Osteomyelitis: Difference between revisions
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== Background == |
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*See also: |
*See also: |
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**[[Acute osteomyelitis]] |
**[[Acute osteomyelitis]] |
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**[[Chronic osteomyelitis]] |
**[[Chronic osteomyelitis]] |
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**[[Osteomyelitis with orthopedic hardware]] |
**[[Osteomyelitis with orthopedic hardware]] |
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=== Microbiology === |
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{| class="wikitable" |
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! colspan="2" |Species |
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!Upper Extremity |
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!Vertebral |
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!Lower Extremity PJI |
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!Trauma of Fracture |
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!Hematogenous |
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!Foot and Ankle |
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|- |
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| colspan="2" |Gram-positive |
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| |
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| |
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| |
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| |
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| |
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| |
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|- |
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| rowspan="6" | |
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|[[Staphylococcus aureus]] |
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|10-40% |
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|15-60% |
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|20-30% |
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|20-40% |
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|40% |
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|45-55% |
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|- |
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|[[Coagulase-negative staphylococci]] |
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|10-20% |
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|5-40% |
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|25-35% |
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|10-40% |
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|<5% |
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|<5% |
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|- |
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|[[Streptococcus]] species |
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|5-10% |
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|5-10% |
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|<5% |
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|5-10% |
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|5-10% |
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|5-20% |
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|- |
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|[[Enterococcus]] species |
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|<5% |
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|5-15% |
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|<5% |
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|5% |
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|<5% |
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|5% |
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|- |
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|[[Diphtheroids]] |
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|<5% |
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|5% |
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|<5% |
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|5% |
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|<5% |
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|<5% |
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|- |
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|[[Cutibacterium acnes]] |
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|30-50% in shoulder |
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|10-15% spinal fusion |
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| |
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| |
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| |
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|- |
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| colspan="2" |Gram-negatives |
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|5-10% |
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|10-40% |
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|5-10% |
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|20% |
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|10-15% |
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|35-55% |
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|- |
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| rowspan="3" | |
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|[[Pseudomonas]] species |
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|<5% |
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|5-10% |
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|<5% |
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|5-10% |
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|5-10% |
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|10-20% |
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|- |
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|[[Enterobacteriaceae]] |
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|<5% |
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|10-20% |
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|<5% |
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|5-20% |
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|5% |
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|10-15% |
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|- |
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|[[HACEK group]] |
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|<5% |
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|<5% |
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|<5% |
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|<5% |
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|<5% |
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|<5% |
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|- |
