Newborn screening in South Africa: the past, present, and plans for the future

Helen L. Malherbe , Jim Bonham , Michelle Carrihill , Karmani Chetty , Engela H. Conradie , Marli Dercksen , Hilary Goeiman , Marianne C. M. Gomes , Brenda Klopper , Neil McKerrow , Carmencita Padilla , Tahir S. Pillay , Bronwyn Roussot , Tumelo M. Satekge , Michael Urban , George van der Watt , Helena Vreede , Dianne Webster , Marco Zampoli , Barend C. Vorster

Rare Disease and Orphan Drugs Journal ›› 2024, Vol. 3 ›› Issue (1) : 7

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Rare Disease and Orphan Drugs Journal ›› 2024, Vol. 3 ›› Issue (1) :7 DOI: 10.20517/rdodj.2023.49
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Newborn screening in South Africa: the past, present, and plans for the future

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Abstract

Worldwide, comprehensive newborn screening (NBS) now includes a clinical examination at birth, hearing screening, pulse oximetry measurement for congenital heart defects, and biochemical screening to identify congenital disorders early in life, preventing irreversible damage, early mortality and enhancing overall health outcomes. This article provides a comprehensive overview of biochemical NBS in South Africa, outlining the history, current status, and future plans for NBS expansion. In South Africa, NBS is fragmented, with some investigations included in neonatal health assessments. Historically, biochemical NBS pilot projects in the country in the 1960s and 1980s focused on phenylketonuria and congenital hypothyroidism (CH). Despite showing initial promise, these programmes were discontinued, largely due to competing health priorities. The current status of biochemical NBS in South Africa is discussed, both for the state and private healthcare sectors, which collectively screen approximately 0.5% of births annually. While recent clinical guidelines provide for a national biochemical NBS programme, implementation has been limited, and guideline adherence remains a challenge. A brief report of a two-day meeting held in Cape Town in February 2023 focusing on biochemical NBS for South Africa is provided. The meeting addressed the importance of NBS, technology requirements, and the need for a comprehensive demonstration project for biochemical CH NBS. Key challenges identified included early newborn post-delivery discharge, technical, logistical, and infrastructure issues, as well as limited financial and human resources. Meeting recommendations included the establishment of a National Advisory Panel for Biochemical NBS, and the development and implementation of a demonstration project for CH biochemical NBS in two provinces.

Keywords

Biochemical newborn screening / congenital hypothyroidism / rare diseases / South Africa

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Helen L. Malherbe, Jim Bonham, Michelle Carrihill, Karmani Chetty, Engela H. Conradie, Marli Dercksen, Hilary Goeiman, Marianne C. M. Gomes, Brenda Klopper, Neil McKerrow, Carmencita Padilla, Tahir S. Pillay, Bronwyn Roussot, Tumelo M. Satekge, Michael Urban, George van der Watt, Helena Vreede, Dianne Webster, Marco Zampoli, Barend C. Vorster. Newborn screening in South Africa: the past, present, and plans for the future. Rare Disease and Orphan Drugs Journal, 2024, 3(1): 7 DOI:10.20517/rdodj.2023.49

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