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
suspected acute peripheral osteomyelitis: low MRSA prevalence
empiric antibiotic therapy
Peripheral osteomyelitis usually occurs in the major long bones (e.g., femur, tibia, humerus), but can occur in other bones too.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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 An acute presentation has a history of <2 weeks.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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 acute osteomyelitis in diabetic foot," below.
Any patient who is systemically unwell should be admitted to the hospital for intravenous antibiotic therapy.
Sepsis should be suspected if there is acute deterioration in a patient in whom there is clinical evidence or strong suspicion of infection. Local sepsis protocols should be followed. See Sepsis in adults.
Blood cultures should be considered in patients with fever suspected of having peripheral bone infection.[1]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 If blood cultures are indicated, samples should be taken before commencing antibiotics.[1]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
Initial antibiotic choice is based on the most likely causative organism, which in turn depends on the patient's age, immunization history, comorbidities, the prevalence of organisms in the community, and antimicrobial sensitivities.
In adults with suspected acute peripheral osteomyelitis in areas of low MRSA prevalence (<10%), empiric therapy options include vancomycin plus a third- or fourth-generation cephalosporin (e.g., ceftriaxone, cefepime). If the patient has a penicillin allergy, vancomycin plus a fluoroquinolone (e.g., ciprofloxacin) may be considered.[99]Spellberg B, Lipsky BA. Systemic antibiotic therapy for chronic osteomyelitis in adults. Clin Infect Dis. 2012 Feb 1;54(3):393-407. https://academic.oup.com/cid/article/54/3/393/304469 http://www.ncbi.nlm.nih.gov/pubmed/22157324?tool=bestpractice.com
If Pseudomonas is suspected, an empiric antibiotic regimen that covers Pseudomonas should be chosen. Hematogenous osteomyelitis caused by Pseudomonas aeruginosa and other Pseudomonas species occurs most often in people who inject drugs.[9]Miller JM, Binnicker MJ, Campbell S, et al. Guide to utilization of the microbiology laboratory for diagnosis of infectious diseases: 2024 update by the Infectious Diseases Society of America (IDSA) and the American Society for Microbiology (ASM). Clin Infect Dis. 2024 Mar 5;ciae104. https://www.doi.org/10.1093/cid/ciae104 http://www.ncbi.nlm.nih.gov/pubmed/38442248?tool=bestpractice.com P aeruginosa is the most common bacterial cause of calcaneal osteomyelitis in patients who develop this infection after stepping on nails while wearing sneakers.[9]Miller JM, Binnicker MJ, Campbell S, et al. Guide to utilization of the microbiology laboratory for diagnosis of infectious diseases: 2024 update by the Infectious Diseases Society of America (IDSA) and the American Society for Microbiology (ASM). Clin Infect Dis. 2024 Mar 5;ciae104. https://www.doi.org/10.1093/cid/ciae104 http://www.ncbi.nlm.nih.gov/pubmed/38442248?tool=bestpractice.com A local infectious disease specialist should be consulted about suitable options.
Fluoroquinolones have been associated with serious, disabling, and potentially irreversible adverse effects, including tendonitis, tendon rupture, arthralgia, neuropathies, and other musculoskeletal or nervous system effects.[102]European Medicines Agency. Quinolone- and fluoroquinolone-containing medicinal products. Nov 2018 [internet publication]. https://www.ema.europa.eu/en/medicines/human/referrals/quinolone-fluoroquinolone-containing-medicinal-products Warnings have also been issued about the increased risk of aortic dissection, significant hypoglycemia, and mental health adverse effects in patients taking fluoroquinolones.[103]US Food and Drug Administration. Safety announcement: FDA reinforces safety information about serious low blood sugar levels and mental health side effects with fluoroquinolone antibiotics; requires label changes. Jul 2018 [internet publication]. https://www.fda.gov/drugs/drug-safety-and-availability/fda-reinforces-safety-information-about-serious-low-blood-sugar-levels-and-mental-health-side [104]US Food and Drug Administration. Drug safety communication: FDA warns about increased risk of ruptures or tears in the aorta blood vessel with fluoroquinolone antibiotics in certain patients. Dec 2018 [internet publication]. https://www.fda.gov/drugs/drug-safety-and-availability/fda-warns-about-increased-risk-ruptures-or-tears-aorta-blood-vessel-fluoroquinolone-antibiotics
Intravenous therapy should be switched to appropriate oral antibiotic therapy when clinically indicated. Once the organism is identified by culture or polymerase chain reaction (PCR), and sensitivity to antibiotics is determined, antibiotic therapy should be narrowed accordingly.
The optimal duration of antimicrobial therapy is not certain.[57]Li HK, Rombach I, Zambellas R, et al; OVIVA Trial Collaborators. 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/10.1056/NEJMoa1710926 http://www.ncbi.nlm.nih.gov/pubmed/30699315?tool=bestpractice.com Response to antibiotic treatment is typically rapid. However, if the affected limb deteriorates or imaging suggests progressive bone destruction, choice of antibiotics should be discussed with microbiology. Surgery should be considered to prevent progression to chronic osteomyelitis.
Examples of antibiotic regimens are provided here; however, local protocols should be followed.
Primary options
vancomycin: 15-20 mg/kg intravenously every 8-12 hours, maximum 2000 mg/day
More vancomycinAdjust dose according to serum vancomycin level. A loading dose of 20-35 mg/kg (maximum 3000 mg/dose) may be considered in seriously ill patients.
-- AND --
ceftriaxone: 1-2 g intravenously every 24 hours
or
cefepime: 1-2 g intravenously every 8-12 hours
Secondary options
vancomycin: 15-20 mg/kg intravenously every 8-12 hours, maximum 2000 mg/day
More vancomycinAdjust dose according to serum vancomycin level. A loading dose of 20-35 mg/kg (maximum 3000 mg/dose) may be considered in seriously ill patients.
and
ciprofloxacin: 400 mg intravenously every 8-12 hours
supportive care
Treatment recommended for ALL patients in selected patient group
The approach to treatment of osteomyelitis is complex, and often requires a multidisciplinary approach, with input from radiologists, vascular and orthopedic surgeons, infectious disease specialists, and wound care and rehabilitation specialists.[96]Fritz JM, McDonald JR. Osteomyelitis: approach to diagnosis and treatment. Phys Sportsmed. 2008 Dec;36(1):nihpa116823. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696389 http://www.ncbi.nlm.nih.gov/pubmed/19652694?tool=bestpractice.com
The affected limb should be elevated and immobilized if necessary. Assessment should be undertaken for deep vein thrombosis, particularly with Staphylococcus aureus osteomyelitis since there is a high risk of venous thromboembolism during the first month following an episode of S aureus bacteremia.[98]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/10.1111/joim.12147 http://www.ncbi.nlm.nih.gov/pubmed/24118528?tool=bestpractice.com See Deep vein thrombosis.
Any comorbidities should be addressed. It is particularly important to maintain strict blood glucose control in any patient with diabetes and a major infection such as osteomyelitis.[37]Lipsky BA, Senneville É, Abbas ZG, et al; International Working Group on the Diabetic Foot (IWGDF). Guidelines on the diagnosis and treatment of foot infection in persons with diabetes (IWGDF 2019 update). Diabetes Metab Res Rev. 2020 Mar;36 Suppl 1:e3280. https://onlinelibrary.wiley.com/doi/10.1002/dmrr.3280 http://www.ncbi.nlm.nih.gov/pubmed/32176444?tool=bestpractice.com See Diabetic foot complications.
Pain relief should be provided to all patients as required. First-line analgesics include acetaminophen and nonsteroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen. For more severe pain, an opioid (e.g., morphine, oxycodone) may be required for a short duration. If longer-term pain relief is required, a pain management specialist should be consulted.
