|Happy New Year! Dr. Bob, ($100 dollars donation)..Please help me with this question being asked three times w/o responses....please help me before conducting more test next week..PLEASE
Jan 3, 2010
Please disregard my earlier question, i wanna donate $100 dollars, not 50 dollars......Sorry to keep writing you this question in the post. I haven't had any responses from you. I know, now, it is new year weekend, i really hope to see your responses before conducting more tests next week....please...
After a possible exposure in late July (fully protected oral/insert sex, likely exposure: a few vaginal fluid reaching(by fingers) the wounds(a few, average size is 0.1 inch by 0.1 inch) due to skin rash on my back thigh, with a few blood 20+ minutes before sex).
I only used FDA approved whole blood Rapid test(Clearview h1/2 stat pak) to test in week 13, 18, 20 and 22.5. They all came negative. Since my likely exposure was in Macao, China, i noticed the common HIV subtypes(A,C,E(or CRFA/E)) there are different as the subtype(B) in the States. Therefore, i have several questions need your professional advices, 1) can modern "Rapid Test" approved by FDA and used in the States detect the antibodies produced by most common HIV-1 group M antibodies? 2) I found out the product instruction of Clearview H1/2 Stat Pak, the website is http://www.invernessmedicalpd.com/pdf/Clearview%20HIV%201-2%20STAT-PAK%20PI_05904.03.pdf" IN page 13&14, it addresses some subtypes that have been evaluated using this assay, I noticed the testes can detect the antibodies produced by individual subtype A and E. If the assay can detect the antibodies produced by individual A and E subtypes, does it mean it can detect CRF A/E? 3)Is different HIV subtype causing different window period? or the conservative window period for all known subtypes is three month? 4)What generation the Clearview H1/2 Stat Pak is? Can my result be conclusive? Do i need more test methods other than rapid test?
i will make a donation ($100 dollars) to your foundation this month. I want to appreciate your answer first and then write you back when i make the donation.
wish you best!! Andy
| Response from Dr. Frascino
2. It detects it as well as other comparable FDA-approved antibody tests.
3. No. The window period is the same.
4. Clearview HIV 1/2 would be a third generation test. (Fourth generation tests combine a p24 antigen test with the antibody test.) Yes, your repeatedly negative results out to 22.5 weeks would be considered definitive and conclusive. Your HIV exposure risk was negligible.
Thank you for your donation to The Robert James Frascino AIDS Foundation (www.concertedeffort.org).
Happy New Year!
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