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Newborn screening in Indonesia
Diet S Rustama1, M Ryadi Fadil, Elly R Harahap
1Department of Child Health, Padjadjaran University School of Medicine, Bandung, Indonesia.
Insights
Indonesia lacks a national newborn screening policy, leaving infants vulnerable to preventable conditions like congenital hypothyroidism (CH). A pilot project identified challenges in screening implementation and follow-up, highlighting the need for improved infrastructure and awareness.
Area of Science:
- Endocrinology
- Public Health
- Neonatal Medicine
Background:
- Newborn screening for congenital hypothyroidism (CH) is not a national policy in Indonesia.
- The incidence of preventable causes of mental retardation, such as CH, is unknown.
- Unidentified CH cases can lead to long-term health issues and developmental delays.
Purpose of the Study:
- To estimate the local incidence of CH in Indonesia.
- To evaluate the challenges associated with implementing a newborn screening program for CH.
- To inform the development of a nationwide CH screening initiative.
Main Methods:
- A pilot study was conducted from June 2000 to August 2001, screening 6,843 neonates.
- Initial screening used cord blood serum (June 2000-Feb 2001), followed by the heel prick method (March 2001-Aug 2001).
- TSH measurement was the primary test, with T4 used for confirmation in elevated TSH cases.
Main Results:
- The heel prick method significantly reduced the recall rate from 3.3% to 0.64%.
- High rates of unsatisfactory samples were observed due to blood collection issues.
- Parental refusal and lack of policy maker awareness hindered program acceptance.
Conclusions:
- Implementing a nationwide CH screening program requires improved infrastructure, particularly for patient recall systems.
- Intensified education and information campaigns for parents and healthcare professionals are crucial.
- Securing a national mandate from the Department of Health is essential for program sustainability.
Abstract:
In Indonesia, newborn screening is not yet a policy, and the incidence of preventable causes of mental retardation detected by newborn screening is not known. Congenital hypothyroidism (CH) is not infrequent. Without a screening program, unrecognized CH patients were neglected for years. Since May 1999, the International Atomic Energy Agency (IAEA) has assisted in starting a CH Newborn Screening Project to estimate the local incidence of CH and to evaluate the problems associated with the screening. In June 2000, a pilot study was conducted using primary TSH measurement, supplemented by T4 in infants with elevated TSH. The target was to screen 12,000 newborn infants, using cord blood serum taken at birth, or a heel prick between 2 to 6 days of age. Between June 2000 and February 2001, 3,534 neonates born in 4 hospitals were screened using cord blood serum taken at birth (recall rate 3.3%). From March 2001 onwards, the heel prick method was used and participating hospitals increased from 4 to 7. Using this approach, until August 2001, 3,309 samples were analysed and the recall rate was much lower (0.64%). The number of unsatisfactory samples was relatively high due to an unstable process of blood collection. Parental refusal and low acceptance of screening among policy makers resulted from lack of awareness of the dangers of CH, and the screening program was not considered a health priority. Recall of patients after screening was a major barrier, with problems in tracking patients arising from urbanization and a high rate of relocation. To advance the CH screening program nationwide, infrastructure must be improved along with the recall system, and education as well as information campaigns for parents and medical professionals must be intensified. The Department of Health must be persuaded to give a national mandate.
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