Osteomyelitis: Difference between revisions
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=== OVIVA Trial === |
=== OVIVA Trial === |
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* Oral therapy non-inferior to intravenous therapy for bone and joint infections requiring 6+ weeks of therapy |
* Oral therapy non-inferior to intravenous therapy for bone and joint infections requiring 6+ weeks of therapy[[CiteRef::li2019or]] |
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* Oral regimens included fluoroquinolones (41%), combination with |
* Oral regimens included [[fluoroquinolones]] (41%), combination with [[ciprofloxacin]]/[[clindamycin]] or [[ciprofloxacin]]/[[doxycycline]] (14%), [[Beta lactam antibiotics|beta lactams]] (15%), [[macrolides]] or [[lincosamides]] (11%), [[tetracyclines]] (9%), and other antibiotics (9%) |
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[[Category:Bone and joint infections]] |
[[Category:Bone and joint infections]] |
Revision as of 15:44, 17 February 2022
Background
- Classified by:
- Acute osteomyelitis (1 to 2 weeks) versus chronic osteomyelitis (3 to 6 months), though this classification is not necessarily helpful
- Etiology and location, including the presence of orthopedic hardware or joint prosthesis
- Cierny-Mader classification based on area of bone involvement
- Type I: medullary
- Type II: superficial
- Type III: localized
- Type IV: diffuse
- Immune status and frailty of host
Microbiology
- Based on 1
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% |
- Polymicrobial infections are more common in trauma-related OM, PJI, and diabetic foot infections
- Poorer outcomes
- Commonly involves Staphylococcus aureus iwht a mix of other bacteria
Diagnosis
- Bone biopsy for histology and culture is the gold standard
- However, diagnosis is usually made based on a combination of physical exam, lab tests, and imaging
- Physical exam findings: fever, constitutional symptoms, sinus tract, joint pain and swelling, cellulitis at the site
- Blood tests: elevated WBC or CRP, positive blood cultures
- Novel tests: alpha-defensin, D-dimer, synolvial IL-6, and synovial CRP
- Imaging: MRI is the most sensitive; can also use bone scan and labelled WBC scan, or plain film x-ray or CT (if more chronic)
Management
- No clinically meaningful differences in bone penetration between classes of antibiotics exist2
- 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 therapy3
- Oral regimens included fluoroquinolones (41%), combination with ciprofloxacin/clindamycin or ciprofloxacin/doxycycline (14%), beta lactams (15%), macrolides or lincosamides (11%), tetracyclines (9%), and other antibiotics (9%)
References
- ^ 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.