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28 - Polycythemia

from Part IV - Specific Conditions Associated with Fetal and Neonatal Brain Injury

Published online by Cambridge University Press:  10 November 2010

Ted S. Rosenkrantz
Affiliation:
University of Connecticut Health Center, Farmington, CT, USA
William Oh
Affiliation:
Department of Pediatrics, Brown University, Providence, RI, USA
David K. Stevenson
Affiliation:
Stanford University School of Medicine, California
William E. Benitz
Affiliation:
Stanford University School of Medicine, California
Philip Sunshine
Affiliation:
Stanford University School of Medicine, California
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Summary

Introduction

Polycythemia and hyperviscosity were first associated with adverse neurologic events and sequelae in a series of case reports. The first case often referenced was published by Wood in 1952 and was followed by a small series of infants with polycythemia and hyperviscosity who displayed multiple problems, including cerebral dysfunction. Since those early reports it has become clear that polycythemia has multiple etiologies which influence whether and which problems may be associated with it in the newborn period. In addition more recent animal and human studies have clarified the relationship between polycythemia and alterations in function of various organs.

Definition

Polycythemia is usually defined in the literature as a hematocrit value ≥ 65% when the blood sample is obtained from a free-flowing, large venous blood vessel such as the inferior vena cava (umbilical vein sample) spun in a centrifuge. Sampling from small vessels with low flow or capillary samples will have higher values. In addition, hematocrits calculated by a Coulter counter will yield comparatively lower values. Independent of sample site or measurement technique, the hematocrit increases over the first 2–4 h of life, gradually returning to the birth value by 12–24 h of age.

Incidence

The incidence of polycythemia varies by definition, altitude of the population, pregnancy risk factors, and techniques involved in the delivery of the fetus, and timing and sampling sites of blood samples.

Type
Chapter
Information
Fetal and Neonatal Brain Injury
Mechanisms, Management and the Risks of Practice
, pp. 578 - 585
Publisher: Cambridge University Press
Print publication year: 2003

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  • Polycythemia
    • By Ted S. Rosenkrantz, University of Connecticut Health Center, Farmington, CT, USA, William Oh, Department of Pediatrics, Brown University, Providence, RI, USA
  • Edited by David K. Stevenson, Stanford University School of Medicine, California, William E. Benitz, Stanford University School of Medicine, California, Philip Sunshine, Stanford University School of Medicine, California
  • Book: Fetal and Neonatal Brain Injury
  • Online publication: 10 November 2010
  • Chapter DOI: https://doi.org/10.1017/CBO9780511544774.030
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  • Polycythemia
    • By Ted S. Rosenkrantz, University of Connecticut Health Center, Farmington, CT, USA, William Oh, Department of Pediatrics, Brown University, Providence, RI, USA
  • Edited by David K. Stevenson, Stanford University School of Medicine, California, William E. Benitz, Stanford University School of Medicine, California, Philip Sunshine, Stanford University School of Medicine, California
  • Book: Fetal and Neonatal Brain Injury
  • Online publication: 10 November 2010
  • Chapter DOI: https://doi.org/10.1017/CBO9780511544774.030
Available formats
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  • Polycythemia
    • By Ted S. Rosenkrantz, University of Connecticut Health Center, Farmington, CT, USA, William Oh, Department of Pediatrics, Brown University, Providence, RI, USA
  • Edited by David K. Stevenson, Stanford University School of Medicine, California, William E. Benitz, Stanford University School of Medicine, California, Philip Sunshine, Stanford University School of Medicine, California
  • Book: Fetal and Neonatal Brain Injury
  • Online publication: 10 November 2010
  • Chapter DOI: https://doi.org/10.1017/CBO9780511544774.030
Available formats
×