Korada M, Pearce M S, Ward Platt M P, Avis E, Turner S, Wastell H, Cheetham T
School of Clinical Medical Sciences (Child Health), Sir James Spence Institute, Royal Victoria Infirmary, Newcastle Upon Tyne, UK.
Arch Dis Child Fetal Neonatal Ed. 2008 Jul;93(4):F286-8. doi: 10.1136/adc.2007.134999. Epub 2008 Feb 5.
Revised UK neonatal screening guidelines recommend that a second blood sample for assay of thyroid stimulating hormone (TSH) be taken when preterm infants reach a postmenstrual age of 36 weeks.
To examine the results of a regional screening programme to see whether a rise in TSH concentration was observed in some preterm infants between the first sample taken around 5 days after delivery and the second sample taken at around 36 weeks.
Whole-blood TSH concentrations in preterm infants born over a 2-year period (April 2005 to March 2007) were assessed, and the number of infants in whom there was a fall or rise to values below or above the local screening threshold (6 mU/l) was determined.
Baseline TSH samples were obtained from 2238 preterm infants (median gestational age 32 weeks, range 21-35) with second samples obtained from 2039 (median gestational 32 weeks, range 23-35). In 19 infants, TSH concentrations fell from above to below the screening threshold, and in five infants values rose from below the screening threshold to 6-10 mU/l. However, TSH concentrations fell to <6 mU/l on a further blood spot in four of these infants, and the remaining infant had a serum TSH of 6.8 mU/l. Three infants had raised TSH concentrations on both occasions with unequivocal hypothyroidism (serum TSH >80 mU/l). The initial TSH concentration in one of these infants was 6-10 mU/l.
No infant with a normal TSH concentration on first sampling had a TSH concentration that rose above 10 mU/l on second sampling, and no infants with a normal TSH concentration on first screening are receiving long-term thyroxine treatment. This study suggests that a second sample may not be necessary with a screening threshold of 6 mU/l.
修订后的英国新生儿筛查指南建议,当早产儿达到36周的月经后年龄时,应采集第二份血样用于检测促甲状腺激素(TSH)。
检查一项区域筛查计划的结果,以确定在一些早产儿出生后约5天采集的第一份样本与36周左右采集的第二份样本之间,TSH浓度是否会升高。
评估了2年期间(2005年4月至2007年3月)出生的早产儿的全血TSH浓度,并确定了TSH值下降或上升至低于或高于当地筛查阈值(6 mU/l)的婴儿数量。
从2238名早产儿(中位胎龄32周,范围21 - 35周)获得了基线TSH样本,从2039名(中位胎龄32周,范围23 - 35周)获得了第二份样本。19名婴儿的TSH浓度从高于筛查阈值降至低于筛查阈值,5名婴儿的值从低于筛查阈值升至6 - 10 mU/l。然而,其中4名婴儿在进一步的血斑检测中TSH浓度降至<6 mU/l,其余1名婴儿的血清TSH为6.8 mU/l。3名婴儿两次检测时TSH浓度均升高,患有明确的甲状腺功能减退症(血清TSH>80 mU/l)。其中1名婴儿的初始TSH浓度为6 - 10 mU/l。
首次采样时TSH浓度正常的婴儿,第二次采样时TSH浓度均未升至高于10 mU/l,且首次筛查TSH浓度正常的婴儿均未接受长期甲状腺素治疗。本研究表明,对于筛查阈值为6 mU/l的情况,可能无需采集第二份样本。