Publication:
Incidence and risk factors of rash associated with efavirenz in HIV-infected patients with preceding nevirapine-associated rash

dc.contributor.authorWeerawat Manosuthien_US
dc.contributor.authorS. Thongyenen_US
dc.contributor.authorN. Chumpathaten_US
dc.contributor.authorK. Muangchanaen_US
dc.contributor.authorS. Sungkanuparphen_US
dc.contributor.otherThailand Ministry of Public Healthen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-08-20T07:00:52Z
dc.date.available2018-08-20T07:00:52Z
dc.date.issued2006-09-01en_US
dc.description.abstractObjective: To determine the incidence and risk factors of rash associated with efavirenz in HIV-infected patients with preceding nevirapine-associated rash. Methods: A retrospective cohort study was conducted in HIV-infected patients diagnosed with nevirapine-associated rash who subsequently received efavirenz between July 2003 and January 2005. Patients were followed up for 3 months after receiving efavirenz. Possible risk factors, including demographics, previous opportunistic infections, CD4 cell count, viral load, severity of nevirapine-associated rash and concurrent drugs, were studied and compared between those who had (group A) and did not have (group B) rash associated with efavirenz. Results: A total of 122 patients (52.5% male) were included in the study, with a mean age of 38.2 years. Median (and interquartile range) CD4 cell count and viral load were 55 (20-167) cells/μL and 86 150 (35 321-700 750) HIV-1 RNA copies/mL, respectively. Of the 122 patients, 10 (8.2%) developed rash associated with efavirenz and all required discontinuation of efavirenz. The baseline characteristics of group A (10 patients) and group B (112 patients) were similar. Median (and interquartile range) time from nevirapine discontinuation to efavirenz initiation was 12 (9-21) days in group A and 11 (7-21) days in group B (P = 0.765). None of the risk factors investigated was associated with developing rash associated with efavirenz. The preceding development of severe nevirapine-associated rash had a trend towards a higher rate in group A than in group B (20.0% vs 10.7%; odds ratio = 2.08; 95% confidence interval 0.39-10.97; P = 0.322). Conclusions: The majority (>90%) of HIV-infected patients with CD4 counts <200 cells/μL who had preceding nevirapine-associated rash could tolerate efavirenz well. Efavirenz may be an option for subsequent use in these patients, particularly in those who had preceding nevirapine-associated rash. © 2006 British HIV Association.en_US
dc.identifier.citationHIV Medicine. Vol.7, No.6 (2006), 378-382en_US
dc.identifier.doi10.1111/j.1468-1293.2006.00396.xen_US
dc.identifier.issn14681293en_US
dc.identifier.issn14642662en_US
dc.identifier.other2-s2.0-33746450002en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/23310
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33746450002&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleIncidence and risk factors of rash associated with efavirenz in HIV-infected patients with preceding nevirapine-associated rashen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33746450002&origin=inwarden_US

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