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Comprehensive Newborn Screening Program: ARAMCO Experience, The National Need and Recommendations

1992; King Faisal Specialist Hospital and Research Centre; Volume: 12; Issue: 3 Linguagem: Inglês

10.5144/0256-4947.1992.235

0975-4466

Yousef K. Abu‐Osba, Ahmad A. Mallouh, Mouhamed Salamah, Richard W. Hann, A. Thalji, Jahed Hamdan, Abed Alrahman Sa'di,

Blood disorders and treatments

Comprehensive screening programs for congenital diseases of newborn infants are lacking at a national or regional level. A comprehensive newborn screening program modified to the needs and resources available was established in ARAMCO Dhahran Health Center. This program includes screening for congenital hypothyroidism, phenylketonuria, abnormal hemoglobins, glucose-6-phosphate dehydrogenase deficienc, and blood group incompatibilities. Several problems were encountered during the operation which required several modifications of the program. The organization and procedures of the program are described. Since the program was started in 1980, more than 70,000 newborn infants have been screened. Valuable epidemiological data have been collected and necessary information for direct clinical use was obtained. A national program to screen all neonates in the Kingdom of Saudi Arabia is achievable and urgently needed. Recommendations based on ARAMCO experience are given.