|Re:rash as a die-off effect
Feb 24, 2002
Thanks for your prompt reply. I have been 100 on with the meds only missing by an hour a couple of times a week. I also don't do drugs, alcohol or smoke and try and maintain a healthy diet. I will get a susceptibility test as soon as my viral load goes over 1000. My doctor tells me that it is not accurate under 1000. Is that not correct? I too suspected the Sustiva but was assured that it was more likely the Combivir. The rash lasted for two weeks after I stopped meds and then cleared for a week and returned full force for another bout. It then gradually cleared and is now gone. This seemed to fit more with a drug that stays in the system longer. This is also the first time I have had an alergic reaction to any drug. I now take Sustiva with Zerit and Epivir and have no side effects at the moment. This would, of course, mean it was the AZT or that the rash was only an inital reaction that has gone away. I guess the reson I was asking was that I am concerned that the virus is gradually building up a resistance to those meds and was considering trying Sustiva and Combivir again since the <400 seemed to come from the first two drugs. Sorry to take up your time again but would really appreciate any further thoughts?
| Response from Dr. Young
Thanks for your question.
In commercial labs, one cannot obtain sufficient viral material to do resistance testing with viral loads less than 1000 copies. This does not mean that technically that it cannot be done, nor does it necessarily mean that the results are unreliable.
As for your drugs, I believe that d4T and ZDV are roughly equivalent from a potency standpoint (though, if anything, d4T might be a little more potent and should be expected to have a greater viral effect). In either case, since the resistance mutations associated with resistance to d4T are essentially the same as those for ZDV; loss of susceptibility to one drug likely means the same for the other.
In the regimen of ZDV (or d4T) with 3TC and efavirenz, one could expect that if resistance was emerging, that the first mutations to arise would be associated with efavirenz resistance (K103N, for example) and soon thereafter 3TC (M184V); resistance to the thymidine analogues (ZDV and d4T) typically arise later.
I think that in the final analysis; I'd certaily keep up the excellent adherence; but we'd need to look at repeat viral loads and your viral resistance profile before making any concrete decisions. Good luck, BY
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