Reports
for NATAP from the
|
7th Annual Conference of the British HIV Association (BHIVA) |
April
27-29, 2001
The Hove Centre, Brighton |
Ethnic and gender differences in non-nucleoside reverse transcriptase inhibitor (NNRTI)-induced rash
C Mazhude, S Jones, PJ Easterbrook, C Taylor The Caldecot Centre, Department of Genito-Urinary Medicine, Kings College Hospital, London, UK
Objective:
To determine the association of ethnic group and sex with the development of
NNRTI-induced rash in a multiethnic cohort of HIV-infected patients.
Methods:
Retrospective record analysis of all patients starting nevirapine (NVP)/efavirenz
(EFV) between Jan 1997 and Jan 2000. Sex, ethnic group and stage of disease
were analysed as potential risk factors for the development of the rash.
Results:
A total of 337 records were analysed, including 285 patients on NVP and 52 on
EFV. Of the 285 on NVP, 130 (46%) were white males, 93 (33%) black females,
48 (17%) black males and 9 (3%) white females. There was no significant difference
in disease stage between the various ethnic groups (24% black females had prior
AIDS-defining events vs. 19% of white males). Of the 285 on NVP, 21 (7%) developed
a rash, and two-thirds of these discontinued as a result. Of those that developed
a rash, 13 (62%) were black females, two (10%) white females, five (24%) white
males and one (5%) black male. Female sex was associated with the highest incident
risk of 15% (black women 14%, white women 22%) vs. 24% for males. Only
two patients with a rash had prior AIDS-defining events. Two-thirds were on
400 mg NVP when the rash occurred. The median time to rash was 15 days (range
239). Three patients developed a StevenJohnson type syndrome (two
black females, one white male). Of nine developing a rash on NVP and switching
to EFV, none had a recurrence. Of the 52 started on EFV, only one white male
developed a rash and the drug was stopped.
Conclusions:
The 7% incidence of rash in those starting NVP falls within ranges described
previously. Female sex is strongly associated with a higher risk of NVP-induced
rash. These data do not suggest a difference in the risk of NVP rash on the
basis of black/white ethnicity. (Commentary from Jules Levin: recent data reported
at the Pharmacology Workshop in the Netherlands suggests that body weight may
be crucial factor and possibly not gender. However, gender differences in pharmacokinetics
or other gender differences may also play a role. Interstingly, although authors
conclude there was no ethnic difference white women had less rash than black
women 62% vs 10%).
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