Treatment for Ringworm (Tinea Infection)
For tinea corporis (body) and tinea cruris (groin), use topical terbinafine or topical naftifine as first-line therapy, applied once or twice daily for 1-2 weeks; for tinea capitis (scalp), oral terbinafine is the preferred treatment at weight-based dosing for 2-4 weeks. 1, 2
Topical Treatment for Tinea Corporis and Tinea Cruris
First-Line Topical Agents
Terbinafine 1% cream is highly effective, achieving clinical cure rates 4.5 times higher than placebo (NNT 3), applied once or twice daily for 1-2 weeks 3, 1
Naftifine 1% cream demonstrates strong efficacy with mycological cure rates 2.4 times higher than placebo (NNT 3), applied once or twice daily for 1-2 weeks 3
Azole antifungals (clotrimazole, miconazole, ketoconazole) are effective alternatives with mycological cure rates 2.9 times higher than placebo for clotrimazole (NNT 2), typically applied twice daily for 2-4 weeks 3
Treatment Duration and Application
Most topical treatments require 2-4 weeks of application, though terbinafine and naftifine may achieve cure with shorter courses of 1-2 weeks 3, 2
Continue treatment for at least one week after clinical symptoms resolve to ensure mycological cure 2
Oral Treatment for Extensive or Resistant Disease
Indications for Oral Therapy
Tinea capitis (scalp ringworm) always requires oral treatment because topical agents cannot penetrate hair follicles adequately 4, 2, 5
Extensive tinea corporis or cruris involving large body surface areas 2
Lack of response to topical treatment after 2-4 weeks 2
Immunocompromised patients 2
Hair follicle involvement (Majocchi's granuloma) 2
Oral Terbinafine (First-Line for Tinea Capitis)
Dosing by weight for children and adults:
- <20 kg: 62.5 mg daily
- 20-40 kg: 125 mg daily
40 kg: 250 mg daily 4
Treatment duration: 2-4 weeks for tinea capitis caused by Trichophyton species 4, 2
Terbinafine is preferred over griseofulvin because it is well-tolerated, effective, and requires shorter treatment duration 2, 4
Alternative Oral Agents
Griseofulvin remains an option, particularly for Microsporum species, dosed at:
- 10-20 mg/kg/day for children
- Treatment duration: 6-8 weeks 4
Itraconazole 5 mg/kg/day for 2-4 weeks or pulse dosing (100 mg daily for 4 weeks) is effective for both Trichophyton and Microsporum species 4
Fluconazole 6 mg/kg once weekly has been used but offers no cost advantage and has more side effects 4
Critical Management Considerations
Avoid Combination Antifungal-Corticosteroid Products
Do not use topical steroid-antifungal combinations as routine first-line therapy, despite slightly higher initial clinical cure rates, because steroids may suppress local immune response and allow deeper fungal invasion 6, 2
If combination products are used for heavily inflamed lesions, limit use to 2 weeks maximum and only in adults, never in children under 12 years or on facial/occluded areas 6
Confirm Diagnosis Before Treatment
Clinical diagnosis alone is unreliable—tinea corporis mimics eczema, and onychomycosis mimics psoriatic or traumatic nail dystrophy 2, 4
Obtain KOH preparation or fungal culture to confirm dermatophyte infection before initiating prolonged oral therapy 2, 4
Treatment Failure Management
If no clinical improvement after 2-4 weeks of appropriate topical therapy, switch to oral antifungals 2
For tinea capitis with treatment failure on terbinafine, switch to itraconazole or griseofulvin (particularly for Microsporum species) 4
Consider emerging resistant tinea infections if standard treatments fail—these may require prolonged oral therapy and specialized testing 2
Adjunctive Measures for Tinea Capitis
Children receiving appropriate oral therapy should attend school or nursery without restriction 4
Screen and treat all family members and close contacts for Trichophyton tonsurans infections 4
Continue treatment until mycological clearance is achieved, not just clinical improvement 4
Special Populations
Pediatric Considerations
Oral terbinafine is safe and effective in children at weight-based dosing 4, 2
Avoid topical steroid-antifungal combinations in children under 12 years due to increased risk of cutaneous adverse effects 6