Refractory mucosal candidiasis in advanced human immunodeficiency virus infection

  • Carl J. Fichtenbaum
  • , Susan Koletar
  • , Constantin Yiannoutsos
  • , Fiona Holland
  • , John Pottage
  • , Susan E. Cohn
  • , Ann Walawander
  • , Peter Frame
  • , Judith Feinberg
  • , Michael Saag
  • , Charles Van der Horst
  • , W. G. Powderly

Research output: Contribution to journalArticlepeer-review

96 Scopus citations

Abstract

We conducted a multicenter, prospective study of the risk factors, natural history, and outcome of fluconazole-refractory mucosal candidiasis (FRMC) in 832 persons with advanced human immunodeficiency virus (HIV) infection (median CD4 cell count, 14/mm3) during 1994-1996. FRMC was defined as mucosal candidiasis that failed to resolve despite 14 days of therapy with daily doses (200 mg) of fluconazole. Thirty-six persons (4.3%) had FRMC (35, oral; 1, esophageal), for an incidence of 4.2 per 100 person-years (859.7 total years of follow-up). In a multivariate model, the use of trimethoprim-sulfamethoxazole within 6 months of enrollment (relative risk [RR], 2.39; P = .04) and the use of fluconazole daily or every other day (RR, 5.64; P = .004) were significantly associated with the development of FRMC. The median survival after the development of FRMC was 32.6 weeks. In conclusion, the annual incidence of FRMC was <5%. Refractory candidiasis was a poor prognostic indicator. Daily or every-other-day use of fluconazole was associated with the development of refractory infection.

Original languageEnglish
Pages (from-to)749-756
Number of pages8
JournalClinical Infectious Diseases
Volume30
Issue number5
DOIs
StatePublished - 2000

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