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Published on: March 14, 2017
Partial exchange transfusion for polycythemia hyperviscosity syndrome
Bridget Hopewell1, Laurie A Steiner, Richard A Ehrenkranz
1Yale University School of Medicine, Yale University School of Medicine, 333 Cedar Street, New Haven, CT 06520, USA.
Insights
Partial exchange transfusion (PET) for polycythemia hyperviscosity syndrome (PHS) in infants showed no change in usage over time. PHS and PET are linked to complications, necessitating further research on their long-term risks and benefits.
Area of Science:
- Neonatology
- Pediatric Hematology
Background:
- Polycythemia hyperviscosity syndrome (PHS) is a condition affecting newborns.
- Risk factors for PHS include maternal diabetes, and it can lead to significant complications.
Purpose of the Study:
- To analyze the trends in partial exchange transfusion (PET) for PHS in infants.
- To evaluate the associated risk factors and complications of PHS and PET.
Main Methods:
- Retrospective review of 141 infants treated with PET for PHS between 1986 and 2007.
- Data collected included patient demographics, PHS risk factors, PET indications, and complications.
Main Results:
- No significant change in the number of PET procedures performed over the 20-year study period.
- Maternal diabetes decreased as a risk factor over time.
- Forty percent of patients experienced PHS complications pre-PET; 18% had PET-related complications. Life-threatening events were rare.
Conclusions:
- PHS remains a concern in neonatal intensive care units, especially in high-risk infants.
- Both PHS and PET are associated with notable complications.
- Further long-term studies are required to fully understand the risks and benefits of PET for PHS.
Abstract:
The objective of this study was to examine the use of partial exchange transfusion (PET) performed for polycythemia hyperviscosity syndrome (PHS) over time. A retrospective review of 141 infants who received a PET for PHS at Yale-New Haven Hospital between 1986 and 2007 was performed, querying maternal and neonatal medical records. Patient demographics, risk factors for PHS, indications for PET, and complications associated with PET and PHS were collected. Overall, there was no change in the number of PET performed over the study period ( R(2)=0.082, P=0.192). Eighty-eight percent of patients had at least one risk factor for PHS, most commonly maternal diabetes. Over time, there was a statistically significant decrease in maternal diabetes as a risk factor for PHS. Forty percent of patients had a significant complication attributed to PHS prior to PET. Eighteen percent of patients had a complication attributed to PET. Life-threatening complications of PHS or PET were rare. In conclusion, PHS continues to be a problem observed in neonatal intensive care units, particularly in at-risk populations. PHS and PET are associated with significant complications. Well-designed studies with long-term follow up are needed to assess the risks and benefits of PET for PHS.
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