• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
[Impact of the COVID-19 pandemic on Neonatal Screening for Congenital Hypothyroidism.].[新型冠状病毒肺炎大流行对先天性甲状腺功能减退症新生儿筛查的影响。]
Rev Esp Salud Publica. 2020 Dec 16;94:e202012176.
2
Cases Referred from the Turkish National Screening Program: Frequency of Congenital Hypothyroidism and Etiological Distribution.来自土耳其国家筛查项目的病例:先天性甲状腺功能减退症的发病率及病因分布
J Clin Res Pediatr Endocrinol. 2019 Sep 3;11(3):240-246. doi: 10.4274/jcrpe.galenos.2019.2018.0255. Epub 2019 Jan 11.
3
A Detailed Analysis of the Factors Influencing Neonatal TSH: Results From a 6-Year Congenital Hypothyroidism Screening Program.新生儿 TSH 影响因素的详细分析:6 年先天性甲状腺功能减退症筛查项目的结果。
Front Endocrinol (Lausanne). 2020 Jul 17;11:456. doi: 10.3389/fendo.2020.00456. eCollection 2020.
4
Diagnostic re-evaluation and predictors of congenital hypothyroidism with eutopic thyroid gland in Jiangxi, China.中国江西正常甲状腺位先天性甲状腺功能减退症的诊断再评估及预测因素。
J Pediatr Endocrinol Metab. 2021 Jun 28;34(9):1139-1146. doi: 10.1515/jpem-2020-0733. Print 2021 Sep 27.
5
High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transients.在土耳其全国筛查项目中,因疑似先天性甲状腺功能减退症而转诊的婴儿中,暂时性先天性甲状腺功能减退症的发生率较高:甲状腺素剂量可能有助于预测暂时性疾病。
J Endocrinol Invest. 2024 Sep;47(9):2213-2224. doi: 10.1007/s40618-024-02348-9. Epub 2024 Mar 28.
6
Current status of the congenital hypothyroidism neonatal screening program in Adana Province, Turkey.土耳其阿达纳省先天性甲状腺功能减退症新生儿筛查项目的现状
J Pediatr Endocrinol Metab. 2018 Jun 27;31(6):619-624. doi: 10.1515/jpem-2017-0433.
7
Congenital hypothyroidism: etiology and growth-development outcome.先天性甲状腺功能减退症:病因及生长发育结局
Acta Med Iran. 2014;52(10):752-6.
8
Thirty years of the newborn screening program in Central Serbia: the missed cases of congenital hypothyroidism.塞尔维亚中部新生儿筛查项目30年:先天性甲状腺功能减退症漏诊病例
Turk J Pediatr. 2019;61(3):319-324. doi: 10.24953/turkjped.2019.03.001.
9
Neonatal screening for congenital hypothyroidism and phenylketonuria in China.中国新生儿先天性甲状腺功能减退症和苯丙酮尿症筛查
World J Pediatr. 2009 May;5(2):136-9. doi: 10.1007/s12519-009-0027-0. Epub 2009 Jul 9.
10
[Diagnosis and follow-up of patients with congenital hypothyroidism detected by neonatal screening].[新生儿筛查发现的先天性甲状腺功能减退症患者的诊断与随访]
An Pediatr (Engl Ed). 2019 Apr;90(4):250.e1-250.e8. doi: 10.1016/j.anpedi.2018.11.002. Epub 2019 Jan 24.

