Apr 3, 2006
I found out my husband is HIV positive. We have had unprotected sex through out our marriage. I have tested 2, 4, 12 weeks post last exposure. These tests were all negative. Do I need to continue to test or is the confirming my negative status. My first test was via donating blood - I was not aware that my husband was positive at this time. Is it true that the blood bank uses a very specific test? My last test at 12 weeks was an p24 and elisa both neg. I am still worried. It was a big surprise with his diagnosis - not expected as he is a healthcare worker and probably got it from a patient. How is it that some get the virus and other's don't? Thanks for a reply.Questions related to HIV transmission, prevention, safer sex, HIV testing and risk should be sent to Dr. Bob at his "Safe Sex and HIV Prevention" expert forum. Please resubmit your question there using the same title and add the phrase, "resubmitted form the Fatigue and Anemia Forum." Thank you.
| Response from Dr. Frascino
For significant HIV exposures, such as your multiple unprotected sex acts with your husband who has now been confirmed to be HIV positive, the CDC recommends a repeat HIV-antibody test at the six-month mark. Certainly your multiple HIV tests up to 12 weeks are very, very encouraging. Regarding blood bank testing, I addressed this question recently and will repost my response from the archives below. As for why some people get HIV and others don't, that's a very complex issue involving both viral factors (viral strain, viral load, etc) and host factors (route of exposure, immune response, etc.). A complete discussion would be beyond the scope of this forum.
Finally, I'm glad you found the right forum to post your question.
Good luck to both you and your husband. Please make sure your husband knows about this site. There's a wealth of information here that might be helpful to you both.
Safe blood transfusion v. Window period Mar 25, 2006
Hi Doc! I have heard that places that accept blood (for storage and transfusion) can know if the blood is infected even if the person donating is at his/her window period. Then why don't they use this technology to straight-away determine if a person is Hiv+ or not? My second question: After sustaining a severe hollow-bore needlestick and laceration while performing a medical procedure on a patient, were you on PEP? Thanks.
Response from Dr. Frascino
The answer to your first question is a bit complex and technical, but I'll try to explain.
Blood donors have been screened for HIV since 1985. Although newer generations of the test have been developed that increase the sensitivity for detecting HIV antibodies, in rare instances infections in donors have been missed. In 2002 the FDA licensed the first NAT (nucleic acid test) for screening blood donors. NAT detects viral genes rather than anti-HIV antibodies or antigens (proteins from the virus). Viral gene detection allows for earlier detection, because the production of detectable antibodies, which is an immune response, requires time. With the use of NAT, the HIV window period has been reduced to approximately 16 days. NAT is FDA-approved only for use in screening donated blood. It is not approved for routine HIV screening for individual patients. There are a number of reasons for this having to do with the sensitivity/specificity of the testing assay and the cost. The purpose of blood-donation screening is to protect the blood supply. Consequently the sensitivity of the screening tests is set so that it will err on the side of protecting the blood supply. In other words, if the test picks up some false positives, no problem. The questionably positive blood can then be discarded. Donors are notified to follow up with their doctors to see if their test was a false positive or if they are truly HIV infected. Again the primary purpose of these tests is not to diagnose patients, but to protect the blood supply. NAT is also extremely expensive. NAT testing is performed on pooled samples. That means usually around 20 donor samples are mixed together and tested as a batch. If the batch tests positive, then each of the 20 donor samples is tested individually by our usual serological testing methods. See, I told you this was a bit confusing.
As for your second question, my occupational exposure was in January 1991. We didn't know much about PEP back then and only a few antiretrovirals were even available. I did take AZT within moments of being stuck and continued it for a full course, but seroconverted nonetheless. The patient I was performing the procedure on had advanced-stage AIDS; consequently, his viral strain was probably resistant to AZT. We didn't have resistance tests back then. I should also point out that PEP, even when taken as directed, isn't always successful in preventing HIV infection.
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