1. Moshe Phillip, M.D., Tadej Battelino, M.D., Eran Atlas, M.Sc., Olga Kordonouri, M.D., Natasa Bratina, M.D., Shahar Miller, B.Sc., Torben Biester, M.D., Magdalena Avbelj Stefanija, M.D., Ido Muller, B.Sc., Revital Nimri, M.D., and Thomas Danne, M.D N Engl J Med 2013; 368:824-833 R1 정수웅 / R3 변종규 / Prof. 우정택 1 Introduction - Prof. 우정택 History of Artificial pancreas Background - R3 변종규 Methods & Results - R1 정수웅 Discussion & Conclusion - R3 변종규

2. The goal of the artificial pancreas  To improve insulin replacement therapy  To avoidance of the complications of hyper-hypoglycemia  To ease the burden of therapy for the insulin-dependent 2

3. Approaches  Medical equipment  Insulin pump  Bioengineering  Bio-artificial pancreas  Implant bioengineered tissue containing islet cells  Gene therapy  DNA change of intestinal cells to become insulin-producing cells 3

4. First insulin pump in 1964 - Dr. Arnold Kadish Continuous subcutaneous insulin infusion (CSII) in 1970s First portable drug infusion pump In 1973 - Dean Kamen First marketable insulin pump in 1983 Sensor-augmented insulin pump 4

5. ► First introduced in the 1960’s by a Los Angeles Physician, Dr. Arnold Kadish.

6. 1974

7. First commercially available portable insulin pump called the Autosyringe “Big Blue Brick” in 1978

8. 1983

9. ACCU-CHEK SPIRIT – ROCHE AMIGO – NIPRO CORPORATION DANA DIABECARE 11S – SOAIL DEVELOPMENT MINIMED PARADIGM REVEL – MEDTRONIC OMNIPOD – INSULET CORPORATION ONE TOUCH PING – ANIMAS CORPORATION

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12. 12 Indication for insulin pump Tx in a T1DM  Continued elevated HbA1C despite MDI  Continued disabling hypoglycemia despite MDI  Among children, elevated HbA1C level and disabling hypoglycemia  In the first trimester of pregnancy or before conception  Target HbA1C levels cannot be achieved. MDI. - multiple daily insulin injections *

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14. Infuses rapid-acting insulin at a slow basal rate, 24 hours a day, patient-activated insulin boosts (boluses) administered at mealtimes Improve glycemic control in patients with type 1 DM  reduce the within-day and between-day glycemic variability Mean glycated hemoglobin levels are significantly lower  about 0.3 to 0.6% between treatments  accompanied by a 10 to 20% reduction in the dose of insulin Severe hypoglycemia was significantly lower than MDI (rate ratio, 4.19; 95% CI, 2.86 to 6.13) 14

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19. Full closed-loop system  insulin is administered according to the glucose readings in a fully automated manner Includes the patient's physical characteristics, insulin delivery regimen, insulin pharmacodynamic parameters Insulin pump can communicate in real time with a personal computer, conducted using the Artificial Pancreas Software (APS) MDLAP system is a promising tool for individualized glucose control of patients with type 1 diabetes 19

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21. Intensive insulin therapy is considered to be the standard treatment for type 1 diabetes Insulin pumps, glucose sensors, or a combination of the two devices (sensor- augmented pump) However, the risk of hypoglycemia is still present with the use of all currently available therapies. Maintenance of nocturnal euglycemia is extremely important and is challenging, since most cases of severe hypoglycemia occur at night. 75% of total hypoglycemic seizures in children and 6% of deaths in patients under the age of 40 years who have type 1 diabetes. 21

22. Fully automated artificial-pancreas systems have been suggested as a means to control nocturnal glucose levels. Such systems can improve glucose control and reduce the risk of nocturnal hypoglycemia in hospital setting Diabetes Wireless Artificial Pancreas Consortium (DREAM) was established to test the MD-Logic Artificial Pancreas system in settings outside the hospital under real-life conditions. The objective of the study was to evaluate the safety and efficacy of the artificial-pancreas system in young persons with type 1 diabetes, in a youth- camp setting. 22

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25. Study participants  10 to 18 years of age  at least a 1 year history of type 1 diabetes  insulin pump therapy for at least 3 months  A glycated hemoglobin level of 7 and 10 %  A body mass index below the 97 th percentile for the patient’s age 25

26. Main exclusion criteria  A concomitant disease  Participation in another study  Pregnancy  A history of diabetic ketoacidosis or severe hypoglycemia within the past month 26

27. artificial pancreas sensor-augmented insulin pump artificial pancreas Group A Group B 1 st night 2 nd night

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29. 29 The first trial with Artificial Pancreas at diabetes camp

30. Primary end point  Total number of episodes of glucose levels < 63mg/dL  Time that glucose level was < 60mg/dL  Overnight glucose level 30

31. Secondary end point  overnight glucose control  overnight glucose variability 31

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35. P value = 0.02 P value = 0.003 No significance

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39. The MD-Logic Artificial Pancreas system reduced risk of hypoglycemia in young persons at an overnight camp. The combined effect of amount of insulin provided, timing of insulin delivery, the presence of an alarm module The early-alert system for the artificial pancreas 39

40. Each treatment was evaluated in a one-night session, may be different in a multinight design Crossover studies have an intrinsic limitation, since the order in which treatments are administered may affect the outcome Glucose-level data were based on sensor readings  Every 3 hours, the assigned medical personnel evaluated capillary blood glucose levels. 40

41. The use of an artificial-pancreas system resulted in less hypoglycemia and tighter control of nocturnal glucose levels than did a sensor-augmented pump system in a youth-camp setting. 41