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Published on: March 19, 2016
Blood transfusions in preterm infants: changes on perfusion index and intermittent hypoxemia
Katrina T Ibonia1, Henrietta S Bada1, Philip M Westgate2
1Division of Neonatology, Department of Pediatrics, University of Kentucky, Lexington, Kentucky.
Insights
Red blood cell (RBC) transfusions improve intermittent hypoxemia (IH) in preterm infants after the first week of life. However, the increase in perfusion index (PI) after transfusion did not correlate with this IH benefit.
Area of Science:
- Neonatal Medicine
- Pediatric Cardiology
- Respiratory Physiology
Background:
- Red blood cell (RBC) transfusions are known to decrease intermittent hypoxemia (IH) in infants after the first week of life.
- Improved perfusion to the respiratory control network is a potential mechanism for this benefit.
- Perfusion index (PI) is a non-invasive measure of perfusion obtained from pulse oximetry.
Purpose of the Study:
- To test the hypothesis that increased PI after RBC transfusion is associated with improved IH.
- To evaluate the predictive value of PI and clinical measures for the effect of RBC transfusion on IH.
Main Methods:
- Prospective enrollment of infants <30 weeks' gestation.
- Monitoring of PI and oxygen saturation (SpO2) using high-resolution pulse oximeters before and after RBC transfusion.
- Analysis of data across three postnatal periods: 1-7 days, 8-28 days, and 4-8 weeks of life.
Main Results:
- A total of 118 transfusions were analyzed.
- IH measures significantly decreased in infants after the first week of life (Epochs 2 and 3).
- PI significantly increased post-transfusion but did not correlate with IH reduction; mechanical ventilation, FiO2, and IH influenced oxygenation effects.
Conclusions:
- RBC transfusion effectively improves IH in preterm infants beyond the first week of life.
- The observed benefit in IH is not directly correlated with the post-transfusion increase in PI.
- Pretransfusion respiratory support and IH severity are predictors of transfusion's impact on oxygenation.
Background:
Red blood cell (RBC) transfusion decreases intermittent hypoxemia (IH) events beyond the first week of life. This benefit may be related to improved perfusion to the respiratory control network. Perfusion index (PI) is a perfusion measure provided by the pulse oximeter. We hypothesized that the benefit in IH after RBC transfusion is associated with an increase in PI. In addition, we assessed the value of PI and clinical measures in predicting the effect of RBC transfusion on IH.
Study Design And Methods:
We prospectively enrolled infants less than 30 weeks' gestation age. PI and oxygen saturation (SpO2 ) were monitored with high-resolution pulse oximeters 24 hours before and after RBC transfusion. Data were analyzed at three postnatal periods: Epoch 1, first week of life (1 to 7 days of life); Epoch 2, 2 to 4 weeks of life (8 to 28 days of life); and Epoch 3, 4 to 8 weeks of life.
Results:
A total of 118 transfusions were analyzed. IH measures significantly decreased after transfusion in Epochs 2 and 3. PI significantly increased after transfusion, but it did not correlate with the decrease in IH measures. Mechanical ventilation, fraction of inspired oxygen (FiO2 ), and IH measures influenced the effects on oxygenation.
Conclusions:
RBC transfusion improved IH after the first week of life. The benefit in IH did not correlate with PI increase after transfusion. Pretransfusion respiratory support and IH measures predicted the effect of transfusion on oxygenation.
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