Plasma nevirapine levels, adverse events and efficacy of antiretroviral therapy among HIV-infected patients concurrently receiving nevirapine-based antiretroviral therapy and fluconazole

<p>Abstract</p> <p>Background</p> <p>The clinical data of plasma NVP level, safety and efficacy of antiretroviral therapy (ART) for the concurrent use of nevirapine (NVP)-based ART and fluconazole (FLU) is scanty.</p> <p>Methods</p> <p>A retrospe...

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Main Authors: Phoorisri Thanongsri, Uttayamakul Sumonmal, Athichathanabadi Chatiya, Manosuthi Weerawat, Sungkanuparph Somnuek
Format: Article
Language:English
Published: BMC 2007-03-01
Series:BMC Infectious Diseases
Online Access:http://www.biomedcentral.com/1471-2334/7/14
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spelling doaj-95624bc32cd548809b561fd7d828d4fd2020-11-25T01:42:42ZengBMCBMC Infectious Diseases1471-23342007-03-01711410.1186/1471-2334-7-14Plasma nevirapine levels, adverse events and efficacy of antiretroviral therapy among HIV-infected patients concurrently receiving nevirapine-based antiretroviral therapy and fluconazolePhoorisri ThanongsriUttayamakul SumonmalAthichathanabadi ChatiyaManosuthi WeerawatSungkanuparph Somnuek<p>Abstract</p> <p>Background</p> <p>The clinical data of plasma NVP level, safety and efficacy of antiretroviral therapy (ART) for the concurrent use of nevirapine (NVP)-based ART and fluconazole (FLU) is scanty.</p> <p>Methods</p> <p>A retrospective study was conducted in patients who were initiated NVP-based ART between October 2004 and November 2005. The objectives were to compare NVP levels, adverse events, and 36-week efficacy of NVP-based ART between patients who did not receive FLU (group A) and those who received FLU 200 mg/day or 400 mg/day (group B).</p> <p>Results</p> <p>There were 122 patients with mean ± SD age of 36 ± 9 years; 81 in group A and 41 in group B. Median (IQR) baseline CD4 cell count was 29 (8–79) cell/mm<sup>3 </sup>in group A and 19 (8–33) cell/mm<sup>3 </sup>in group B (<it>P </it>= 0.102). Baseline characteristics between the two groups were similar. Mean ± SD NVP levels were 6.5 ± 3.0 mg/L in group A and 11.4 ± 6.1 mg/L in group B(<it>P </it>< 0.001). One (2.4%) patient in group B developed clinical hepatitis (<it>P </it>= 0.336). Six (7.4%) patients in group A developed NVP-related skin rashes (<it>P </it>= 0.096). There were no differences in term of 36-week antiviral efficacy between the two groups (<it>P </it>> 0.05).</p> <p>Conclusion</p> <p>Co-administration of NVP and daily dosage of FLU (200 mg/day and 400 mg/day) results in markedly increased trough plasma NVP level when compared to the administration of NVP alone. The concurrent use of NVP and FLU in very advanced HIV-infected patients is well-tolerated. The immunological and virological responses are favorable.</p> http://www.biomedcentral.com/1471-2334/7/14
collection DOAJ
language English
format Article
sources DOAJ
author Phoorisri Thanongsri
Uttayamakul Sumonmal
Athichathanabadi Chatiya
Manosuthi Weerawat
Sungkanuparph Somnuek
spellingShingle Phoorisri Thanongsri
Uttayamakul Sumonmal
Athichathanabadi Chatiya
Manosuthi Weerawat
Sungkanuparph Somnuek
Plasma nevirapine levels, adverse events and efficacy of antiretroviral therapy among HIV-infected patients concurrently receiving nevirapine-based antiretroviral therapy and fluconazole
BMC Infectious Diseases
author_facet Phoorisri Thanongsri
Uttayamakul Sumonmal
Athichathanabadi Chatiya
Manosuthi Weerawat
Sungkanuparph Somnuek
author_sort Phoorisri Thanongsri
title Plasma nevirapine levels, adverse events and efficacy of antiretroviral therapy among HIV-infected patients concurrently receiving nevirapine-based antiretroviral therapy and fluconazole
title_short Plasma nevirapine levels, adverse events and efficacy of antiretroviral therapy among HIV-infected patients concurrently receiving nevirapine-based antiretroviral therapy and fluconazole
title_full Plasma nevirapine levels, adverse events and efficacy of antiretroviral therapy among HIV-infected patients concurrently receiving nevirapine-based antiretroviral therapy and fluconazole
title_fullStr Plasma nevirapine levels, adverse events and efficacy of antiretroviral therapy among HIV-infected patients concurrently receiving nevirapine-based antiretroviral therapy and fluconazole
title_full_unstemmed Plasma nevirapine levels, adverse events and efficacy of antiretroviral therapy among HIV-infected patients concurrently receiving nevirapine-based antiretroviral therapy and fluconazole
title_sort plasma nevirapine levels, adverse events and efficacy of antiretroviral therapy among hiv-infected patients concurrently receiving nevirapine-based antiretroviral therapy and fluconazole
publisher BMC
series BMC Infectious Diseases
issn 1471-2334
publishDate 2007-03-01
description <p>Abstract</p> <p>Background</p> <p>The clinical data of plasma NVP level, safety and efficacy of antiretroviral therapy (ART) for the concurrent use of nevirapine (NVP)-based ART and fluconazole (FLU) is scanty.</p> <p>Methods</p> <p>A retrospective study was conducted in patients who were initiated NVP-based ART between October 2004 and November 2005. The objectives were to compare NVP levels, adverse events, and 36-week efficacy of NVP-based ART between patients who did not receive FLU (group A) and those who received FLU 200 mg/day or 400 mg/day (group B).</p> <p>Results</p> <p>There were 122 patients with mean ± SD age of 36 ± 9 years; 81 in group A and 41 in group B. Median (IQR) baseline CD4 cell count was 29 (8–79) cell/mm<sup>3 </sup>in group A and 19 (8–33) cell/mm<sup>3 </sup>in group B (<it>P </it>= 0.102). Baseline characteristics between the two groups were similar. Mean ± SD NVP levels were 6.5 ± 3.0 mg/L in group A and 11.4 ± 6.1 mg/L in group B(<it>P </it>< 0.001). One (2.4%) patient in group B developed clinical hepatitis (<it>P </it>= 0.336). Six (7.4%) patients in group A developed NVP-related skin rashes (<it>P </it>= 0.096). There were no differences in term of 36-week antiviral efficacy between the two groups (<it>P </it>> 0.05).</p> <p>Conclusion</p> <p>Co-administration of NVP and daily dosage of FLU (200 mg/day and 400 mg/day) results in markedly increased trough plasma NVP level when compared to the administration of NVP alone. The concurrent use of NVP and FLU in very advanced HIV-infected patients is well-tolerated. The immunological and virological responses are favorable.</p>
url http://www.biomedcentral.com/1471-2334/7/14
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