Posttransfusion Haematocrit Equilibration: Timing Posttransfusion Haematocrit Check in Neonates at the National Hospital, Abuja, Nigeria

Anaemia is a common morbidity in the NICU and often requires transfusion of packed red blood cells. Haematocrit equilibration following red cell transfusion occurs over time ultimately resulting in a stable packed cell volume (PCV). Knowledge of this equilibration process is pertinent in the accurat...

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Main Authors: L. I. Audu, A. T. Otuneye, A. B. Mairami, L. J. Mshelia, V. E. Nwatah
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:International Journal of Pediatrics
Online Access:http://dx.doi.org/10.1155/2015/175867
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author L. I. Audu
A. T. Otuneye
A. B. Mairami
L. J. Mshelia
V. E. Nwatah
author_facet L. I. Audu
A. T. Otuneye
A. B. Mairami
L. J. Mshelia
V. E. Nwatah
author_sort L. I. Audu
collection DOAJ
description Anaemia is a common morbidity in the NICU and often requires transfusion of packed red blood cells. Haematocrit equilibration following red cell transfusion occurs over time ultimately resulting in a stable packed cell volume (PCV). Knowledge of this equilibration process is pertinent in the accurate timing of posttransfusion (PT) PCV. We conducted a prospective study to determine an appropriate timing for PT PCV estimation on 47 stable anaemic babies at the Neonatal Unit of National Hospital, Abuja. Values of PCV were determined before transfusion and at 1, 6, 12, 24, and 48 hours posttransfusion. Forty of the recruited neonates and young infants were analyzed. Their gestational age range was 26 to 40 weeks. 1-hour PT PCV (48.5% ± 5.5%) was similar to the 6-hour PT PCV (47.8% ± 5.6%) P=0.516, but both were significantly different from the 12-hour (46.8% ± 5.9%), 24-hour (45.9 ± 5.8%), and 48-hour (45.4% ± 6.2%) PT PCVs. The 12-hour PT PCV was similar to the 24-hour and 48-hour PT PCVs (P=0.237 and 0.063, resp.). We concluded that, in stable nonhaemorrhaging and nonhaemolysing young infants, the estimated timing of haematocrit equilibration and, consequently, posttransfusion PCV is 12 hours after red blood cell transfusion.
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spelling doaj-art-5eebc1757a7843399fb7577bf21cb8312025-02-03T05:48:09ZengWileyInternational Journal of Pediatrics1687-97401687-97592015-01-01201510.1155/2015/175867175867Posttransfusion Haematocrit Equilibration: Timing Posttransfusion Haematocrit Check in Neonates at the National Hospital, Abuja, NigeriaL. I. Audu0A. T. Otuneye1A. B. Mairami2L. J. Mshelia3V. E. Nwatah4Neonatal Unit, National Hospital Abuja, Plot 132, National Hospital Road, Central Business District, PMB 425, Abuja, NigeriaNeonatal Unit, National Hospital Abuja, Plot 132, National Hospital Road, Central Business District, PMB 425, Abuja, NigeriaNeonatal Unit, National Hospital Abuja, Plot 132, National Hospital Road, Central Business District, PMB 425, Abuja, NigeriaNeonatal Unit, National Hospital Abuja, Plot 132, National Hospital Road, Central Business District, PMB 425, Abuja, NigeriaNeonatal Unit, National Hospital Abuja, Plot 132, National Hospital Road, Central Business District, PMB 425, Abuja, NigeriaAnaemia is a common morbidity in the NICU and often requires transfusion of packed red blood cells. Haematocrit equilibration following red cell transfusion occurs over time ultimately resulting in a stable packed cell volume (PCV). Knowledge of this equilibration process is pertinent in the accurate timing of posttransfusion (PT) PCV. We conducted a prospective study to determine an appropriate timing for PT PCV estimation on 47 stable anaemic babies at the Neonatal Unit of National Hospital, Abuja. Values of PCV were determined before transfusion and at 1, 6, 12, 24, and 48 hours posttransfusion. Forty of the recruited neonates and young infants were analyzed. Their gestational age range was 26 to 40 weeks. 1-hour PT PCV (48.5% ± 5.5%) was similar to the 6-hour PT PCV (47.8% ± 5.6%) P=0.516, but both were significantly different from the 12-hour (46.8% ± 5.9%), 24-hour (45.9 ± 5.8%), and 48-hour (45.4% ± 6.2%) PT PCVs. The 12-hour PT PCV was similar to the 24-hour and 48-hour PT PCVs (P=0.237 and 0.063, resp.). We concluded that, in stable nonhaemorrhaging and nonhaemolysing young infants, the estimated timing of haematocrit equilibration and, consequently, posttransfusion PCV is 12 hours after red blood cell transfusion.http://dx.doi.org/10.1155/2015/175867
spellingShingle L. I. Audu
A. T. Otuneye
A. B. Mairami
L. J. Mshelia
V. E. Nwatah
Posttransfusion Haematocrit Equilibration: Timing Posttransfusion Haematocrit Check in Neonates at the National Hospital, Abuja, Nigeria
International Journal of Pediatrics
title Posttransfusion Haematocrit Equilibration: Timing Posttransfusion Haematocrit Check in Neonates at the National Hospital, Abuja, Nigeria
title_full Posttransfusion Haematocrit Equilibration: Timing Posttransfusion Haematocrit Check in Neonates at the National Hospital, Abuja, Nigeria
title_fullStr Posttransfusion Haematocrit Equilibration: Timing Posttransfusion Haematocrit Check in Neonates at the National Hospital, Abuja, Nigeria
title_full_unstemmed Posttransfusion Haematocrit Equilibration: Timing Posttransfusion Haematocrit Check in Neonates at the National Hospital, Abuja, Nigeria
title_short Posttransfusion Haematocrit Equilibration: Timing Posttransfusion Haematocrit Check in Neonates at the National Hospital, Abuja, Nigeria
title_sort posttransfusion haematocrit equilibration timing posttransfusion haematocrit check in neonates at the national hospital abuja nigeria
url http://dx.doi.org/10.1155/2015/175867
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