Leprosy Treatment
For leprosy, the World Health Organization-recommended multidrug therapy (MDT) is the definitive treatment: rifampin 600mg monthly supervised plus dapsone 100mg daily for paucibacillary disease (6 months), or rifampin 600mg monthly supervised, clofazimine 300mg monthly supervised plus 50mg daily, and dapsone 100mg daily for multibacillary disease (12 months). 1, 2, 3
Classification and Treatment Selection
The treatment regimen depends on disease classification:
- Paucibacillary leprosy (tuberculoid, indeterminate, borderline tuberculoid with <5 skin lesions): Rifampin 600mg monthly supervised + dapsone 100mg daily for 6 months 1, 4
- Multibacillary leprosy (lepromatous, borderline lepromatous, borderline with ≥5 skin lesions): Rifampin 600mg monthly supervised + clofazimine 300mg monthly supervised plus 50mg daily + dapsone 100mg daily for 12 months 1, 2, 3
Pre-Treatment Screening Requirements
Before initiating therapy, mandatory screening includes:
- G6PD deficiency testing before dapsone due to hemolytic anemia and methemoglobinemia risk 1, 2, 3
- Baseline ECG before clofazimine to assess QT interval 2, 3
- Baseline complete blood count and liver function tests 2, 3
Monitoring During Treatment
Regular monitoring is essential:
- Complete blood count and liver function tests during dapsone therapy to detect hemolytic anemia, methemoglobinemia, nausea, and hepatotoxicity 2, 3, 4
- ECG monitoring at 2 weeks after clofazimine initiation and when adding any QT-prolonging medications 2, 3
- Clinical assessment for treatment response, expecting lesion flattening by 4-6 weeks 2, 3
Critical Treatment Principles
MDT must not be interrupted for skin complications, wound healing, or leprosy reactions. 2, 3 This is a common pitfall that worsens outcomes.
Managing Leprosy Reactions
Leprosy reactions are immunological phenomena distinct from treatment failure:
- Type 1 reversal reactions: Treat with corticosteroids while continuing MDT 2, 3
- Type 2 erythema nodosum leprosum: Requires anti-inflammatory management but continuation of MDT 2, 3
These reactions require adding anti-inflammatory therapy, not stopping antibiotics. 2, 3
Special Populations
Pregnancy
Treatment should continue during pregnancy as benefits outweigh risks, with close monitoring required. 2, 3 All three drugs (rifampin, dapsone, clofazimine) can be used.
Pediatric Patients
Clofazimine has been well-tolerated in pediatric leprosy trials at 1-2 mg/kg/day (maximum 100mg daily). 3 Dapsone and rifampin doses are correspondingly reduced based on weight. 4
Medication-Specific Guidance
Dapsone
- Dosage: 100mg daily in adults, proportionally reduced in children 4
- Side effects: Hemolysis, methemoglobinemia, nausea, vomiting 3, 4
- Influenced by acetylation rates; high acetylators may require dose adjustment 4
Clofazimine
- Dosage: 50-100mg daily with meals or milk to maximize absorption 3
- Available as 100mg capsules that cannot be split 3
- Causes pink to brownish-black skin discoloration in 75-100% of patients within 1-4 weeks, resolving 6-12 months after stopping 3
- Other adverse effects: Ichthyosis, gastrointestinal intolerance, QT prolongation 3
Rifampin
Dapsone Resistance
Suspect secondary dapsone resistance when lepromatous or borderline lepromatous patients relapse clinically and bacteriologically with solid-staining bacilli in new active lesions. 4 If no response occurs within 3-6 months of supervised therapy, resistance should be considered confirmed and alternative drugs used. 4
Common Pitfalls to Avoid
- Premature discontinuation due to leprosy reactions worsens outcomes; reactions require anti-inflammatory therapy while continuing MDT 2, 3
- Failure to screen for G6PD deficiency before dapsone can lead to life-threatening hemolytic anemia 1, 2, 3
- Inadequate QT monitoring with clofazimine, especially when combined with other QT-prolonging medications 2, 3
- Confusing leprosy reactions with treatment failure leads to inappropriate MDT discontinuation 2, 3