A few weeks ago I post a question about a probably exposure to blood from a HIV infected patient ( Superficial
cutCuts and puncture wounds on the
handHand or foot spasms
Hand tremor using gloves ). Your response was very
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Clear-atadine
Clear-atadine children's and alleviate my anxiety. I am agree with you that the new EIA assay can reduce dramatically the window period. The problem is that usually in USA the Labs don’t use the third generation test, and the CDC knows it, is that the reason for its official 6 months window period and the 97% of seroconversion at 3 months. I was tested with Labcorp And I was surprised when found that they use
firstFirst progesterone mc10
First progesterone mc5
First-progesterone vgs 100
First-progesterone vgs 200
First-progesterone vgs 25
First-progesterone vgs 400
First-progesterone vgs 50
First-testosterone
First-testosterone mc generation assay (This test uses a viral lysate as the
antigenCea
Histocompatibility antigen test
Hla-b27 antigen
Psa source and detects antibodies by specific immune binding and subsequent
colorColor blindness
Color blindness tests
Color vision test development (enzyme immunoassay (EIA) technology).
Check Labcorp webite: http://www.labcorp.com/datasets/labcorp/html/chapter/mono/se028900.htm
The third generation use the follow Methodology: ELISA III technology is the antigen sandwich method in which an enzyme (alkaline phosphatase or horseradish peroxidase) is conjugated to an HIV antigen (similar to the immobilized antigen on the solid phase). The antibody in the sample is "sandwiched" between two antigen molecules, one immobilized on the solid phase and one containing the enzyme.
So I think that in USA the window period is 6 months because the old test.
I did an extensive search and almost all the other countries around the world use a 3 months window period but they use third generation assay, is a public health law.
If you check in the officials health web sites of countries like Australia, UK, France, Germany, Sweden, Spain, New Zealand, Switzerland, South Africa, Chile, Argentina, Colombia, Mexico, Brazil, Denmark, Norway, Finland, China, etc. All this countries are using the third generation test and 3 months window period. Even some of this countries check always for HIV 1, 2 and Group O. ( Routine )
But in USA I don’t know why we are using the old test, maybe for occult economics or business reasons.
I was tested at 4,7 and 12 weeks (Negative) with the Labcorp EIA (first generation), I know that with a third generation is enough but that is not my case and maybe everybody here have the same situation. What is your opinion?
Thank you for your time
Interesting info:
http://www.phppo.cdc.gov/dls/ila/cd/cambodia0704/day1/3-UpdateOnHivTesting.ppt
http://www.faetc.org/PowerPoint/AAHIVM-Nov-1-2003/02-Kurtyka-HIV-Testing-and-Superinfection-11-01-03.ppt
http://www.aidsportugal.com/article.php?sid=980
http://www.phppo.cdc.gov/mlp/pdf/labhiv/MBusch.pdf
Check this journal
http://www.aidsonline.com/pt/re/aids/fulltext.00002030-200010200-00014.htm;jsessionid=DUANX2Yg1NjNADh7fDphQTJEGsJSkP13lgxGBDrOIUM0yn1Tckfx!-1932480194!-949856144!9001!-1
I called my lab today. They could not tell me what generation of the test they are using. The only thing they know for sure that it is an ELISA enzyme liked essay test. They said they consider their procedure are gold standard. I dont blame them for not knowing. They are chemists not doctors. They told me that they test for both HIV1-HIV2 by default. This made me feel that they are very up to date with this issue. I have the Doctor in this forum and Dr. Bob at theBody.com who are HIV experts. They said 12 week is conclusive. This is enough for me to believe in my 12 week result. I am HIV negative.
Most other websites indicate that a negative HIV test at 12 weeks is conclusive regardless of vintage. You are obviously HIV negative.
"we are using the latest automated CMIA (chemiluminescent microparticle immunoassay) technology for our Anti-HIV 1&2 screening. This ARC HIV Ag/Ab Combo assay will have better sensitivity and specificity for the simultaneous qualitative detection of HIV p24 antigen and antibodies to HIV type 1 (Group M & Group O) and/or HIV type 2, if comparing to other screening methods like the manual ELISA 3rd generation etc"
Is this test is standard ELISA test
How accurate after 5 weeks and a half, please?
How accurate after 5 weeks and a half, please?