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Re: 'tripple-scan' blood testFrom: Katya (anonymous@obgyn.net)Wed, 5 Mar 2003 22:00:44 -0600 (CST)
Dear Liz, Let me try to explain the triple screen business. Triple test is excellent for detecting trisomy 13 and spina bifida. However, it's a pretty lousy test to detect Down's syndrome. The reason it's used so widely is because it's the only Down's syndrome test, flaws and all, that presents no risk to the baby or to the mother. Basically, triple test is able to subdivide babies into 2 groups. The first group - about 5% of the population, I think - contains 60% of all the Down's syndrome cases. About 1% of the women in that small group carry babies afflicted with Down's syndrome. The second group - 95% of the population - contains the other 40% of Down's syndrome babies. So you (or anyone) can have a Down's syndrome baby even if the triple screen comes back with a low likelyhood for problems, it's just very unlikely. Since detecting Down's syndrome without amnio is so difficult, you take the worst possible predictive result you have (in your case, the ultrasound) and run with it. There are 2 other methods - CVS (you are too late for that) and amniosynthesis. Amnio carries a 1:200 miscarriage penalty, 1:1000 if done at by an experienced doctor a special facility (hint: do amnio in a special facility). Dr. Braun indicated that you have a 1-3:100 chance of having a Down's syndrome baby. If that's too high for you, then you can get amniosynthesis. If you can live with the risk, don't get amniosynthesis. OK, this may be more info than you need,
-- Katya (not a doctor, just a biochemist)
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