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早期诊断和全民医疗保健的迫切需求:对印度尼西亚先天性肾上腺皮质增生症患儿家长系列访谈的见解

An urgent need for early diagnosis and universal health care: insights from a series of interviews with parents of children living with congenital adrenal hyperplasia in Indonesia.

作者信息

Pulungan Aman, Puteri Helena Arnetta, Waladhiyaputri Vahira, Chandra Angelina Patricia, Ratnasari Amajida Fadia, Idaayen Fatima, Fadiana Ghaisani, Armstrong Kate, Utari Agustini

机构信息

Department of Child Health, Universitas Indonesia, Jakarta, Indonesia.

International Pediatric Association, Chicago, USA.

出版信息

Clin Pediatr Endocrinol. 2025 Apr;34(2):105-114. doi: 10.1297/cpe.2024-0051. Epub 2025 Feb 27.

Abstract

Congenital adrenal hyperplasia (CAH) presents significant health challenges and requires a timely diagnosis and comprehensive treatment. This qualitative study assessed the experiences of parents of children with CAH in Indonesia, and focused on the challenges associated with delayed diagnosis. In-depth interviews with 40 parents of children with CAH from 9 Indonesian provinces were conducted between December 2022 and January 2023. The results revealed parents experienced challenges due to the absence of a newborn screening program (NBS) and the minimal capacity of healthcare professionals to diagnose CAH. Parents reported having emotional stress, financial challenges, and social stigma. Fludrocortisone and 17-OHP are not covered by the national health insurance, thus financial challenges prevailed. The impact of late diagnosis was also notable in their children; parents reported that their children had tendencies to self-isolate, insecurities, temperamental behavior, and masculine behavior (for females). These findings emphasize the critical need for the NBS to implement early diagnosis, increase healthcare professionals' capacity to diagnose CAH, and ensure accessible and affordable healthcare policies for patients with CAH. Addressing these gaps is essential for improving the quality of life for children with CAH and their families in Indonesia.

摘要

先天性肾上腺皮质增生症(CAH)带来了重大的健康挑战,需要及时诊断和综合治疗。这项定性研究评估了印度尼西亚CAH患儿家长的经历,并聚焦于与诊断延迟相关的挑战。2022年12月至2023年1月期间,对来自印度尼西亚9个省份的40名CAH患儿家长进行了深入访谈。结果显示,由于缺乏新生儿筛查项目(NBS)以及医疗专业人员诊断CAH的能力有限,家长们面临诸多挑战。家长们报告称存在情绪压力、经济困难和社会耻辱感。氢化可的松和17-OHP不在国家医疗保险覆盖范围内,因此经济困难普遍存在。诊断延迟对他们孩子的影响也很显著;家长们报告说,他们的孩子有自我隔离的倾向、不安全感、喜怒无常的行为以及(女性患儿的)男性化行为。这些发现强调了新生儿筛查项目实施早期诊断、提高医疗专业人员诊断CAH的能力以及确保为CAH患者提供可及且负担得起的医疗政策的迫切需求。弥补这些差距对于改善印度尼西亚CAH患儿及其家庭的生活质量至关重要。

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