Cyanosis screening: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
Line 14: | Line 14: | ||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
[[Category:Primary care]] | |||
[[Category: |
Latest revision as of 04:09, 26 December 2020
Cyanosis Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Cyanosis screening On the Web |
American Roentgen Ray Society Images of 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.