• Ingolf Griebsch, Rachel L Knowles, Jacqueline Brown, Catherine Bull, Christopher Wren, and Carol A Dezateux.
• Department of Social Medicine, University of Bristol, UK. Ingolf.Griebsch@merck.de
• Int J Technol Assess Health Care. 2007 Jan 1;23(2):192-204.

ObjectivesCongenital heart defects (CHD) are an important cause of death and morbidity in early childhood, but the effectiveness of alternative newborn screening strategies in preventing the collapse or death--before diagnosis--of infants with treatable but life-threatening defects is uncertain. We assessed their effectiveness and efficiency to inform policy and research priorities.MethodsWe compared the effectiveness of clinical examination alone and clinical examination with either pulse oximetry or screening echocardiography in making a timely diagnosis of life-threatening CHD or in diagnosing clinically significant CHD. We contrasted their cost-effectiveness, using a decision-analytic model based on 100,000 live births, and assessed future research priorities using value of information analysis.ResultsClinical examination alone, pulse oximetry, and screening echocardiography achieved 34.0, 70.6, and 71.3 timely diagnoses per 100,000 live births, respectively. This finding represents an additional cost per additional timely diagnosis of 4,894 pounds and 4,496,666 pounds for pulse oximetry and for screening echocardiography. The equivalent costs for clinically significant CHD are 1,489 pounds and 36,013 pounds, respectively. Key determinants of cost-effectiveness are detection rates and screening test costs. The false-positive rate is very high with screening echocardiography (5.4 percent), but lower with pulse oximetry (1.3 percent) or clinical examination alone (.5 percent).ConclusionsAdding pulse oximetry to clinical examination is likely to be a cost-effective newborn screening strategy for CHD, but further research is required before this policy can be recommended. Screening echocardiography is unlikely to be cost-effective, unless the detection of all clinically significant CHD is considered beneficial and a 5 percent false-positive rate acceptable.

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