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Lived experience of CamAPS FX closed loop system in youth with type 1 diabetes and their parents.
Hood, Korey K; Garcia-Willingham, Natasha; Hanes, Sarah; Tanenbaum, Molly L; Ware, Julia; Boughton, Charlotte K; Allen, Janet M; Wilinska, Malgorzata E; Tauschmann, Martin; Denvir, Louise; Thankamony, Ajay; Campbell, Fiona; Wadwa, R Paul; Buckingham, Bruce A; Davis, Nikki; DiMeglio, Linda A; Mauras, Nelly; Besser, Rachel E J; Ghatak, Atrayee; Weinzimer, Stuart A; Fox, D Steven; Kanapka, Lauren; Kollman, Craig; Sibayan, Judy; Beck, Roy W; Hovorka, Roman.
Afiliação
  • Hood KK; Stanford University School of Medicine, Stanford Diabetes Research Center, Stanford, California, USA.
  • Garcia-Willingham N; Stanford University School of Medicine, Stanford Diabetes Research Center, Stanford, California, USA.
  • Hanes S; Stanford University School of Medicine, Stanford Diabetes Research Center, Stanford, California, USA.
  • Tanenbaum ML; Stanford University School of Medicine, Stanford Diabetes Research Center, Stanford, California, USA.
  • Ware J; Wellcome Trust-MRC Institute of Metabolic Science, University of Cambridge, Cambridge, UK.
  • Boughton CK; Department of Paediatrics, University of Cambridge, Cambridge, UK.
  • Allen JM; Wellcome Trust-MRC Institute of Metabolic Science, University of Cambridge, Cambridge, UK.
  • Wilinska ME; Department of Diabetes & Endocrinology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Tauschmann M; Wellcome Trust-MRC Institute of Metabolic Science, University of Cambridge, Cambridge, UK.
  • Denvir L; Wellcome Trust-MRC Institute of Metabolic Science, University of Cambridge, Cambridge, UK.
  • Thankamony A; Department of Paediatrics, University of Cambridge, Cambridge, UK.
  • Campbell F; Wellcome Trust-MRC Institute of Metabolic Science, University of Cambridge, Cambridge, UK.
  • Wadwa RP; Department of Paediatrics, University of Cambridge, Cambridge, UK.
  • Buckingham BA; Department of Paediatric Diabetes and Endocrinology, Nottingham University Hospitals NHS Trust, Nottingham, UK.
  • Davis N; Department of Paediatrics, University of Cambridge, Cambridge, UK.
  • DiMeglio LA; Department of Paediatric Diabetes, Leeds Children's Hospital, Leeds, UK.
  • Mauras N; Barbara Davis Center for Childhood Diabetes, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
  • Besser REJ; Stanford University School of Medicine, Stanford Diabetes Research Center, Stanford, California, USA.
  • Ghatak A; Department of Paediatric Endocrinology and Diabetes, Southampton Children's Hospital, Southampton General Hospital, Southampton, UK.
  • Weinzimer SA; Department of Pediatrics, Division of Pediatric Endocrinology and Diabetology, Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, Indiana, USA.
  • Fox DS; Division of Endocrinology, Diabetes & Metabolism, Nemours Children's Health, Jacksonville, Florida, USA.
  • Kanapka L; Oxford University Hospitals NHS Foundation Trust, NIHR Oxford Biomedical Research Centre, Oxford, UK.
  • Kollman C; University of Oxford, Department of Paediatrics, Oxford, UK.
  • Sibayan J; Alder Hey Children's Hospital, Liverpool, UK.
  • Beck RW; Department of Pediatrics, Yale University, New Haven, Connecticut, USA.
  • Hovorka R; Department of Pharmaceutical and Health Economics, School of Pharmacy, University of Southern California, Los Angeles, California, USA.
Diabetes Obes Metab ; 24(12): 2309-2318, 2022 12.
Article em En | MEDLINE | ID: mdl-35837984
ABSTRACT

AIM:

To examine changes in the lived experience of type 1 diabetes after use of hybrid closed loop (CL), including the CamAPS FX CL system. MATERIALS AND

METHODS:

The primary study was conducted as an open-label, single-period, randomized, parallel design contrasting CL versus insulin pump (with or without continuous glucose monitoring). Participants were asked to complete patient-reported outcomes before starting CL and 3 and 6 months later. Surveys assessed diabetes distress, hypoglycaemia concerns and quality of life. Qualitative focus group data were collected at the completion of the study.

RESULTS:

In this sample of 98 youth (age range 6-18, mean age 12.7 ± 2.8 years) and their parents, CL use was not associated with psychosocial benefits overall. However, the subgroup (n = 12) using the CamAPS FX system showed modest improvements in quality of life and parent distress, reinforced by both survey (p < .05) and focus group responses. There were no negative effects of CL use reported by study participants.

CONCLUSIONS:

Closed loop use via the CamAPS FX system was associated with modest improvements in aspects of the lived experience of managing type 1 diabetes in youth and their families. Further refinements of the system may optimize the user experience.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 1 Tipo de estudo: Clinical_trials / Qualitative_research Limite: Adolescent / Child / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 1 Tipo de estudo: Clinical_trials / Qualitative_research Limite: Adolescent / Child / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article