibiotic regimen based on results of radiologically guided biopsy.
If the flare-ups are back to back with a matter of days between them, escalate the therapy to long-term antibiotic suppression.
Long-term suppressive antibiotic usage needs to be balanced against significant risk of poor adherence, adverse effects, drug interactions, and developing antimicrobial resistance.
ln some cases, rather than achieving cure, limited surgery to reduce the infective load, followed by long-term antibiotic suppression, may be an option (e.g., when existing implants provide a challenging reconstructive problem).
Consider – curative surgery plus intravenous antibiotic therapy
curative surgery plus intravenous antibiotic therapy
Additional treatment recommended for SOME patients in selected patient group
Surgery in a patient with chronic osteomyelitis is complex and often warrants technical expertise and multidisciplinary input. Staged reconstruction is sometimes needed. For further details, see the section on Chronic osteomyelitis in the Management Recommendations section of this topic.
Plan the surgical approach using imaging. Plain film x-ray and magnetic resonance imaging (MRI) are particularly useful in accessing the sequestrum and avoiding unnecessary damage to the healthy bone when making a window to enter the medullary canal. MRI is also helpful in identifying localised active disease when the normal morphology of the bone is disrupted.
In general, operative principles include:
Use of a tourniquet wherever possible
Excision of any sinus with an ellipse of skin in the line of the incision
Thorough debridement and excision of all infected tissue
Meticulous microbiological and histological sampling early during the procedure
Obtaining uncontaminated representative samples to diagnose the causative organism and rule out other potential differentials, such as tumour, is essential.
Dead space management to prevent the formation of haematoma
Haematoma increases infection recurrence rates.
Stabilisation of the bone, when there is instability or risk of fracture, usually with an external fixator
Attaining immediate soft-tissue coverage with healthy vascularised tissue that can deliver systemic antibiotics.
Once sampling has been completed, antibiotics are given. Initial intravenous antibiotic therapy appropriate to the flora encountered in the hospital’s region must be continued until a definitive regimen is selected based on the intraoperative culture results.
A protocol using a glycopeptide and a carbapenem antibiotic postoperatively in 166 cases of osteomyelitis debridement showed coverage of 96% of all organisms subsequently cultured.[74]Dudareva M, Hotchen AJ, Ferguson J, et al. The microbiology of chronic osteomyelitis: changes over ten years. J Infect. 2019 Sep;79(3):189-98. http://www.ncbi.nlm.nih.gov/pubmed/31319142?tool=bestpractice.com This study revealed that one third of organisms cultured were resistant to a penicillin-based empirical antibiotic regimens. The carbapenem is usually stopped after 48 hours' culture if no gram-negative organisms have been cultured at that point.
If the patient does not respond to standard therapy, atypical organisms or fungal infections should be considered.
The optimal duration of antimicrobial therapy after surgery is not certain. If the osteomyelitic bone has been fully resected, a shorter course of antibiotic therapy (2-6 weeks) may be adequate as long as operative wounds are healing without any signs of infection.
Choose a patient group to see our recommendations
Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups. See disclaimer
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