本文引用的文献

1
[Diagnosis and follow-up of patients with congenital hypothyroidism detected by neonatal screening].[新生儿筛查发现的先天性甲状腺功能减退症患者的诊断与随访]
An Pediatr (Engl Ed). 2019 Apr;90(4):250.e1-250.e8. doi: 10.1016/j.anpedi.2018.11.002. Epub 2019 Jan 24.
2
[Fifty years of neonatal screening for congenital diseases in Spain].[西班牙五十年先天性疾病新生儿筛查]
An Pediatr (Engl Ed). 2019 Apr;90(4):205-206. doi: 10.1016/j.anpedi.2018.11.013. Epub 2018 Dec 21.
3
Screening for congenital hypothyroidism: a worldwide view of strategies.先天性甲状腺功能减退症的筛查:策略的全球视角。
Best Pract Res Clin Endocrinol Metab. 2014 Mar;28(2):175-87. doi: 10.1016/j.beem.2013.05.008. Epub 2013 Jun 18.
4
European Society for Paediatric Endocrinology consensus guidelines on screening, diagnosis, and management of congenital hypothyroidism.欧洲儿科内分泌学会关于先天性甲状腺功能减退症筛查、诊断和管理的共识指南。
J Clin Endocrinol Metab. 2014 Feb;99(2):363-84. doi: 10.1210/jc.2013-1891. Epub 2014 Jan 21.
5
Congenital hypothyroidism.先天性甲状腺功能减退症。
Orphanet J Rare Dis. 2010 Jun 10;5:17. doi: 10.1186/1750-1172-5-17.
6
How should we be treating children with congenital hypothyroidism?我们应该如何治疗先天性甲状腺功能减退症患儿?
J Pediatr Endocrinol Metab. 2007 May;20(5):559-78. doi: 10.1515/jpem.2007.20.5.559.
7
Update of newborn screening and therapy for congenital hypothyroidism.先天性甲状腺功能减退症的新生儿筛查与治疗进展
Pediatrics. 2006 Jun;117(6):2290-303. doi: 10.1542/peds.2006-0915.
8
A population-based study on the frequency of additional congenital malformations in infants with congenital hypothyroidism: data from the Italian Registry for Congenital Hypothyroidism (1991-1998).一项基于人群的关于先天性甲状腺功能减退症婴儿中其他先天性畸形发生频率的研究:来自意大利先天性甲状腺功能减退症登记处的数据(1991 - 1998年)
J Clin Endocrinol Metab. 2002 Feb;87(2):557-62. doi: 10.1210/jcem.87.2.8235.
9
Influence of timing and dose of thyroid hormone replacement on development in infants with congenital hypothyroidism.甲状腺激素替代治疗的时机和剂量对先天性甲状腺功能减退症患儿发育的影响。
J Pediatr. 2000 Mar;136(3):292-7. doi: 10.1067/mpd.2000.103351.
10
Maternal thyroid deficiency during pregnancy and subsequent neuropsychological development of the child.孕期母亲甲状腺功能减退与儿童随后的神经心理发育
N Engl J Med. 1999 Aug 19;341(8):549-55. doi: 10.1056/NEJM199908193410801.

[新型冠状病毒肺炎大流行对先天性甲状腺功能减退症新生儿筛查的影响。]

[Impact of the COVID-19 pandemic on Neonatal Screening for Congenital Hypothyroidism.].

作者信息

Mora Sitja Marina, Sanz Fernández María, Carrascón González-Pinto Lucía, Rodríguez Sánchez Amparo

机构信息

Unidad de Endocrinología Infantil. Hospital General Universitario Gregorio Marañón. Madrid. España.

出版信息

Rev Esp Salud Publica. 2020 Dec 16;94:e202012176.

PMID:33323923
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11583069/
Abstract

OBJECTIVE

The purpose of this paper was to describe the diagnosis, treatment and follow-up of patients diagnosed with congenital hypothyroidism (CH) by the Neonatal Screening Program in the Autonomous Community of Madrid during the state of alarm due to the COVID-19 health crisis.

METHODS

The data were extracted from the retrospective analysis of patients diagnosed with CH and treated at the Clinical Diagnosis and Follow-up Center of CH located in the Pediatric Endocrinology Unit of the General University Hospital Gregorio Marañon.

RESULTS

During the period between March 14 and June 21, 2020, 7 neonates were diagnosed with congenital hypothyroidism. The Screening Center contacted the Clinical Diagnosis and Follow-up Center urgently, with the location and clinical assessment of the patient on the same day, performing the usual complementary examinations in all of them according to clinical pathway. The median age of diagnosis was 15.5 days (range 7.00-24.00). The subsequent clinical and analytical follow-up was carried out in all cases according to the recommended times. All patients presented normalization of the thyroid function after two weeks of treatment.

CONCLUSIONS

All patients seen at the Congenital Hypothyroidism Clinical Diagnosis and Follow-up Center during the alarm state period were diagnosed, treated and reevaluated following the usual clinical pathways without incidents. The current epidemiological situation of the COVID-19 pandemic has revealed the correct functioning of the circuit of the Congenital Hypothyroidism Screening Program in less favorable circumstances.

摘要

目的

本文旨在描述在因新冠疫情处于警戒状态期间,马德里自治区新生儿筛查项目诊断出的先天性甲状腺功能减退症(CH)患者的诊断、治疗及随访情况。

方法

数据来自对在格雷戈里奥·马拉尼翁综合大学医院儿科内分泌科的先天性甲状腺功能减退症临床诊断与随访中心确诊并接受治疗的患者的回顾性分析。

结果

在2020年3月14日至6月21日期间,7名新生儿被诊断为先天性甲状腺功能减退症。筛查中心紧急联系了临床诊断与随访中心,于当天提供了患者的位置及临床评估信息,并按照临床路径对所有患者进行了常规的补充检查。诊断时的中位年龄为15.5天(范围7.00 - 24.00)。随后所有病例均按照推荐时间进行了临床及分析随访。所有患者在治疗两周后甲状腺功能均恢复正常。

结论

在警戒状态期间,先天性甲状腺功能减退症临床诊断与随访中心诊治的所有患者均按照常规临床路径进行了诊断、治疗及重新评估,未出现意外情况。新冠疫情当前的流行病学形势显示,先天性甲状腺功能减退症筛查项目流程在不利情况下仍能正常运行。