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Perspectives on HAART: switch maintenance therapy
1Regional Infectious Diseases Unit, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK.
Insights
Switching from protease inhibitors in highly active antiretroviral therapy (HAART) improves adherence and metabolic profiles. However, potential side effects like hypersensitivity and rashes necessitate careful patient selection for successful viral suppression.
Area of Science:
- Antiretroviral Therapy
- HIV Treatment Adherence
- Metabolic Syndrome in HIV
Background:
- Highly active antiretroviral therapy (HAART) regimens often include protease inhibitors (PIs).
- Discontinuing PIs can improve patient adherence and quality of life.
- Metabolic complications are a concern in patients on long-term HAART.
Purpose of the Study:
- To evaluate the impact of switching from PIs in HAART on adherence, metabolic profiles, and virological suppression.
- To identify patient subgroups who may benefit from PI discontinuation.
- To assess the potential risks and benefits of switching antiretroviral therapy components.
Main Methods:
- Review of switch studies comparing PI-based HAART with alternative regimens.
- Analysis of adherence data, metabolic parameters (insulin resistance, triglycerides), and virological outcomes.
- Assessment of side effect profiles associated with PI discontinuation and alternative drug classes.
Main Results:
- Switching from PIs is associated with improved adherence and quality of life.
- A trend towards improved metabolic profiles, particularly reduced insulin resistance and triglyceride levels, is observed after PI discontinuation.
- Virological suppression can be maintained if achieved for at least six months prior to the switch and in patients without prior suboptimal HAART exposure.
- Peripheral wasting is linked to nucleoside analogues, and modification of HAART is not recommended for isolated fat accumulation.
Conclusions:
- Discontinuing PIs in HAART can enhance adherence and metabolic health while preserving virological suppression in selected patients.
- Switching may preserve PIs for future use.
- Potential side effects of switching include hypersensitivity, rashes, and hepatic or neuropsychiatric events, requiring careful monitoring.
Abstract:
Switch studies have been carried out to explore changes in side effects in adherence. Discontinuing the protease inhibitor (PI) component of highly active antiretroviral therapy (HAART) regimen is often associated with improved adherence and improved quality of life. Following switching from a PI to a non-nucleoside reverse transcriptase inhibitor or abacavir, there is however a clear trend toward an improved metabolic profile particularly in insulin resistance and triglyceride levels when patients discontinue their PI. Peripheral wasting is likely to be associated with nucleoside analogues and for individuals with isolated fat accumulation, modification of HAART is not recommended. Virological suppression can be maintained following switch if adequate suppression of the virus has been achieved for at least six months prior to switch and the patient has not been previously exposed to suboptimal HAART. Discontinuing the PI preserves this class of agents for future use. Switching however may be associated with other side effects; hypersensitivity, skin rashes, hepatic or neuropsychiatric events.
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