Diabetic Ketoacidosis at Onset of Type 1 Diabetes and Glycemic Outcomes with Closed-Loop Insulin Delivery

被引:4
作者
Lakshman, Rama [1 ,11 ]
Najami, Mazin [1 ]
Allen, Janet M. [1 ,2 ]
Ware, Julia [1 ,2 ]
Wilinska, Malgorzata E. [1 ,2 ]
Hartnell, Sara [3 ]
Thankamony, Ajay [2 ]
Randell, Tabitha [4 ]
Ghatak, Atrayee [5 ]
Besser, Rachel E. J. [6 ,7 ]
Elleri, Daniela [8 ]
Trevelyan, Nicola [9 ]
Campbell, Fiona M. [10 ]
Hovorka, Roman [1 ,2 ]
Boughton, Charlotte K. [1 ,3 ]
机构
[1] Univ Cambridge, Wellcome MRC Inst Metab Sci, Cambridge, England
[2] Univ Cambridge, Dept Psychol, Cambridge, England
[3] Cambridge Univ Hosp NHS Fdn Trust, Wolfson Diabet & Endocrine Clin, Cambridge, England
[4] Nottingham Childrens Hosp, Dept Paediat Diabet & Endocrinol, Nottingham, England
[5] Alder Hey Childrens NHS Fdn Trust, Dept Diabet, Liverpool, England
[6] Univ Oxford, Dept Paediat, Oxford, England
[7] John Radcliffe Hosp, NIHR Oxford Biomed Res Ctr, Oxford, England
[8] Royal Hosp Sick Children, Dept Diabet, Edinburgh, Scotland
[9] Southampton Childrens Hosp, Paediat Diabet, Southampton, England
[10] Leeds Childrens Hosp, Dept Paediat Diabet, Leeds, England
[11] Univ Cambridge, Wellcome MRC Inst Metab Sci, Cambridge CB2 0QQ, England
关键词
Type; 1; diabetes; Artificial pancreas; Closed-loop systems; Diabetic ketoacidosis; CHILDREN; ADOLESCENTS; PREDICTOR; HBA(1C);
D O I
10.1089/dia.2023.0307
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The presence of diabetic ketoacidosis (DKA) at diagnosis of type 1 diabetes (T1D) is associated with higher glycated hemoglobin levels over time. We evaluated whether hybrid-closed loop (HCL) therapy from onset of T1D could prevent the adverse impact of DKA at diagnosis on long-term glycemic outcomes. This was a posthoc analysis from 51 adolescents using HCL from diagnosis of T1D as part of the CLOuD trial (NCT02871089). We compared glycemic and insulin metrics between adolescents with (n = 17) and without (n = 34) DKA at diagnosis. Participants with and without DKA at diagnosis had similar time in target glucose range 3.9-10.0 mmol/L (70-180 mg/dL), time below range (<3.9 mmol/L, <70 mg/dL) and HbA1c at 6, 12, and 24 months. While insulin requirements at 6 months were higher in those with DKA at diagnosis, this was not statistically significant after adjusting for bodyweight. Residual C-peptide secretion was similar between groups. We conclude that HCL therapy may mitigate against the negative glycemic effects of DKA at T1D diagnosis.
引用
收藏
页码:198 / 202
页数:5
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