Primary options
acetaminophen: 325-1000 mg orally every 4-6 hours when required, maximum 4000 mg/day
OR
ibuprofen: 400 mg orally every 4-6 hours when required, maximum 2400 mg/day
Secondary options
morphine sulfate: 10-30 mg orally (immediate-release) every 4 hours when required; 2.5 to 10 mg subcutaneously/intravenously/intramuscularly every 2-6 hours when required; adjust dose according to response
OR
oxycodone: 5-15 mg orally (immediate-release) every 4-6 hours when required, adjust dose according to response
surgery
Treatment recommended for SOME patients in selected patient group
Response to antibiotic therapy is typically rapid. However, if the affected limb deteriorates or imaging suggests progressive bone destruction, the choice of antibiotics should be discussed with microbiology. Surgery should be considered to prevent progression to chronic osteomyelitis. Once dead bone or a biofilm has become established, antibiotics alone cannot cure the infection and thorough surgical debridement is required.
empiric antibiotic therapy
Peripheral osteomyelitis usually occurs in the major long bones (e.g., femur, tibia, humerus), but can occur in other bones too.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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 An acute presentation has a history of <2 weeks.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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
Sepsis should be suspected if there is acute deterioration in a patient in whom there is clinical evidence or strong suspicion of infection. Local sepsis protocols should be followed. See Sepsis in children.
Blood cultures should be considered in all children, in line with European Society For Paediatric Infectious Diseases (ESPID) recommendations.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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
Most children are admitted to the hospital for intravenous therapy.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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 Some centers may use outpatient parenteral antimicrobial therapy with the insertion of a peripheral-inserted central line.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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 children with presumed acute hematogenous osteomyelitis who appear ill or have rapidly progressive infection, the Infectious Diseases Society of America (IDSA) recommends that empiric antimicrobial therapy should be started immediately rather than withholding antibiotics until invasive diagnostic procedures are performed.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com In children with presumed acute hematogenous osteomyelitis who are not clinically ill and for whom an aspirate or biopsy by invasive diagnostic procedure is being planned prior to initiating antibiotics, the IDSA recommends that antibiotics should be withheld for no more than 48-72 hours.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com
Initial antibiotic choice is based on the most likely causative organism, which in turn depends on the patient's age, immunization history, comorbidities, the prevalence of organisms in the community, and antimicrobial sensitivities.
Empiric therapy options for children with suspected acute peripheral osteomyelitis in areas of low MRSA prevalence (<10%) include nafcillin, oxacillin, or cefazolin.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com Vancomycin is a common initial choice for children who are critically ill at presentation, regardless of regional MRSA prevalence.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com
In the presence of a clinical presentation, physical examination, exposure history, or other risk factors that either are inconsistent with Staphylococcus aureus infection or suggest need for coverage for other organisms, additional empiric antimicrobial coverage for pathogens other than S aureus may be warranted. For example, additional coverage may be indicated in younger children (<4 years) for Kingella kingae or children with underlying hemoglobinopathies who have increased risk for Salmonella spp. infection.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com [9]Miller JM, Binnicker MJ, Campbell S, et al. Guide to utilization of the microbiology laboratory for diagnosis of infectious diseases: 2024 update by the Infectious Diseases Society of America (IDSA) and the American Society for Microbiology (ASM). Clin Infect Dis. 2024 Mar 5;ciae104. https://www.doi.org/10.1093/cid/ciae104 http://www.ncbi.nlm.nih.gov/pubmed/38442248?tool=bestpractice.com [12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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
Pseudomonas is a rare cause of osteomyelitis in young children, unless there is trauma or puncture of the foot. If Pseudomonas is suspected, an empiric antibiotic regimen that covers Pseudomonas should be chosen. A local infectious disease specialist should be consulted about suitable options. The IDSA notes that non-fluoroquinolone antibiotics are preferred for children, owing to concerns for cartilage/tendon injury noted in animal toxicity studies of fluoroquinolones.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com
Switching from intravenous to oral antibiotics after 2-4 days should be considered when the child has been afebrile for 24-48 hours, shows clinical improvement with reduced pain, inflammation, and improved mobility, and has a C-reactive protein (CRP) level that has decreased by at least 30% of the highest value.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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 children who respond well to initial treatment, early transition from intravenous to oral therapy (after 3 days to 1 week) may be as effective as longer courses of intravenous antibiotics.[100]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 [101]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 In children with acute hematogenous osteomyelitis presumed or proven to be caused by S aureus who have had an uncomplicated course and respond to initial therapy, the IDSA suggests a 3- to 4-week duration of antibiotics (parenteral plus oral) rather than a longer course.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com Longer duration may be necessary for other pathogens, including more virulent strains of S aureus, and for complicated cases.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com
Examples of antibiotic regimens are provided here; however, local protocols should be followed.
Primary options
nafcillin: 100-200 mg/kg/day intravenously given in divided doses every 4-6 hours, maximum 12 g/day
OR
oxacillin: 100-200 mg/kg/day intravenously given in divided doses every 4-6 hours, maximum 12 g/day
OR
cefazolin: 25-100 mg/kg/day intravenously given in divided doses every 6-8 hours, maximum 6 g/day
Secondary options
vancomycin: children 1-2 months of age: 45-60 mg/kg/day intravenously given in divided doses every 6-8 hours; children 3 months to 11 years of age: 60-80 mg/kg/day intravenously given in divided doses every 6 hours, maximum 3000 mg/day; children ≥12 years of age: 60-70 mg/kg/day intravenously given in divided doses every 6-8 hours, maximum 3000 mg/day
More vancomycinAdjust dose according to serum vancomycin level. A loading dose may be considered in seriously ill patients.
supportive care
Treatment recommended for ALL patients in selected patient group
The approach to treatment of osteomyelitis is complex, and often requires a multidisciplinary approach, with input from radiologists, vascular and orthopedic surgeons, infectious disease specialists, and wound care and rehabilitation specialists.[96]Fritz JM, McDonald JR. Osteomyelitis: approach to diagnosis and treatment. Phys Sportsmed. 2008 Dec;36(1):nihpa116823. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696389 http://www.ncbi.nlm.nih.gov/pubmed/19652694?tool=bestpractice.com
The affected limb should be elevated and immobilized if necessary. Assessment should be undertaken for deep vein thrombosis, particularly with Staphylococcus aureus osteomyelitis since there is a high risk of venous thromboembolism during the first month following an episode of S aureus bacteremia.[98]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/10.1111/joim.12147 http://www.ncbi.nlm.nih.gov/pubmed/24118528?tool=bestpractice.com See Deep vein thrombosis.
Any comorbidities should be addressed. It is particularly important to maintain strict blood glucose control in any patient with diabetes and a major infection such as osteomyelitis.[37]Lipsky BA, Senneville É, Abbas ZG, et al; International Working Group on the Diabetic Foot (IWGDF). Guidelines on the diagnosis and treatment of foot infection in persons with diabetes (IWGDF 2019 update). Diabetes Metab Res Rev. 2020 Mar;36 Suppl 1:e3280. https://onlinelibrary.wiley.com/doi/10.1002/dmrr.3280 http://www.ncbi.nlm.nih.gov/pubmed/32176444?tool=bestpractice.com Diabetic foot infections are uncommon in children. Specialist advice should be sought. See Diabetic foot complications.
Pain relief should be provided to all patients as required. First-line analgesics include acetaminophen and nonsteroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen. Rectal administration of acetaminophen can provide pain relief longer than intravenous administration in children.[97]Verghese ST, Hannallah RS. Acute pain management in children. J Pain Res. 2010 Jul 15;3:105-23. https://www.dovepress.com/getfile.php?fileID=6955 http://www.ncbi.nlm.nih.gov/pubmed/21197314?tool=bestpractice.com For more severe pain, an opioid (e.g., morphine, oxycodone) may be required for a short duration. If longer-term pain relief is required, a pain management specialist should be consulted.
