Efavirenz challenge in patients with nevirapine induced Stevens-Johnson Syndrome

Background: Non-nucleoside reverse transcriptase inhibitors (NNRTI) are recommended as part of first-line treatment by the World Health Organisation (WHO) for antiretroviral treatment (ART) naïve subjects. Due to reports of cross-toxicity between nevirapine (NVP) and efavirenz (EFV), there is reluct...

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Main Authors: Thandekile C. Manzini, Bernadett I. Gosnell, Melanie-Anne A. John, Mahomed Y. S. Moosa
Format: Article
Language:English
Published: AOSIS 2016-12-01
Series:Southern African Journal of Infectious Diseases
Subjects:
Online Access:https://sajid.co.za/index.php/sajid/article/view/75
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spelling doaj-544c9d55578b487290dfe936b6f0f7592020-11-24T21:56:44ZengAOSISSouthern African Journal of Infectious Diseases2312-00532313-18102016-12-0131411912110.4102/sajid.v31i4.7567Efavirenz challenge in patients with nevirapine induced Stevens-Johnson SyndromeThandekile C. Manzini0Bernadett I. Gosnell1Melanie-Anne A. John2Mahomed Y. S. Moosa3Department of Infectious Diseases, University of KwaZulu-Natal, DurbanDepartment of Infectious Diseases, University of KwaZulu-Natal, DurbanEnhancing Care Foundation, South Africa, Department of Infectious Diseases, University of KwaZulu-Natal, DurbanDepartment of Infectious Diseases, University of KwaZulu-Natal, DurbanBackground: Non-nucleoside reverse transcriptase inhibitors (NNRTI) are recommended as part of first-line treatment by the World Health Organisation (WHO) for antiretroviral treatment (ART) naïve subjects. Due to reports of cross-toxicity between nevirapine (NVP) and efavirenz (EFV), there is reluctance to substitute EFV for NVP when serious toxicity occurs. In such cases lopinavir/ritonavir (LPV/r) remains the only alternative. We report on our experience of patients with Stevens-Johnson Syndrome (SJS) secondary to NVP who were challenged with EFV under careful supervision. Methods: A retrospective chart review of patients who presented with SJS presumed to be secondary to NVP who were challenged with EFV and were followed up for at least 2 months. Results: The study included 13 patients. All were female, median age 28 years and median weight 66.5 kg. The median CD4 cell count at ART initiation was 160 cells/μl. Twelve patients (92%) developed a rash within 4 weeks of NVP. The median alanine transaminase at SJS presentation was 30 U/l. The median time to EFV challenge was 30 days. The median hospital stay for SJS was 30 days and median follow up was 19 months. Eleven (85%) patients tolerated co-trimoxazole rechallenge, two had no prior exposure. Median hospital stay for EFV challenge was additional 10 days. Twelve patients (92%) tolerated the EFV challenge. One patient developed a pruritic maculo-papular eruption within 3 days of challenge which led to discontinuation of EFV. Conclusion: The risk of recurrence of SJS with EFV challenge in patients with NVP induced SJS is low. It is safe to challenge patients with EFV with careful observation.https://sajid.co.za/index.php/sajid/article/view/75efavirenznevirapinestevens-johnson syndrome
collection DOAJ
language English
format Article
sources DOAJ
author Thandekile C. Manzini
Bernadett I. Gosnell
Melanie-Anne A. John
Mahomed Y. S. Moosa
spellingShingle Thandekile C. Manzini
Bernadett I. Gosnell
Melanie-Anne A. John
Mahomed Y. S. Moosa
Efavirenz challenge in patients with nevirapine induced Stevens-Johnson Syndrome
Southern African Journal of Infectious Diseases
efavirenz
nevirapine
stevens-johnson syndrome
author_facet Thandekile C. Manzini
Bernadett I. Gosnell
Melanie-Anne A. John
Mahomed Y. S. Moosa
author_sort Thandekile C. Manzini
title Efavirenz challenge in patients with nevirapine induced Stevens-Johnson Syndrome
title_short Efavirenz challenge in patients with nevirapine induced Stevens-Johnson Syndrome
title_full Efavirenz challenge in patients with nevirapine induced Stevens-Johnson Syndrome
title_fullStr Efavirenz challenge in patients with nevirapine induced Stevens-Johnson Syndrome
title_full_unstemmed Efavirenz challenge in patients with nevirapine induced Stevens-Johnson Syndrome
title_sort efavirenz challenge in patients with nevirapine induced stevens-johnson syndrome
publisher AOSIS
series Southern African Journal of Infectious Diseases
issn 2312-0053
2313-1810
publishDate 2016-12-01
description Background: Non-nucleoside reverse transcriptase inhibitors (NNRTI) are recommended as part of first-line treatment by the World Health Organisation (WHO) for antiretroviral treatment (ART) naïve subjects. Due to reports of cross-toxicity between nevirapine (NVP) and efavirenz (EFV), there is reluctance to substitute EFV for NVP when serious toxicity occurs. In such cases lopinavir/ritonavir (LPV/r) remains the only alternative. We report on our experience of patients with Stevens-Johnson Syndrome (SJS) secondary to NVP who were challenged with EFV under careful supervision. Methods: A retrospective chart review of patients who presented with SJS presumed to be secondary to NVP who were challenged with EFV and were followed up for at least 2 months. Results: The study included 13 patients. All were female, median age 28 years and median weight 66.5 kg. The median CD4 cell count at ART initiation was 160 cells/μl. Twelve patients (92%) developed a rash within 4 weeks of NVP. The median alanine transaminase at SJS presentation was 30 U/l. The median time to EFV challenge was 30 days. The median hospital stay for SJS was 30 days and median follow up was 19 months. Eleven (85%) patients tolerated co-trimoxazole rechallenge, two had no prior exposure. Median hospital stay for EFV challenge was additional 10 days. Twelve patients (92%) tolerated the EFV challenge. One patient developed a pruritic maculo-papular eruption within 3 days of challenge which led to discontinuation of EFV. Conclusion: The risk of recurrence of SJS with EFV challenge in patients with NVP induced SJS is low. It is safe to challenge patients with EFV with careful observation.
topic efavirenz
nevirapine
stevens-johnson syndrome
url https://sajid.co.za/index.php/sajid/article/view/75
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