Prenatal diagnosis of chromosomal abnormalities in a resource-poor setting
dc.contributor.author | Geerts L. | |
dc.date.accessioned | 2011-05-15T16:16:41Z | |
dc.date.available | 2011-05-15T16:16:41Z | |
dc.date.issued | 2008 | |
dc.description.abstract | Objective: To compare the efficacy and efficiency of systematic, ultrasound-based risk adjustment using a published algorithm with that of a maternal age cutoff of 37 years for the prenatal detection of chromosomal abnormalities (especially autosomal trisomies). Methods: These approaches were compared in a retrospective study of 136 chromosomal abnormalities confirmed by karyotyping prenatally (n = 46) or postnatally (n = 90). There were 114 autosomal trisomies. Results: Maternal age was known for 103 fetuses with confirmed abnormalities. The ultrasound-based risk adjustment approach was more sensitive for autosomal trisomy (93.9% vs 44.1%), and karyotyping for younger women with abnormalities on ultrasound was more effective than routine karyotyping in older women (1 trisomy detected in 13.5 vs 42.8 samples, P < 0.001). A lack of screening was the main reason for the postnatal diagnosis. Conclusion: Ultrasound-based risk adjustment was the more effective approach. © 2008 International Federation of Gynecology and Obstetrics. | |
dc.description.version | Article | |
dc.identifier.citation | International Journal of Gynecology and Obstetrics | |
dc.identifier.citation | 103 | |
dc.identifier.citation | 1 | |
dc.identifier.issn | 00207292 | |
dc.identifier.other | 10.1016/j.ijgo.2008.05.028 | |
dc.identifier.uri | http://hdl.handle.net/10019.1/13891 | |
dc.subject | article | |
dc.subject | chromosome aberration | |
dc.subject | conception | |
dc.subject | controlled study | |
dc.subject | human | |
dc.subject | karyotyping | |
dc.subject | maternal age | |
dc.subject | prenatal diagnosis | |
dc.subject | priority journal | |
dc.subject | risk assessment | |
dc.subject | screening | |
dc.subject | trisomy | |
dc.subject | ultrasound | |
dc.subject | Adolescent | |
dc.subject | Adult | |
dc.subject | Age Factors | |
dc.subject | Algorithms | |
dc.subject | Chromosome Disorders | |
dc.subject | Female | |
dc.subject | Health Services Accessibility | |
dc.subject | Humans | |
dc.subject | Karyotyping | |
dc.subject | Middle Aged | |
dc.subject | Pregnancy | |
dc.subject | Retrospective Studies | |
dc.subject | Risk Adjustment | |
dc.subject | Sensitivity and Specificity | |
dc.subject | Trisomy | |
dc.subject | Ultrasonography, Prenatal | |
dc.subject | Young Adult | |
dc.title | Prenatal diagnosis of chromosomal abnormalities in a resource-poor setting | |
dc.type | Article |