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1.
Prenat Diagn ; 25(9): 740-5, 2005 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-16170842

RESUMEN

Prenatal screening and diagnosis in a twin pregnancy is not straightforward. Once a twin pregnancy has been identified, women and their partners need time to consider the implications and decide whether they wish the pregnancy to be screened for Down syndrome or neural tube defects. We discuss here how multiple marker screening for Down syndrome and alpha-fetoprotein screening for neural tube defects can be carried out, given that this is the parents' chosen option and that the health professionals involved are capable of performing a diagnosis and selective feticide, should this arise.


Asunto(s)
Síndrome de Down/diagnóstico , Defectos del Tubo Neural/diagnóstico , Diagnóstico Prenatal , Gemelos , Gonadotropina Coriónica Humana de Subunidad beta/sangre , Síndrome de Down/sangre , Reacciones Falso Positivas , Femenino , Humanos , Cuello/diagnóstico por imagen , Cuello/embriología , Defectos del Tubo Neural/sangre , Embarazo , Trimestres del Embarazo , Proteína Plasmática A Asociada al Embarazo/metabolismo , Ultrasonografía Prenatal
2.
J Med Screen ; 12(4): 197-201, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-16417697

RESUMEN

OBJECTIVE: To determine the quantitative effect on overall screening performance (detection rate for a given false-positive rate) of using several moderately strong, independent risk factors in combination as screening markers. SETTING: Theoretical statistical analysis. METHODS: For the purposes of this analysis, it was assumed that all risk factors were independent, had Gaussian distributions with the same standard deviation in affected and unaffected individuals and had the same screening performance. We determined the overall screening performance associated with using an increasing number of risk factors together, with each risk factor having a detection rate of 10%, 15% or 20% for a 5% false-positive rate. The overall screening performance was estimated as the detection rate for a 5% false-positive rate. RESULTS: Combining the risk factors increased the screening performance, but the gain in detection at a constant false-positive rate was relatively modest and diminished with the addition of each risk factor. Combining three risk factors, each with a 15% detection rate for a 5% false-positive rate, yields a 28% detection rate. Combining five risk factors increases the detection rate to 39%. If the individual risk factors have a detection rate of 10% for a 5% false-positive rate, it would require combining about 15 such risk factors to achieve a comparable overall detection rate (41%). CONCLUSION: It is intuitively thought that combining moderately strong risk factors can substantially improve screening performance. For example, most cardiovascular risk factors that may be used in screening for ischaemic heart disease events, such as serum cholesterol and blood pressure, have a relatively modest screening performance (about 15% detection rate for a 5% false-positive rate). It would require the combination of about 15 or 20 such risk factors to achieve detection rates of about 80% for a 5% false-positive rate. This is impractical, given the risk factors so far discovered, because there are too few risk factors and their associations with disease are too weak.


Asunto(s)
Tamizaje Masivo/métodos , Factores de Riesgo , Biomarcadores , Métodos Epidemiológicos , Reacciones Falso Positivas , Humanos
3.
Prenat Diagn ; 23(7): 588-92, 2003 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-12868090

RESUMEN

A method is described to combine the ultrasound marker nuchal translucency (NT) with serum markers so that they can be used together in prenatal screening for Down syndrome in twin pregnancies. For monochorionic twin pregnancies (taken as monozygous), the two fetus-specific NT measurements are averaged before risk is calculated and before the contribution of the serum markers is incorporated. For dichorionic twin pregnancies (taken as dizygous), the risk for each fetus based on the individual NT measurements is calculated, the two fetus-specific risks are added together, and then the contribution of the serum markers is incorporated. In this way, all the screening markers can be used in combination to produce a pregnancy-specific "pseudo-risk", rather than a fetus-specific pseudo-risk. We refer to pseudo-risk because in the absence of sufficient data on the screening markers in affected twin pregnancies, a true risk estimate cannot be calculated. Tentative estimates are given of screening performance in twins using NT, the combined test (NT with first-trimester serum markers), and the integrated test (NT with first- and second-trimester serum markers), all interpreted with maternal age.


Asunto(s)
Síndrome de Down/diagnóstico , Síndrome de Down/etiología , Diagnóstico Prenatal , Gemelos , Biomarcadores/sangre , Gonadotropina Coriónica Humana de Subunidad beta/sangre , Síndrome de Down/sangre , Síndrome de Down/diagnóstico por imagen , Femenino , Humanos , Cuello/diagnóstico por imagen , Cuello/embriología , Embarazo , Trimestres del Embarazo , Proteína Plasmática A Asociada al Embarazo/metabolismo , Factores de Riesgo , Ultrasonografía Prenatal , alfa-Fetoproteínas/metabolismo
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