Literature DB >> 20505782

Patient Characteristics and Treatment Outcome Associated with Protease Inhibitor (PI) use in the Asia-Pacific Region.

Sanjay Pujari1, Preeyaporn Srasuebkul, Somnuek Sungkanuparph, Poh Lian Lim, Nagalingeswaran Kumarasamy, John Chuah, Ritesh N Kumar, Yi-Ming A Chen, Shinichi Oka, Jun Yong Choi, Man-Po Lee, Praphan Phanuphak, Adeeba Kamarulzaman, Christopher Lee, Zhang Fujie, Rosanna Ditangco, Vonthanak Saphonn, Thira Sirisanthana, Tuti Parwati Merati, Jeff Smith, Matthew G Law.   

Abstract

OBJECTIVES: Regimens containing protease inhibitors (PI) are less commonly used in developing countries due to high cost and less availability. We evaluated characteristics of patients initiating PI-based therapy according to previous antiretroviral (ARV) exposure; factors associated with initiating a PI-containing regimen using newer versus older PIs, and proportion of patients with detectable viral loads (VL) after initiating a PI-based regimen.
METHODS: This analysis includes all patients who have initiated a PI-based regimen. ARV exposure was categorised: naïve (no previous ARV), 1st, 2nd, >/= 3rd switches; a switch was defined as starting or stopping any drug in a regimen. Newer PIs were defined as those approved by the US FDA after 1 January 2000. Detectable VL at 12 months was defined as VL >/= 400 copies/mL. Characteristics at PI initiation were evaluated. Logistic regression was used to determine factors associated with initiating a newer PI and detectable VL at 12 months after PI initiation.
RESULTS: 1106 patients initiated PI-based therapy; of these, 618 (56%) were naïve patients. Overall, 22% (176) of patients had detectable VL at 12 months following the PI initiation. Being from a high income country (vs. mid/low income, OR = 1.80, p = 0.034) were more likely to be associated with detectable VL.
CONCLUSION: The use of PIs in this cohort is dictated by accessibility and affordability issues particularly for the newer PIs. Short-term virological outcomes following PI-therapy in our cohort were good, and were associated with CD4 count at time of initiation.

Entities:  

Year:  2009        PMID: 20505782      PMCID: PMC2875551          DOI: 10.4172/jaa.1000004

Source DB:  PubMed          Journal:  J Antivir Antiretrovir


  24 in total

1.  Efficacy and safety of indinavir/ritonavir 400/100 mg twice daily plus two nucleoside analogues in treatment-naive HIV-1-infected patients with CD4+ T-cell counts <200 cells/mm3: 96-week outcomes.

Authors:  Piroon Mootsikapun; Ploenchan Chetchotisakd; Siriluck Anunnatsiri; Parichat Boonyaprawit
Journal:  Antivir Ther       Date:  2005

2.  Drug resistance after failure of initial antiretroviral therapy in resource-limited countries.

Authors:  Joel E Gallant
Journal:  Clin Infect Dis       Date:  2006-12-27       Impact factor: 9.079

Review 3.  Antiretroviral therapy : optimal sequencing of therapy to avoid resistance.

Authors:  Jorge L Martinez-Cajas; Mark A Wainberg
Journal:  Drugs       Date:  2008       Impact factor: 9.546

4.  Mortality in the highly active antiretroviral therapy era: changing causes of death and disease in the HIV outpatient study.

Authors:  Frank J Palella; Rose K Baker; Anne C Moorman; Joan S Chmiel; Kathleen C Wood; John T Brooks; Scott D Holmberg
Journal:  J Acquir Immune Defic Syndr       Date:  2006-09       Impact factor: 3.731

5.  Durable efficacy of tipranavir-ritonavir in combination with an optimised background regimen of antiretroviral drugs for treatment-experienced HIV-1-infected patients at 48 weeks in the Randomized Evaluation of Strategic Intervention in multi-drug reSistant patients with Tipranavir (RESIST) studies: an analysis of combined data from two randomised open-label trials.

Authors:  Charles B Hicks; Pedro Cahn; David A Cooper; Sharon L Walmsley; Christine Katlama; Bonaventura Clotet; Adriano Lazzarin; Margaret A Johnson; Dietmar Neubacher; Douglas Mayers; Hernan Valdez
Journal:  Lancet       Date:  2006-08-05       Impact factor: 79.321

6.  Predictors of incomplete adherence, virologic failure, and antiviral drug resistance among HIV-infected adults receiving antiretroviral therapy in Tanzania.

Authors:  Habib O Ramadhani; Nathan M Thielman; Keren Z Landman; Evaline M Ndosi; Feng Gao; Jennifer L Kirchherr; Rekha Shah; Humphrey J Shao; Susan C Morpeth; Jonathan D McNeill; John F Shao; John A Bartlett; John A Crump
Journal:  Clin Infect Dis       Date:  2007-10-22       Impact factor: 9.079

7.  Initiating highly active antiretroviral therapy with newer protease inhibitors is associated with better survival compared to first-generation protease inhibitors or nevirapine.

Authors:  Heidi M Crane; Stephen E Van Rompaey; Mari M Kitahata
Journal:  AIDS Patient Care STDS       Date:  2007-12       Impact factor: 5.078

8.  Prevalence of HIV-1 drug resistance after failure of a first highly active antiretroviral therapy regimen in KwaZulu Natal, South Africa.

Authors:  Vincent C Marconi; Henry Sunpath; Zhigang Lu; Michelle Gordon; Kofi Koranteng-Apeagyei; Jane Hampton; Steve Carpenter; Janet Giddy; Douglas Ross; Helga Holst; Elena Losina; Bruce D Walker; Daniel R Kuritzkes
Journal:  Clin Infect Dis       Date:  2008-05-15       Impact factor: 9.079

9.  Virological response to darunavir/ritonavir-based regimens in antiretroviral-experienced patients (PREDIZISTA study).

Authors:  Isabelle Pellegrin; Linda Wittkop; Laurence Morand Joubert; Didier Neau; Diane Bollens; Mojgan Bonarek; Pierre-Marie Girard; Hervé Fleury; Bart Winters; Marie-Claude Saux; Jean-Luc Pellegrin; Rodolphe Thiébaut; Dominique Breilh
Journal:  Antivir Ther       Date:  2008

10.  Evolution of drug resistance in HIV-infected patients remaining on a virologically failing combination antiretroviral therapy regimen.

Authors:  Alessandro Cozzi-Lepri; Andrew N Phillips; Lidia Ruiz; Bonaventura Clotet; Clive Loveday; Jesper Kjaer; Helene Mens; Nathan Clumeck; Ludmila Viksna; Francisco Antunes; Ladislav Machala; Jens D Lundgren
Journal:  AIDS       Date:  2007-03-30       Impact factor: 4.177

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