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Challenges in Treating Mycobacterium chelonae/abscessus Prosthetic Joint Infection
Divita Singh1, Mikayla Johnson2, Caleah S Kitchens3
1Pharmacy Practice, 306709Howard University College of Pharmacy, Washington, DC, USA.
Abstract:
Prosthetic joint infections (PJIs) remain a major complication of arthroplasty, most of which are caused by Staphylococcus aureus and gram-negative bacteria. Unfortunately, cultures are false negative in upward of 7 percent of patients with suspected PJIs, and commonly in infections caused by rare rapidly growing mycobacterium (RGM) species. Guidelines recommend 6 months of antimycobacterial therapy for bone diseases caused by RGM, with empiric therapy consists of an oral macrolide (clarithromycin or azithromycin) plus tobramycin and imipenem-cilastatin. Definitive treatment of PJI due to RGM should be guided by antimicrobial susceptibility, however, most microbiology laboratories are unable to differentiate between M. chelonae and M. abscessus. Furthermore, treatment of M. chelonae PJI is challenging due to multidrug resistance and the dearth of oral antibiotics for therapy. This case report investigates a patient with PJI caused by M. chelonae and M. abscessus. The initial treatment with imipenem-cilastatin was complicated by drug induced seizures, further limiting therapy options.
Insights
Prosthetic joint infections (PJIs) caused by rare rapidly growing mycobacteria (RGM) are challenging. This case highlights diagnostic and treatment difficulties, including drug resistance and limited oral options for Mycobacterium chelonae PJI.
Area of Science:
- Infectious Diseases
- Orthopedic Surgery
- Microbiology
Background:
- Prosthetic joint infections (PJIs) are a significant complication of arthroplasty.
- Staphylococcus aureus and gram-negative bacteria are common causative agents.
- Rare rapidly growing mycobacteria (RGM) can also cause PJIs, often with false-negative cultures.
Observation:
- Guidelines recommend 6 months of antimycobacterial therapy for RGM bone diseases.
- Empiric therapy includes macrolides, tobramycin, and imipenem-cilastatin.
- Microbiology labs struggle to differentiate M. chelonae and M. abscessus, complicating definitive treatment.
Findings:
- This case report details a PJI caused by both M. chelonae and M. abscessus.
- Initial treatment with imipenem-cilastatin led to drug-induced seizures, limiting therapeutic choices.
- Mycobacterium chelonae PJI presents challenges due to multidrug resistance and a lack of oral antibiotics.
Implications:
- Accurate diagnostics are crucial for effective RGM PJI management.
- Novel therapeutic strategies are needed to address multidrug-resistant RGM.
- Further research into differentiating and treating M. chelonae and M. abscessus PJIs is warranted.
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