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      ISPAD Clinical Practice Consensus Guidelines 2018: Diabetes technologies

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          Current state of type 1 diabetes treatment in the U.S.: updated data from the T1D Exchange clinic registry.

          To examine the overall state of metabolic control and current use of advanced diabetes technologies in the U.S., we report recent data collected on individuals with type 1 diabetes participating in the T1D Exchange clinic registry. Data from 16,061 participants updated between 1 September 2013 and 1 December 2014 were compared with registry enrollment data collected from 1 September 2010 to 1 August 2012. Mean hemoglobin A1c (HbA1c) was assessed by year of age from 75 years. The overall average HbA1c was 8.2% (66 mmol/mol) at enrollment and 8.4% (68 mmol/mol) at the most recent update. During childhood, mean HbA1c decreased from 8.3% (67 mmol/mol) in 2-4-year-olds to 8.1% (65 mmol/mol) at 7 years of age, followed by an increase to 9.2% (77 mmol/mol) in 19-year-olds. Subsequently, mean HbA1c values decline gradually until ∼30 years of age, plateauing at 7.5-7.8% (58-62 mmol/mol) beyond age 30 until a modest drop in HbA1c below 7.5% (58 mmol/mol) in those 65 years of age. Severe hypoglycemia (SH) and diabetic ketoacidosis (DKA) remain all too common complications of treatment, especially in older (SH) and younger patients (DKA). Insulin pump use increased slightly from enrollment (58-62%), and use of continuous glucose monitoring (CGM) did not change (7%). Although the T1D Exchange registry findings are not population based and could be biased, it is clear that there remains considerable room for improving outcomes of treatment of type 1 diabetes across all age-groups. Barriers to more effective use of current treatments need to be addressed and new therapies are needed to achieve optimal metabolic control in people with type 1 diabetes.
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            Effectiveness of sensor-augmented insulin-pump therapy in type 1 diabetes.

            Recently developed technologies for the treatment of type 1 diabetes mellitus include a variety of pumps and pumps with glucose sensors. In this 1-year, multicenter, randomized, controlled trial, we compared the efficacy of sensor-augmented pump therapy (pump therapy) with that of a regimen of multiple daily insulin injections (injection therapy) in 485 patients (329 adults and 156 children) with inadequately controlled type 1 diabetes. Patients received recombinant insulin analogues and were supervised by expert clinical teams. The primary end point was the change from the baseline glycated hemoglobin level. At 1 year, the baseline mean glycated hemoglobin level (8.3% in the two study groups) had decreased to 7.5% in the pump-therapy group, as compared with 8.1% in the injection-therapy group (P<0.001). The proportion of patients who reached the glycated hemoglobin target (<7%) was greater in the pump-therapy group than in the injection-therapy group. The rate of severe hypoglycemia in the pump-therapy group (13.31 cases per 100 person-years) did not differ significantly from that in the injection-therapy group (13.48 per 100 person-years, P=0.58). There was no significant weight gain in either group. In both adults and children with inadequately controlled type 1 diabetes, sensor-augmented pump therapy resulted in significant improvement in glycated hemoglobin levels, as compared with injection therapy. A significantly greater proportion of both adults and children in the pump-therapy group than in the injection-therapy group reached the target glycated hemoglobin level. (Funded by Medtronic and others; ClinicalTrials.gov number, NCT00417989.) 2010 Massachusetts Medical Society
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              Outpatient glycemic control with a bionic pancreas in type 1 diabetes.

              The safety and effectiveness of automated glycemic management have not been tested in multiday studies under unrestricted outpatient conditions.
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                Author and article information

                Journal
                Pediatric Diabetes
                Pediatr Diabetes
                Wiley
                1399543X
                October 2018
                October 2018
                October 01 2018
                : 19
                : 302-325
                Affiliations
                [1 ]Department of Pediatrics, Yale School of Medicine; Yale University; New Haven Connecticut
                [2 ]Wellcome Trust-MRC Institute of Metabolic Science; University of Cambridge; Cambridge UK
                [3 ]Department of Paediatrics; University of Cambridge; Cambridge UK
                [4 ]UMC-University Children's Hospital; Ljubljana Slovenia
                [5 ]Faculty of Medicine, University of Ljubljana; Ljubljana Slovenia
                [6 ]Department of Paediatrics; University of Otago; Christchurch New Zealand
                [7 ]University of Colorado Denver, Barbara Davis Center; Aurora Colorado
                [8 ]Medical Sciences Department; University of Antofagasta and Antofagasta Regional Hospital; Antofagasta Chile
                [9 ]Department of Psychiatry & Behavioral Sciences; Stanford University School of Medicine; Palo Alto California
                [10 ]Department of Pediatrics; Stanford University School of Medicine; Palo Alto California
                Article
                10.1111/pedi.12731
                30039513
                edaaf980-32b3-49a0-b73c-b6b7a7f18d77
                © 2018

                http://doi.wiley.com/10.1002/tdm_license_1.1

                http://onlinelibrary.wiley.com/termsAndConditions#vor

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