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| colspan="2" |Fungal |
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|<5% |
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|<5% |
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|<5% |
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|<5% |
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|<5% |
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|<5% |
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|- |
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| colspan="2" |Polymicrobial |
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|10-25% |
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|15-30% |
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|10-20% |
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|20-30% |
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|20 |
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|30-80% |
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|} |
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==Management== |
==Management== |
Revision as of 15:01, 17 February 2022
Background
Microbiology
Species | Upper Extremity | Vertebral | Lower Extremity PJI | Trauma of Fracture | Hematogenous | Foot and Ankle | |
---|---|---|---|---|---|---|---|
Gram-positive | |||||||
Staphylococcus aureus | 10-40% | 15-60% | 20-30% | 20-40% | 40% | 45-55% | |
Coagulase-negative staphylococci | 10-20% | 5-40% | 25-35% | 10-40% | <5% | <5% | |
Streptococcus species | 5-10% | 5-10% | <5% | 5-10% | 5-10% | 5-20% | |
Enterococcus species | <5% | 5-15% | <5% | 5% | <5% | 5% | |
Diphtheroids | <5% | 5% | <5% | 5% | <5% | <5% | |
Cutibacterium acnes | 30-50% in shoulder | 10-15% spinal fusion | |||||
Gram-negatives | 5-10% | 10-40% | 5-10% | 20% | 10-15% | 35-55% | |
Pseudomonas species | <5% | 5-10% | <5% | 5-10% | 5-10% | 10-20% | |
Enterobacteriaceae | <5% | 10-20% | <5% | 5-20% | 5% | 10-15% | |
HACEK group | <5% | <5% | <5% | <5% | <5% | <5% | |
Fungal | <5% | <5% | <5% | <5% | <5% | <5% | |
Polymicrobial | 10-25% | 15-30% | 10-20% | 20-30% | 20 | 30-80% |
Management
- No clinically meaningful differences in bone penetration between classes of antibiotics exist1
- Bioavailability likely still important
- Empiric antimicrobials should generally cover MRSA, susceptible Gram-positives, and common Gram-negatives
- For example, vancomycin plus ceftriaxone
Parenteral Antimicrobials
Organism | Antimicrobial Options |
---|---|
MSSA | nafcillin 2 g IV q4h |
oxacillin 2 g IV q4h | |
cefazolin 2 g IV q8h | |
flucloxacillin 2 g IV q6h | |
ceftriaxone 2 g IV q24h | |
MRSA | vancomycin 20 mg/kg load followed by 15-20 mg IV q8-12h |
daptomycin 6 to 10 mg/kg IV daily | |
teicoplanin 12 mg/kg IV q12h for 3 to 5 doses followed by q24h | |
Adjunctive staphylococcal agent | rifampin 300 to 450 mg PO bid |
fusidic acid 500 mg PO tid | |
Gram-negative bacteria | ciprofloxacin 750 mg PO big to 400 mg IV q12h |
levofloxacin 750 mg PO/IV daily | |
ceftriaxone 2 g IV q24h | |
ceftazidime 2 g IV q8h | |
cefepime 2 g IV q8-12h | |
ertapenem 1 g IV q24h | |
meropenem 1 g IV q8h | |
Pseudomonas aeruginosa | ciprofloxacin 400 mg IV q8h |
Enterococcus | ampicillin 12 g continuous IV q24h |
ampicillin 2 g IV q4h | |
penicillin G 20 to 24 million units continuous IV q24h | |
penicillin G 3-4 million units IV q4h | |
vancomycin 20 mg/kg IV load followed by 15 mg/kg IV q12h (max 2 g per dose) | |
daptomycin 6 to 10 mg/kg IV daily | |
teicoplanin 12 mg/kg IV q12h for 3 to 5 doses, followed by q24h | |
ampicillin as above, PLUS ceftriaxone 2 g IV q12-24h | |
penicillin-susceptible streptococci | ampicillin 12 g continuous IV q24h |
ampicillin 2 g IV q4h | |
penicillin G 20 to 24 million units continuous IV q24h | |
penicillin G 3-4 million units IV q4h | |
ceftriaxone 2 g IV q24h | |
vancomycin 20 mg/kg IV load followed by 15 mg/kg IV q12h (max 2 g per dose) | |
Cutibacterium acnes | penicillin G 20 to 24 million units continuous IV q24h |
penicillin G 3-4 million units IV q4h | |
ceftriaxone 2 g IV q24h |
Oral Antimicrobials
Organism | Antibiotic Options |
---|---|
MSSA | cefadroxil 500 to 1000 mg PO bid |
cephalexin 500 mg PO tid to qid, or 1000 mg PO bid to tid | |
dicloxacillin 500 mg PO tid to qid | |
flucloxaxillin 500 mg PO tid to qid | |
MRSA | TMP-SMX DS 1 tablet PO bid |
doxycycline 100 mg PO bid | |
minocycline 100 mg PO bid | |
clindamycin 600 mg PO tid | |
Gram-negative bacteria | TMP-SMX DS 1 tablet PO bid |
ciprofloxacin 500 mg PO bid | |
levofloxacin 500 mg PO daily | |
penicillin-susceptible streptococci and enterococci | amoxicillin 500 mg PO bid to tid |
penicillin VK 500 mg PO bid to tid | |
Cutibacterium acnes | amoxicillin 500 mg PO bid to tid |
penicillin VK 500 mg PO bid to tidO |
OVIVA Trial
- Oral therapy non-inferior to intravenous therapy for bone and joint infections requiring 6+ weeks of therapy
- Oral regimens included fluoroquinolones (41%), combination with cipro/clinda or cipro/doxy (14%), beta lactams (15%), macrolides or lincosamides (11%), tetracyclines (9%), and other antibiotics (9%)
References
- ^ George Cierny, Jon T. Mader, Johan J. Penninck. The Classic: A Clinical Staging System for Adult Osteomyelitis. Clinical Orthopaedics and Related Research. 2003;414:7-24. doi:10.1097/01.blo.0000088564.81746.62.
- ^ Elysia A. Masters, Benjamin F. Ricciardi, Karen L. de Mesy Bentley, T. Fintan Moriarty, Edward M. Schwarz, Gowrishankar Muthukrishnan. Skeletal infections: microbial pathogenesis, immunity and clinical management. Nature Reviews Microbiology. 2022. doi:10.1038/s41579-022-00686-0.
- ^ Cornelia B. Landersdorfer, Jürgen B. Bulitta, Martina Kinzig, Ulrike Holzgrabe, Fritz Sörgel. Penetration of Antibacterials into Bone. Clinical Pharmacokinetics. 2009;48(2):89-124. doi:10.2165/00003088-200948020-00002.
- ^ Ho-Kwong Li, Ines Rombach, Rhea Zambellas, A. Sarah Walker, Martin A. McNally, Bridget L. Atkins, Benjamin A. Lipsky, Harriet C. Hughes, Deepa Bose, Michelle Kümin, Claire Scarborough, Philippa C. Matthews, Andrew J. Brent, Jose Lomas, Roger Gundle, Mark Rogers, Adrian Taylor, Brian Angus, Ivor Byren, Anthony R. Berendt, Simon Warren, Fiona E. Fitzgerald, Damien J.F. Mack, Susan Hopkins, Jonathan Folb, Helen E. Reynolds, Elinor Moore, Jocelyn Marshall, Neil Jenkins, Christopher E. Moran, Andrew F. Woodhouse, Samantha Stafford, R. Andrew Seaton, Claire Vallance, Carolyn J. Hemsley, Karen Bisnauthsing, Jonathan A.T. Sandoe, Ila Aggarwal, Simon C. Ellis, Deborah J. Bunn, Rebecca K. Sutherland, Gavin Barlow, Cushla Cooper, Claudia Geue, Nicola McMeekin, Andrew H. Briggs, Parham Sendi, Elham Khatamzas, Tri Wangrangsimakul, T.H. Nicholas Wong, Lucinda K. Barrett, Abtin Alvand, C. Fraser Old, Jennifer Bostock, John Paul, Graham Cooke, Guy E. Thwaites, Philip Bejon, Matthew Scarborough. Oral versus Intravenous Antibiotics for Bone and Joint Infection. New England Journal of Medicine. 2019;380(5):425-436. doi:10.1056/nejmoa1710926.