Description

If a neonate has polycythemia, then the cause needs to be determined and the clinical severity determined.


 

Diagnosis of polycythemia:

(1) A hematocrit in a capillary blood sample > 65%.

(2) Confirmation with testing done on a venous blood sample.

 

Evaluation of the patient:

(1) Evaluate the neonate for dehydration.

(2) Evaluate the neonate for symptoms related to the polycythemia and hyperviscosity.

 

Management:

(1) If the neonate is dehydrated, then rehydrate and retest.

(2) If the neonate is symptomatic or if the hematocrit is > 75%, then perform a partial exchange transfusion (see Chapter 05).

(3) If the neonate is asymptomatic and the hematocrit is <= 75% then consider hydration, monitor for symptoms and treat any reversible causes.

 


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