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Wider intraoperative glycemic fluctuation increases risk of acute kidney injury after pediatric cardiac surgery

Objective: The association between poor intraoperative glycemic control and postoperative acute kidney injury (AKI) in adult cardiac surgery has been observed, but data in the pediatrics remain unknown. We performed a hypothesis that intraoperative hyperglycemia and/or wider glycemic fluctuation wer...

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Autores principales: Hu, Guo-Huang, Duan, Lian, Jiang, Meng, Zhang, Cheng-Liang, Duan, Yan-Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6225368/
https://www.ncbi.nlm.nih.gov/pubmed/30396300
http://dx.doi.org/10.1080/0886022X.2018.1532908
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author Hu, Guo-Huang
Duan, Lian
Jiang, Meng
Zhang, Cheng-Liang
Duan, Yan-Ying
author_facet Hu, Guo-Huang
Duan, Lian
Jiang, Meng
Zhang, Cheng-Liang
Duan, Yan-Ying
author_sort Hu, Guo-Huang
collection PubMed
description Objective: The association between poor intraoperative glycemic control and postoperative acute kidney injury (AKI) in adult cardiac surgery has been observed, but data in the pediatrics remain unknown. We performed a hypothesis that intraoperative hyperglycemia and/or wider glycemic fluctuation were associated with the incidence of postoperative AKI in pediatric cardiac surgery. Methods: A retrospective study was performed in pediatrics who underwent cardiac surgery from 2013 to 2016. Perioperative glycemic data up to 48 hours after surgery were collected and analyzed. Patients with AKI were matched 1:1 with patients without AKI by a propensity score. Variables of demographic data, preoperative renal function and glycemic level, perioperative cardiac condition were matched. Results: The incidence of AKI was 11.5% (118/1026), with 53.4% (63/118), 30.5% (36/118), and 16.1% (19/118) categorized as AKIN stages I, II, and III, respectively. Children who experienced AKI were younger and cyanotic, underwent more complex surgeries, had higher peak intraoperative glucose levels, wider intraoperative glycemic fluctuation, greater inotropic scores and more transfusions, and poor outcomes (all p < .05). After matching, the AKI group had significantly wider intraoperative glycemic fluctuation (p < .05). Logistic regression showed intraoperative glycemic fluctuation was one of the risk factors for AKI (p = .033) and degree of AKI severity stage increased when the glycemic fluctuation increased (p < .01). Conclusions: Wider intraoperative glycemic fluctuation, but not hyperglycemia, was associated with an increased incidence of postoperative AKI after pediatric cardiac surgery.
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spelling pubmed-62253682018-11-13 Wider intraoperative glycemic fluctuation increases risk of acute kidney injury after pediatric cardiac surgery Hu, Guo-Huang Duan, Lian Jiang, Meng Zhang, Cheng-Liang Duan, Yan-Ying Ren Fail Clinical Study Objective: The association between poor intraoperative glycemic control and postoperative acute kidney injury (AKI) in adult cardiac surgery has been observed, but data in the pediatrics remain unknown. We performed a hypothesis that intraoperative hyperglycemia and/or wider glycemic fluctuation were associated with the incidence of postoperative AKI in pediatric cardiac surgery. Methods: A retrospective study was performed in pediatrics who underwent cardiac surgery from 2013 to 2016. Perioperative glycemic data up to 48 hours after surgery were collected and analyzed. Patients with AKI were matched 1:1 with patients without AKI by a propensity score. Variables of demographic data, preoperative renal function and glycemic level, perioperative cardiac condition were matched. Results: The incidence of AKI was 11.5% (118/1026), with 53.4% (63/118), 30.5% (36/118), and 16.1% (19/118) categorized as AKIN stages I, II, and III, respectively. Children who experienced AKI were younger and cyanotic, underwent more complex surgeries, had higher peak intraoperative glucose levels, wider intraoperative glycemic fluctuation, greater inotropic scores and more transfusions, and poor outcomes (all p < .05). After matching, the AKI group had significantly wider intraoperative glycemic fluctuation (p < .05). Logistic regression showed intraoperative glycemic fluctuation was one of the risk factors for AKI (p = .033) and degree of AKI severity stage increased when the glycemic fluctuation increased (p < .01). Conclusions: Wider intraoperative glycemic fluctuation, but not hyperglycemia, was associated with an increased incidence of postoperative AKI after pediatric cardiac surgery. Taylor & Francis 2018-11-06 /pmc/articles/PMC6225368/ /pubmed/30396300 http://dx.doi.org/10.1080/0886022X.2018.1532908 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Hu, Guo-Huang
Duan, Lian
Jiang, Meng
Zhang, Cheng-Liang
Duan, Yan-Ying
Wider intraoperative glycemic fluctuation increases risk of acute kidney injury after pediatric cardiac surgery
title Wider intraoperative glycemic fluctuation increases risk of acute kidney injury after pediatric cardiac surgery
title_full Wider intraoperative glycemic fluctuation increases risk of acute kidney injury after pediatric cardiac surgery
title_fullStr Wider intraoperative glycemic fluctuation increases risk of acute kidney injury after pediatric cardiac surgery
title_full_unstemmed Wider intraoperative glycemic fluctuation increases risk of acute kidney injury after pediatric cardiac surgery
title_short Wider intraoperative glycemic fluctuation increases risk of acute kidney injury after pediatric cardiac surgery
title_sort wider intraoperative glycemic fluctuation increases risk of acute kidney injury after pediatric cardiac surgery
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6225368/
https://www.ncbi.nlm.nih.gov/pubmed/30396300
http://dx.doi.org/10.1080/0886022X.2018.1532908
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