Prosthetic joint infection: Difference between revisions
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==Background== |
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===Microbiology=== |
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*Hip and knee |
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**Early (<3 months): [[Staphylococcus aureus]] (38%), aerobic [[Gram-negative bacilli]] (24%), [[coagulase-negative staphylococci]] (22%), [[Enterococcus]] (10%), and [[Streptococcus]] (4%), [[anaerobes]] including [[Cutibacterium acnes]] (3%), culture-negative (10%); 31% are polymicrobial |
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**Overall: [[Staphylococcus aureus]] (27%), [[coagulase-negative staphylococci]] (27%), aerobic [[Gram-negative bacilli]] (9%), [[Streptococcus]] (8%), [[anaerobes]] including [[Cutibacterium acnes]] (4%), [[Enterococcus]] (3%), culture-negative (14%); 15% are polymicrobial |
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*Shoulder: [[coagulase-negative staphylococci]] (42%), [[Cutibacterium acnes]] (24%), [[Staphylococcus aureus]] (18%), aerobic [[Gram-negative bacilli]] (10%), others, culture-negative (15%); polymicrobial in 16% |
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*Elbow: [[Staphylococcus aureus]] (42%), [[coagulase-negative staphylococci]] (41%), others, culture-negative (5%); polymicrobial in 3% |
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===Epidemiology=== |
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*Complicates about 2% of [[arthroplasty]] |
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**2% of hip and knee arthroplasties |
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**1% of shoulder arthroplasties |
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===Pathophysiology=== |
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*Bacteria grown on the prosthesis in a [[biofilm]], making it resistant to medical management |
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==Clinical Manifestations== |
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*Most commonly occur within the 3 months after arthroplasty (early); 70% within the first two years |
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*Should be suspected when there is a sinus tract, persistent wound drainage, acute onset of pain, or chronic pain after a pain-free interval |
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=== Prognosis === |
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* Recurrent rates after DAIR are 9% (with 12 weeks of antibiotics) to 18% (with 6 weeks)[[CiteRef::bernard2021an]] |
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*In a large observational study, about 30-40% overall have recurrence |
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**DAIR success was highest with early post-implant infection and lower with late acute and chronic infections |
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**Knee joint and [[Staphylococcus aureus]] were associated with lower success[[CiteRef::davis2022pr]] |
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==Diagnosis== |
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*Routine investigations should include ESR, CRP, plain film x-ray, diagnostic arthrocentesis, and blood cultures (if fever or other systemic symptom) |
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**If clinically stable, try to obtain arthrocentesis samples before antibiotics |
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**Other imaging should not be used routinely |
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*Diagnosis is made most definitively by histopathology of periprosthetic tissue biopsy, and supported by positive intraoperative tissue cultures |
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**Should take 3 to 6 intraoperative samples |
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**If clinically stable, try to obtain tissue cultures before starting antibiotics |
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*A definitive diagnosis of PJI requires any of the following: |
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**Sinus tract that communicates with the prosthesis |
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**Acute inflammation on histopathology of intraoperatic periprosthetic tissue sample |
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**Periprosthetic purulence without other cause |
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**Two or more intraoperative cultures with identical organism, though a single positive culture may be sufficient in some cases |
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*A diagnosis of PJI may still be possible if the above criteria are not met but clinical suspicion remains |
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=== 2018 Definition of Periprosthetic Hip and Knee Infection[[CiteRef::parvizi2018th]] === |
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{| class="wikitable" |
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!Criterion |
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!Points |
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!Interpretation |
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|- |
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! colspan="3" |Major Criteria |
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|- |
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|Two positive cultures of the same organism |
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|N/A |
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| rowspan="2" |Infected |
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|- |
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|Sinus tract with evidence of communication to the joint or visualization of the prosthesis |
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|N/A |
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|- |
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! colspan="3" |Minor Preoperative Criteria |
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|- |
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|Elevated serum CRP or D-dimer |
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|2 |
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| rowspan="6" |≥6: infected |
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2-5: possibly infected |
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≤1: not infected |
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|- |
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|Elevated serum ESR |
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|1 |
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|- |
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|Elevated synovial WBC count or LE |
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|3 |
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|- |
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|Positive synovial alpha-defensin |
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|3 |
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|- |
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|Elevated synovial PMN % |
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|2 |
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|- |
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|Elevated synovial CRP |
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|1 |
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|- |
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! colspan="3" |Intraoperative Criteria for Inconclusive Preoperative Scores |
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|- |
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|Preoperative score |
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| - |
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| rowspan="4" |≥6: infected |
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4-5: inconclusive |
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≤3: not infected |
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|- |
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|Positive histology |
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|3 |
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|- |
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|Positive purulence |
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|3 |
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|- |
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|Single positive culture |
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|2 |
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|} |
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{| class="wikitable" |
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! rowspan="2" |Marker |
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! colspan="2" |Cutoff |
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|- |
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!Chronic >90 days |
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!Acute <90 days |
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|- |
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|Serum CRP (mg/dL) |
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|1 |
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|10 |
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|- |
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|Serum D-dimer (ng/mL) |
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|860 |
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|860 |
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|- |
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|Serum ESR (mm/h) |
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|30 |
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| - |
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|- |
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|Synovial WBC (cells/μL) |
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|3000 |
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|10 000 |
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|- |
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|Synovial PMN (%) |
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|80 |
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|90 |
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|- |
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|Synovial CRP (mg/L) |
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|6.9 |
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|6.9 |
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|- |
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|Synovial alpha-defensin |
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|1 |
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|1 |
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|} |
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* The above criteria may be inaccurate in patients with adverse local tissue reaction (ALTR), crystalline deposition arthropathy, inflammatory arthopathy flare, or infection with slow-growing organisms such as [[Cutibacterium acnes]] and [[coagulase-negative staphylococci]] |
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==Management== |
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===Surgical Management=== |
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*Ultimately the decision of whether and how to treat surgically rests with the orthopedic surgeon |
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*Options include: |
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**Debridement and implant retention (DAIR), preferred if well-fixed prosthesis, no sinus tract, susceptible to oral antibiotics, joint age <30 days, and symptoms <3 weeks |
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**One-stage replacement |
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**Two-stage replacement, where the prosthesis is removed and replaced with a cement spacer, the infection is treated, and then a new prosthesis is placed |
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*Antibiotic-impregnated cement is often used for the spacer |
