[危重患者肠内营养期间血糖的处理]。

Yang Liu, Wei He, Hua Zhou, Tong Li, Yuan Xu
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引用次数: 0

摘要

目的:探讨一种有效、安全的肠内营养(EN)患者胰岛素给药从静脉泵入过渡到皮下注射的方案。方法:采用前瞻性随机对照研究。将2008年9月至2009年2月在北京同仁医院重症监护病房(ICU)住院的危重患者随机分为两组,实验组的能量供给达到总能量需求的一半。试验组(n=44):该方案应用于甘精胰岛素和常规胰岛素注射;对照组(n=43):采用常规胰岛素皮下注射方案。目标血糖范围为4.4 ~ 7.8 mmol/L (80 ~ 140 mg/dl)。如果两次血糖≥11.1 mmol/L,胰岛素给药方式由皮下注射改为静脉泵入,采用电脑化血糖控制方案。如胰岛素输注速度小于3u /h且持续时间大于6小时,血糖≤7.8 mmol/L,则再次改为皮下注射。记录一般信息和所有血糖调节数据进行分析。结果:两组一般资料、平均血糖及血糖变化在基线时无差异。共分析了1689份血糖记录。实验组的平均血糖明显低于对照组(7.58±1.17 mmol/L vs. 9.40±1.74 mmol/L)。结论:与常规胰岛素皮下注射方案相比,该方案甘精胰岛素联合常规胰岛素皮下注射可有效控制危重患者EN期间的血糖水平。该方案显著减少了葡萄糖变化和测量次数。这有助于胰岛素从静脉泵入到皮下注射的传递。
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[Management of blood glucose during enteral nutrition in critical patients].

Objective: To investigate an effective and safe protocol for enteral nutrition (EN) patients permitting successfully transmit insulin administration from venous pump-in to subcutaneous injection.

Methods: A prospective randomized control study was conducted. Critical patients admitted to intensive care unit (ICU) of Beijing Tongren Hospital from September 2008 to February 2009 were randomly divided into two groups when the energy provided by EN up to half of the total energy requirement. Experiment group (n=44): the protocol was applied for insulin glargine and regular insulin injection; control group (n=43): protocol was applied for subcutaneous regular insulin injection. Target glucose range was 4.4-7.8 mmol/L (80-140 mg/dl). If blood glucose ≥11.1 mmol/L was maintained twicely, the approach of insulin administration would convert from subcutaneous injection to venous pump-in using the computerized glucose control protocol. If the infusion rate of insulin was less than 3 U/h and lasted more than 6 hours, blood glucose ≤7.8 mmol/L, insulin administration was switched to subcutaneous injection again. The general information and all glucose regulation data were recorded for analysis.

Results: The two groups did not differ at baseline for the general information, mean blood glucose and the glucose variation. A total of 1689 blood glucose records were analyzed. The mean blood glucose in experiment group, and was significantly lower than that in control group(7.58±1.17 mmol/L vs. 9.40±1.74 mmol/L, P<0.05). The rate of glucose values within target range in experiment group was significantly higher than that in control group [49.72% (534/1074) vs. 35.61% (219/615), P<0.01]. The glucose standard deviation (SD) in experiment group was significantly lower than that in control group (1.89±0.52 mmol/L vs. 2.17±0.94 mmol/L, P<0.05). The number of measurements needed per patient per day was significantly reduced in experiment group compared with control group (7.51±1.31 vs. 8.15±0.97, P<0.05). The ratio of patients converted to venous pump-in was significantly decreased in experiment group compared with control group (9.09% vs. 44.19%, P<0.01). Hypoglycemia (≤3.3 mmol/L) did not different between experiment group and control group [0.74% (8/1074) vs. 0.49% (3/615), P=0.75].

Conclusions: Compared with the conventional subcutaneous insulin injection protocol, this protocol with insulin glargine combined regular insulin subcutaneous injection can control the glucose level effectively during EN in critical patients. The glucose variation and the numbers of measurements were significantly reduced by this protocol. It is helpful for the insulin transmission from venous pump-in to subcutaneous injection.

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