skip nav
National Prevention Information Network
Search Help
Other Searches: Search Organizations | Search Materials | Search Campaign Resources | Search Funding
español
Share Share this page on Twitter Share this page on Facebook Share this page on LinkedIn View more options to share this page E-mail this page to a colleague Print this page


<< Back

News

Simplifying HAART Regimen Fails to Maintain HIV-1 Viral Suppression

Abstract
A pilot study by Harold P. Katner, MD, of Mercer University School of Medicine in Macon, Ga., and colleagues assessed the durability of HIV-1 virologic suppression in persons who changed from a lopinavir/ritonavir-based triple highly active antiretroviral therapy (HAART) regimen once or twice a day to lopinavir/ritonavir monotherapy once daily. This was an observational cohort study to determine the proportion of subjects who sustained virologic suppression through the 48th week following their switch to the daily lopinavir/ritonavir monotherapy. Researchers presented the study at IDWeek 2012, a joint meeting of the Infectious Diseases Society of America (IDSA), the Society for Health and Epidemiology of America (SHEA), the HIV Medicine Association (HIVMA), and the Pediatric Infectious Diseases Society (PIDS). A total of 13 individuals began lopinavir/ritonavir-based HAART therapy and maintained HIV-1 viral loads ?75 copies/mL) for 48 weeks before enrollment in the study; three failed screening—two due to elevated viral loads and one because of an inability to tolerate lopinavir/ritonavir daily. The research continued with 10 individuals, two female and six male African Americans and one male and one female Caucasian. Subjects were 27–53 years old, and the mean duration of their therapy before de-escalation was 252 weeks (105–413 weeks). Mean CD4 count at baseline was 338 cells/m3 (range 120–512 cells/m3). Subjects received frequent clinical, virologic, and immunologic monitoring. One subject completed 48 weeks of daily lopinavir/ritonavir monotherapy and one withdrew at 22 weeks after experiencing two detectable viral loads five weeks apart. Four subjects had virologic failure, one of whom developed multiple nucleoside and protease inhibitor mutations. The study was terminated. None of the subjects reported severe adverse events.
Source
http://www.empr.com
Date of Publication
10/21/2012
Author
Debra Hughes
Article Type
General media
Article Category
Medical News

Disclaimer: NPIN provides this information as a public service only. The views and information provided about the materials, funding opportunities, and organizations do not necessarily state or reflect those of the U.S. Department of Health and Human Services, CDC, or NPIN.

cdcnpin.org News Record #60629

<< Back

CDCNPIN.org

Contact Us
About Us
HIV Content Notice
Privacy Policy
Policies & Disclaimers
Site Index
Help Using the CDC NPIN Web Site

CDC NPIN Searches

Search Organizations
Search Materials
Search Funding Opportunities
Search Campaign Resources
Help Using the CDC NPIN Searches

CDC NPIN Resources

hivtest.cdc.gov
m.hivtest.cdc.gov
findtbresources.org
STD Awareness Microsite
findstdtest.org
AIDS Gov Logo and Link CDC Logo and Link