Primary options
acetaminophen: 10-15 mg/kg orally/rectally every 4-6 hours when required, maximum 75 mg/kg/day
OR
ibuprofen: 5-10 mg/kg orally every 6-8 hours when required, maximum 40 mg/kg/day
Secondary options
morphine sulfate: consult specialist for guidance on dose
OR
oxycodone: consult specialist for guidance on dose
surgery
Treatment recommended for SOME patients in selected patient group
Pediatric orthopedic advice should be sought. In children with acute hematogenous osteomyelitis who present with sepsis or have a rapidly progressive infection, the Infectious Diseases Society of America (IDSA) recommends that debridement of the infected bone and any associated abscesses should be performed as soon as possible after diagnosis, rather than treating with medical therapy alone.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com The European Society for Paediatric Infectious Diseases (ESPID) recommends that surgery should be considered in the following situations: persistent or recurring fever after 3-4 days; periosteal abscess with persistent fever and raised CRP; sequestration; MRSA or Panton-Valentine leukocidin (PVL)-positive S aureus; chronic osteomyelitis; prosthetic material.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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 Once dead bone or a biofilm has become established, antibiotics alone cannot cure the infection and thorough surgical debridement is required.
suspected acute peripheral osteomyelitis: high MRSA prevalence
empiric antibiotic therapy
Peripheral osteomyelitis usually occurs in the major long bones (e.g., femur, tibia, humerus), but can occur in other bones too.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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 An acute presentation has a history of <2 weeks.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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 acute osteomyelitis in diabetic foot," below.
Any patient who is systemically unwell should be admitted to the hospital for intravenous antibiotic therapy.
Sepsis should be suspected if there is acute deterioration in a patient in whom there is clinical evidence or strong suspicion of infection. Local sepsis protocols should be followed. See Sepsis in adults.
Blood cultures should be considered in patients with fever suspected of having peripheral bone infection.[1]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 If blood cultures are indicated, samples should be taken before commencing antibiotics.[1]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
Initial antibiotic choice is based on the most likely causative organism, which in turn depends on the patient's age, immunization history, comorbidities, the prevalence of organisms in the community, and antimicrobial sensitivities.
In adults with suspected acute peripheral osteomyelitis in areas of high MRSA prevalence (>10%), vancomycin is the drug of choice. Daptomycin is a reasonable alternative if the patient cannot tolerate vancomycin or if vancomycin is contraindicated.
Fluoroquinolones have been associated with serious, disabling, and potentially irreversible adverse effects, including tendonitis, tendon rupture, arthralgia, neuropathies, and other musculoskeletal or nervous system effects.[102]European Medicines Agency. Quinolone- and fluoroquinolone-containing medicinal products. Nov 2018 [internet publication]. https://www.ema.europa.eu/en/medicines/human/referrals/quinolone-fluoroquinolone-containing-medicinal-products Warnings have also been issued about the increased risk of aortic dissection, significant hypoglycemia, and mental health adverse effects in patients taking fluoroquinolones.[103]US Food and Drug Administration. Safety announcement: FDA reinforces safety information about serious low blood sugar levels and mental health side effects with fluoroquinolone antibiotics; requires label changes. Jul 2018 [internet publication]. https://www.fda.gov/drugs/drug-safety-and-availability/fda-reinforces-safety-information-about-serious-low-blood-sugar-levels-and-mental-health-side [104]US Food and Drug Administration. Drug safety communication: FDA warns about increased risk of ruptures or tears in the aorta blood vessel with fluoroquinolone antibiotics in certain patients. Dec 2018 [internet publication]. https://www.fda.gov/drugs/drug-safety-and-availability/fda-warns-about-increased-risk-ruptures-or-tears-aorta-blood-vessel-fluoroquinolone-antibiotics
Intravenous therapy should be switched to appropriate oral antibiotic therapy when clinically indicated. Once the organism is identified by culture or polymerase chain reaction (PCR), and sensitivity to antibiotics is determined, antibiotic therapy should be narrowed accordingly.
The optimal duration of antimicrobial therapy is not certain.[57]Li HK, Rombach I, Zambellas R, et al; OVIVA Trial Collaborators. 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/10.1056/NEJMoa1710926 http://www.ncbi.nlm.nih.gov/pubmed/30699315?tool=bestpractice.com Response to antibiotic treatment is typically rapid. However, if the affected limb deteriorates or imaging suggests progressive bone destruction, choice of antibiotics should be discussed with microbiology. Surgery should be considered to prevent progression to chronic osteomyelitis.
Examples of antibiotic regimens are provided here; however, local protocols should be followed.
Primary options
vancomycin: 15-20 mg/kg intravenously every 8-12 hours, maximum 2000 mg/day
More vancomycinA loading dose of 20-35 mg/kg (maximum 3000 mg/dose) may be considered in seriously ill patients. Adjust dose according to serum vancomycin level.
Secondary options
daptomycin: 6 mg/kg intravenously every 24 hours
supportive care
Treatment recommended for ALL patients in selected patient group
The approach to treatment of osteomyelitis is complex, and often requires a multidisciplinary approach, with input from radiologists, vascular and orthopedic surgeons, infectious disease specialists, and wound care and rehabilitation specialists.[96]Fritz JM, McDonald JR. Osteomyelitis: approach to diagnosis and treatment. Phys Sportsmed. 2008 Dec;36(1):nihpa116823. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696389 http://www.ncbi.nlm.nih.gov/pubmed/19652694?tool=bestpractice.com
The affected limb should be elevated and immobilized if necessary. Assessment should be undertaken for deep vein thrombosis, particularly with Staphylococcus aureus osteomyelitis since there is a high risk of venous thromboembolism during the first month following an episode of S aureus bacteremia.[98]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/10.1111/joim.12147 http://www.ncbi.nlm.nih.gov/pubmed/24118528?tool=bestpractice.com See Deep vein thrombosis.
Any comorbidities should be addressed. It is particularly important to maintain strict blood glucose control in any patient with diabetes and a major infection such as osteomyelitis.[37]Lipsky BA, Senneville É, Abbas ZG, et al; International Working Group on the Diabetic Foot (IWGDF). Guidelines on the diagnosis and treatment of foot infection in persons with diabetes (IWGDF 2019 update). Diabetes Metab Res Rev. 2020 Mar;36 Suppl 1:e3280. https://onlinelibrary.wiley.com/doi/10.1002/dmrr.3280 http://www.ncbi.nlm.nih.gov/pubmed/32176444?tool=bestpractice.com See Diabetic foot complications.
Pain relief should be provided to all patients as required. First-line analgesics include acetaminophen and nonsteroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen. For more severe pain, an opioid (e.g., morphine, oxycodone) may be required for a short duration. If longer-term pain relief is required, a pain management specialist should be consulted.
Primary options
acetaminophen: 325-1000 mg orally every 4-6 hours when required, maximum 4000 mg/day
OR
ibuprofen: 400 mg orally every 4-6 hours when required, maximum 2400 mg/day
Secondary options
morphine sulfate: 10-30 mg orally (immediate-release) every 4 hours when required; 2.5 to 10 mg subcutaneously/intravenously/intramuscularly every 2-6 hours when required; adjust dose according to response
OR
oxycodone: 5-15 mg orally (immediate-release) every 4-6 hours when required, adjust dose according to response
surgery
Treatment recommended for SOME patients in selected patient group
Response to antibiotic therapy is typically rapid. However, if the affected limb deteriorates or imaging suggests progressive bone destruction, the choice of antibiotics should be discussed with microbiology. Surgery should be considered to prevent progression to chronic osteomyelitis. Once dead bone or a biofilm has become established, antibiotics alone cannot cure the infection and thorough surgical debridement is required.
empiric antibiotic therapy
Peripheral osteomyelitis usually occurs in the major long bones (e.g., femur, tibia, humerus), but can occur in other bones too.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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 An acute presentation has a history of <2 weeks.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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
Sepsis should be suspected if there is acute deterioration in a patient in whom there is clinical evidence or strong suspicion of infection. Local sepsis protocols should be followed. See Sepsis in children.
