2011
DOI: 10.1177/193229681100500514
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Usage and Effectiveness of the Low Glucose Suspend Feature of the Medtronic Paradigm Veo Insulin Pump

Abstract: The LGS feature was on for most of the patient days in the study. Most LGS episodes lasted for <10 min. Use of the LGS feature significantly reduced exposure to hypoglycemia. Profound hyperglycemia resulting from LGS episodes lasting >115 min was not observed.

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Cited by 80 publications
(63 citation statements)
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“…[7][8][9] In studies of sensor-augmented pumps with a low glucose suspend feature (Paradigm VeoÔ; Medtronic Diabetes), no significant ketosis or ketoacidosis has been reported in thousands of 2-h nocturnal pump suspensions. [10][11][12][13] On intervention nights (algorithm operational), glucose levels tended to be lower on nights with pump suspension compared with nights without pump suspension, reflecting that there were lower glucose levels on nights triggering a suspension. However, not unexpectedly, when comparing all intervention nights (with and without pump suspension) with control nights, mean overnight glucose and morning fasting glucose levels tended to be higher on the intervention nights.…”
Section: Discussionmentioning
confidence: 99%
“…[7][8][9] In studies of sensor-augmented pumps with a low glucose suspend feature (Paradigm VeoÔ; Medtronic Diabetes), no significant ketosis or ketoacidosis has been reported in thousands of 2-h nocturnal pump suspensions. [10][11][12][13] On intervention nights (algorithm operational), glucose levels tended to be lower on nights with pump suspension compared with nights without pump suspension, reflecting that there were lower glucose levels on nights triggering a suspension. However, not unexpectedly, when comparing all intervention nights (with and without pump suspension) with control nights, mean overnight glucose and morning fasting glucose levels tended to be higher on the intervention nights.…”
Section: Discussionmentioning
confidence: 99%
“…This system contains hypoglycemic alarms for predicted and threshold levels of hypoglycemia but no remote telemedicine capabilities. 26 A remote warning system for use by CGM device users who might be experiencing unrecognized nocturnal hypoglycemia was approved by the FDA. The system consists of a monitor for the patient, a power supply, and a transmitter to send information to a second monitor at the bedside of another person in the house.…”
Section: Closed-loop Systemsmentioning
confidence: 99%
“…To date, there has been little evaluation of the efficacy and safety of this function in the prevention of severe hypoglycaemias [37,38].…”
Section: Hypoglycaemia and Glucose Variabilitymentioning
confidence: 99%