5.1 Cyanotic heart disease and tetralogy of Fallot spells
Introduction
Cyanosis is a bluish discolouration of skin and mucous membranes due to excessive concentration of reduced haemoglobin in the blood.1 Cyanosis is evident when deoxygenated haemoglobin in the cutaneous veins reaches approximately 5 g dL–1.2 Deoxygenated haemoglobin may occur either from arterial blood desaturation or increased oxygen extraction by peripheral tissue. Central cyanosis is produced as a result of arterial desaturation, i.e. aortic blood carrying deoxygenated haemoglobin. Isolated peripheral cyanosis may result from excessive deoxy-haemoglobin caused by extensive oxygen extraction.1 Haemoglobin level affects the presence of cyanosis. Cyanosis is detected at a higher oxygen saturation in children with polycythaemia and is more difficult to detect in children with severe anaemia. Causes of cyanosis are listed in Table 5.1.1.
Differential diagnosis |
Arterial oxygen desaturation (central cyanosis [pO2 <50 mmHg]) |
Increased capillary oxygen extraction (peripheral cyanosis) |
Abnormal haemoglobin (not related to level of oxygenation) |
Cyanotic congenital heart disease
Cyanotic congenital heart disease (CHD) generally presents in the neonatal period. In the newborn, mild cyanosis (mild hypoxia SaO2 >85%) may be difficult to detect clinically. Other confounding factors may be acrocyanosis (a normal finding, which may last 72 hours), polycythaemia (giving the appearance of cyanosis) and dark skin (cyanosis is more difficult to detect). Cyanosis is better appreciated in natural light than in artificial light.
Arterial oxygen saturation should always be assessed with pulse oximetry when considering cyanosis in the newborn. The hyperoxia test may help distinguish cyanosis caused by cyanotic heart defects from other defects.2–4,8
Hyperoxia test

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