Neugeborenenhypothyreosescreening in Deutschland. Retrospektive Analyse der Entwicklung von betroffenen Kindern am Beispiel des Bundeslandes Hessen
| العنوان: | Neugeborenenhypothyreosescreening in Deutschland. Retrospektive Analyse der Entwicklung von betroffenen Kindern am Beispiel des Bundeslandes Hessen |
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| المؤلفون: | B. Höpfner, N Koehler, S. Höpfner, E. W. Rauterberg |
| المصدر: | Klinische Pädiatrie. 219:206-211 |
| بيانات النشر: | Georg Thieme Verlag KG, 2007. |
| سنة النشر: | 2007 |
| مصطلحات موضوعية: | Program evaluation, Pediatrics, medicine.medical_specialty, medicine.diagnostic_test, Cross-sectional study, business.industry, Incidence (epidemiology), Retrospective cohort study, medicine.disease, Thyroid function tests, Hypoplasia, Congenital hypothyroidism, Pediatrics, Perinatology and Child Health, medicine, Etiology, business |
| الوصف: | Background Since widespread screenings for hypothyreosis were started in 1981 in Germany, the numbers of mental and physical handicaps due to hypothyroidism are reduced markedly. The aim of this study is to evaluate the actual efficiency of the newborn screenings in Germany using in the federal state "Hessen". Methods/subjects All children born between 1988 and 1992 with suspicions laboratory results in the screening examination were contacted personally and statements concerning the screening itself and the physical and mental development were gathered from their parents, doctors and teachers. Results 99.1% of all hessian newborns born between 1988 and 1992 were included into the screening for hypothyreosis. The incidence of congenital hypothyreosis in general was 1:3 313. An etiological classification was possible in 77% of the patients which is divided as follows: 40% athyreosis, 24% hypoplasia of the thyroid, 8% dyshormonogenesis, 5% ektopia of the thyroid. In 67% of the cases hormone substitution was initiated during the first 14 days of life. In 23.9% it was started in the third week, in 6.8% in the fourth week and only in 2.3% of the patients treatment was started later on. The physical development of the children with congenital hypothyreosis can be regarded as widely normal. The school achievement was moderately retarded even when treatment was started in the early neonatal period. Conclusions The screening for hypothyreosis is well established in Hessen concerning tracking, organisation and analysis. There are short comings concerning the follow ups of children with suspicions findings, which shall be overcome by creating a new position. The long-term-follow-up according to the guidelines of the "Arbeitsgemeinschaft Padiatrische Endokrinologie" is of central interest. Furthermore compliance is improved by regular personal counselling with the parents. |
| تدمد: | 1439-3824 0300-8630 |
| URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_________::695751a17d101349a3f5f3416a808c1b https://doi.org/10.1055/s-2006-921579 |
| رقم الأكسشن: | edsair.doi...........695751a17d101349a3f5f3416a808c1b |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 14393824 03008630 |
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