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**Usually [[vancomycin]] 2 to 8 g per 40 g cement, or an [[Aminoglycosides|aminoglycoside]] |
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***No clear guidelines for dosing |
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**No clear evidence of effectiveness, but recommended in all revisions for [[septic arthritis]] |
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**Releases over a period of two to three days |
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===Antimicrobial Therapy=== |
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{| class="wikitable" |
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!Surgical Management |
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!Species |
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!Location |
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!Duration IV<sup>*</sup> |
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!Total Duration |
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!Adjunctive Rifampin |
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!Chronic Suppressive Therapy |
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|- |
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| rowspan="6" |debridement and retention |
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| rowspan="5" |[[Staphylococcus]] |
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|knee |
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| rowspan="5" |2-6 weeks |
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|6 months |
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| rowspan="5" |yes; 4-6 weeks IV if not given |
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|± |
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|- |
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|hip |
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| rowspan="4" |3 months |
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|± |
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|- |
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|elbow |
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|± |
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|- |
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|shoulder |
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|± |
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|- |
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|ankle |
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|± |
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|- |
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|species other than [[staphylococci]] |
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|— |
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|4-6 weeks |
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|12 weeks<sup>†</sup> |
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| |
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|± |
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|- |
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|resection ± reimplantation |
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|— |
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|— |
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|4-6 weeks |
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| |
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| |
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| |
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|- |
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| rowspan="2" |1-stage exchange |
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|[[Staphylococcus]] |
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|— |
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|2-6 weeks |
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|3 months |
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|yes; 4-6 weeks IV if not given |
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|± |
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|- |
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|species other than staphylococci |
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|— |
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|4-6 weeks |
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|3 months |
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| |
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|± |
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|- |
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|amputation with source control |
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|— |
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|— |
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|24-48 hours |
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| |
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| |
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| |
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|- |
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|amputation without source control |
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|— |
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|— |
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|4-6 weeks |
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| |
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| |
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| |
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|} |
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*<sup>*</sup> IV therapy includes highly bioavailable oral therapy |
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*<sup>†</sup> per DAPITO trial[[CiteRef::bernard2021an]] |
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===Intravenous and Highly Bioavailable Oral Therapy=== |
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====Choice of Antimicrobial==== |
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* Increasing evidence suggests that regimens of [[fluoroquinolone]] plus [[rifampin]] has the lowest risk of recurrence, and should likely be the preferred regimen in staphylococcal infections with susceptible organisms |
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{| class="wikitable" |
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|+IDSA guideline-based antimicrobial recommendations |
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!Species |
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!Preferred Antimicrobials |
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!Alternative Antimicrobials |
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|- |
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|[[Staphylococcus]] (oxacillin-susceptible) |
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|[[nafcillin]] or [[cefazolin]] or [[ceftriaxone]] |
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|[[vancomycin]] or [[daptomycin]] or [[linezolid]] |
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|- |
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|[[Staphylococcus]] (oxacillin-resistant) |
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|[[vancomycin]] |
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|[[daptomycin]] |
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|- |
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|[[Enterococcus]] (penicillin-susceptible) |
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|[[penicillin G]] or [[ampicillin]] |
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|[[vancomycin]] or [[daptomycin]] or [[linezolid]] |
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|- |
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|[[Pseudomonas aeruginosa]] |
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|[[cefepime]] or [[meropenem]] |
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|[[ciprofloxacin]] or [[ceftazidime]] |
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|- |
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|[[Enterobacter]] |
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|[[cefepime]] |
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|[[ciprofloxacin]] |
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|- |
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|[[Enterobacteriaceae]] |
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|[[ampicillin]] or [[ceftriaxone]] or [[ciprofloxacin]] |
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| |
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|- |
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|β-hemolytic streptococci |
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|[[penicillin G]] or [[ceftriaxone]] |
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|[[vancomycin]] |
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|- |
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|[[Cutibacterium acnes]] |
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|[[penicillin G]] or [[ceftriaxone]] |
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|[[clindamycin]] or [[vancomycin]] |
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|} |
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====Dosing==== |
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{| class="wikitable" |
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!Antimicrobial |
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!Dose |
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|- |
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|[[ampicillin]] |
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|12 g IV q24h continuously or split q4h |
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|- |
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|[[cefazolin]] |
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|1-2 g IV q8h |
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|- |
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|[[cefepime]] |
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|2 g IV q12h |
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|- |
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|[[ceftazidime]] |
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|2 g IV q8h |
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|- |
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|[[ceftriaxone]] |
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|2 g IV q24h |
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|- |
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|[[ciprofloxacin]] |
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|750 mg PO bid |
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|- |
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|[[ciprofloxacin]] |
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|400 mg IV q12h |
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|- |
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|[[clindamycin]] |
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|300-450 mg PO qid |
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|- |
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|[[clindamycin]] |
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|600-900 mg IV q8h |
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|- |
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|[[daptomycin]] |
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|6 mg/kg IV q24h |
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|- |
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|[[ertapenem]] |
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|1 g IV q24h |
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|- |
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|[[linezolid]] |
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|600 mg PO/IV q12h |
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|- |
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|[[meropenem]] |
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|1 g IV q8h |
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|- |
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|[[nafcillin]] |
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|1.5-2 g IV q4-6h |
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|- |
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|[[penicillin G]] |
