Polycythemia
Deirdre O’Reilly
KEY POINTS
Polycythemia and hyperviscosity of the blood in newborns may lead to symptoms such as hypoglycemia, poor feeding, and irritability; yet, most newborns with polycythemia are asymptomatic.
Partial exchange transfusion to reduce hematocrit should be considered for newborns with levels >65%.
Partial exchange transfusion will likely treat symptoms if they are present but has not been shown to affect neurodevelopmental outcome.
As the central venous hematocrit rises, there is increased viscosity and decreased blood flow. When the hematocrit increases to >60%, there is decreased oxygen delivery (Fig. 46.1). Newborns have larger, irregularly shaped red blood cells (RBC) with different membrane characteristics than the RBCs of adults. As viscosity increases, there is impairment of tissue oxygenation and decreased glucose in plasma, leading to increased risk of microthrombus formation. If these events occur in the cerebral cortex, kidneys, or adrenal glands, significant damage may result. Hypoxia and acidosis increase viscosity and deformity further. Poor perfusion increases the possibility of thrombosis.
I. DEFINITIONS
A. Polycythemia is defined as venous hematocrit of at least 65%. Hematocrit measurements vary greatly with site of sample, and capillary hematocrit may be up to 20% higher than venous. Hematocrit initially rises after birth from placental transfer of RBCs and then decreases to baseline by approximately 24 hours. The mean venous hematocrit of term infants is 53% in cord blood, 60% at 2 hours of age, 57% at 6 hours of age, and 52% at 12 to 18 hours of age.
B. Hyperviscosity is defined as viscosity >2 standard deviations greater than the mean. Blood viscosity, as described by Poiseuille, is the ratio of shear stress to shear rate and is dependent on such factors as the pressure gradient along the vessel, radius, length, and flow. The relationship between hematocrit and viscosity is nearly linear below a hematocrit of 60%, but viscosity increases exponentially at a hematocrit of 70% or greater (Fig. 46.1).
Other factors affect blood viscosity, including plasma proteins such as fibrinogen, local blood flow, and pH. The hyperviscosity syndrome is usually seen only in infants with venous hematocrits above 60%.
II. INCIDENCE. The incidence of polycythemia is 1% to 5% in term newborns. Polycythemia is increased in babies that have intrauterine growth restriction (IUGR), are small for gestational age (SGA), and are born postterm.
III. CAUSES OF POLYCYTHEMIA
A. Placental red cell transfusion
1. Delayed cord clamping may occur either intentionally or in unattended deliveries.
a. When the cord is clamped within 1 minute after birth, the blood volume of the infant is approximately 80 mL/kg.
b. When the cord is clamped 2 minutes after delivery, the blood volume of the infant is 90 mL/kg.
c. In newborns with polycythemia, blood volume per kilogram of body weight varies inversely in relation to birth weight (Fig. 46.2).
2. Cord stripping (thereby pushing more blood into the infant)
3. Holding the baby below the mother at delivery
4. Maternal-to-fetal transfusion is diagnosed with the Kleihauer-Betke stain technique of acid elution to detect maternal cells in the circulation of the newborn (see Chapter 45).