How many times have you started to have a conversation with someone about Hepatitis C only to have it blow up in your face? Have you ever heard someone say something about Hep C that didn't seem quite right to you? You were probably right something was amiss. A discussion about Hepatitis C can...
As per Wikipedia, the definition of a stigma is as follows: "Stigma is a word that originally means a "sign", "point", or "branding mark"." Wikipedia goes on to call stigma "A badge of shame, a physical mark of infamy or disgrace." Damn that w...
Recently, the CDC (Center for Disease Control) issued a statement that all Baby Boomers should be tested for Hepatitis C. The question often comes up as to why this particular segment of people is so vulnerable. What does being born between 1945 and 1965 have to do with Hepatitis C? What was di...
Buyer Beware! There are several snake oil salesmen out there who are claiming to have cured their own Hepatitis C with herbs, supplements and parking lot gravel. Okay, maybe not the parking lot gravel but it might as well be. What you need to remember is that there are two different types of...
Most every adult woman (and an occasional man) has enjoyed a manicure and a pedicure at a nail salon or spa. That 30 minute pedicure can be so relaxing but are you aware of the danger lurking in that nail salon? Although few individuals recognize the medical risks associated with this common pr...
Second-line antiretroviral therapy in South Africa achieves durable viral suppression in three-quarters of patients and is associated with an increase in CD4 cell count, investigators report in the online edition of the Journal of Acquired Immune Deficiency Syndromes. Therapy was based on a boosted protease inhibitor (lopinavir/ritonavir, Kaletra).
Unsurprisingly, adherence was associated with virological outcomes, with each 10% improvement in the rate of adherence more than doubling the chances of achieving an undetectable viral load.
An increasing proportion of people who have started HIV therapy in resource-limited settings have experienced first-line treatment failure. Second-line options are limited, and are usually based on a ritonavir-boosted protease inhibitor, which is taken in combination with two drugs in the NRTI class.
There is currently little information on the virological efficacy and durability of second-line treatment in poorer countries. However, it is important that this is established, and that an understanding is achieved of the factors associated with the effectiveness of such treatment.
“An improved understanding of second-line ART [antiretroviral therapy] in resource-limited settings will be critical in maximizing the durability of second-line regimens, preventing disease progression and reducing long-term AIDS-related mortality in high HIV-prevalence countries without access to third-line ART regimens,” explain the authors.
They therefore designed a study monitoring the outcomes of 136 patients who initiated second-line therapy in Durban, South Africa. This treatment consisted of lopinavir/ritonavir, which was taken in combination with two NRTIs (usually AZT and enteric-coated ddI). The investigators also conducted analyses to see which factors were associated with the efficacy of this treatment.
All the patients had experience of first-line therapy (usually efavirenz [Sustiva, Stocrin] with d4T and 3TC).
The median duration of first-line treatment was 13 months. At the time therapy was changed, the patients had a median CD4 cell count of 153 cells/mm3 and a median viral load of approximately 28,500 copies/ml.
Adherence in the six months before this therapy was discontinued had been poor. The median rate (calculated by pharmacy refill) was just 67%. The investigators believe that this low rate may have been partly due to the toxic effects of d4T, a drug which is no longer used in routine HIV therapy.
Switching to second-line treatment was associated with a significant improvement in adherence. In the first six months after the treatment change, the median rate of adherence was 100%. Adherence remained high throughout follow-up; the median rate at month 12 being 92%, which increased to 96% at month 24.
Almost three-quarters of patients (74%) had an undetectable viral load (below 50 copies/ml) six months after switching treatment. This rate of suppression changed little during the two years of the study.
Factors associated with viral suppression after twelve months of therapy were evaluated by the investigators. A higher rate of adherence was independently associated with an increased chance of an undetectable viral load at this time point. Each 10% increase in adherence more then doubled the chances of virological suppression (OR = 2.5; 95% CI, 1.3-4.8, p = 0.01).
Time to virological suppression was most rapid in patients who took 90% or more of their doses (p = 0.01).
Adherence of this level was associated with rates of virological suppression at months 6, 12, 18 and 24 of 73, 87, 93 and 97% respectively. In contrast, the rates of suppression at these time points for patients who took fewer than 80% of their doses were just 20, 44, 67 and 83% respectively.
Changing to second-line therapy also had immunological benefits. Median CD4 cell count increased to 228 cells/mm3 six months after switching therapy and continued to increase during follow-up, reaching a median of 330 cells/mm3 at month 24.
“The switch to second-line ART in South Africa was associated with an improvement in adherence and a rapid immunological recovery,” comment the authors.
However, they express concern that approximately one quarter of patients continued to have a detectable viral load. “Median adherence was not uniformly > 90% after initiation of second-line ART and differences in second-line adherence help explain why some patients… achieved virologic suppression after switch and other patients did not.”
They therefore conclude: “Novel adherence interventions may usefully target patients with second-line ART failure who – given a low likelihood of failure with major protease inhibitor resistance mutations – have a high likelihood of achieving viral suppression.”
Please sign the ATC Salvage Therapy Petition Join us in asking Congressman Alcee Hastings and Congresswomen Maxine Waters to send a ‘Dear Colleague’ letter to Anthony Fauci, Director of NIAID, asking for the federal facilitation of apricitabine (ATC). ATC is a phase III nucleoside reverse transcriptase inhibitor (NRTI) that has been shown to be safe and effective in treating people with HIV. It works against viruses that are resistant to several other nukes and could ...
Researchers from Johns Hopkins Children’s Center, the University of Mississippi Medical Center and the University of Massachusetts Medical School announced today at CROI2013 the discovery of the first infant functionally cured of HIV. The baby, a female now two and a half years old, received 3 HIV medications when brought to the hospital at 30 hours old. Viral load tests were performed during the first few weeks that showed a rapidly decreasing viral load which reached ...
At the 19th International AIDS Conference (AIDS 2012) in Washington D.C., the CDC reported that only 1 out of 4 HIV patients in the U.S. have HIV under control, which is defined as complete viral suppression. Warning bells should be ringing in the scientific and HIV advocacy communities. While much progress has been made in the last three decades in the treatment of HIV, tens of thousands of people living with HIV (PLWH) are currently struggling to construct viable treat...
Paige Rawl is 17 and HIV positive, but while her life has been shaped by HIV it isn't ruled by it. When Paige Rawl starts her senior year at Indianapolis’s Herron High School next month, she'll be cheer captain and a member of the student government and prom committee. This summer, the 17-year-old held down a part-time job at Hollister, hawking the popular Southern California-inspired clothing brand. The all-American girl — who happens to be HIV positive. Paige was in...
The HIV community has been abuzz with the August FDA approval of what had been termed “the Quad”, the second one-pill-once-a-day combination antiretroviral drug. Marketed by Gilead under the name Stribild, the drug contains two NRTIs (tenofovir and emtricitabine), an integrase inhibitor (elvitegravir) and an integrase booster (cobicistat) and is approved for use in treatment naïve patients with either drug resistant or wild type virus. In comparison to Atripla, the first...

Bristol-Myers Squibb Company (NYSE: BMY) today announced that the U.S. Food and Drug Administration (FDA) has approved a supplemental new drug application (sNDA) for SUSTIVA® (efavirenz), including dosing recommendations for...

California and other states would be pressured to amend or repeal criminal laws that single out HIV-positive people under a bipartisan bill co-authored and introduced this week by Rep. Barbara...
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At HIV Haven we wish to provide our readers with vital cutting edge information to help expand HIV knowledge and promote activism, particularly that which works towards an end to the HIV pandemic. It is our desire to bring to you the scientific, medical and social advances that given the appropriate attention and support, could change the course of the HIV pandemic, lessen the devastating effects of HIV and AIDS, better the quality and quantity of life for people living with HIV and even yield an eventual end to the HIV pandemic. We also provide the basics of HIV transmission and treatment.
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