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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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 |
work_keys_str_mv |
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