The Participation of Perinatal Diagnostics in Decreasing the
Incidence of Congenital Malformations in the Czech Republic
Gregor V.1,2, Šípek A.3,4, Mašátová D.5
1Oddělení lékařské genetiky, Fakultní Thomayerova nemocnice, Praha, ředitel Ing. J. Pubrdle 2Institut postgraduálního vzdělávání ve zdravotnictví, Katedra lékařské genetiky, Praha, vedoucí prof. MUDr. P. Goetz, CSc. 3Ústav pro péči o matku a dítě, Praha, ředitel doc. MUDr. J. Feyereisl, CSc. 4Institut postgraduálního vzdělávání ve zdravotnictví, Katedra gynekologicko-porodnická, Praha, vedoucí doc. MUDr. J. Feyereisl, CSc. 5Ústav zdravotnických informací a statistiky České republiky, Praha, ředitelka Mgr. V. Mazánková |
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Summary:
Objectve: An analysis of prenatal diagnostics of congenital malformations in the year 2002
and an analysis of the proportion of prenatal diagnostics in the total incidence of congenital
malformations in the Czech Republic in the years 1994 – 2002.
Design: A retrospective study.
Setting: Department of Medical Genetics, Faculty Thomayer Hospital, Prague.
Materials and Methods: The data were obtained from Dept. of Medical Genetics wards (28
departments) – congenital malformations were detected during prenatal diagnostics, and
other data were obtained from the Institute of Medical Information and Statistics of the Czech
Republic, the National Registry of Inborn Defects – Congenital Malformations in Newborns. From
the available material the authors selected six types of congenital malformations (anencephaly,
spina bifi da, omphalocoele, gastroschisis, renal agenesis/hypoplasia, Down syndrome) for a more
detailed analysis.
Results: In the period of 1994-2002 a total of 3,621 pregnancies with congenital malformations
were detected and terminated and 1,351 fetuses were prenatally diagnosed, but the pregnancy
was not terminated. The prenatal detection of inborn errors is gradually increasing. A detailed
analysis of prenatal diagnostics in 2002 indicated that chromosomal aberrations were diagnosed
most frequently (307 cases), of which Down syndrome was most frequent (108 cases). The next
most frequent defects were those of urinary tract (agenesis or renal hypoplasia 13 times, kidney
cystosis 25 times, hydronephrosis 31 times, other congenital malformations 10 times), congenital
heart malformations (dealt with in another presentation), defects of neural tube (anencephaly
18 times, encephalocoele 6 times, spina bifi da 22 times), congenital malformations of skeletal and
muscular system (46 times) and defects of abdominal wall (omphalocoele 10 times, gastoschisis
25 times).
A detailed analysis of six types of congenital malformations revealed that prenatal detection of
congenital malformations increases with time and prenatal diagnostics signifi cantly participates
in the total detection of congenital malformations. The percentage of prematurely terminated
pregnancies from the total number of diagnosed malformations is almost 100% in anencephaly,
50-60% in spina bifi da, 50-60% in omphalocoele, 70-90% in gastroschisis, 20-30% in renal agenesis/
hypoplasia and 60-70% in Down syndrome.
Conclusion: In the period of observation there were increasing numbers of prenatally diagnosed
congenital malformations. A difference develops between the total number of prenatally
diagnosed cases and those diagnosed prenatally and terminated. There is an increasing number
of non-terminated cases (decision of the pregnant woman, multiple pregnancies, late detection of
the congenital malformations). The effi ciency of prenatal diagnosis in the observed period was in
the range of 50-100% in relation to the type and severity of the congenital malformations.
Key words:
congenital malformations, prenatal diagnostics, anencephaly, spina bifi da,
omphalocoele, gastroschisis, renal agenesis and hypoplasia, Down syndrome
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