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Would you suggest a restart?

Posted: Jul 7, 2002

QUESTION:

Many of our patients are off meds due to side effects. For one pateint of mine it's been 10 months and I thought all is well,until I read this article below. Does this finding change your ideas on stopping meds? I copied the paragraph that discussed this and ommitted the entire artice.I hope you can offer an opinion on whether you would restart meds based only on this data:

NIH NEWS: HIV Selectively Suppresses Anti-HIV Defense Cells National Institute of Allergy and Infectious Diseases National Institutes of Health - Wednesday, May 1, 2002 Contact: Jeff Minerd, (301) 402-1663 - jminerd@niaid.nih.gov http://ww2.aegis.org/news/niaid/2002/NI020501.html This experiment shows that HIV continuously and preferentially infects mature HIV-specific helper T cells as they try to fight off the virus," say Dr. Koup. "In one patient, over half of all his infected CD4+ T cells were HIV-specific."

This finding means that clinicians should consider the possible negative consequences of structured therapy interruptions that allow virus levels to rebound, says lead study author Daniel Douek, M.D., Ph.D., chief of the VRC's Human Immunology Section. "Although short courses of structured intermittent therapy do not result in increased levels of HIV," he says, "longer regimens that permit the viral load to increase may result in long-term damage of the immune system's ability to fight off HIV."


  

RESPONSE FROM:   

    Thanks for your sage question.

    This is one of the most challenging areas of HIV medicine- namely the pros and cons of antiretroviral therapy for persons with relatively high CD4 cell counts.

    The article that you cite raises the point that with continuing CD4 cell depletion, there is very likely depletion of the very CD4 cells that recognize and therefore are responsible for attack of HIV-infected cells. This would raise the point that if one were to wait too long, the ability to reconstitute meaningful HIV-specific immunity wanes.

    There is also recent information that suggests that the risk of certain kinds of malignancies appear to increase with lower CD4 cell nadirs. This coupled to recent data (Lichtenstein, 2002) from the HOPS cohort that suggest that the risk of new development of lipoatrophy is related to CD4 count nadir (less than 200)would seem to point out that there are HIV-related complications that may increase, the longer one waits to initiate therapy (or waits to reinitiate therapy).

    Of course, the story is more complicated than just this. There is risk of other complications that relate to time on therapy, clearly the most significant (at least to me) is that of the developement of drug resistance. Adherence (or more importantly, risk of sub-optimal adherence) would be a strong factor in the decision to resume therapy or not. It is also very important that while on therapy, that you receive optimal counsel and monitoring about the therapy that you are on.

    In the end analysis, I don't think that we have definative answers as to the best approach for every person. In the absence of proof of global risks and benefits, I'll provide the best possible counsel and defer to patient's desires (this operates under the premise of patient autonomy). For patients like you who are a motivated, very adherent patient, and understand the risks and potential benefits of resuming therapy, I would have little reason not to support that decision (indeed, I have several patients in my practice who have done exactly that).

    I hope that this helps, good luck and stay in touch. BY




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