Abstract
Poor adherence to combined antiretroviral therapy (cART) has been shown to be a major determinant of virologic failure, emergence of drug resistant virus, disease progression, hospitalizations, mortality, and health care costs. While high adherence levels can be achieved in both resource-rich and resource-limited settings following initiation of cART, long-term adherence remains a challenge regardless of available resources. Barriers to optimal adherence may originate from individual (biological, socio-cultural, behavioral), pharmacological, and societal factors. Although patients and providers should continuously strive for maximum adherence to cART, there is accumulating evidence that each class of antiretroviral therapy has specific adherence-drug resistance relationship characteristics allowing certain regimens more flexibility than others. There is not a universally accepted measure for cART adherence, since each method has distinct advantages and disadvantages including cost, complexity, accuracy, precision, intrusiveness and bias. Development of a real-time cART adherence monitoring tool will enable the development of novel, pre-emptive adherence-improving strategies. The application of these strategies may ultimately prove to be the most cost-effective method to reduce morbidity and mortality for the individual and decrease the likelihood of HIV transmission and emergence of resistance in the community.
Keywords:HIV,antiretroviral therapy adherence,virologic failure,drug resistance,outcomes,resource-rich and resource-limited settings,flexibility,complexity,real-time cART adherence monitoring tool,morbidity and mortality,cART,protease inhibitor,test and treat,HIV prevention strategies
Infectious Disorders - Drug Targets
Title: HIV Treatment Adherence, Drug Resistance, Virologic Failure: Evolving Concepts
Volume: 11Issue: 2
Author(s):Jean B. Nachega, Vincent C. Marconi, Gert U. van Zyl, Edward M. Gardner, Wolfgang Preiser, Steven Y. Hong, Edward J. Mills and Robert Gross
Affiliation:
Keywords:HIV,antiretroviral therapy adherence,virologic failure,drug resistance,outcomes,resource-rich and resource-limited settings,flexibility,complexity,real-time cART adherence monitoring tool,morbidity and mortality,cART,protease inhibitor,test and treat,HIV prevention strategies
Abstract: Poor adherence to combined antiretroviral therapy (cART) has been shown to be a major determinant of virologic failure, emergence of drug resistant virus, disease progression, hospitalizations, mortality, and health care costs. While high adherence levels can be achieved in both resource-rich and resource-limited settings following initiation of cART, long-term adherence remains a challenge regardless of available resources. Barriers to optimal adherence may originate from individual (biological, socio-cultural, behavioral), pharmacological, and societal factors. Although patients and providers should continuously strive for maximum adherence to cART, there is accumulating evidence that each class of antiretroviral therapy has specific adherence-drug resistance relationship characteristics allowing certain regimens more flexibility than others. There is not a universally accepted measure for cART adherence, since each method has distinct advantages and disadvantages including cost, complexity, accuracy, precision, intrusiveness and bias. Development of a real-time cART adherence monitoring tool will enable the development of novel, pre-emptive adherence-improving strategies. The application of these strategies may ultimately prove to be the most cost-effective method to reduce morbidity and mortality for the individual and decrease the likelihood of HIV transmission and emergence of resistance in the community.
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B. Nachega Jean, C. Marconi Vincent, U. van Zyl Gert, M. Gardner Edward, Preiser Wolfgang, Y. Hong Steven, J. Mills Edward and Gross Robert, HIV Treatment Adherence, Drug Resistance, Virologic Failure: Evolving Concepts, Infectious Disorders - Drug Targets 2011; 11 (2) .https://dx.doi.org/10.2174/187152611795589663
DOI https://dx.doi.org/10.2174/187152611795589663 | Print ISSN 1871-5265 |
Publisher Name Bentham Science Publisher | Online ISSN 2212-3989 |
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