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土耳其先天性甲状腺功能减退症国家新生儿筛查项目的建立与发展。

Establishment and development of a national newborn screening programme for congenital hypothyroidism in Turkey.

作者信息

Dilli Dilek, Çzbaş Sema, Acıcan Deniz, Yamak Nergiz, Ertek Mustafa, Dilmen Uğur

机构信息

Dr. Sami Ulus Maternity and Children Research and Training Hospital, Department of Neonatology, Ankara, Turkey.

出版信息

J Clin Res Pediatr Endocrinol. 2013;5(2):73-9. doi: 10.4274/Jcrpe.929.

Abstract

OBJECTIVE

To assess the Turkish National Newborn Screening Programme (NNSP) for congenital hypothyroidism (CH). Retrospective study based on the data from NNSP.

METHODS

Since December 2006, a nationwide screening programme for CH has been conducted in Turkey by the Turkish Directorate of Public Health (TDPH) in cooperation with several institutions. We evaluated the database between January 2008 and July 2010 of this programme. According to the methodology of the NNSP, between three and five days of age (or at discharge from the hospital, if this occurs earlier) blood specimens were routinely collected from neonates on filter paper, by puncturing the heel. The accepted thyroid-stimulating hormone cut-off level for recall was 20 mU/L initially and 15 mU/L subsequently. The incidence of possible CH by years was reported.

RESULTS

During the evaluation period, 3223765 newborns were tested. The mean annual incidence of possible CH showed a gradual increase over the years (1:888 in 2008, 1:592 in 2009, and 1:469 in 2010). Regional differences were noted. Although the mean age of blood sampling did not change by years, the mean age at notification for suspected CH decreased from 19.2 to 15.7 days from 2008 to 2010.

CONCLUSIONS

We reported the first assessment of NNSP in Turkey. An improvement in performance measures for the CH screening programme has been noted. Knowledge on incidence of confirmed CH is not yet available in the database.

摘要

目的

评估土耳其全国先天性甲状腺功能减退症(CH)新生儿筛查项目(NNSP)。基于NNSP数据进行回顾性研究。

方法

自2006年12月起,土耳其公共卫生总局(TDPH)与多家机构合作在全国开展了CH筛查项目。我们评估了该项目2008年1月至2010年7月的数据库。根据NNSP的方法,在新生儿出生三至五天(或若出院较早,则在出院时),通过足跟采血,常规采集滤纸上的血样。最初召回的促甲状腺激素临界值为20 mU/L,随后为15 mU/L。报告了各年份可能患CH的发病率。

结果

在评估期间,共检测了3223765名新生儿。可能患CH的年平均发病率逐年呈逐渐上升趋势(2008年为1:888,2009年为1:592,2010年为1:469)。注意到存在地区差异。虽然采血的平均年龄没有逐年变化,但疑似CH的通报平均年龄从2008年的19.2天降至2010年的15.7天。

结论

我们报告了对土耳其NNSP的首次评估。已注意到CH筛查项目的绩效指标有所改善。数据库中尚无确诊CH发病率的相关信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71cd/3701925/26faee0291d4/JCRPE-5-73-g5.jpg

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