11Jul 2023
Implementation of Rapid Genome Sequencing for Critically Ill Infants With Complex Congenital Heart Disease

Implementation of Rapid Genome Sequencing for Critically Ill Infants With Complex Congenital Heart Disease

In a prospective evaluation, Rapid genome sequencing (rGS) was used to improve the care of 48 infants with complex congenital heart disease (CHD) in a cardiac neonatal intensive care unit. The results showed that rGS diagnosed genetic disorders in 27% of cases and led to changes in management in 62% of cases with diagnostic results. This study emphasizes the importance of rGS in CHD and calls for further research on its implementation for a broader population of infants with CHD.

  • #cardiology

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