AUDIT OF A SCREENING SERVICE FOR FETAL ABNORMALITIES USING EARLY ULTRASOUND SCANNING AND MATERNAL SERUM ALPHA-FETOPROTEIN ESTIMATION COMBINED WITH SELECTIVE DETAILED SCANNING
Se. Chambers et al., AUDIT OF A SCREENING SERVICE FOR FETAL ABNORMALITIES USING EARLY ULTRASOUND SCANNING AND MATERNAL SERUM ALPHA-FETOPROTEIN ESTIMATION COMBINED WITH SELECTIVE DETAILED SCANNING, Ultrasound in obstetrics & gynecology, 5(3), 1995, pp. 168-173
Citations number
NO
Categorie Soggetti
Acoustics,"Obsetric & Gynecology","Radiology,Nuclear Medicine & Medical Imaging
The objective of the study was the evaluation of a screening service f
or fetal abnormality using early ultrasound scanning to date and estab
lish viability of the pregnancy combined with maternal serum alpha-fet
oprotein estimation at 16 weeks and thereafter selective detailed scan
ning at 18-20 weeks based on clinical indication. The study was design
ed to be retrospective, emphasizing the possibility of diagnosis. Earl
y scans were performed by radiographers and radiologists, detailed one
s by radiologists and obstetricians with subspeciality training in pre
natal diagnosis. The study was carried out in the ultrasound departmen
t of a large University Hospital. The subjects studied were all cases
of abnormality identified pre- or postnatally in women delivering in t
he hospital over 4 years and to whom the screening service applied. In
formation was obtained from ultrasound and maternity records, birth no
tifications, pathology and autopsy reports and a special needs registe
r. Cases were classified as not detectable, potentially detectable and
usually detectable. Major fetal anomalies numbered 255 (total deliver
ies 19 497), a prevalence of 1.3%; 130 (51%) were diagnosed by ultraso
und with 64% before 24 weeks and 36% later. Eleven chromosomal anomali
es (4%) were diagnosed by genetic methods and 114 (45%) anomalies were
not diagnosed antenatally. The sensitivity of the program was 37% bef
ore 24 weeks. Chromosomal anomalies, lesions of the central nervous sy
stem and cardiac defects were most common, followed by lesions of the
gastrointestinal and urinary tracts. A large proportion of the detecte
d and detectable anomalies were lethal. The implementation of a policy
of routine scans at 18-20 weeks for fetal abnormality would be justif
ied if it led to improved obstetric decision-making, reduction in chil
d handicap and less parental suffering. A routine scan applied to our
population might not have achieved these except in a comparatively sma
ll number of cases.