Comparative genomic hybridization, a widely used method for screening for genomic imbalances, suffers from a lack of standardized evaluation. In order to compare a recently proposed data-driven procedure with the commonly used fixed cutoff values, we tested 257 events by both procedures as well as b
False positive results in a neuroblastoma screening programme
β Scribed by Bell, Susan ;Parker, Louise ;Craft, Alan W. ;Dale, Gordon ;McGill, Andrew C. ;Seviour, John ;Cole, Michael ;Smith, Julian
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 347 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0098-1532
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Twenty thousand, eight hundred and twentyβnine babies were screened for neuroblastoma at 6 months of age by measuring homovanillic (HVA) and vanillylmandelic (VMA) acid in urine and ratioing these to creatinine. Using a βcut offβοΈ of the mean + 3 SD, 10 were found to be positive. Two were found on evaluation to have neuroblastoma and in the remaining 8 the raised levels of HVA and/or VMA returned to normal. Only one of the 8 false positive babies was absolutely normal, most having a chronic disorder or illness. Utilising new centiles which relate HVA and VMA to creatinine, only 3 of the 8 would have remained positive, a false positive rate of 0.01%. The false negative rate would have remained unchanged.
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