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Persistent hyperglycemia is an independent predictor of outcome in acute myocardial infarction
BACKGROUND: Elevated blood glucose values are a prognostic factor in myocardial infarction (MI) patients. The unfavourable relation between hyperglycemia and outcome is known for admission glucose and fasting glucose after admission. These predictors are single measurements and thus not indicative o...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1802732/ https://www.ncbi.nlm.nih.gov/pubmed/17284309 http://dx.doi.org/10.1186/1475-2840-6-2 |
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author | van der Horst, Iwan CC Nijsten, Maarten WN Vogelzang, Mathijs Zijlstra, Felix |
author_facet | van der Horst, Iwan CC Nijsten, Maarten WN Vogelzang, Mathijs Zijlstra, Felix |
author_sort | van der Horst, Iwan CC |
collection | PubMed |
description | BACKGROUND: Elevated blood glucose values are a prognostic factor in myocardial infarction (MI) patients. The unfavourable relation between hyperglycemia and outcome is known for admission glucose and fasting glucose after admission. These predictors are single measurements and thus not indicative of overall hyperglycemia. Increased persistent hyperglycemia may better predict adverse events in MI patients. METHODS: In a prospective study of MI patients treated with primary percutaneous coronary intervention (PCI) frequent blood glucose measurements were obtained to investigate the relation between glucose and the occurrence of major adverse cardiac events (MACE) at 30 days follow-up. MACE was defined as death, recurrent infarction, repeat primary coronary intervention, and left ventricular ejection fraction equal to or smaller than 30%. RESULTS: MACE occurred in 89 (21.3%) out 417 patients. In 17 patients (4.1%) it was a fatal event. A mean of 7.4 glucose determinations were available per patient. Mean +/- SD admission glucose was 10.1 +/- 3.7 mmol/L in patients with a MACE versus 9.1 +/- 2.7 mmol/L in event-free patients (P = 0.0024). Mean glucose during the first two days after admission was 9.0 +/- 2.8 mmol/L in patients with MACE compared to 8.1 +/- 2.0 mmol/L in event free patients (P < 0.0001). The area under the receiver operator characteristic curve was 0.64 for persistent hyperglycemia and 0.59 for admission glucose. Persistent hyperglycemia emerged as a significant independent predictor (P < 0.001). CONCLUSION: Persistent hyperglycemia in MI has a stronger relation with 30-day MACE than elevated glucose at admission. |
format | Text |
id | pubmed-1802732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-18027322007-02-22 Persistent hyperglycemia is an independent predictor of outcome in acute myocardial infarction van der Horst, Iwan CC Nijsten, Maarten WN Vogelzang, Mathijs Zijlstra, Felix Cardiovasc Diabetol Original Investigation BACKGROUND: Elevated blood glucose values are a prognostic factor in myocardial infarction (MI) patients. The unfavourable relation between hyperglycemia and outcome is known for admission glucose and fasting glucose after admission. These predictors are single measurements and thus not indicative of overall hyperglycemia. Increased persistent hyperglycemia may better predict adverse events in MI patients. METHODS: In a prospective study of MI patients treated with primary percutaneous coronary intervention (PCI) frequent blood glucose measurements were obtained to investigate the relation between glucose and the occurrence of major adverse cardiac events (MACE) at 30 days follow-up. MACE was defined as death, recurrent infarction, repeat primary coronary intervention, and left ventricular ejection fraction equal to or smaller than 30%. RESULTS: MACE occurred in 89 (21.3%) out 417 patients. In 17 patients (4.1%) it was a fatal event. A mean of 7.4 glucose determinations were available per patient. Mean +/- SD admission glucose was 10.1 +/- 3.7 mmol/L in patients with a MACE versus 9.1 +/- 2.7 mmol/L in event-free patients (P = 0.0024). Mean glucose during the first two days after admission was 9.0 +/- 2.8 mmol/L in patients with MACE compared to 8.1 +/- 2.0 mmol/L in event free patients (P < 0.0001). The area under the receiver operator characteristic curve was 0.64 for persistent hyperglycemia and 0.59 for admission glucose. Persistent hyperglycemia emerged as a significant independent predictor (P < 0.001). CONCLUSION: Persistent hyperglycemia in MI has a stronger relation with 30-day MACE than elevated glucose at admission. BioMed Central 2007-02-06 /pmc/articles/PMC1802732/ /pubmed/17284309 http://dx.doi.org/10.1186/1475-2840-6-2 Text en Copyright © 2007 van der Horst et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Investigation van der Horst, Iwan CC Nijsten, Maarten WN Vogelzang, Mathijs Zijlstra, Felix Persistent hyperglycemia is an independent predictor of outcome in acute myocardial infarction |
title | Persistent hyperglycemia is an independent predictor of outcome in acute myocardial infarction |
title_full | Persistent hyperglycemia is an independent predictor of outcome in acute myocardial infarction |
title_fullStr | Persistent hyperglycemia is an independent predictor of outcome in acute myocardial infarction |
title_full_unstemmed | Persistent hyperglycemia is an independent predictor of outcome in acute myocardial infarction |
title_short | Persistent hyperglycemia is an independent predictor of outcome in acute myocardial infarction |
title_sort | persistent hyperglycemia is an independent predictor of outcome in acute myocardial infarction |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1802732/ https://www.ncbi.nlm.nih.gov/pubmed/17284309 http://dx.doi.org/10.1186/1475-2840-6-2 |
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