Daptomycin treatment in patients with resistant staphylococcal periprosthetic joint infection

Yu-Jui Chang1, Mel S Lee1,2, Chen-Hsiang Lee2,3

  • 1Department of Orthopedic Surgery, Kaohsiung Chang Gung Memorial Hospital, No 123, Ta Pei Road, Niao Sung Dist, Kaohsiung, Taiwan.

BMC Infectious Diseases
|December 1, 2017
PubMed
Abstract

Insights

Daptomycin effectively treated resistant staphylococcal periprosthetic joint infections (PJI) in 87.5% of patients when vancomycin failed or was contraindicated. This antibiotic is a viable option for complex PJI cases.

Area of Science:

  • Infectious Diseases
  • Orthopedic Surgery
  • Pharmacology

Background:

  • Resistant staphylococcal infections pose significant challenges in treating periprosthetic joint infections (PJI).
  • Vancomycin use in PJI has been associated with higher failure rates.
  • Alternative treatments are crucial for patients with resistant PJI.

Purpose of the Study:

  • To evaluate the clinical dosage, efficacy, and safety of daptomycin for resistant staphylococcal PJI.
  • To assess daptomycin as a treatment option when glycopeptides are unsuitable.
  • To analyze treatment outcomes in patients with hip or knee PJI.

Main Methods:

  • Retrospective study of 16 patients with hip or knee PJI treated with daptomycin (January 2013 - December 2014).
  • Daptomycin was administered when glycopeptides were contraindicated (resistance, adverse reactions, CKD) or failed.
  • Minimum follow-up of 2 years was required.

Main Results:

  • Median daptomycin dose was 8.3 mg/kg/day for 14 days.
  • Overall treatment success rate was 87.5% (14/16 patients) at a median follow-up of 27 months.
  • Acute PJI success rate was 80%, chronic PJI success rate was 91%.
  • One patient had transient AST elevation; no severe side effects like myositis or rhabdomyolysis were observed.

Conclusions:

  • High-dose daptomycin, combined with surgery, is effective for resistant staphylococcal PJI.
  • Daptomycin presents a valuable alternative for PJI patients unsuitable for glycopeptide therapy.
  • Further prospective studies are warranted to confirm these findings.

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