What is Mycobacterium chelonae and how is it treated?

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Mycobacterium chelonae: Overview and Treatment

What is Mycobacterium chelonae?

M. chelonae is a rapidly growing nontuberculous mycobacterium that primarily causes skin, bone, and soft tissue infections, with treatment being substantially easier than its close relative M. abscessus. 1

Key Organism Characteristics

  • Ubiquitous environmental organism found in water and soil that enters through direct inoculation via trauma, surgery, or contaminated medical procedures 1, 2
  • Rapid growth distinguishes it from slow-growing mycobacteria, allowing culture identification within days rather than weeks 1
  • Critical to differentiate from M. abscessus since therapy for M. chelonae is potentially easier 1

Clinical Presentations

Primary Manifestations (Most Common)

Skin, bone, and soft tissue disease are the most important clinical manifestations 1:

  • Localized infections at puncture wound sites, surgical sites, or traumatic injuries 1
  • Nosocomial infections including post-injection abscesses, infections after liposuction, augmentation mammaplasty, cardiac bypass surgery 1, 3
  • Chronic granulomatous infections of tendon sheaths, bursae, joints, and bones after direct inoculation 1
  • Catheter-related infections involving long-term intravenous or peritoneal catheters 1

Ocular Disease

  • M. chelonae is the most frequently reported etiologic agent in LASIK-associated keratitis 1
  • Associated with contact lens wear and ocular surgery 1
  • Outcome for vision is typically poor, often requiring corneal transplant 1

Disseminated Disease

  • Occurs primarily in immunocompromised patients, particularly those with advanced HIV (very low CD4 counts), organ transplantation (especially renal), or hematologic malignancies 4, 5
  • Presents with characteristic skin lesions 1
  • Extremely rare in immunocompetent individuals, where infections tend to remain localized 4, 2

Pulmonary Disease

  • Less common cause of pulmonary disease than M. abscessus 1
  • Symptoms and radiographic presentation similar to M. abscessus and M. fortuitum 1

Antimicrobial Susceptibility Profile

M. chelonae demonstrates predictable susceptibility patterns that guide treatment selection 1:

  • Tobramycin: 100% susceptibility (more active than amikacin for M. chelonae) 1
  • Clarithromycin: 100% susceptibility 1
  • Linezolid: 90% susceptibility 1
  • Imipenem: 60% susceptibility (preferred over cefoxitin, to which M. chelonae is uniformly resistant) 1
  • Amikacin: 50% susceptibility 1
  • Doxycycline: 25% susceptibility 1, 6
  • Ciprofloxacin: 20% susceptibility 1
  • Additional agents: clofazimine 1

Treatment Recommendations

Skin and Soft Tissue Infections

Mild, Localized Disease

For uncomplicated skin disease, clarithromycin monotherapy at 500 mg twice daily for 6 months achieved cure in 92% of patients in the only clinical treatment trial 1. However, one patient (8%) relapsed with mutational resistance to clarithromycin 1.

Serious Skin, Bone, and Soft Tissue Disease

A minimum of 4 months of combination drug therapy is necessary to provide high likelihood of cure and minimize macrolide resistance risk 1, 6:

  • Initial combination therapy with clarithromycin plus a second agent based on susceptibility (tobramycin or imipenem preferred) 1, 6
  • For bone infections: 6 months of therapy is recommended 1
  • Surgery is generally indicated with extensive disease, abscess formation, or where drug therapy is difficult 1, 6
  • Removal of foreign bodies (breast implants, catheters) is important or essential to recovery 1

Treatment Failure or Persistent Infection

Complete surgical excision of affected tissue combined with optimized antimicrobial therapy is the treatment of choice 6:

  • Obtain new cultures during excision for updated susceptibility testing 6
  • Consider parenteral agents like tobramycin (100% susceptibility) or imipenem (60% susceptibility) 6
  • Continue combination therapy for at least 4-6 months post-excision 6
  • If surgery contraindicated, use aggressive parenteral therapy with tobramycin plus imipenem for at least 12 months of negative cultures 6

Corneal Infections

First-line treatment involves topical and oral agents 1:

  • Amikacin, fluoroquinolones, clarithromycin, and azithromycin are usual drugs of choice depending on susceptibility 1
  • Many patients require corneal transplant for vision recovery or infection cure 1

Pulmonary Disease

Optimal therapy for M. chelonae lung disease is unknown 1:

  • Based on in vitro susceptibilities, a regimen including clarithromycin with a second agent (based on susceptibilities) would likely be successful 1
  • Treatment duration should follow principles established for other nontuberculous mycobacterial lung infections 1

Disseminated Disease in Immunocompromised Patients

Effective treatment involves combination antibiotics with clarithromycin and azithromycin as long-term therapy, plus linezolid and tigecycline for acute dissemination management 5:

  • Clarithromycin and azithromycin form the backbone of long-term treatment 5
  • Linezolid and tigecycline added for managing acute disseminated disease 5
  • Prolonged multi-drug therapy essential for successful outcomes 2

Critical Clinical Pitfalls

Diagnostic Challenges

  • Prolonged skin lesions resistant to standard antibiotics should raise suspicion for M. chelonae in both immunocompromised and immunocompetent patients 7
  • Tissue biopsy is the most sensitive means of obtaining specimens for culture; fine needle aspiration or incision/drainage may lead to fistula formation with chronic drainage 1
  • Only 50-82% of excised nodes yield positive cultures even with compatible histopathology 1
  • Nonspecific symptoms (pain, erythema, draining subcutaneous nodules) make diagnosis difficult without prior suspicion 3

Treatment Considerations

  • Monotherapy risks macrolide resistance development; combination therapy should be used initially for serious infections 1, 6
  • Inadequate drug penetration into lymph nodes may contribute to treatment failure 6
  • Long-term follow-up is essential to ensure complete eradication 4
  • Doxycycline has only 25% susceptibility and may explain treatment failures when used 6

Timeframe for Disease Progression

  • Initial localized infection develops within days to weeks after inoculation 4
  • Proximal lymph node involvement may occur within 2-10 months if inadequately treated 4
  • Spread to distant lymph nodes would be exceptionally rare and take many months to years 4

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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