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Individual variation in unfractionated heparin dosing after pediatric cardiac surgery
We aimed to identify attributing factors to the interindividual variabilities of the infusion rates in unfractionated heparin therapy. We included patients who required unfractionated heparin therapy to achieve the target APTT after cardiac surgery between May 2014 and February 2018. Fifty-nine pati...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655810/ https://www.ncbi.nlm.nih.gov/pubmed/33173059 http://dx.doi.org/10.1038/s41598-020-76547-8 |
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author | Hikino, Keiko Koido, Masaru Ide, Kentaro Nishimura, Nao Terao, Chikashi Mushiroda, Taisei Nakagawa, Satoshi |
author_facet | Hikino, Keiko Koido, Masaru Ide, Kentaro Nishimura, Nao Terao, Chikashi Mushiroda, Taisei Nakagawa, Satoshi |
author_sort | Hikino, Keiko |
collection | PubMed |
description | We aimed to identify attributing factors to the interindividual variabilities of the infusion rates in unfractionated heparin therapy. We included patients who required unfractionated heparin therapy to achieve the target APTT after cardiac surgery between May 2014 and February 2018. Fifty-nine patients were included, of whom 8 underwent Blalock-Taussig shunt; 27, Glenn procedure; 19, Fontan procedure; 3, mechanical valve replacement; and 2, Rastelli procedure. Previously reported variables that influenced the response to unfractionated heparin treatment were initially compared, which included age; weight; sex; type of surgery; platelet count; fibrinogen, antithrombin III, total protein, albumin, alanine transaminase, and creatinine levels; and use of fresh frozen plasma. The type of surgical procedure was found to be significantly associated with the differences in heparin infusion rate (P = 0.00073). Subsequently, the variance explained by these factors was estimated through a selection based on the minimum Akaike information criterion value; models constructed by various combinations of the surgery types were compared. The model including the Blalock-Taussig shunt, Glenn procedure, and mechanical valve replacement showed the highest summed variance explained (29.1%). More than 70% of the interindividual variability in initial heparin maintenance dosing was unexplained. |
format | Online Article Text |
id | pubmed-7655810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76558102020-11-12 Individual variation in unfractionated heparin dosing after pediatric cardiac surgery Hikino, Keiko Koido, Masaru Ide, Kentaro Nishimura, Nao Terao, Chikashi Mushiroda, Taisei Nakagawa, Satoshi Sci Rep Article We aimed to identify attributing factors to the interindividual variabilities of the infusion rates in unfractionated heparin therapy. We included patients who required unfractionated heparin therapy to achieve the target APTT after cardiac surgery between May 2014 and February 2018. Fifty-nine patients were included, of whom 8 underwent Blalock-Taussig shunt; 27, Glenn procedure; 19, Fontan procedure; 3, mechanical valve replacement; and 2, Rastelli procedure. Previously reported variables that influenced the response to unfractionated heparin treatment were initially compared, which included age; weight; sex; type of surgery; platelet count; fibrinogen, antithrombin III, total protein, albumin, alanine transaminase, and creatinine levels; and use of fresh frozen plasma. The type of surgical procedure was found to be significantly associated with the differences in heparin infusion rate (P = 0.00073). Subsequently, the variance explained by these factors was estimated through a selection based on the minimum Akaike information criterion value; models constructed by various combinations of the surgery types were compared. The model including the Blalock-Taussig shunt, Glenn procedure, and mechanical valve replacement showed the highest summed variance explained (29.1%). More than 70% of the interindividual variability in initial heparin maintenance dosing was unexplained. Nature Publishing Group UK 2020-11-10 /pmc/articles/PMC7655810/ /pubmed/33173059 http://dx.doi.org/10.1038/s41598-020-76547-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Hikino, Keiko Koido, Masaru Ide, Kentaro Nishimura, Nao Terao, Chikashi Mushiroda, Taisei Nakagawa, Satoshi Individual variation in unfractionated heparin dosing after pediatric cardiac surgery |
title | Individual variation in unfractionated heparin dosing after pediatric cardiac surgery |
title_full | Individual variation in unfractionated heparin dosing after pediatric cardiac surgery |
title_fullStr | Individual variation in unfractionated heparin dosing after pediatric cardiac surgery |
title_full_unstemmed | Individual variation in unfractionated heparin dosing after pediatric cardiac surgery |
title_short | Individual variation in unfractionated heparin dosing after pediatric cardiac surgery |
title_sort | individual variation in unfractionated heparin dosing after pediatric cardiac surgery |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655810/ https://www.ncbi.nlm.nih.gov/pubmed/33173059 http://dx.doi.org/10.1038/s41598-020-76547-8 |
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