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. 2018 Sep 4;30(3):138–146. doi: 10.5371/hp.2018.30.3.138

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.