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通过新生儿筛查确诊的先天性甲状腺功能减退症的初级保健提供者管理

Primary Care Provider Management of Congenital Hypothyroidism Identified Through Newborn Screening.

作者信息

Rosenthal N A, Bezar E, Mann S, Bachrach L K, Banerjee S, Geffner M E, Gottschalk M, Shapira S K, Hasegawa L, Feuchtbaum L

机构信息

California Department of Public Health, Genetic Disease Screening Program, USA.

Public Health Foundation Enterprises, USA.

出版信息

Ann Thyroid Res. 2017;3(1):95-101. Epub 2017 Apr 18.

Abstract

OBJECTIVE

To assess Primary Congenital Hypothyroidism (CH) management patterns and feasibility of providing long-term care for patients with CH identified through newborn screening by Primary Care Providers (PCPs) in California and Hawaii.

STUDY DESIGN

A survey was mailed to all physicians (N=823) listed as the referral doctor for confirmed patients with CH identified through newborn screening programs in both states between 01/01/2009-12/31/2013. Information was collected on CH management patterns, barriers to providing care, and knowledge on CH treatment. Descriptive statistics and bivariate logistic regression results were reported.

RESULTS

206 PCPs completed the survey. Among these, 78% currently have patients with CH and 91% indicated willingness to provide long-term care to new patients with CH. Among PCPs currently caring for patients with CH, 17% managed CH by themselves with limited assistance from endocrinologists; 63% were involved in managing CH but endocrinologists played a larger role than PCPs; 19% were not involved in CH care. Only 49% of PCPs correctly answered questions regarding recommended follow-up frequencies and 23% knew the correct age for a trial off levothyroxine for suspected transient CH. Top two perceived barriers to providing long-term care included "need guidance or support from endocrinologists" (61%) and "not familiar with CH treatment guidelines" (28%).

CONCLUSION

The majority of PCPs surveyed are willing to provide long-term care to patients with CH, but need support from endocrinologists and increased knowledge about current treatment guidelines.

摘要

目的

评估加利福尼亚州和夏威夷州基层医疗服务提供者(PCP)对通过新生儿筛查确诊的原发性先天性甲状腺功能减退症(CH)患者的管理模式以及提供长期护理的可行性。

研究设计

向2009年1月1日至2013年12月31日期间两州通过新生儿筛查项目确诊为CH的患者的所有转诊医生(共823名)邮寄了一份调查问卷。收集了关于CH管理模式、提供护理的障碍以及CH治疗知识等方面的信息。报告了描述性统计和双变量逻辑回归结果。

结果

206名基层医疗服务提供者完成了调查。其中,78%目前有CH患者,91%表示愿意为新的CH患者提供长期护理。在目前照料CH患者的基层医疗服务提供者中,17%在内分泌科医生的有限协助下自行管理CH;63%参与CH管理,但内分泌科医生比基层医疗服务提供者发挥的作用更大;19%未参与CH护理。只有49%的基层医疗服务提供者正确回答了关于推荐随访频率的问题,23%知道疑似暂时性CH停用左甲状腺素的正确年龄。提供长期护理的两大主要障碍是“需要内分泌科医生的指导或支持”(61%)和“不熟悉CH治疗指南”(28%)。

结论

接受调查的大多数基层医疗服务提供者愿意为CH患者提供长期护理,但需要内分泌科医生的支持以及增加对当前治疗指南的了解。

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