Herden S, Willgerodt H, Rotzsch W
Institut für Klinische Chemie und Laboratoriumsdiagnostik des Bereiches Medizin, Universität Leipzig.
Kinderarztl Prax. 1993 Mar;61(2):48-52.
The development of neonatal screening for congenital hypothyroidism in the GDR and particularly in Saxony after German reunification is described in this paper. The results of the studies and the experiences in respect of realisation and organisation of the screening for hypothyroidism in the screening centre of Leipzig are discussed. Measurement of TSH in the blood spot of about 65,000 newborn yielded an incidence rate of congenital hypothyroidism of 1:3,200. The onset of therapy within the first three weeks of life has been ensured until now since no children with congenital hypothyroidism were involved in cases of occasionally delayed blood sampling and/or postal delay. However, there has been some organisational disparity due to individually different handling of health insurance fund payments of screening fees for hypothyroidism in Saxony and also in the other federal states. The disadvantages of this lack of uniform regulations are explained. Neonatal screening for evidence of congenital adrenal hyperplasia by determining 17-alpha-hydroxyprogesterone, is under preparation.
本文描述了民主德国,特别是德国统一后萨克森州先天性甲状腺功能减退症新生儿筛查的发展情况。讨论了莱比锡筛查中心甲状腺功能减退症筛查的研究结果以及实施和组织方面的经验。对约65000名新生儿血斑进行促甲状腺激素检测,先天性甲状腺功能减退症的发病率为1:3200。由于偶尔的采血延迟和/或邮寄延迟的病例中没有先天性甲状腺功能减退症患儿,到目前为止已确保在出生后的前三周内开始治疗。然而,由于萨克森州以及其他联邦州对甲状腺功能减退症筛查费用的医疗保险基金支付处理方式存在个体差异,出现了一些组织上的差异。解释了缺乏统一规定的弊端。通过测定17-α-羟孕酮进行先天性肾上腺皮质增生症证据的新生儿筛查正在筹备中。