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|20-24 MU IV q24h continuously or split q4h |
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|- |
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|[[vancomycin]] |
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|15 mg/kg IV q12h |
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|} |
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==== Adjunctive Rifamycins ==== |
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* Adjunctive [[rifampin]] 300 to 450 mg twice daily is usually added for staphylococcal infection where strong contraindications do not exist[[CiteRef::zimmerli2018ro]] |
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* Alternatively , can potentially use [[rifabutin]] 300 mg PO daily[[CiteRef::doub2020ri]] |
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=== Management after DAIR === |
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* Mostly 12 weeks of antibiotics (24 weeks for staphylococcal knee infections), as in above table |
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* DAPITO trial showed inferiority of 6 weeks compared to 12 weeks after DAIR[[CiteRef::bernard2021an]] |
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==== Chronic Suppressive Therapy ==== |
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*Sometimes considered after debridement and implant retention |
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*Duration unclear; 3-12 months or indefinite |
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*In people in whom there is recurrence, it tends to recur within 4 months of discontinuing suppressive therapy |
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*Chronic suppression is recommended where there is a high risk of recurrence or where the consequences of recurrence would be devastating |
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**High-risk bacteria like [[Staphylococcus aureus]] or [[Multidrug-resistant Gram-negative bacteria]] |
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**Limited life expectancy |
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**Prior treatment failure |
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**Poor candidate for future surgeries |
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*Reassess the suppressive therapy every 6 to 12 months |
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{| class="wikitable" |
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!Microorganism |
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!Preferred treatment |
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!Alternative treatment |
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|- |
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|[[Staphylococcus]] (oxacillin-susceptible) |
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|[[Cephalexin]] 500 mg PO tid to qid; |
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[[Cefadroxil]] 500 mg PO bid |
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|[[Dicloxacillin]] 500 mg PO tid to qid; |
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[[Clindamycin]] 300 mg PO qid; |
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[[Amoxicillin-clavulanic acid]] 500mg PO tid |
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|- |
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|[[Staphylococcus]] (oxacillin-resistant) |
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|[[TMP-SMX]] DS 1 tab PO bid; |
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[[Doxycycline]] 100 mg PO bid |
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| |
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|- |
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|[[β-hemolytic streptococci]] |
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|[[Penicillin V]] 500 mg PO bid to qid; |
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[[Amoxicillin]] 500 mg PO tid |
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|[[Cephalexin]] 500 mg PO tid to qid |
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|- |
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|[[Enterococcus]] (penicillin-susceptible) |
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|[[Penicillin V]] 500 mg PO bid to qid; |
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[[Amoxicillin]] 500 mg PO tid |
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| |
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|- |
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|[[Pseudomonas aeruginosa]] |
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|[[Ciprofloxacin]] 250-500 mg PO bid |
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| |
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|- |
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|[[Enterobacteriaceae]] |
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|[[TMP-SMX]] DS 1 tab PO bid |
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|Beta-lactam, if susceptible |
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|- |
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|[[Cutibacterium]] |
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|[[Penicillin V]] 500 mg PO bid to qid; |
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[[Amoxicillin]] 500 mg PO tid |
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|[[Cephalexin]] 500 mg PO tid to qid; |
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[[Doxycycline]] 100 mg PO bid |
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|} |
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=== Management With One-Stage Replacement === |
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* Duration 6 to 12 weeks of antibiotics |
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=== Management With Two-Stage Replacement === |
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* Initially 6 to 12 weeks of antibiotics, followed by a 2+ week antibiotic holiday, then reimplantation |
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===Intra-Articular Infusion=== |
