Literature DB >> 12793844

Low nevirapine plasma concentrations predict virological failure in an unselected HIV-1-infected population.

Theodora E M S de Vries-Sluijs1, Jeanne P Dieleman, Dennis Arts, Alwin D R Huitema, Jos H Beijnen, Martin Schutten, Marchina E van der Ende.   

Abstract

OBJECTIVE: To assess the relationship between plasma nevirapine concentrations and plasma HIV-1 RNA response in HIV-1-infected patients.
DESIGN: An observational cohort analysis.
METHODS: Plasma samples were obtained on a routine basis from 189 patients receiving nevirapine 200mg twice daily, and plasma nevirapine concentrations were measured with reversed phase high performance liquid chromatography. Patients were divided into two groups based on plasma nevirapine concentrations below (and equal to) or above 3 mg/L. The association between steady-state nevirapine concentrations and plasma HIV-1 RNA was determined by multivariate analysis.
RESULTS: Out of 189 patients, 13 (7%) had low nevirapine plasma concentrations and 176 patients had concentrations above 3 mg/L. In total, 22 (12%) patients showed virological failure and 8 patients (4%) discontinued nevirapine because of adverse effects. The risk of failure in patients with nevirapine plasma concentrations </=3mg/L was increased (relative risk 5.0, 95% CI 1.8-13.7). Rashes and liver enzyme elevations each occurred in 8% of patients.
CONCLUSIONS: Low nevirapine drug concentrations are predictive of virological failure.

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Year:  2003        PMID: 12793844     DOI: 10.2165/00003088-200342060-00009

Source DB:  PubMed          Journal:  Clin Pharmacokinet        ISSN: 0312-5963            Impact factor:   6.447


  18 in total

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3.  Study finds AIDS patients live longer when their doctors have more experience treating HIV.

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Authors:  P T Nieuwkerk; M A Sprangers; D M Burger; R M Hoetelmans; P W Hugen; S A Danner; M E van Der Ende; M M Schneider; G Schrey; P L Meenhorst; H G Sprenger; R H Kauffmann; M Jambroes; M A Chesney; F de Wolf; J M Lange
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5.  Experience with nevirapine in previously treated HIV-1-infected individuals.

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6.  Hepatotoxicity in HIV-1-infected patients receiving nevirapine-containing antiretroviral therapy.

Authors:  E Martínez; J L Blanco; J A Arnaiz; J B Pérez-Cuevas; A Mocroft; A Cruceta; M A Marcos; A Milinkovic; M A García-Viejo; J Mallolas; X Carné; A Phillips; J M Gatell
Journal:  AIDS       Date:  2001-07-06       Impact factor: 4.177

7.  The effect of plasma drug concentrations on HIV-1 clearance rate during quadruple drug therapy.

Authors:  R M Hoetelmans; M H Reijers; G J Weverling; R W ten Kate; F W Wit; J W Mulder; H M Weigel; P H Frissen; M Roos; S Jurriaans; H Schuitemaker; F de Wolf; J H Beijnen; J M Lange
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Authors:  David M Burger; Patricia W H Hugen; Rob E Aarnoutse; Richard M W Hoetelmans; Marielle Jambroes; Pythia T Nieuwkerk; Gerrit Schreij; Margriet M E Schneider; Marchina E van der Ende; Joep M A Lange
Journal:  Ther Drug Monit       Date:  2003-02       Impact factor: 3.681

9.  Rapid determination of nevirapine in human plasma by ion-pair reversed-phase high-performance liquid chromatography with ultraviolet detection.

Authors:  R P van Heeswijk; R M Hoetelmans; P L Meenhorst; J W Mulder; J H Beijnen
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10.  High-dose nevirapine: safety, pharmacokinetics, and antiviral effect in patients with human immunodeficiency virus infection.

Authors:  D Havlir; S H Cheeseman; M McLaughlin; R Murphy; A Erice; S A Spector; T C Greenough; J L Sullivan; D Hall; M Myers
Journal:  J Infect Dis       Date:  1995-03       Impact factor: 5.226

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Authors:  Karen Dahri; Mary H H Ensom
Journal:  Clin Pharmacokinet       Date:  2007       Impact factor: 6.447

Review 4.  Pharmacokinetic optimization of antiretroviral therapy in children and adolescents.

Authors:  Michael N Neely; Natella Y Rakhmanina
Journal:  Clin Pharmacokinet       Date:  2011-03       Impact factor: 6.447

5.  Suboptimal nevirapine steady-state pharmacokinetics during intrapartum compared with postpartum in HIV-1-seropositive Ugandan women.

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6.  Determinants of virological outcome and adverse events in African children treated with paediatric nevirapine fixed-dose-combination tablets.

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Review 8.  Dose adjustment of the non-nucleoside reverse transcriptase inhibitors during concurrent rifampicin-containing tuberculosis therapy: one size does not fit all.

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9.  Pharmacokinetic and safety evaluation of BILR 355, a second-generation nonnucleoside reverse transcriptase inhibitor, in healthy volunteers.

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10.  Novel method to assess antiretroviral target trough concentrations using in vitro susceptibility data.

Authors:  Edward P Acosta; Kay L Limoli; Lan Trinh; Neil T Parkin; Jennifer R King; Jodi M Weidler; Ighovwerha Ofotokun; Christos J Petropoulos
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