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Intramuscular Triamcinolone Acetonide Versus Oral Minipulse Dexamethasone in Active Vitiligo: An Observational Study
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Background:
Systemic corticosteroids, particularly oral minipulse dexamethasone (OMP-D), are commonly used to stabilize active vitiligo. Intramuscular triamcinolone acetonide (IMTA), though effective in other dermatoses, has limited studies for vitiligo.
Objectives:
To compare the efficacy and safety of IMTA versus OMP-D in adults with active vitiligo.
Methods:
This observational study included patients aged 18 to 60 years with clinically active vitiligo. Patients received either IMTA 40 mg monthly or OMP-D 2.5 mg twice weekly for 3 months. Vitiligo extent score (VES) and adverse events were assessed at baseline, months 1, 2, 3, and 6. Biochemical parameters were evaluated at baseline and month 3.
Results:
Nineteen patients (9 in the IMTA group and 10 in the OMP-D group) were included. All patients achieved disease stabilization within the first month. The IMTA group showed an earlier onset of repigmentation, evidenced by a significant reduction in VES at month 1. By months 2, 3, and 6, both groups demonstrated significant reductions in VES compared to baseline. Notably, at months 2 and 3, the OMP-D group exhibited a more pronounced decrease in VES (
P
≤ .01) than the IMTA group (
P
≤ .05). One patient in the IMTA group began to experience vitiligo relapse at month 6. Both treatments were well-tolerated. Cortisol suppression was observed in 1 patient from each group.
Conclusions:
IMTA shows promising results, comparable in efficacy and safety to OMP-D for active vitiligo, achieving early disease stabilization and repigmentation. IMTA represents a practical first-line alternative for active vitiligo management.
Title: Intramuscular Triamcinolone Acetonide Versus Oral Minipulse Dexamethasone in Active Vitiligo: An Observational Study
Description:
Background:
Systemic corticosteroids, particularly oral minipulse dexamethasone (OMP-D), are commonly used to stabilize active vitiligo.
Intramuscular triamcinolone acetonide (IMTA), though effective in other dermatoses, has limited studies for vitiligo.
Objectives:
To compare the efficacy and safety of IMTA versus OMP-D in adults with active vitiligo.
Methods:
This observational study included patients aged 18 to 60 years with clinically active vitiligo.
Patients received either IMTA 40 mg monthly or OMP-D 2.
5 mg twice weekly for 3 months.
Vitiligo extent score (VES) and adverse events were assessed at baseline, months 1, 2, 3, and 6.
Biochemical parameters were evaluated at baseline and month 3.
Results:
Nineteen patients (9 in the IMTA group and 10 in the OMP-D group) were included.
All patients achieved disease stabilization within the first month.
The IMTA group showed an earlier onset of repigmentation, evidenced by a significant reduction in VES at month 1.
By months 2, 3, and 6, both groups demonstrated significant reductions in VES compared to baseline.
Notably, at months 2 and 3, the OMP-D group exhibited a more pronounced decrease in VES (
P
≤ .
01) than the IMTA group (
P
≤ .
05).
One patient in the IMTA group began to experience vitiligo relapse at month 6.
Both treatments were well-tolerated.
Cortisol suppression was observed in 1 patient from each group.
Conclusions:
IMTA shows promising results, comparable in efficacy and safety to OMP-D for active vitiligo, achieving early disease stabilization and repigmentation.
IMTA represents a practical first-line alternative for active vitiligo management.
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