An insight into Indonesia's progress for newborn screening program: What is currently going on

Abstract

Objectives: In this literature review, we describe the progress of Indonesia's NBS program (which is heavily centered on CH screening), its current pilot projects, and what lies ahead for this program. Setting: Since its conception began with congenital hypothyroidism (CH) screening, Indonesia has experienced plodding progress in NBS. There is a shortage of literature discussing the history, or the lack of, and journey of NBS in Indonesia. Methods: We searched for literature in Pubmed and Google Scholar with keywords such as “Newborn Screening, “Neonatal Screening,'' “Indonesia,'' “Asia Pacific,'' “Congenital Hypothyroidism,'' “Congenital Adrenal Hyperplasia,””Critical Congenital Heart Disease,” “Hearing Loss,” and “Inborn Error of Metabolism.” Results: The only mandatory and regulated NBS program in Indonesia is congenital hypothyroid (CH) screening, with some pilot projects being conducted on screening for congenital adrenal hyperplasia (CAH), critical congenital heart disease (CCHD), hearing loss, and to a lesser extent, inborn error of metabolisms (IEMs). Conclusion: Despite the evidence and benefits, the government does not mandate or regulate newborn diseases such as CHD, CAH, hearing loss, and IEMs. The lack of regulation exists despite multiple pilot projects and studies showing a benefit in at least trying to screen newborns for those conditions.

Keywords

• Congenital adrenal hyperplasia
• Congenital hypothyroid
• Critical congenital heart disease
• Indonesia
• Newborn screening