The Role of Thyroid Scintigraphy in Infants with Congenital Hypothyroidism: Our Experience at Royal Hospital, Oman

Asya S Al-Busaidi, Naima K Al-Bulushi, K. Al-Nabhani
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Abstract

Objectives: The early diagnosis and treatment of congenital hypothyroidism is critical, to avoid detrimental outcomes such as mental retardation. Thyroid stimulating hormone (TSH) level is the usual diagnostic screening test; however, thyroid scintigraphy helps identify etiologies of the disease there by determining different management plans. The aim of this descriptive retrospective study is to evaluate thyroid scintigraphy findings in newborns and children with biochemical evidence of congenital hypothyroid and to assess the impact of thyroid scintigraphy findings on the long-term management of those patients. Methods: Retrospective review of 101 infants with congenital hypothyroidism (CH) who were initially diagnosed biochemically, and then underwent thyroid scintigraphy, between 2010 and 2015 at a tertiary hospital in Oman. Patients’ data was collected from the hospitals’ database and then analyzed using statistical package for social sciences (SPSS). Results: 8.9 % (9/101) patients had the thyroid scintigraphy up to 7 days of life, whereas 91.1% (92/101), were performed after the age of 3 years. The performed scintigraphy revealed five different findings which included dyshormonogenesis, ectopia, agenesis, reduced and normal % of Tc-99m pertechnetate uptake in the thyroid gland. The most common cause of congenital hypothyroidism in this cohort was ectopic sublingual thyroid, 32.6% (33/101), and the ratio of female to male was 1.29:1, in keeping with international figures. However, in this cohort the Dyshormonogenesis was the cause of congenital hypothyroid in 29.7% (30/101) patients, which is higher than that known internationally and can be probably attributed to the high rate of consanguineous marriage in the country. 39.6% (40/101) patients required alteration in management (increase or decrease thyroid hormone dosage, start, or discontinue the treatment) based of thyroid scintigraphy, US and serial TFT. There was a statistical significance (p-value= 0.000) between scan findings and the need to change the treatment plan following the scan. Conclusion: Thyroid scintigraphy is an essential part of screening program for congenital hypothyroidism and useful in differentiating the causes of congenital hypothyroidism thus essential for proper management plans. We, therefore, highly advise to increase the awareness of early utilization of thyroid scintigraphy in congenital hypothyroidism screening.
甲状腺显像在先天性甲状腺功能减退婴儿中的作用:我们在阿曼皇家医院的经验
目的:早期诊断和治疗先天性甲状腺功能减退症至关重要,以避免智力低下等不良后果。促甲状腺激素(TSH)水平是常用的诊断筛查试验;然而,甲状腺显像通过确定不同的治疗方案来帮助确定疾病的病因。本描述性回顾性研究的目的是评估有先天性甲状腺功能减退生化证据的新生儿和儿童的甲状腺显像结果,并评估甲状腺显像结果对这些患者长期治疗的影响。方法:回顾性分析2010 - 2015年阿曼某三级医院101例先天性甲状腺功能减退症(CH)患儿经生化诊断后行甲状腺显像检查的病例。从医院数据库中收集患者数据,然后使用社会科学统计软件包(SPSS)进行分析。结果:8.9%(9/101)的患者在出生后7天内进行了甲状腺显像检查,而91.1%(92/101)的患者在3岁后进行了甲状腺显像检查。显像显示了五种不同的结果,包括激素生成障碍、异位、发育不全、甲状腺Tc-99m高技术酸盐摄取百分比降低和正常。本队列中最常见的先天性甲状腺功能减退病因为舌下甲状腺异位,占32.6%(33/101),男女比例为1.29:1,与国际数据一致。然而,在本队列中,29.7%(30/101)的患者是先天性甲状腺功能低下的原因,这一比例高于国际上已知的水平,可能与我国高近亲结婚率有关。39.6%(40/101)的患者需要改变管理(增加或减少甲状腺激素剂量,开始或停止治疗),基于甲状腺显像,US和连续TFT。扫描结果与扫描后需要改变治疗方案之间有统计学意义(p值= 0.000)。结论:甲状腺显像是先天性甲状腺功能减退症筛查的重要组成部分,有助于鉴别先天性甲状腺功能减退症的病因,为制定适当的治疗方案提供依据。因此,我们强烈建议在先天性甲状腺功能减退筛查中提高早期使用甲状腺显像的意识。
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