Treatment of herpes zoster. Recombinant alpha interferon versus acyclovir

Int J Dermatol. 1988 Apr;27(3):193-7. doi: 10.1111/j.1365-4362.1988.tb04932.x.

Abstract

Sixty-four patients received systemic alpha-interferon (10 million units subcutaneously daily) and 63 received systemic acyclovir (5 mg/kg body weight intravenously thrice daily) in a randomized study of acute herpes zoster. Start of healing, complete healing, development of new skin lesions in the primarily affected and in other dermatomes, and degree and duration of pain were evaluated. Both drugs proved equally clinically efficient without statistically different findings between the two groups; herpes zoster neuralgia was not prevented by either interferon or acyclovir therapy. Minor clinical side effects occurred slightly more frequently during interferon treatment and included fever and nausea. Transient and moderate leukopenia was observed in nearly all patients in the interferon group.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Acyclovir / adverse effects
  • Acyclovir / therapeutic use*
  • Aged
  • Clinical Trials as Topic
  • Female
  • Fever / chemically induced
  • Herpes Zoster / drug therapy*
  • Humans
  • Interferon Type I / adverse effects
  • Interferon Type I / therapeutic use*
  • Leukopenia / chemically induced
  • Male
  • Middle Aged
  • Nausea / chemically induced
  • Random Allocation
  • Recombinant Proteins / therapeutic use

Substances

  • Interferon Type I
  • Recombinant Proteins
  • Acyclovir