North American Blastomycosis (Option B) Has the More Established Treatment Protocol
North American blastomycosis caused by Blastomyces dermatitidis has comprehensive, evidence-based treatment guidelines established by the Infectious Diseases Society of America, making it the clear choice for a more established treatment protocol. 1
Why North American Blastomycosis Has Superior Treatment Protocols
Comprehensive Guideline Development
- The IDSA published detailed clinical practice guidelines specifically for North American blastomycosis in 2000 and updated them in 2008, providing systematic treatment recommendations for multiple clinical scenarios 1
- These guidelines address pulmonary disease, disseminated extrapulmonary disease, CNS involvement, immunosuppressed patients, and special populations including pregnant women and children 1
- The guidelines use a formal evidence grading system (IDSA-USPHS grading) to rank recommendations, providing transparency about evidence quality 1
Well-Defined Treatment Algorithms
For mild to moderate pulmonary or disseminated disease:
- Oral itraconazole 200 mg three times daily for 3 days, then once or twice daily for 6-12 months is the established first-line therapy 1
- Serum itraconazole levels should be measured after 2 weeks to ensure adequate drug exposure (target >1.0 μg/mL) 1, 2
For moderately severe to severe disease:
- Lipid formulation amphotericin B at 3-5 mg/kg/day or amphotericin B deoxycholate at 0.7-1 mg/kg/day for 1-2 weeks until improvement 1
- Step-down to oral itraconazole 200 mg three times daily for 3 days, then twice daily for at least 12 months 1
For CNS blastomycosis:
- Lipid formulation amphotericin B at 5 mg/kg/day for 4-6 weeks 1
- Followed by oral azole therapy (fluconazole 800 mg/day, itraconazole 200 mg 2-3 times daily, or voriconazole 200-400 mg twice daily) for at least 12 months until CSF abnormalities resolve 1
Special Population Considerations
Immunosuppressed patients:
- Initial therapy with lipid formulation amphotericin B 3-5 mg/kg/day or amphotericin B deoxycholate 0.7-1 mg/kg/day for 1-2 weeks 1
- Life-long suppressive therapy with itraconazole 200 mg daily may be required if immunosuppression cannot be reversed 1
Pregnant women:
- Lipid formulation amphotericin B 3-5 mg/kg/day is recommended, as azoles should be avoided due to teratogenicity 1
Children:
- Amphotericin B deoxycholate 0.7-1.0 mg/kg/day or lipid formulation 3-5 mg/kg/day for severe disease 1
- Itraconazole 10 mg/kg/day (maximum 400 mg/day) for mild to moderate infection for 6-12 months 1
Geographic and Epidemiologic Clarity
- North American blastomycosis has well-defined endemic regions: southeastern and south-central states bordering the Mississippi and Ohio Rivers, midwestern states and Canadian provinces bordering the Great Lakes, and areas adjacent to the St. Lawrence Seaway 1
- Multiple studies have documented areas of hyperendemicity and point-source outbreaks, providing clear epidemiologic data 1
Diagnostic Standards
- Established diagnostic methods include culture growth of the mold phase, histopathological identification of the distinctive yeast form, and detection of cell wall antigens in urine or serum 3, 4
- The characteristic broad-based budding yeast form is well-described and readily identifiable 5
Important Clinical Caveats
Drug Interaction Considerations
- For patients on proton pump inhibitors, fluconazole 400-800 mg daily is preferred over itraconazole capsules, as itraconazole requires gastric acidity for absorption 2
- Itraconazole solution may be used as an alternative if capsules are problematic 2
Monitoring Requirements
- Hepatic enzymes should be monitored before starting azole therapy, at 2 and 4 weeks, then every 3 months 2
- Serum itraconazole levels must be checked after 2 weeks to ensure therapeutic exposure 1, 2
Treatment Duration
- Osteoarticular blastomycosis requires at least 12 months of therapy 1
- Immunocompromised patients may require longer treatment courses 2
Agents to Avoid
- Echinocandins (caspofungin, micafungin, anidulafungin) have poor activity against B. dermatitidis and should not be used 2
In contrast, South American blastomycosis (paracoccidioidomycosis) lacks the same level of systematic guideline development and evidence-based treatment protocols that characterize North American blastomycosis management. 1