Pregled bibliografske jedinice broj: 672584
Oesophageal atresia : prevalence, prenatal diagnosis and associated anomalies in 23 European regions
Oesophageal atresia : prevalence, prenatal diagnosis and associated anomalies in 23 European regions // Archives of disease in childhood, 97 (2012), 3; 227-232 doi:10.1136/archdischild-2011-300597 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 672584 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Oesophageal atresia : prevalence, prenatal diagnosis and associated anomalies in 23 European regions
Autori
Pedersen, R.N. ; Calzolari, E. ; Husby, S. ; Garne, E. ; EUROCAT Working group
Izvornik
Archives of disease in childhood (0003-9888) 97
(2012), 3;
227-232
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
oesphageal atresia
Sažetak
Objectivre was to describe prevalence, prenatal diagnosis and epidemiological data on oesophageal atresia from 23 well-defined European regions and compare the prevalence between these regions. Population-based study using data from a large European database for surveillance of congenital anomalies (EUROCAT) for two decades (1987-2006). SETTINGS: Twenty-three participating registries based on multiple sources of information including information about live births, fetal deaths with gestational age ≥20 weeks and terminations of pregnancy. 1222 cases of oesophageal atresia in a population of 5 019 804 births. The overall prevalence was 2.43 cases per 10 000 births (95% CI 2.30 to 2.57). There were regional differences in prevalence ranging from 1.27 to 4.55. Prenatal detection rates varied by registry from >50% of cases to <10% of cases. A total of 546 cases (44.7%) had an isolated oesophageal anomaly, 386 (31.6%) were multiple malformed and 290 (23.7%) had an association or a syndrome. There were 1084 live born cases (88.7%), 43 cases were fetal deaths and 95 cases were terminations of pregnancy. One-week survival for live births was 86.9% and 99.2% if the gestational age was ≥38 weeks and isolated oesophageal atresia was present. Males accounted for 57.3% of all cases and 38.5% of live born cases were born with gestational age <37 weeks. There were regional differences in prevalence of oesophageal atresia in Europe. Half of all cases had associated anomalies. Prenatal detection rate increased from 26% to 36.5% over the two decades. Survival in infants with isolated oesophageal atresia born at term is high.
Izvorni jezik
Engleski
POVEZANOST RADA
Projekti:
072-1083107-0365 - Istraživanje epidemiologijskih i genetičkih osnova prirođenih mana (Barišić, Ingeborg, MZOS ) ( CroRIS)
Ustanove:
Klinika za dječje bolesti Medicinskog fakulteta
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE