Effectiveness of home or hospital initiation of treatment at diagnosis for children with type 1 diabetes (DECIDE trial): a multicentre individually randomised controlled trial

Gregory, John W., Townson, Julia, Channon, Sue, Cohen, David, Longo, Mirella, Davies, Justin, Nicola, Harman, Hood, Kerenza, Pickles, Timothy, Playle, Rebecca, Tabitha, Randell, Robling, Michael, Morro, Touray, Trevelyan, Nicola, Warner, Justin and Lowes, Lesley 2019. Effectiveness of home or hospital initiation of treatment at diagnosis for children with type 1 diabetes (DECIDE trial): a multicentre individually randomised controlled trial. BMJ Open 9 , e032317. 10.1136/bmjopen-2019-032317

Preview

PDF - Published Version Available under License Creative Commons Attribution Non-commercial. Download (609kB) | Preview

Abstract

Objective: To determine whether, in children with newly diagnosed type 1 diabetes who were not acutely unwell, management at home for initiation of insulin treatment and education of the child and family, would result in improved clinical and psychological outcomes at 2 years postdiagnosis. Design: A multicentre randomised controlled trial (January 2008/October 2013). Setting: Eight paediatric diabetes centres in England, Wales and Northern Ireland. Participants: 203 clinically well children aged under 17 years, with newly diagnosed type 1 diabetes and their carers. Intervention: Management of the initiation period from diagnosis at home, for a minimum of 3 days, to include at least six supervised injections and delivery of pragmatic educational care. Main outcome measures: Primary outcome was glycosylated haemoglobin (HbA1c) concentration at 24 months postdiagnosis. Secondary outcomes included coping, anxiety, quality of life and use of NHS resources. Results: 203 children, newly diagnosed, were randomised to commence management at home (n=101) or in hospital (n=102). At the 24 month primary end point, there was one withdrawal and a follow-up rate of 194/202 (96%). Mean HbA1c in the home treatment arm was 72.1 mmol/mol and in the hospital treated arm 72.6 mmol/mol. There was a negligible difference between the mean HbA1c levels in the two arms adjusted for baseline (1.01, 95% CI 0.93 to 1.09). There were mostly no differences in secondary outcomes at 24 months, apart from better child self-esteem in the home-arm. No home-arm children were admitted to hospital during initiation and there were no adverse events at that time. The number of investigations was higher in hospital patients during the follow-up period. There were no differences in insulin regimens between the two arms. Conclusions: There is no evidence of a difference between home-based and hospital-based initiation of care in children newly diagnosed with type 1 diabetes across relevant outcomes.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Medicine Centre for Trials Research (CNTRR)
Additional Information:	This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial.
Publisher:	BMJ Publishing Group
ISSN:	2044-6055
Date of First Compliant Deposit:	4 November 2019
Date of Acceptance:	4 November 2019
Last Modified:	15 Jan 2021 10:00
URI:	http://orca-mwe.cf.ac.uk/id/eprint/126566

Citation Data

Cited 1 time in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item