Cyanosis screening
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sara Zand, M.D.[2]
Overview
Prenatal echocardiography and genetic testing are useful methods for early detection of cyanotic congenital heart disease.Postnatal pulse oximetry is recommended for diagnosis of cyanotic congenital heart disease
Screening
- Prenatal echocardiography and genetic testing are useful methods for early detection of cyanotic congenital heart disease.
- Postnatal pulse oximetry is recommended for diagnosis of cyanotic congenital heart disease.[1]
References
- ↑ Liu, Xiwang; Xu, Weize; Yu, Jiangen; Shu, Qiang (2019). “Screening for congenital heart defects: diversified strategies in current China”. World Journal of Pediatric Surgery. 2 (1): e000051. doi:10.1136/wjps-2019-000051. ISSN 2516-5410.
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