Cyanosis diagnostic study of choice: Difference between revisions
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::* Insufficient [[pulmonary blood flow]] such as increased [[pulmonary vascular resistance]], [[ congenital heart disease]] | ::* Insufficient [[pulmonary blood flow]] such as increased [[pulmonary vascular resistance]], [[ congenital heart disease]] | ||
::* unusual pattern of [[pulmonary blood flow]] such as [[transposition of great arteries]] (TGA), [[total anomalous pulmonary venous connection]] (TAPVC), [[pulmonary arteriovenous malformation]] | ::* unusual pattern of [[pulmonary blood flow]] such as [[transposition of great arteries]] (TGA), [[total anomalous pulmonary venous connection]] (TAPVC), [[pulmonary arteriovenous malformation]] | ||
==References== | ==References== | ||
Revision as of 07:27, 21 October 2020
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
Diagnostic Study of Choice
- Echocardiography is the gold standard test for the diagnosis of cyanotic congenital heart diseases.[1]
Diagnostic Criteria
- The diagnosis of cyanosis is made when the following diagnostic criteria are met:
- Transient bluish discoloration of hands and feet in the neonate or acrocyanosis
- Response to oxygen therapy in peripheral cyanosis
- NO response to oxygen therapy in central cyanosis
- Discoloration of hands and feet in peripheral cyanosis
- Discoloration of mucous membrane and lips in central cyanosis
- The diagnosis of central cyanosis in the neonate is made when at least one of the following diagnostic criteria are met:
- Insufficient pulmonary oxygen intake such as respiratory failure, upper airway obstruction, hypoventilation
- Insufficient pulmonary blood flow such as increased pulmonary vascular resistance, congenital heart disease
- unusual pattern of pulmonary blood flow such as transposition of great arteries (TGA), total anomalous pulmonary venous connection (TAPVC), pulmonary arteriovenous malformation
References
- ↑ Deeg KH (April 2015). "Echocardiographic differential diagnosis of the cyanotic newborn". Ultraschall Med. 36 (2): 104–18, quiz 119–20. doi:10.1055/s-0034-1385493. PMID 25474186.