Blood cultures should be considered in all children, in line with European Society For Paediatric Infectious Diseases (ESPID) recommendations.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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
Most children are admitted to the hospital for intravenous therapy.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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 Hospital admission may be particularly important in regions with a high rate of MRSA or Panton-Valentine leukocidin (PVL)-positive Staphylococcus aureus, worse clinical severity, and in high-risk patients (e.g., infants, immunocompromised children).[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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 Some centers may use outpatient parenteral antimicrobial therapy with the insertion of a peripheral-inserted central line.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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 children with presumed acute hematogenous osteomyelitis who appear ill or have rapidly progressive infection, the Infectious Diseases Society of America (IDSA) recommends that empiric antimicrobial therapy should be started immediately rather than withholding antibiotics until invasive diagnostic procedures are performed.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com In children with presumed acute hematogenous osteomyelitis who are not clinically ill and for whom an aspirate or biopsy by invasive diagnostic procedure is being planned prior to initiating antibiotics, the IDSA recommends that antibiotics should be withheld for no more than 48-72 hours.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com
Initial antibiotic choice is based on the most likely causative organism, which in turn depends on the patient's age, immunization history, comorbidities, the prevalence of organisms in the community, and antimicrobial sensitivities.
For children with suspected acute peripheral osteomyelitis in areas of high MRSA prevalence (>10%), vancomycin or clindamycin may be considered.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com Vancomycin is a common initial choice for children who are critically ill at presentation, regardless of regional MRSA prevalence.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com
In the presence of a clinical presentation, physical examination, exposure history, or other risk factors that either are inconsistent with S aureus infection or suggest need for coverage for other organisms, additional empiric antimicrobial coverage for pathogens other than S aureus may be warranted. For example, additional coverage may be indicated in younger children (<4 years) for Kingella kingae or children with underlying hemoglobinopathies who have increased risk for Salmonella spp. infection.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com [9]Miller JM, Binnicker MJ, Campbell S, et al. Guide to utilization of the microbiology laboratory for diagnosis of infectious diseases: 2024 update by the Infectious Diseases Society of America (IDSA) and the American Society for Microbiology (ASM). Clin Infect Dis. 2024 Mar 5;ciae104. https://www.doi.org/10.1093/cid/ciae104 http://www.ncbi.nlm.nih.gov/pubmed/38442248?tool=bestpractice.com [12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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
Pseudomonas is a rare cause of osteomyelitis in young children, unless there is trauma or puncture of the foot. If Pseudomonas is suspected, an empiric antibiotic regimen that covers Pseudomonas should be chosen. A local infectious disease specialist should be consulted about suitable options. The IDSA notes that non-fluoroquinolone antibiotics are preferred for children, owing to concerns for cartilage/tendon injury noted in animal toxicity studies of fluoroquinolones.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com
Switching from intravenous to oral antibiotics after 2-4 days should be considered when the child has been afebrile for 24-48 hours, shows clinical improvement with reduced pain, inflammation, and improved mobility, and has a C-reactive protein (CRP) level that has decreased by at least 30% of the highest value.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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 children who respond well to initial treatment, early transition from intravenous to oral therapy (after 3 days to 1 week) may be as effective as longer courses of intravenous antibiotics.[100]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 [101]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 In children with acute hematogenous osteomyelitis presumed or proven to be caused by S aureus who have had an uncomplicated course and respond to initial therapy, the IDSA suggests a 3- to 4-week duration of antibiotics (parenteral plus oral) rather than a longer course.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com Longer duration may be necessary for other pathogens, including more virulent strains of S aureus, and for complicated cases.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com
Examples of antibiotic regimens are provided here; however, local protocols should be followed.
Primary options
vancomycin: children 1-2 months of age: 45-60 mg/kg/day intravenously given in divided doses every 6-8 hours; children 3 months to 11 years of age: 60-80 mg/kg/day intravenously given in divided doses every 6 hours, maximum 3000 mg/day; children ≥12 years of age: 60-70 mg/kg/day intravenously given in divided doses every 6-8 hours, maximum 3000 mg/day
More vancomycinAdjust dose according to serum vancomycin level. A loading dose may be considered in seriously ill patients.
OR
clindamycin: 25-40 mg/kg/day intravenously given in divided doses every 6-8 hours, maximum 4.8 g/day
supportive care
Treatment recommended for ALL patients in selected patient group
The approach to treatment of osteomyelitis is complex, and often requires a multidisciplinary approach, with input from radiologists, vascular and orthopedic surgeons, infectious disease specialists, and wound care and rehabilitation specialists.[96]Fritz JM, McDonald JR. Osteomyelitis: approach to diagnosis and treatment. Phys Sportsmed. 2008 Dec;36(1):nihpa116823. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696389 http://www.ncbi.nlm.nih.gov/pubmed/19652694?tool=bestpractice.com
The affected limb should be elevated and immobilized if necessary. Assessment should be undertaken for deep vein thrombosis, particularly with Staphylococcus aureus osteomyelitis since there is a high risk of venous thromboembolism during the first month following an episode of S aureus bacteremia.[98]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/10.1111/joim.12147 http://www.ncbi.nlm.nih.gov/pubmed/24118528?tool=bestpractice.com See Deep vein thrombosis.
Any comorbidities should be addressed. It is particularly important to maintain strict blood glucose control in any patient with diabetes and a major infection such as osteomyelitis.[37]Lipsky BA, Senneville É, Abbas ZG, et al; International Working Group on the Diabetic Foot (IWGDF). Guidelines on the diagnosis and treatment of foot infection in persons with diabetes (IWGDF 2019 update). Diabetes Metab Res Rev. 2020 Mar;36 Suppl 1:e3280. https://onlinelibrary.wiley.com/doi/10.1002/dmrr.3280 http://www.ncbi.nlm.nih.gov/pubmed/32176444?tool=bestpractice.com Diabetic foot infections are uncommon in children. Specialist advice should be sought. See Diabetic foot complications.
Pain relief should be provided to all patients as required. First-line analgesics include acetaminophen and nonsteroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen. Rectal administration of acetaminophen can provide pain relief longer than intravenous administration in children.[97]Verghese ST, Hannallah RS. Acute pain management in children. J Pain Res. 2010 Jul 15;3:105-23. https://www.dovepress.com/getfile.php?fileID=6955 http://www.ncbi.nlm.nih.gov/pubmed/21197314?tool=bestpractice.com For more severe pain, an opioid (e.g., morphine, oxycodone) may be required for a short duration. If longer-term pain relief is required, a pain management specialist should be consulted.
