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DOI 10.23750/abm.v90i2.8485

Медицинская библиотека · Acta bio-medica : Atenei Parmensis · 2019

Newborn screening in Nigeria: Associating the screening of congenital hypothyroidism and sickle cell disease can be a winning choice?

Yarhere Iroro Enameguolo, Jaja Tamunopriye, Briggs Datonye, Iughetti Lorenzo

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Аннотация

UNLABELLED: ntroduction: Nigeria like many African countries has tried to start the newborn screening for congenital hypothyroidism and many failed. Since sickle cell disease is more common in Nigeria, the hypothesis is that incorporating it into a screening programme for congenital hypothyroidism will improve the uptake of the programme by parents and government.

METHODS

Different aspects of newborn screening with difficulties and challenges in running newborn screening were identified and discussed.

RESULT: Identifying that for newborn screening to be successful, several key factors have to be put in place including but not limited to organizational structure, system thinking, finance, legislative and political will. A proper recall system for test positives and diagnostic/confirmatory test must be put in place before the programme starts. Since several other screening programmes like sickle cell disease, cervical and breast cancer have run successfully in Nigeria, incorporating one of them into the newborn screening for CH can make the programme succeed as there will be better uptake by the population and the policy makers.

CONCLUSION

The difficulty in establishing a newborn screening programme in Nigeria stem from health care financing, organizing the programme from screening through to recall and treatment, and ultimately, prevention of diseases.

Для цитирования: Yarhere Iroro Enameguolo, Jaja Tamunopriye, Briggs Datonye, Iughetti Lorenzo. Newborn screening in Nigeria: Associating the screening of congenital hypothyroidism and sickle cell disease can be a winning choice?. Acta bio-medica : Atenei Parmensis. 2019. DOI: 10.23750/abm.v90i2.8485.

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