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*Used in veterinary practice for decades, but only used experimentally in humans |
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*Intraoperatively insert two Hickman catheters into the intraarticular space |
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**Two catheters used to ensure that at least one will remain viable for the duration |
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*[[Vancomycin]] |
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**May precipitate local inflammatory response necessitating holding it for several days |
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==Further Reading== |
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*Prosthetic Joint Infection. ''Clin Micro Rev''. 2014;27(2):302-345. doi: [https://doi.org/10.1128/CMR.00111-13 10.1128/CMR.00111-13] |
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* Microbiology of polymicrobial prosthetic joint infection. ''Diagnostic Microbio Infect Dis''. 2019;94(3):255-259. doi: [https://doi.org/10.1016/j.diagmicrobio.2019.01.006 10.1016/j.diagmicrobio.2019.01.006] |
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*Diagnosis and Management of Prosthetic Joint Infection: Clinical Practice Guidelines by the IDSA. ''Clin Infect Dis''. 2013;56(1):e1-25. doi: [https://doi.org/10.1093/cid/cis803 10.1093/cid/cis803] |
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[[Category:Bone and joint infections]] |
[[Category:Bone and joint infections]] |
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[[Category:Infectious diseases]] |
Latest revision as of 17:18, 27 September 2024
Background
Microbiology
- Hip and knee
- Early (<3 months): Staphylococcus aureus (38%), aerobic Gram-negative bacilli (24%), coagulase-negative staphylococci (22%), Enterococcus (10%), and Streptococcus (4%), anaerobes including Cutibacterium acnes (3%), culture-negative (10%); 31% are polymicrobial
- Overall: Staphylococcus aureus (27%), coagulase-negative staphylococci (27%), aerobic Gram-negative bacilli (9%), Streptococcus (8%), anaerobes including Cutibacterium acnes (4%), Enterococcus (3%), culture-negative (14%); 15% are polymicrobial
- Shoulder: coagulase-negative staphylococci (42%), Cutibacterium acnes (24%), Staphylococcus aureus (18%), aerobic Gram-negative bacilli (10%), others, culture-negative (15%); polymicrobial in 16%
- Elbow: Staphylococcus aureus (42%), coagulase-negative staphylococci (41%), others, culture-negative (5%); polymicrobial in 3%
Epidemiology
- Complicates about 2% of arthroplasty
- 2% of hip and knee arthroplasties
- 1% of shoulder arthroplasties
Pathophysiology
- Bacteria grown on the prosthesis in a biofilm, making it resistant to medical management
Clinical Manifestations
- Most commonly occur within the 3 months after arthroplasty (early); 70% within the first two years
- Should be suspected when there is a sinus tract, persistent wound drainage, acute onset of pain, or chronic pain after a pain-free interval
Prognosis
- Recurrent rates after DAIR are 9% (with 12 weeks of antibiotics) to 18% (with 6 weeks)1
- In a large observational study, about 30-40% overall have recurrence
- DAIR success was highest with early post-implant infection and lower with late acute and chronic infections
- Knee joint and Staphylococcus aureus were associated with lower success2
Diagnosis
- Routine investigations should include ESR, CRP, plain film x-ray, diagnostic arthrocentesis, and blood cultures (if fever or other systemic symptom)
- If clinically stable, try to obtain arthrocentesis samples before antibiotics
- Other imaging should not be used routinely
- Diagnosis is made most definitively by histopathology of periprosthetic tissue biopsy, and supported by positive intraoperative tissue cultures
- Should take 3 to 6 intraoperative samples
- If clinically stable, try to obtain tissue cultures before starting antibiotics
- A definitive diagnosis of PJI requires any of the following:
- Sinus tract that communicates with the prosthesis
- Acute inflammation on histopathology of intraoperatic periprosthetic tissue sample
- Periprosthetic purulence without other cause
- Two or more intraoperative cultures with identical organism, though a single positive culture may be sufficient in some cases
- A diagnosis of PJI may still be possible if the above criteria are not met but clinical suspicion remains
2018 Definition of Periprosthetic Hip and Knee Infection3
Criterion | Points | Interpretation |
---|---|---|
Major Criteria | ||
Two positive cultures of the same organism | N/A | Infected |
Sinus tract with evidence of communication to the joint or visualization of the prosthesis | N/A | |
Minor Preoperative Criteria | ||
Elevated serum CRP or D-dimer | 2 | ≥6: infected
2-5: possibly infected ≤1: not infected |
Elevated serum ESR | 1 | |
Elevated synovial WBC count or LE | 3 | |
Positive synovial alpha-defensin | 3 | |
Elevated synovial PMN % | 2 | |
Elevated synovial CRP | 1 | |
Intraoperative Criteria for Inconclusive Preoperative Scores | ||
Preoperative score | - | ≥6: infected
4-5: inconclusive ≤3: not infected |
Positive histology | 3 | |
Positive purulence | 3 | |
Single positive culture | 2 |
Marker | Cutoff | |
---|---|---|
Chronic >90 days | Acute <90 days | |
Serum CRP (mg/dL) | 1 | 10 |
Serum D-dimer (ng/mL) | 860 | 860 |
Serum ESR (mm/h) | 30 | - |
Synovial WBC (cells/μL) | 3000 | 10 000 |
Synovial PMN (%) | 80 | 90 |
Synovial CRP (mg/L) | 6.9 | 6.9 |
Synovial alpha-defensin | 1 | 1 |
- The above criteria may be inaccurate in patients with adverse local tissue reaction (ALTR), crystalline deposition arthropathy, inflammatory arthopathy flare, or infection with slow-growing organisms such as Cutibacterium acnes and coagulase-negative staphylococci
Management
Surgical Management
- Ultimately the decision of whether and how to treat surgically rests with the orthopedic surgeon
- Options include:
- Debridement and implant retention (DAIR), preferred if well-fixed prosthesis, no sinus tract, susceptible to oral antibiotics, joint age <30 days, and symptoms <3 weeks
- One-stage replacement
- Two-stage replacement, where the prosthesis is removed and replaced with a cement spacer, the infection is treated, and then a new prosthesis is placed
