Fuloria M, Friedberg M A, DuRant R H, Aschner J L
Department of Pediatrics and Brenner Center for Child and Adolescent Health, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
Pediatrics. 1998 Dec;102(6):1401-6. doi: 10.1542/peds.102.6.1401.
A retrospective medical record review of 13 consecutive, hyperglycemic, extremely low birth weight (ELBW) infants treated with continuous insulin infusions revealed a 14- to 24-hour delay (mean, 19 hours) in blood glucose normalization despite stepwise increases in insulin infusion rates.
This in vitro study examined the effects of flow rate and insulin priming on insulin recovery from polyvinyl chloride (PVC) tubing and polyethylene (PE)-lined PVC tubing infused with a standard insulin stock solution.
Stock insulin solution (0.2 U/mL) was infused through microbore PVC or PE-lined tubing at flow rates of 0.05 and 0.2 mL/h. To determine if saturation of nonspecific binding sites would alter effluent insulin concentration, we compared insulin recovery from tubing previously flushed with the stock solution and tubing primed with 5 U/mL of insulin for 20 minutes. Effluent samples, which were collected at baseline and at six time points during a 24-hour period, were immediately frozen at -20 degreesC. Insulin concentration was measured by IMx immunoassay. Data were analyzed using general linear modeling with repeated measures.
At 0.05 mL/h flow rate, insulin recovery from unprimed PVC tubing at 1, 2, 4, and 8 hours was 17%, 11%, 27%, and 55%, respectively, with 100% recovery at 24 hours. From insulin-primed tubing, insulin recovery was approximately 70% at 1, 2, and 4 hours, and close to 100% at 8 hours. At a faster flow rate of 0.2 mL/h, insulin recovery at 1, 2, 4, and 8 hours was 22%, 38%, 67%, and 75% vs 42%, 85%, 91% and 95% from unprimed and insulin-primed PVC tubing, respectively. Similar results were obtained from unprimed and insulin-primed PE-lined tubing at 0.2 mL/h flow rate.
Priming of microbore tubing with 5 U/mL of insulin solution for 20 minutes to block nonspecific binding sites enhances delivery of a standard insulin stock at infusion rates typically used to treat hyperglycemic ELBW infants. We conclude that priming the tubing with a higher concentration of insulin before initiation of standard insulin infusion therapy should accelerate achievement of steady-state insulin delivery and correction of hyperglycemia in ELBW infants.
一项对13例连续接受持续胰岛素输注治疗的高血糖极低出生体重(ELBW)婴儿的回顾性病历审查显示,尽管胰岛素输注速率逐步增加,但血糖正常化仍延迟了14至24小时(平均19小时)。
这项体外研究检查了流速和胰岛素预充对从输注标准胰岛素储备溶液的聚氯乙烯(PVC)管和内衬聚乙烯(PE)的PVC管中回收胰岛素的影响。
将储备胰岛素溶液(0.2 U/mL)以0.05和0.2 mL/h的流速通过微孔PVC管或内衬PE的管进行输注。为了确定非特异性结合位点的饱和是否会改变流出液胰岛素浓度,我们比较了先前用储备溶液冲洗过的管和用5 U/mL胰岛素预充20分钟的管中的胰岛素回收率。在基线和24小时内的六个时间点采集的流出液样本立即在-20℃下冷冻。通过IMx免疫测定法测量胰岛素浓度。使用重复测量的一般线性模型分析数据。
在流速为0.05 mL/h时,未预充的PVC管在1、2、4和8小时的胰岛素回收率分别为17%、11%、27%和55%,24小时时回收率为100%。从胰岛素预充管中,胰岛素在1、2和4小时的回收率约为70%,8小时时接近100%。在0.2 mL/h的较快流速下,未预充和胰岛素预充的PVC管在1、2、4和8小时的胰岛素回收率分别为22%、38%、67%和75%,而在胰岛素预充管中分别为42%、85%、91%和95%。在流速为0.2 mL/h时,未预充和胰岛素预充的内衬PE的管也获得了类似结果。
用5 U/mL胰岛素溶液对微孔管预充20分钟以阻断非特异性结合位点,可增强在通常用于治疗高血糖ELBW婴儿的输注速率下标准胰岛素储备的输送。我们得出结论,在开始标准胰岛素输注治疗前用更高浓度的胰岛素对管进行预充,应能加速ELBW婴儿达到稳态胰岛素输送并纠正高血糖。