Primary options
acetaminophen: 10-15 mg/kg orally/rectally every 4-6 hours when required, maximum 75 mg/kg/day
OR
ibuprofen: 5-10 mg/kg orally every 6-8 hours when required, maximum 40 mg/kg/day
Secondary options
morphine sulfate: consult specialist for guidance on dose
OR
oxycodone: consult specialist for guidance on dose
surgery
Treatment recommended for SOME patients in selected patient group
Pediatric orthopedic advice should be sought. In children with acute hematogenous osteomyelitis who present with sepsis or have a rapidly progressive infection, the Infectious Diseases Society of America (IDSA) recommends that debridement of the infected bone and any associated abscesses should be performed as soon as possible after diagnosis, rather than treating with medical therapy alone.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com The European Society for Paediatric Infectious Diseases (ESPID) recommends that surgery should be considered in the following situations: persistent or recurring fever after 3-4 days; periosteal abscess with persistent fever and raised CRP; sequestration; MRSA or Panton-Valentine leukocidin (PVL)-positive S aureus; chronic osteomyelitis; prosthetic material.[12]Saavedra-Lozano J, Falup-Pecurariu O, Faust SN, et al. Bone and joint infections. 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 Once dead bone or a biofilm has become established, antibiotics alone cannot cure the infection and thorough surgical debridement is required.
suspected acute native vertebral osteomyelitis
empiric antibiotic therapy
In adults with suspected native vertebral osteomyelitis who have a normal and stable neurologic examination and stable hemodynamics, empirical antimicrobial therapy should not be given until a microbiologic diagnosis is established.[13]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
Sepsis should be suspected if there is acute deterioration in a patient in whom there is clinical evidence or strong suspicion of infection. Local sepsis protocols should be followed. See Sepsis in adults.
In adults with suspected native vertebral osteomyelitis and neurologic compromise, the Infectious Diseases Society of America (IDSA) recommends immediate surgical intervention and initiation of empiric antimicrobial therapy instead of withholding antimicrobial therapy prior to an image-guided diagnostic aspiration biopsy.[13]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 In suspected native vertebral osteomyelitis without neurologic compromise, the IDSA recommends that whenever possible, initiation of antibiotic therapy should be delayed for a limited period of time until bone cultures can be obtained.[13]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 Pending further studies, the IDSA recommends that holding antibiotics when feasible for 1-2 weeks is reasonable in these circumstances.[13]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
Initial antibiotic choice is based on the most likely causative organism, which in turn depends on the patient's age, immunization history, comorbidities, the prevalence of organisms in the community, and antimicrobial sensitivities. Local protocols should be consulted. The following regimens are based on recommendations from the IDSA. The antibiotic regimen should cover staphylococci (including MRSA), streptococci, and gram-negative bacilli. An example of a suitable regimen is vancomycin plus a third- or fourth-generation cephalosporin (e.g., ceftriaxone, cefepime) or a carbapenem (e.g., meropenem) depending on risk of a resistant organism. For patients with an allergy or intolerance to first-line options, daptomycin plus a fluoroquinolone (e.g., ciprofloxacin) should be given.[13]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 Pseudomonas is suspected, an empiric antibiotic regimen that covers Pseudomonas should be chosen. A local infectious disease specialist should be consulted about suitable options.
Fluoroquinolones have been associated with serious, disabling, and potentially irreversible adverse effects, including tendonitis, tendon rupture, arthralgia, neuropathies, and other musculoskeletal or nervous system effects.[102]European Medicines Agency. Quinolone- and fluoroquinolone-containing medicinal products. Nov 2018 [internet publication]. https://www.ema.europa.eu/en/medicines/human/referrals/quinolone-fluoroquinolone-containing-medicinal-products Warnings have also been issued about the increased risk of aortic dissection, significant hypoglycemia, and mental health adverse effects in patients taking fluoroquinolones.[103]US Food and Drug Administration. Safety announcement: FDA reinforces safety information about serious low blood sugar levels and mental health side effects with fluoroquinolone antibiotics; requires label changes. Jul 2018 [internet publication]. https://www.fda.gov/drugs/drug-safety-and-availability/fda-reinforces-safety-information-about-serious-low-blood-sugar-levels-and-mental-health-side [104]US Food and Drug Administration. Drug safety communication: FDA warns about increased risk of ruptures or tears in the aorta blood vessel with fluoroquinolone antibiotics in certain patients. Dec 2018 [internet publication]. https://www.fda.gov/drugs/drug-safety-and-availability/fda-warns-about-increased-risk-ruptures-or-tears-aorta-blood-vessel-fluoroquinolone-antibiotics
Empiric antifungal and antimycobacterial therapy should not be prescribed in most situations.[13]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
Examples of antibiotic regimens are provided here; however, local protocols should be followed.
Primary options
vancomycin: 15-20 mg/kg intravenously every 8-12 hours, maximum 2000 mg/day
More vancomycinAdjust dose according to serum vancomycin level. A loading dose of 20-35 mg/kg (maximum 3000 mg/dose) may be considered in seriously ill patients.
-- AND --
ceftriaxone: 1-2 g intravenously every 24 hours
or
cefepime: 1-2 g intravenously every 8-12 hours
or
meropenem: 1 g intravenously every 8 hours
Secondary options
daptomycin: 6 mg/kg intravenously every 24 hours
and
ciprofloxacin: 400 mg intravenously every 8-12 hours
supportive care
Treatment recommended for ALL patients in selected patient group
The approach to treatment of osteomyelitis is complex, and often requires a multidisciplinary approach, with input from radiologists, vascular and orthopedic surgeons, infectious disease specialists, and wound care and rehabilitation specialists.[96]Fritz JM, McDonald JR. Osteomyelitis: approach to diagnosis and treatment. Phys Sportsmed. 2008 Dec;36(1):nihpa116823. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696389 http://www.ncbi.nlm.nih.gov/pubmed/19652694?tool=bestpractice.com
Assessment should be undertaken for deep vein thrombosis, particularly with Staphylococcus aureus osteomyelitis since there is a high risk of venous thromboembolism during the first month following an episode of S aureus bacteremia.[98]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/10.1111/joim.12147 http://www.ncbi.nlm.nih.gov/pubmed/24118528?tool=bestpractice.com See Deep vein thrombosis.
Any comorbidities should be addressed. It is particularly important to maintain strict blood glucose control in any patient with diabetes and a major infection such as osteomyelitis.[37]Lipsky BA, Senneville É, Abbas ZG, et al; International Working Group on the Diabetic Foot (IWGDF). Guidelines on the diagnosis and treatment of foot infection in persons with diabetes (IWGDF 2019 update). Diabetes Metab Res Rev. 2020 Mar;36 Suppl 1:e3280. https://onlinelibrary.wiley.com/doi/10.1002/dmrr.3280 http://www.ncbi.nlm.nih.gov/pubmed/32176444?tool=bestpractice.com See Diabetic foot complications.
Pain relief should be provided to all patients as required. First-line analgesics include acetaminophen and nonsteroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen. For more severe pain, an opioid (e.g., morphine, oxycodone) may be required for a short duration. If longer-term pain relief is required, a pain management specialist should be consulted.
Primary options
acetaminophen: 325-1000 mg orally every 4-6 hours when required, maximum 4000 mg/day
OR
ibuprofen: 400 mg orally every 4-6 hours when required, maximum 2400 mg/day
Secondary options
morphine sulfate: 10-30 mg orally (immediate-release) every 4 hours when required; 2.5 to 10 mg subcutaneously/intravenously/intramuscularly every 2-6 hours when required; adjust dose according to response
OR
oxycodone: 5-15 mg orally (immediate-release) every 4-6 hours when required, adjust dose according to response
surgery
Treatment recommended for SOME patients in selected patient group
In adults with suspected native vertebral osteomyelitis and neurologic compromise with or without impending sepsis or hemodynamic instability, the Infectious Diseases Society of America (IDSA) recommends immediate surgical intervention and initiation of empiric antimicrobial therapy instead of withholding antimicrobial therapy prior to an image-guided diagnostic aspiration biopsy.[13]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 intervention is required for progressive neurologic deficits, progressive deformity, and spinal instability with or without pain or recurrent bloodstream infection (without alternative source) despite adequate antimicrobial therapy.[13]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
empiric antibiotic therapy
For children with suspected spondylodiscitis or vertebral osteomyelitis, advice on empiric antibiotic regimens should be sought from microbiology and from an infectious disease specialist.