- Antibiotic-impregnated cement is often used for the spacer
- Usually vancomycin 2 to 8 g per 40 g cement, or an aminoglycoside
- No clear guidelines for dosing
- No clear evidence of effectiveness, but recommended in all revisions for septic arthritis
- Releases over a period of two to three days
- Usually vancomycin 2 to 8 g per 40 g cement, or an aminoglycoside
Antimicrobial Therapy
Surgical Management | Species | Location | Duration IV* | Total Duration | Adjunctive Rifampin | Chronic Suppressive Therapy |
---|---|---|---|---|---|---|
debridement and retention | Staphylococcus | knee | 2-6 weeks | 6 months | yes; 4-6 weeks IV if not given | ± |
hip | 3 months | ± | ||||
elbow | ± | |||||
shoulder | ± | |||||
ankle | ± | |||||
species other than staphylococci | — | 4-6 weeks | 12 weeks† | ± | ||
resection ± reimplantation | — | — | 4-6 weeks | |||
1-stage exchange | Staphylococcus | — | 2-6 weeks | 3 months | yes; 4-6 weeks IV if not given | ± |
species other than staphylococci | — | 4-6 weeks | 3 months | ± | ||
amputation with source control | — | — | 24-48 hours | |||
amputation without source control | — | — | 4-6 weeks |
- * IV therapy includes highly bioavailable oral therapy
- † per DAPITO trial1
Intravenous and Highly Bioavailable Oral Therapy
Choice of Antimicrobial
- Increasing evidence suggests that regimens of fluoroquinolone plus rifampin has the lowest risk of recurrence, and should likely be the preferred regimen in staphylococcal infections with susceptible organisms
Species | Preferred Antimicrobials | Alternative Antimicrobials |
---|---|---|
Staphylococcus (oxacillin-susceptible) | nafcillin or cefazolin or ceftriaxone | vancomycin or daptomycin or linezolid |
Staphylococcus (oxacillin-resistant) | vancomycin | daptomycin |
Enterococcus (penicillin-susceptible) | penicillin G or ampicillin | vancomycin or daptomycin or linezolid |
Pseudomonas aeruginosa | cefepime or meropenem | ciprofloxacin or ceftazidime |
Enterobacter | cefepime | ciprofloxacin |
Enterobacteriaceae | ampicillin or ceftriaxone or ciprofloxacin | |
β-hemolytic streptococci | penicillin G or ceftriaxone | vancomycin |
Cutibacterium acnes | penicillin G or ceftriaxone | clindamycin or vancomycin |
Dosing
Antimicrobial | Dose |
---|---|
ampicillin | 12 g IV q24h continuously or split q4h |
cefazolin | 1-2 g IV q8h |
cefepime | 2 g IV q12h |
ceftazidime | 2 g IV q8h |
ceftriaxone | 2 g IV q24h |
ciprofloxacin | 750 mg PO bid |
ciprofloxacin | 400 mg IV q12h |
clindamycin | 300-450 mg PO qid |
clindamycin | 600-900 mg IV q8h |
daptomycin | 6 mg/kg IV q24h |
ertapenem | 1 g IV q24h |
linezolid | 600 mg PO/IV q12h |
meropenem | 1 g IV q8h |
nafcillin | 1.5-2 g IV q4-6h |
penicillin G | 20-24 MU IV q24h continuously or split q4h |
vancomycin | 15 mg/kg IV q12h |
Adjunctive Rifamycins
- Adjunctive rifampin 300 to 450 mg twice daily is usually added for staphylococcal infection where strong contraindications do not exist4
- Alternatively , can potentially use rifabutin 300 mg PO daily5
Management after DAIR
- Mostly 12 weeks of antibiotics (24 weeks for staphylococcal knee infections), as in above table
- DAPITO trial showed inferiority of 6 weeks compared to 12 weeks after DAIR1
Chronic Suppressive Therapy
- Sometimes considered after debridement and implant retention
- Duration unclear; 3-12 months or indefinite
- In people in whom there is recurrence, it tends to recur within 4 months of discontinuing suppressive therapy
- Chronic suppression is recommended where there is a high risk of recurrence or where the consequences of recurrence would be devastating
- High-risk bacteria like Staphylococcus aureus or Multidrug-resistant Gram-negative bacteria
- Limited life expectancy
- Prior treatment failure
- Poor candidate for future surgeries
- Reassess the suppressive therapy every 6 to 12 months
Microorganism | Preferred treatment | Alternative treatment |
---|---|---|
Staphylococcus (oxacillin-susceptible) | Cephalexin 500 mg PO tid to qid;
Cefadroxil 500 mg PO bid |
Dicloxacillin 500 mg PO tid to qid;
Clindamycin 300 mg PO qid; Amoxicillin-clavulanic acid 500mg PO tid |
Staphylococcus (oxacillin-resistant) | TMP-SMX DS 1 tab PO bid;
Doxycycline 100 mg PO bid |
|
β-hemolytic streptococci | Penicillin V 500 mg PO bid to qid;
Amoxicillin 500 mg PO tid |
Cephalexin 500 mg PO tid to qid |
Enterococcus (penicillin-susceptible) | Penicillin V 500 mg PO bid to qid;
Amoxicillin 500 mg PO tid |
|
Pseudomonas aeruginosa | Ciprofloxacin 250-500 mg PO bid | |
Enterobacteriaceae | TMP-SMX DS 1 tab PO bid | Beta-lactam, if susceptible |
Cutibacterium | Penicillin V 500 mg PO bid to qid;
Amoxicillin 500 mg PO tid |
Cephalexin 500 mg PO tid to qid;
Doxycycline 100 mg PO bid |
Management With One-Stage Replacement
- Duration 6 to 12 weeks of antibiotics
Management With Two-Stage Replacement
- Initially 6 to 12 weeks of antibiotics, followed by a 2+ week antibiotic holiday, then reimplantation
Intra-Articular Infusion
- Used in veterinary practice for decades, but only used experimentally in humans
- Intraoperatively insert two Hickman catheters into the intraarticular space
- Two catheters used to ensure that at least one will remain viable for the duration
- Vancomycin
- May precipitate local inflammatory response necessitating holding it for several days
Further Reading
- Prosthetic Joint Infection. Clin Micro Rev. 2014;27(2):302-345. doi: 10.1128/CMR.00111-13
- Microbiology of polymicrobial prosthetic joint infection. Diagnostic Microbio Infect Dis. 2019;94(3):255-259. doi: 10.1016/j.diagmicrobio.2019.01.006
- Diagnosis and Management of Prosthetic Joint Infection: Clinical Practice Guidelines by the IDSA. Clin Infect Dis. 2013;56(1):e1-25. doi: 10.1093/cid/cis803
References
- ^ Werner Zimmerli, Parham Sendi. Role of Rifampin against Staphylococcal Biofilm InfectionsIn Vitro, in Animal Models, and in Orthopedic-Device-Related Infections. Antimicrobial Agents and Chemotherapy. 2018;63(2):e01746-18. doi:10.1128/aac.01746-18.
- ^ James B. Doub, Emily L. Heil, Afua Ntem-Mensah, Renaldo Neeley, Patrick R. Ching. Rifabutin Use in Staphylococcus Biofilm Infections: A Case Series. Antibiotics. 2020;9(6):326. doi:10.3390/antibiotics9060326.