Charting the Course: Towards a Comprehensive Newborn Screening Program in India

Author:

Kapoor Seema1ORCID,Gupta Amit Kumar1ORCID,Thelma B. K.2

Affiliation:

1. Genetic & Metabolic Lab, Division of Genetics, Department of Pediatrics, Lok Nayak Hospital & Maulana Azad Medical College, New Delhi 110002, India

2. Department of Genetics, University of Delhi South Campus, New Delhi 110021, India

Abstract

Integrating health interventions in a growing economy like India, with a birth cohort of 27 million/year, one-fifth of all childbirths, and approximately one-third of neonatal deaths globally, is a challenge. While mortality statistics are vital, intact survival and early preventive healthcare, such as newborn screening (NBS), are paramount. The appalling lack of information about the precise burden of metabolic errors at the state/national level or a mandated program encouraged a feasibility study of NBS in a prospective newborn cohort recruited in Delhi State (November 2014–April 2017) using a public–private partnership mode. The major determinants for effective implementation of universal NBS at the national level and limitations encountered are discussed in this report. Data to generate the ‘core’ panel for screening, sustained training of healthcare personnel, dissemination of the power of NBS to ensure neonatal/societal health to the public, and a ‘national policy’ emerge as priorities in a developing country.

Funder

Science and Engineering Research Board, Govt of India

Publisher

MDPI AG

Reference30 articles.

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