Sepsis should be suspected if there is acute deterioration in a patient in whom there is clinical evidence or strong suspicion of infection. Local sepsis protocols should be followed. See Sepsis in children.
supportive care
Treatment recommended for ALL patients in selected patient group
The approach to treatment of osteomyelitis is complex, and often requires a multidisciplinary approach, with input from radiologists, vascular and orthopedic surgeons, infectious disease specialists, and wound care and rehabilitation specialists.[96]Fritz JM, McDonald JR. Osteomyelitis: approach to diagnosis and treatment. Phys Sportsmed. 2008 Dec;36(1):nihpa116823. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696389 http://www.ncbi.nlm.nih.gov/pubmed/19652694?tool=bestpractice.com
Assessment should be undertaken for deep vein thrombosis, particularly with Staphylococcus aureus osteomyelitis since there is a high risk of venous thromboembolism during the first month following an episode of S aureus bacteremia.[98]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/10.1111/joim.12147 http://www.ncbi.nlm.nih.gov/pubmed/24118528?tool=bestpractice.com See Deep vein thrombosis.
Any comorbidities should be addressed. It is particularly important to maintain strict blood glucose control in any patient with diabetes and a major infection such as osteomyelitis.[37]Lipsky BA, Senneville É, Abbas ZG, et al; International Working Group on the Diabetic Foot (IWGDF). Guidelines on the diagnosis and treatment of foot infection in persons with diabetes (IWGDF 2019 update). Diabetes Metab Res Rev. 2020 Mar;36 Suppl 1:e3280. https://onlinelibrary.wiley.com/doi/10.1002/dmrr.3280 http://www.ncbi.nlm.nih.gov/pubmed/32176444?tool=bestpractice.com Diabetic foot infections are uncommon in children. Specialist advice should be sought. See Diabetic foot complications.
Pain relief should be provided to all patients as required. First-line analgesics include acetaminophen and nonsteroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen. Rectal administration of acetaminophen can provide pain relief longer than intravenous administration in children.[97]Verghese ST, Hannallah RS. Acute pain management in children. J Pain Res. 2010 Jul 15;3:105-23. https://www.dovepress.com/getfile.php?fileID=6955 http://www.ncbi.nlm.nih.gov/pubmed/21197314?tool=bestpractice.com For more severe pain, an opioid (e.g., morphine, oxycodone) may be required for a short duration. If longer-term pain relief is required, a pain management specialist should be consulted.
Primary options
acetaminophen: 10-15 mg/kg orally/rectally every 4-6 hours when required, maximum 75 mg/kg/day
OR
ibuprofen: 5-10 mg/kg orally every 6-8 hours when required, maximum 40 mg/kg/day
Secondary options
morphine sulfate: consult specialist for guidance on dose
OR
oxycodone: consult specialist for guidance on dose
surgery
Treatment recommended for SOME patients in selected patient group
Indications for surgical management of pediatric spinal disease include lack of response to antibiotics, progressive kyphosis, or neurologic compromise.[105]Brown R, Hussain M, McHugh K, et al. Discitis in young children. J Bone Joint Surg Br. 2001 Jan;83(1):106-11. https://boneandjoint.org.uk/Article/10.1302/0301-620X.83B1.0830106/pdf http://www.ncbi.nlm.nih.gov/pubmed/11245515?tool=bestpractice.com In practice, if spondylodiscitis or vertebral osteomyelitis is suspected in a child, advice should be sought from pediatrics and/or pediatric orthopedics, depending on local resources.
suspected acute osteomyelitis in diabetic foot
empiric antibiotic therapy
Antibiotic therapy without surgical resection of the bone should be considered in patients with diabetes and uncomplicated forefoot osteomyelitis, for whom there is no other indication for surgical treatment.[37]Lipsky BA, Senneville É, Abbas ZG, et al; International Working Group on the Diabetic Foot (IWGDF). Guidelines on the diagnosis and treatment of foot infection in persons with diabetes (IWGDF 2019 update). Diabetes Metab Res Rev. 2020 Mar;36 Suppl 1:e3280. https://onlinelibrary.wiley.com/doi/10.1002/dmrr.3280 http://www.ncbi.nlm.nih.gov/pubmed/32176444?tool=bestpractice.com Samples should be taken for microbiologic testing before, or as close as possible to, the start of antibiotic therapy.[36]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19
Sepsis should be suspected if there is acute deterioration in a patient in whom there is clinical evidence or strong suspicion of infection. Local sepsis protocols should be followed. See Sepsis in adults.
Empiric antibiotic therapy in patients with suspected diabetic foot infection should be commenced as soon as possible. Antibiotic agents should be chosen from among those that have demonstrated efficacy for osteomyelitis in clinical studies.[36]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19 [37]Lipsky BA, Senneville É, Abbas ZG, et al; International Working Group on the Diabetic Foot (IWGDF). Guidelines on the diagnosis and treatment of foot infection in persons with diabetes (IWGDF 2019 update). Diabetes Metab Res Rev. 2020 Mar;36 Suppl 1:e3280. https://onlinelibrary.wiley.com/doi/10.1002/dmrr.3280 http://www.ncbi.nlm.nih.gov/pubmed/32176444?tool=bestpractice.com
The duration of antibiotic treatment for diabetic foot osteomyelitis should be for no longer than 6 weeks. If the infection does not clinically improve within the first 2-4 weeks, the need for collecting a bone specimen for culture, undertaking surgical resection, or selecting an alternative antibiotic regimen should be reconsidered.[37]Lipsky BA, Senneville É, Abbas ZG, et al; International Working Group on the Diabetic Foot (IWGDF). Guidelines on the diagnosis and treatment of foot infection in persons with diabetes (IWGDF 2019 update). Diabetes Metab Res Rev. 2020 Mar;36 Suppl 1:e3280. https://onlinelibrary.wiley.com/doi/10.1002/dmrr.3280 http://www.ncbi.nlm.nih.gov/pubmed/32176444?tool=bestpractice.com
For more information, see Diabetic foot complications.
supportive care
Treatment recommended for ALL patients in selected patient group
Advice should be sought from the multidisciplinary foot care service.[36]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19 [42]Lipsky BA, Berendt AR, Cornia PB, et al. 2012 Infectious Diseases Society of America clinical practice guideline for the diagnosis and treatment of diabetic foot infections. Clin Infect Dis. 2012 Jun;54(12):e132-73. https://academic.oup.com/cid/article/54/12/e132/455959 http://www.ncbi.nlm.nih.gov/pubmed/22619242?tool=bestpractice.com This is a limb-threatening or life-threatening diabetic foot problem.[36]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19 Diabetic foot care teams can include (or should have ready access to) specialists in various fields; patients with a diabetic foot infection may especially benefit from consultation with an infectious disease or clinical microbiology specialist and a surgeon with experience and interest in managing diabetic foot infections.[42]Lipsky BA, Berendt AR, Cornia PB, et al. 2012 Infectious Diseases Society of America clinical practice guideline for the diagnosis and treatment of diabetic foot infections. Clin Infect Dis. 2012 Jun;54(12):e132-73. https://academic.oup.com/cid/article/54/12/e132/455959 http://www.ncbi.nlm.nih.gov/pubmed/22619242?tool=bestpractice.com
Patients with probable diabetic foot osteomyelitis with concomitant soft tissue infection should be urgently evaluated for the need for surgery as well as intensive postoperative medical and surgical follow-up.[37]Lipsky BA, Senneville É, Abbas ZG, et al; International Working Group on the Diabetic Foot (IWGDF). Guidelines on the diagnosis and treatment of foot infection in persons with diabetes (IWGDF 2019 update). Diabetes Metab Res Rev. 2020 Mar;36 Suppl 1:e3280. https://onlinelibrary.wiley.com/doi/10.1002/dmrr.3280 http://www.ncbi.nlm.nih.gov/pubmed/32176444?tool=bestpractice.com
The affected limb should be elevated and immobilized if necessary. Assessment should be undertaken for deep vein thrombosis, particularly with Staphylococcus aureus osteomyelitis since there is a high risk of venous thromboembolism during the first month following an episode of S aureus bacteremia.[98]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/10.1111/joim.12147 http://www.ncbi.nlm.nih.gov/pubmed/24118528?tool=bestpractice.com See Deep vein thrombosis.
