Treatment of human brucellosis with rifampin plus minocycline

J Chemother. 2003 Jun;15(3):248-52. doi: 10.1179/joc.2003.15.3.248.

Abstract

In order to evaluate the efficacy and tolerability of a high intravenous dose of rifampin plus oral minocycline (administered daily for 3 weeks) for the treatment of acute brucellosis, we retrospectively reviewed the outcome of 239 consecutive patients (135 adults and 104 children) diagnosed and treated over a 17-year period in Italy. The combination used resulted in 100% response and a relapse rate lower than 2%. Fifty-two (30 adults and 22 children) (29.8%) complained of mild adverse effects including an increase in aspartate aminotransferase (>250 IU) observed in 12 cases and considered related to rifampin and in 11 cases a reversible hyperpigmentation of the tongue attributed to minocycline. A randomized prospective comparative study should be performed to confirm our encouraging results.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Brucella / classification
  • Brucella / drug effects*
  • Brucellosis / diagnosis
  • Brucellosis / drug therapy*
  • Child
  • Child, Preschool
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Drug Therapy, Combination / administration & dosage*
  • Female
  • Follow-Up Studies
  • Humans
  • Infusions, Intravenous
  • Italy
  • Male
  • Middle Aged
  • Minocycline / administration & dosage*
  • Recurrence
  • Retrospective Studies
  • Rifampin / administration & dosage*
  • Risk Assessment
  • Treatment Outcome

Substances

  • Minocycline
  • Rifampin