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The JewelPUMP™ (JP) is a new patch pump based on a microelectromechanical system that operates without any plunger. The study aimed to evaluate the infusion accuracy of the JP in vitro and in vivo. For the in vitro studies, commercially available pumps meeting the ISO standard were compared to the JP: the MiniMed® Paradigm® 712 (MP), Accu-Chek® Combo (AC), OmniPod® (OP), Animas® Vibe™ (AN). Pump accuracy was measured over 24 hours using a continuous microweighing method, at 0.1 and 1 IU/h basal rates. The occlusion alarm threshold was measured after a catheter occlusion. The JP, filled with physiological serum, was then tested in 13 patients with type 1 diabetes simultaneously with their own pump for 2 days. The weight difference was used to calculate the infused insulin volume. The JP showed reduced absolute median error rate in vitro over a 15-minute observation window compared to other pumps (1 IU/h): ±1.02

作者:Sophie, Borot;Sylvia, Franc;Justine, Cristante;Alfred, Penfornis;Pierre-Yves, Benhamou;Bruno, Guerci;Hélène, Hanaire;Eric, Renard;Yves, Reznik;Chantal, Simon;Guillaume, Charpentier

来源:Journal of diabetes science and technology 2014 年 8卷 6期

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作者:
Sophie, Borot;Sylvia, Franc;Justine, Cristante;Alfred, Penfornis;Pierre-Yves, Benhamou;Bruno, Guerci;Hélène, Hanaire;Eric, Renard;Yves, Reznik;Chantal, Simon;Guillaume, Charpentier
来源:
Journal of diabetes science and technology 2014 年 8卷 6期
标签:
catheter occlusion continuous subcutaneous insulin infusion (CSII) insulin delivery accuracy insulin pump insulin therapy microelectromechanical system (MEMS) patch pump type 1 diabetes
The JewelPUMP™ (JP) is a new patch pump based on a microelectromechanical system that operates without any plunger. The study aimed to evaluate the infusion accuracy of the JP in vitro and in vivo. For the in vitro studies, commercially available pumps meeting the ISO standard were compared to the JP: the MiniMed® Paradigm® 712 (MP), Accu-Chek® Combo (AC), OmniPod® (OP), Animas® Vibe™ (AN). Pump accuracy was measured over 24 hours using a continuous microweighing method, at 0.1 and 1 IU/h basal rates. The occlusion alarm threshold was measured after a catheter occlusion. The JP, filled with physiological serum, was then tested in 13 patients with type 1 diabetes simultaneously with their own pump for 2 days. The weight difference was used to calculate the infused insulin volume. The JP showed reduced absolute median error rate in vitro over a 15-minute observation window compared to other pumps (1 IU/h): ±1.02