Any comorbidities should be addressed. It is particularly important to maintain strict blood glucose control in any patient with diabetes and a major infection such as osteomyelitis.[37]Lipsky BA, Senneville É, Abbas ZG, et al; International Working Group on the Diabetic Foot (IWGDF). Guidelines on the diagnosis and treatment of foot infection in persons with diabetes (IWGDF 2019 update). Diabetes Metab Res Rev. 2020 Mar;36 Suppl 1:e3280. https://onlinelibrary.wiley.com/doi/10.1002/dmrr.3280 http://www.ncbi.nlm.nih.gov/pubmed/32176444?tool=bestpractice.com
Pain relief should be provided to all patients as required. First-line analgesics include acetaminophen and nonsteroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen. For more severe pain, an opioid (e.g., morphine, oxycodone) may be required for a short duration. If longer-term pain relief is required, a pain management specialist should be consulted.
Primary options
acetaminophen: 325-1000 mg orally every 4-6 hours when required, maximum 4000 mg/day
OR
ibuprofen: 400 mg orally every 4-6 hours when required, maximum 2400 mg/day
Secondary options
morphine sulfate: 10-30 mg orally (immediate-release) every 4 hours when required; 2.5 to 10 mg subcutaneously/intravenously/intramuscularly every 2-6 hours when required; adjust dose according to response
OR
oxycodone: 5-15 mg orally (immediate-release) every 4-6 hours when required, adjust dose according to response
surgery
Treatment recommended for SOME patients in selected patient group
Patients who have probable diabetic foot osteomyelitis with concomitant soft tissue infection should be urgently evaluated for surgical intervention as well as intensive postoperative medical and surgical follow-up.[37]Lipsky BA, Senneville É, Abbas ZG, et al; International Working Group on the Diabetic Foot (IWGDF). Guidelines on the diagnosis and treatment of foot infection in persons with diabetes (IWGDF 2019 update). Diabetes Metab Res Rev. 2020 Mar;36 Suppl 1:e3280. https://onlinelibrary.wiley.com/doi/10.1002/dmrr.3280 http://www.ncbi.nlm.nih.gov/pubmed/32176444?tool=bestpractice.com
During surgery to resect bone for diabetic foot osteomyelitis, obtaining a specimen of bone for culture (and, if possible, histopathology) at the stump of the resected bone should be considered to identify if there is residual bone infection.
referral to specialist
Diabetic foot infections are uncommon in children. Specialist advice should be sought from the multidisciplinary foot care service.[36]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19 [42]Lipsky BA, Berendt AR, Cornia PB, et al. 2012 Infectious Diseases Society of America clinical practice guideline for the diagnosis and treatment of diabetic foot infections. Clin Infect Dis. 2012 Jun;54(12):e132-73. https://academic.oup.com/cid/article/54/12/e132/455959 http://www.ncbi.nlm.nih.gov/pubmed/22619242?tool=bestpractice.com Patients with a diabetic foot infection may particularly benefit from consultation with an infectious disease or clinical microbiology specialist and a surgeon with experience and interest in managing diabetic foot infections.[42]Lipsky BA, Berendt AR, Cornia PB, et al. 2012 Infectious Diseases Society of America clinical practice guideline for the diagnosis and treatment of diabetic foot infections. Clin Infect Dis. 2012 Jun;54(12):e132-73. https://academic.oup.com/cid/article/54/12/e132/455959 http://www.ncbi.nlm.nih.gov/pubmed/22619242?tool=bestpractice.com See Diabetic foot complications.
confirmed acute peripheral osteomyelitis: adults and children
pathogen-targeted antibiotic therapy
When microbiologic results are available, the antibiotic should be reviewed and changed accordingly, using a narrow-spectrum antibiotic, if appropriate.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com [13]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
Response to antibiotic treatment is typically rapid. However, if the limb deteriorates or imaging suggests progressive bone destruction, choice of antibiotics should be discussed with microbiology. Surgery should be considered to prevent progression to chronic osteomyelitis. Once dead bone or a biofilm has become established, antibiotics alone cannot cure the infection and thorough surgical debridement is required.
The optimal duration of antimicrobial therapy for osteomyelitis is not certain.[57]Li HK, Rombach I, Zambellas R, et al; OVIVA Trial Collaborators. 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/10.1056/NEJMoa1710926 http://www.ncbi.nlm.nih.gov/pubmed/30699315?tool=bestpractice.com However, the IDSA makes recommendations for some types of osteomyelitis. For instance, in children with acute hematogenous osteomyelitis presumed or proven to be caused by Staphylococcus aureus who have had an uncomplicated course and responded to initial therapy, the IDSA suggests a 3- to 4-week duration of antibiotics (parenteral plus oral) rather than a longer course.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com Longer durations of antibiotics may be necessary for other pathogens, including more virulent strains of S aureus, and for complicated cases.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com
confirmed acute native vertebral osteomyelitis: adults and children
pathogen-targeted antibiotic therapy
When microbiologic results are available, the antibiotic should be reviewed and changed accordingly, using a narrow-spectrum antibiotic, if appropriate.
Most patients with confirmed bacterial native vertebral osteomyelitis should receive 6 weeks of parenteral or highly bioavailable oral antimicrobial therapy.[13]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
In suspected native vertebral osteomyelitis, when the etiologic 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.[57]Li HK, Rombach I, Zambellas R, et al; OVIVA Trial Collaborators. 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/10.1056/NEJMoa1710926 http://www.ncbi.nlm.nih.gov/pubmed/30699315?tool=bestpractice.com Therefore, targeted antibiotic therapy may need to be started when polymerase chain reaction (PCR) results are available and infection has been confirmed, regardless of whether culture and sensitivity results are available. Local antibiotic protocols should be consulted with advice from microbiology in endemic areas. Evaluation by a spine surgeon and an infectious disease specialist should be sought in nonendemic areas.[13]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 A total duration of 3 months of antimicrobial therapy is recommended for most patients with native vertebral osteomyelitis caused by Brucella species.[13]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 more information, see Brucellosis.
confirmed acute osteomyelitis in diabetic foot: adults and children
pathogen-targeted antibiotic therapy
When microbiologic results are available, the antibiotic should be reviewed and changed accordingly, using a narrow-spectrum antibiotic, if appropriate.
Advice should be sought from the multidisciplinary foot care service.[36]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19 [42]Lipsky BA, Berendt AR, Cornia PB, et al. 2012 Infectious Diseases Society of America clinical practice guideline for the diagnosis and treatment of diabetic foot infections. Clin Infect Dis. 2012 Jun;54(12):e132-73. https://academic.oup.com/cid/article/54/12/e132/455959 http://www.ncbi.nlm.nih.gov/pubmed/22619242?tool=bestpractice.com This is a limb-threatening or life-threatening diabetic foot problem.[36]National Institute for Health and Care Excellence. Diabetic foot problems: prevention and management. Oct 2019 [internet publication]. https://www.nice.org.uk/guidance/ng19 Patients with a diabetic foot infection may particularly benefit from consultation with an infectious disease or clinical microbiology specialist and a surgeon with experience and interest in managing diabetic foot infections.[42]Lipsky BA, Berendt AR, Cornia PB, et al. 2012 Infectious Diseases Society of America clinical practice guideline for the diagnosis and treatment of diabetic foot infections. Clin Infect Dis. 2012 Jun;54(12):e132-73. https://academic.oup.com/cid/article/54/12/e132/455959 http://www.ncbi.nlm.nih.gov/pubmed/22619242?tool=bestpractice.com Diabetic foot infections are uncommon in children. Specialist advice should be sought. See Diabetic foot complications.
chronic osteomyelitis
clinical assessment, disease staging, optimization of comorbidities
When there is dead bone, or a biofilm has become established, antibiotics alone cannot cure the infection and surgery is required for full cure.
