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入院时血糖水平并不能改善心肌梗死后6个月和5年时的GRACE评分。

Admission glucose does not improve GRACE score at 6 months and 5 years after myocardial infarction.

作者信息

de Mulder Maarten, van der Ploeg Tjeerd, de Waard Guus A, Boersma Eric, Umans Victor A

机构信息

Department of Cardiology, Medical Centre Alkmaar, Alkmaar, The Netherlands.

出版信息

Cardiology. 2011;120(4):227-34. doi: 10.1159/000335715. Epub 2012 Feb 15.

DOI:10.1159/000335715
PMID:22343543
Abstract

OBJECTIVE

Admission plasma glucose (APG) is a biomarker that predicts mortality in myocardial infarction (MI) patients. Therefore, APG may improve risk stratification based on the GRACE risk score.

METHODS

We collected data on baseline characteristics and long-term (median 55 months) outcome of 550 MI patients who entered our hospital in 2003 and 2006. We determined the GRACE risk score at admission for each patient, which was entered in a logistic regression model, together with APG, to evaluate their prognostic value for 6-month and 5-year mortality.

RESULTS

Patients with APG ≥7.8 mmol/l had a higher mortality than those with APG levels <7.8 mmol/l; 6 months: 13.7 versus 3.6%, p value <0.001; 5 years: 20.4 versus 11.1%, p value 0.003. After adjustment for the GRACE risk score variables, APG appeared a significant predictor of 6-month and 5-year mortality, adjusted OR 1.17 (1.06-1.29) and 1.12 (1.03-1.22). The combination of the GRACE risk score and APG increased the model's performance (discrimination C-index 0.87 vs. 0.85), although the difference was not significant (p = 0.095). Combining the GRACE risk score and APG reclassified 12.9% of the patients, but the net reclassification improvement was nonsignificant (p = 0.146).

CONCLUSION

APG is a predictor of 6-month and 5-year mortality, each mmol/l increase in APG being associated with a mortality increase of 17 and 12%, respectively, independent of the GRACE risk score. However, adding APG to the GRACE model did not result in significantly improved clinical risk stratification.

摘要

目的

入院时血浆葡萄糖(APG)是预测心肌梗死(MI)患者死亡率的生物标志物。因此,APG可能会改善基于GRACE风险评分的风险分层。

方法

我们收集了2003年和2006年入院的550例MI患者的基线特征和长期(中位55个月)结局数据。我们确定了每位患者入院时的GRACE风险评分,并将其与APG一起纳入逻辑回归模型,以评估它们对6个月和5年死亡率的预后价值。

结果

APG≥7.8 mmol/l的患者死亡率高于APG水平<7.8 mmol/l的患者;6个月时:分别为13.7%和3.6%,p值<0.001;5年时:分别为20.4%和11.1%,p值0.003。在对GRACE风险评分变量进行调整后,APG似乎是6个月和5年死亡率的显著预测因素,调整后的OR分别为1.17(1.06 - 1.29)和1.12(1.03 - 1.22)。GRACE风险评分与APG的联合提高了模型的性能(区分C指数为0.87对0.85),尽管差异不显著(p = 0.095)。将GRACE风险评分与APG相结合对12.9%的患者进行了重新分类,但净重新分类改善不显著(p = 0.146)。

结论

APG是6个月和5年死亡率的预测因素,APG每增加1 mmol/l,死亡率分别增加17%和12%,独立于GRACE风险评分。然而,将APG添加到GRACE模型中并未导致临床风险分层得到显著改善。

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