1 Pharmaceutical Care Division, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
2 College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
JPEN J Parenter Enteral Nutr. 2017 Sep;41(7):1110-1118. doi: 10.1177/0148607116644710. Epub 2016 Apr 18.
Hyperglycemia is a major complication of parenteral nutrition (PN). Guidelines for hyperglycemia management in noncritically ill patients cite basal insulin administration but do not recommend a regimen. The GLUCOSE-in-PN study aimed to compare the efficacy of glargine insulin versus continuously infused regular insulin in PN (RI-in-PN) to achieve glycemic control in noncritically ill surgical patients with diabetes who were receiving PN.
This prospective randomized open-label study was conducted at King Faisal Specialist Hospital and Research Centre. Noncritically ill surgical patients with diabetes who were receiving PN were randomized to receive basal glargine insulin or RI-in-PN on day 4 of PN support. Mean blood glucose levels were compared on study days 5-9. The percentages of blood glucose measurements at goal were compared between groups.
Sixty-seven PN treatment episodes were analyzed. There were no statistically significant differences in mean glucose levels between groups on any study day ( P > .1). Overall glycemic control rates were 52.24% (glargine insulin) and 47.76% (RI-in-PN; P = .06). A significantly higher percentage of hyperglycemia was observed on day 5 for glargine insulin versus RI-in-PN (22.39% vs 5.97%, P = .0059). Blood glucose measurements indicated 6 hypoglycemic events: 2 for glargine insulin (5.7%) and 4 for RI-in-PN (11.4%; P > .1).
Both glargine insulin and RI-in-PN are effective basal insulin modalities for blood glucose control in noncritically ill surgical patients with diabetes who are receiving PN. Uncontrolled hyperglycemic events occurred more frequently with glargine insulin, and the rate of hypoglycemia was acceptable for both regimens.
高血糖是肠外营养(PN)的主要并发症。非危重症患者高血糖管理指南引用基础胰岛素给药,但不推荐具体方案。GLUCOSE-in-PN 研究旨在比较甘精胰岛素与持续输注常规胰岛素在 PN(RI-in-PN)中的疗效,以实现接受 PN 的糖尿病非危重症外科患者的血糖控制。
这项前瞻性随机开放标签研究在法伊萨尔国王专科医院和研究中心进行。接受 PN 的糖尿病非危重症外科患者在 PN 支持的第 4 天随机接受基础甘精胰岛素或 RI-in-PN。比较研究第 5-9 天的平均血糖水平。比较两组之间目标血糖测量的百分比。
分析了 67 个 PN 治疗期。任何研究日均无组间平均血糖水平的统计学差异(P>.1)。总体血糖控制率分别为甘精胰岛素 52.24%(52.24%)和 RI-in-PN 47.76%(P=.06)。甘精胰岛素组第 5 天的高血糖发生率明显高于 RI-in-PN 组(22.39% vs 5.97%,P=.0059)。血糖测量显示 6 例低血糖事件:甘精胰岛素 2 例(5.7%),RI-in-PN 4 例(11.4%;P>.1)。
甘精胰岛素和 RI-in-PN 均为接受 PN 的糖尿病非危重症外科患者血糖控制的有效基础胰岛素方式。甘精胰岛素组发生未控制的高血糖事件更为频繁,两种方案的低血糖发生率均可接受。