Table 3. Antimicrobial Treatment of Periprosthetic Joint Infection.
Microorganism | Antibiotic (dose), check pathogen susceptibility | Duration | Followed by |
---|---|---|---|
Staphylococcus spp. | |||
Oxacillin-/methicillin-susceptible | Cefazolin (3×2 g, i.v.)*+Rifampin (2×450 mg, p.o.) | 2 wk | According to susceptibility, Levofloxacin (2×500 mg, p.o.) or Cotrimoxazol (3×960 mg, p.o.) or Doxycyclin (2×100 mg, p.o.) +Rifampin(2×450 mg, p.o.) |
Oxacillin-/methicillin-resistant | Vancomycin (2×1 g, i.v.)†+Rifampin (2×450 mg. p.o.) | 2 wk | Same combination as above for oxacillin-/methicillin-susceptible staphylococci |
Rifampicin-resistant§ | Vancomycin (2×1 g, i.v.)† | 2 wk | Long-term suppression for ≥1 yr, depending on susceptibility (e.g., with cotrimoxazol, doxycycline or clindamycin) |
Streptococcus spp. | Penicillin G (4×5 million U, i.v.)* or Ceftriaxon (1×2 g, i.v.) | 2 wk | Amoxicillin (3×1,000 mg, p.o.) or Levofloxacin (2×500 mg, p.o.) (consider suppression for 1 year) |
Enterococcus spp. | |||
Penicillin-susceptible | Ampicillin (4×2 g, i.v.)*+Gentamicin (2×60-80 mg, i.v.)‡ | 2–3 wk | Amoxicillin (3×1,000 mg, p.o.) |
Penicillin-resistant§ | Vancomycin (2×1 g, i.v.)† or +Gentamicin (2×60-80 mg, i.v.)‡ | 2–4 wk | Linezolid (2×600 mg, p.o.), maximum 4 wk |
Vancomycin-resistant | Individual; removal of the implant or life-long suppression necessary | ||
Gram-negative bacteria | |||
Enterobacteriaceae (Escherichia coli, Klebsiella, Enterobacter, etc.) | Ciprofloxacin (2×750 mg, p.o.) | ||
Nonfermenters (Pseudomonas aeruginosa, Acinetobacter spp.) | Piperacillin/tazobactam (3×4.5 g, i.v.) or Meropenem (3×1 g, i.v.) or Ceftazidim (3×2 g, i.v.)+Gentamicin (1×240 mg, i.v.) | 2–3 wk | Ciprofloxacin (2×750 mg, p.o.) |
Ciprofloxacin-resistant§ | Depending on susceptibility: meropenem (3×1 g), colistin (3×3 million U) and/or fosfomycin (3×5 g), i.v. | Oral suppression | |
Anaerobes | |||
Gram-positive anaerobes (Propionibacterium, Peptostreptococcus, Finegoldia magna) | Penicillin G (4×5 million U, i.v.)* or Ceftriaxon (1×2 g, i.v.)+Rifampin (2×450 mg, p.o.) | 2 wk | Levofloxacin (2×500 mg, p.o.) or Amoxicillin (3×1,000 mg, p.o.)+Rifampin (2×450 mg, p.o.) |
Gram-negative anaerobes (Bacteroides) | Clindamycin (3×600 mg, i.v.) | 2 wk | Metronidazol (3×500 mg, p.o.) |
Candida spp. | |||
Fluconazole-susceptible§ | Caspofungin (1×50 mg, 1st day: 70 mg; i.v.) | 2 wk | Fluconazole (1×400 mg, suppression for ≥1 year; p.o.) |
Fluconazole-resistant§ | Individual (e.g., with voriconazole 2×200 mg, p.o.); removal of the implant or long-term suppression |
Total duration of therapy: 12 weeks, usually 2 weeks intravenously, followed by oral route.
Laboratory testing 2 times/weekly: leukocytes, C-reactive protein, creatinine/estimated glomerular filtration rate, liver enzymes (AST/SGOT and ALT/SGPT).
Dose-adjustment according to renal function and body weight (<40 kg or >100 kg); the dosages needed renal adjustment are in bold.
i.v.: intravenously; p.o.: per oral.
Rifampin is administered only after the new prosthesis is implanted, wounds are dry and drains are removed; in patients aged >75 years, the rifampicin dose should be reduced to 2×300 mg, p.o.
*In case of anaphylaxis (such as Quincke's edema, bronchospasm, anaphylactic shock) or cephalosporin allergy: vancomycin (21 g, i.v.).
†Check vancomycin trough concentration (take blood before next dose) at least 1 time/week; therapeutic range, 15–20 µg/mL.
‡Give only, if gentamicin high-level (HL) is tested susceptible (consult your microbiology laboratory). In gentamicin HL-resistant enterococci: gentamicin is exchanged with ceftriaxone (1×2 g, i.v.).
§Difficult-to-treat.