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Prenatal ultrasound detection of abdominal wall defects: Associated malformations, chromosomal abnormalities and perinatal outcome (CROSBI ID 512274)

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Barišić, Ingeborg ; Clementi, Maurizio ; Haeusler, Martin ; Gjergja, Romana ; Stoll, Claude and EUROSCAN Study Group Prenatal ultrasound detection of abdominal wall defects: Associated malformations, chromosomal abnormalities and perinatal outcome // Reproductive toxicology. 2002. str. 87-88

Podaci o odgovornosti

Barišić, Ingeborg ; Clementi, Maurizio ; Haeusler, Martin ; Gjergja, Romana ; Stoll, Claude and EUROSCAN Study Group

engleski

Prenatal ultrasound detection of abdominal wall defects: Associated malformations, chromosomal abnormalities and perinatal outcome

OBJECTIVES: Evaluation of the current effectiveness of routine prenatal ultrasound screening in detecting abdominal wall defects and associated conditions in unselected population across Europe. Analysis of the impact of associated malformations, syndromes, and chromosomal abnormalities on pregnancy outcome and parental decisions concerning termination of pregnancy (TOP). METHODS: 19 Congenital Malformation Registries from 11 European countries collected data on the family history, mother, fetus/infant, results of prenatal scans and outcome of pregnancy. The study period was 30 months (01/07/96 to 31/12/98) and total number of monitored pregnancies 690, 123. RESULTS: From the total of 243 abdominal wall defects, associated malformations were found in 56.2 % (77/137) of omphalocele and 22.6% (24/106) of gastroschisis. Overall 25 % (34/137)of fetuses with omphalocele had an abnormal karyotype, 31.4 % (43/137) had a recognisable syndrome, association, or an unspecified pattern of malformations. Of the 106 gastroschisis, 15 (14%) had aditional abnormalities. Only 2 (2%)cases could be atributted to a chromosomal and 7 (7%) to a recognisable nonchromosomal syndrome. Prenatal ultrasound examination detected 75 % (103/137) of omphalocele and 83% (88/106) of gastroschisis. The detection rate was higher and the mean gestational age at detection lower in multiple affected fetuses. In 51 (37%) cases with omphalocele and in 31 (29%) with gastroschisis, parents opted for TOP. PČroportion of TOP was higher in multiple affected fetuses compared to syndromic, chromosomal, and multiple cases. CONCLUSION: A high proportion of abdominal wall defects is associated with concurrent malformations and/or chromosomal abnormalities. Associated conditions clearly influence perinatal outcome. Therefore, a detailed search for other structural malformations and karyotyping should be performed whenever an abdominal wall defect is identified.

abdominal wall defects; omphalocele; gastroschisis; prenatal diagnosis; ultrasound

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Podaci o prilogu

87-88.

2002.

nije evidentirano

objavljeno

Podaci o matičnoj publikaciji

Reproductive toxicology

0890-6238

Podaci o skupu

Nepoznat skup

poster

29.02.1904-29.02.2096

Povezanost rada

Kliničke medicinske znanosti, Javno zdravstvo i zdravstvena zaštita

Indeksiranost