[前瞻性观察研究探讨血糖水平和变异性与危重患者预后的关系]。

Xu Liu, Di-fen Wang, Jie Xiong
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引用次数: 3

摘要

目的探讨危重患者血糖水平及变异性与预后的关系。方法采用前瞻性研究。对2011年6月至2012年1月入住重症监护病房(ICU)的成人非糖尿病患者进行血糖监测及预后观察。血糖监测终端为入ICU后72 h,转ICU结束后28 d观察预后。计算转入ICU时的急性生理和慢性健康评估II(APACHE II)评分和血糖变异性[血糖标准差(SD)、平均绝对血糖波动幅度(MAGE)和血糖不稳定指数(GLI)]。根据预后将患者分为死亡组和生存组,比较两组患者APACHE II评分、平均血糖和血糖变异性。根据血糖水平将患者分为不同的组,比较各组间APACHE II评分、血糖变异性和28天死亡率。结果共入组85例。与生存组(n=58)、死亡组(n=27)比较,APACHEⅱ评分(28.9±6.6 vs. 23.8±5.9)、平均血糖(11.9±2.9 mmol/L vs. 9.4±1.8 mmol/L)、血糖SD(3.7±1.6 mmol/L vs. 2.4±1.0 mmol/L)、MAGE(0.86±0.46 mmol/L vs. 0.54±0.25 mmol/L)、GLI(255.9±232.7 vs. 111.7±110.9)均升高(P11.1 mmol/L组(n=22)均高于≤11.1 mmol/L组(n=63、2.3±0.9 mmol/L、0.5±0.2 mmol/L、91.9±91.2、20.6%,均P0.05)。结论血糖变异性与危重患者28天死亡率相关,并可与APACHE II评分一样预测死亡率。
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[Prospective observational study exploring the relationship between the levels and variability of blood glucose and the prognosis of critical patients].
OBJECTIVE To explore the relationship between the levels and variability of blood glucose and the prognosis of critical patients. METHODS A prospective study was conducted. Blood glucose monitoring and prognosis observation were performed for the adult nondiabetic patients admitted in intensive care unit (ICU) from June 2011 to January 2012. Blood glucose monitoring terminal was 72 hours after admitting in ICU, prognosis was observed for 28 days after the end of turning into ICU. Acute physiology and chronic health evaluation II(APACHE II) scores when transferred into ICU and blood glucose variability [standard deviation (SD) of blood glucose, mean absolute blood glucose fluctuation amplitude (MAGE) and glycemic instability index (GLI)] were calculated. Patients were divided into death group and survival group according to the outcome, and the APACHE II score, mean blood glucose and blood glucose variability were compared between the two groups. Patients were divided into different groups based on the blood glucose, and the APACHE II score, blood glucose variability and 28-day mortality were compared among groups. RESULTS Total 85 cases were enrolled. Compared with survivor group (n=58), in death group (n=27), APACHE II score (28.9±6.6 vs. 23.8±5.9), mean blood glucose (11.9±2.9 mmol/L vs. 9.4±1.8 mmol/L), SD of blood glucose (3.7±1.6 mmol/L vs. 2.4±1.0 mmol/L), MAGE (0.86±0.46 mmol/L vs. 0.54±0.25 mmol/L) and GLI (255.9±232.7 vs. 111.7±110.9) were increased (all P<0.05). SD of blood glucose (4.3±1.4 mmol/L), MAGE (1.1±0.4 mmol/L), GLI (345.3±210.3) and 28-day mortality (63.6%) in blood glucose >11.1 mmol/L group (n=22) were higher than those in ≤11.1 mmol/L group (n=63, 2.3±0.9 mmol/L, 0.5±0.2 mmol/L, 91.9±91.2, 20.6%, respectively, all P<0.05) and 7.8-11.1 mmol/L group (n=52, 2.3±0.9 mmol/L, 0.5±0.2 mmol/L, 85.2±66.4, 25.0%, respectively, all P<0.05). There were no significant differences between 7.8-11.1 mmol/L group and <7.8 mmol/L group (n=11) in SD of blood glucose (2.0±0.9 mmol/L), MAGE (0.5±0.3 mmol/L), GLI (123.8±166.7) and 28-day mortality (0, all P>0.05). CONCLUSION Blood glucose variability is associated with critical patient's 28-day mortality, and may predict mortality as good as APACHE II score.
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