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Examination of the Percentage of Immature Platelet Fraction in Term and Preterm Infants at Birth
BACKGROUND: Reticulated platelets (RPs) are newly synthesized platelets. Recently, an automatic method was established to detect RPs as a percentage of the immature platelet fraction (IPF%). Although, neonates often develop thrombocytopenia at some time during their hospitalization, the details of I...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3883212/ https://www.ncbi.nlm.nih.gov/pubmed/24404529 http://dx.doi.org/10.4103/2249-4847.123095 |
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author | Yuko, Sakurai Takeda, Tomohiro Hirota, Atsushi Hisaeda, Yoshiya Amakata, Syusuke Nakao, Atsushi Kawakami, Tadashi |
author_facet | Yuko, Sakurai Takeda, Tomohiro Hirota, Atsushi Hisaeda, Yoshiya Amakata, Syusuke Nakao, Atsushi Kawakami, Tadashi |
author_sort | Yuko, Sakurai |
collection | PubMed |
description | BACKGROUND: Reticulated platelets (RPs) are newly synthesized platelets. Recently, an automatic method was established to detect RPs as a percentage of the immature platelet fraction (IPF%). Although, neonates often develop thrombocytopenia at some time during their hospitalization, the details of IPF% in neonates remain unclear. We, therefore, studied the relations between IPF% and other factors to gain a more detailed understanding of IPF% in neonates. METHODS: The following clinical data were obtained from the medical records of 105 neonates who met our inclusion criteria: Gestational age, birth weight, IPF% and platelet count of neonatal peripheral blood at birth, and perinatal data. The subjects were divided into three groups: Group A, birth weight standard deviation score (SDS) ≥ −2 standard deviation (SD) and ≤ +2 SD; Group S, < −2 SD; and Group L, > +2 SD. RESULTS: IPF% correlated negatively with platelet count at birth in the whole study population. IPF% was 2.8 ± 1.3% in term neonates, and IPF correlated negatively with gestational age and birth weight. Platelet count correlated positively with birth weight SDS in the whole study population and in Group S. IPF% correlated negatively with birth weight SDS in the whole study population and in Group S. In neonates with a platelet count below 25 × 10(4)/μl, IPF% correlated negatively with platelet count. Among other neonates, however, IPF% remained almost constant. CONCLUSION: Monitoring of IPF% is useful for estimating the function of thrombocytopoiesis in neonates and preterm infants. |
format | Online Article Text |
id | pubmed-3883212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38832122014-01-08 Examination of the Percentage of Immature Platelet Fraction in Term and Preterm Infants at Birth Yuko, Sakurai Takeda, Tomohiro Hirota, Atsushi Hisaeda, Yoshiya Amakata, Syusuke Nakao, Atsushi Kawakami, Tadashi J Clin Neonatol Original Article BACKGROUND: Reticulated platelets (RPs) are newly synthesized platelets. Recently, an automatic method was established to detect RPs as a percentage of the immature platelet fraction (IPF%). Although, neonates often develop thrombocytopenia at some time during their hospitalization, the details of IPF% in neonates remain unclear. We, therefore, studied the relations between IPF% and other factors to gain a more detailed understanding of IPF% in neonates. METHODS: The following clinical data were obtained from the medical records of 105 neonates who met our inclusion criteria: Gestational age, birth weight, IPF% and platelet count of neonatal peripheral blood at birth, and perinatal data. The subjects were divided into three groups: Group A, birth weight standard deviation score (SDS) ≥ −2 standard deviation (SD) and ≤ +2 SD; Group S, < −2 SD; and Group L, > +2 SD. RESULTS: IPF% correlated negatively with platelet count at birth in the whole study population. IPF% was 2.8 ± 1.3% in term neonates, and IPF correlated negatively with gestational age and birth weight. Platelet count correlated positively with birth weight SDS in the whole study population and in Group S. IPF% correlated negatively with birth weight SDS in the whole study population and in Group S. In neonates with a platelet count below 25 × 10(4)/μl, IPF% correlated negatively with platelet count. Among other neonates, however, IPF% remained almost constant. CONCLUSION: Monitoring of IPF% is useful for estimating the function of thrombocytopoiesis in neonates and preterm infants. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3883212/ /pubmed/24404529 http://dx.doi.org/10.4103/2249-4847.123095 Text en Copyright: © Journal of Clinical Neonatology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Yuko, Sakurai Takeda, Tomohiro Hirota, Atsushi Hisaeda, Yoshiya Amakata, Syusuke Nakao, Atsushi Kawakami, Tadashi Examination of the Percentage of Immature Platelet Fraction in Term and Preterm Infants at Birth |
title | Examination of the Percentage of Immature Platelet Fraction in Term and Preterm Infants at Birth |
title_full | Examination of the Percentage of Immature Platelet Fraction in Term and Preterm Infants at Birth |
title_fullStr | Examination of the Percentage of Immature Platelet Fraction in Term and Preterm Infants at Birth |
title_full_unstemmed | Examination of the Percentage of Immature Platelet Fraction in Term and Preterm Infants at Birth |
title_short | Examination of the Percentage of Immature Platelet Fraction in Term and Preterm Infants at Birth |
title_sort | examination of the percentage of immature platelet fraction in term and preterm infants at birth |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3883212/ https://www.ncbi.nlm.nih.gov/pubmed/24404529 http://dx.doi.org/10.4103/2249-4847.123095 |
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