The following need to be undertaken:
Assessment of the degree of disease allowing accurate clinical staging (using the Cierny-Mader classification).[2]Cierny G 3rd, Mader JT, Penninck JJ. A clinical staging system for adult osteomyelitis. Clin Orthop Relat Res. 2003 Sep;(414):7-24. http://www.ncbi.nlm.nih.gov/pubmed/12966271?tool=bestpractice.com
Full discussion with the patient about the treatment options and the potential associated risks.
Diagnostic tests to assess general health and the condition of the limb (blood tests, scanning, angiography, image-guided biopsy).
Optimization of any comorbidities (e.g., anemia of chronic disease; coagulopathies; diabetes mellitus, control of which is often difficult in the context of uncontrolled infection and may require hospitalization for optimization before surgery; vascular insufficiency, which may need to be addressed before healing to ensure optimal healing; sickle cell disease - exchange transfusion may be needed before embarking on surgery to minimize the risks of bone infarct, sickle crisis, and wound healing problems caused by an anesthetic). Poor nutritional status, smoking, and substance dependence also need to be addressed.
surgery
Treatment recommended for ALL patients in selected patient group
Patients who are surgical candidates and who wish to attempt cure need full surgical debridement. Details of the debridement surgery undertaken depend on the type of infection according to the Cierny-Mader classification and the clinical circumstances.[2]Cierny G 3rd, Mader JT, Penninck JJ. A clinical staging system for adult osteomyelitis. Clin Orthop Relat Res. 2003 Sep;(414):7-24. http://www.ncbi.nlm.nih.gov/pubmed/12966271?tool=bestpractice.com Samples should always be taken for microbiology and histology assessment, preferably before antibiotic therapy is started.[4]Woods CR, Bradley JS, Chatterjee A, et al. Clinical practice guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. J Pediatric Infect Dis Soc. 2021 Sep 23;10(8):801-44. https://academic.oup.com/jpids/article/10/8/801/6338658 http://www.ncbi.nlm.nih.gov/pubmed/34350458?tool=bestpractice.com Surgical excision of all affected necrotic tissue is necessary to eradicate infection.
At the end of debridement, the whole operative field is likely to be contaminated with bacteria disseminated during surgery.[108]Cierny G 3rd, Mader JT. The surgical treatment of adult osteomyelitis. In: Evarts CMC, ed. Surgery of the musculoskeletal system. New York: Churchill Livingstone; 1983:4337-79. Bone is an unyielding tissue, so any defect will remain and will fill with hematoma, providing an ideal environment for the propagation of bacteria and allowing early biofilm development. Various antibiotic-containing materials have been used to fill bony defects. A local antibiotic carrier can achieve high local antibiotic concentrations without systemic toxicity, because they can elute high concentrations of antibiotic locally, often in the order of 10-100 times the minimum inhibitory concentration of the organisms that are present.[111]Mayberry-Carson KJ, Tober-Meyer B, Smith JK, et al. Bacterial adherence and glycocalyx formation in osteomyelitis experimentally induced with Staphylococcus aureus. Infect Immun. 1984 Mar;43(3):825-33. https://journals.asm.org/doi/epdf/10.1128/iai.43.3.825-833.1984 http://www.ncbi.nlm.nih.gov/pubmed/6199302?tool=bestpractice.com [112]Walenkamp GH, Vree TB, van Rens TJ. Gentamicin-PMMA beads: pharmacokinetic and nephrotoxicological study. Clin Orthop Relat Res. 1986 Apr;(205):171-83. http://www.ncbi.nlm.nih.gov/pubmed/3516500?tool=bestpractice.com
Following debridement the bone may be unstable and need temporary support with a monolateral frame to prevent fracture and aid postoperative rehabilitation.[47]Mader JT, Calhoun JH, Lazzarini L. Adult long bone osteomyelitis. In: Mader JT, Calhoun JH, eds. Musculoskeletal infections. New York, NY: Marcel Dekker; 2003:149-82. Staged reconstruction is sometimes needed.
systemic antibiotics
Treatment recommended for ALL patients in selected patient group
Intravenous antibiotics are started once intraoperative sampling has been completed. An empiric regimen appropriate to the flora encountered in the hospital's region is appropriate. A protocol using a glycopeptide and a carbapenem showed coverage of 96% of all organisms subsequently cultured.[107]Sheehy SH, Atkins BA, Bejon P, et al. The microbiology of chronic osteomyelitis: prevalence of resistance to common empirical anti-microbial regimens. J Infect. 2010 May;60(5):338-43. http://www.ncbi.nlm.nih.gov/pubmed/20230854?tool=bestpractice.com This same study revealed that one third of organisms cultured were resistant to a penicillin-based empiric antibiotic regime. The carbapenem is usually stopped after 48 hours' culture if no gram-negative organisms have been cultured at that point. Once full intraoperative culture results are known, a definitive regimen can be selected.
The optimal duration of antimicrobial therapy is not certain. If the osteomyelitic bone has been fully resected, a course of antibiotic therapy lasting 2-6 weeks may be adequate as long as operative wounds are healing without any signs of infection. This can be an appropriate course of oral antibiotics, based on microbial cultures and sensitivities.
One multicenter, randomized controlled trial of 1054 patients demonstrated that oral antibiotic therapy is noninferior to intravenous antibiotic therapy following surgical treatment of bone or joint infection.[57]Li HK, Rombach I, Zambellas R, et al; OVIVA Trial Collaborators. 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/10.1056/NEJMoa1710926 http://www.ncbi.nlm.nih.gov/pubmed/30699315?tool=bestpractice.com
rehabilitation
Treatment recommended for ALL patients in selected patient group
Functional rehabilitation should be arranged.
individualized treatment
Treatment recommended for ALL patients in selected patient group
Full cure may involve complex surgery with potential complications, staged reconstruction, antimicrobial drug reactions, and prolonged time in treatment and rehabilitation. Therefore, an approach that controls current symptoms, but with the possibility of later recurrence, may be a more attractive option for some patients.
In group C patients under the Cierny-Mader classification (patients who are so severely compromised that treatment has an unacceptable risk-benefit ratio, or those with few symptoms from their infection) it is reasonable to withhold treatment or just to treat symptomatic flare-ups with short antibiotic courses. Selection of an appropriate antibiotic regime can be informed by radiologically guided biopsy.
Biopsy-guided or empiric antibiotic therapy may be considered in some cases where the patient is unfit for surgery, or unwilling to have surgery. This is unlikely to cure chronic infection but it may alleviate symptoms. If a trial of therapy is successful, long-term suppression may be considered. Long-term suppressive antibiotic usage needs to be balanced against the significant risk of poor adherence, adverse effects, and drug interactions. More studies are needed to determine the best antibiotic regimen and duration of therapy.
Limited surgery may be an option for patients who are not candidates for curative limb salvage surgery (e.g., those with implants in situ that would provide a challenging reconstructive problem if they were removed). While not effecting a cure, it may reduce the infective load.
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