Adherence to metformin is reduced during school holidays and weekends in children with type 1 diabetes participating in a randomised controlled trial.


Journal

Archives of disease in childhood
ISSN: 1468-2044
Titre abrégé: Arch Dis Child
Pays: England
ID NLM: 0372434

Informations de publication

Date de publication:
09 2019
Historique:
received: 27 09 2018
revised: 16 03 2019
accepted: 24 04 2019
pubmed: 13 5 2019
medline: 17 3 2020
entrez: 13 5 2019
Statut: ppublish

Résumé

Non-adherence to treatment in childhood chronic illness has serious consequences for health and healthcare costs. Accurate detailed objective data on adherence are minimal in this age group. To evaluate medication adherence using electronic monitoring systems in children with type 1 diabetes (T1D). A cohort study of 90 T1D children (aged 13.6±2.5 years, 41 males) from two paediatric diabetes clinics, participated in a 12-month double-blind, randomised, placebo-controlled trial (1:1 allocation). This cohort provided 28 336 days of study observations; 7138 school holiday and 8875 weekend/public holiday days. Adherence to intervention (metformin (n=45) or placebo (n=45)) was measured objectively by Medication Event Monitoring Systems (MEMS) including proportion of medication doses taken and daily adherence patterns and by tablet count at 3, 6 and 12 months. The trial was completed in June 2015. There was an average (SD) of 363.3 (42) days of MEMS observations available for each study participant (94.1 (12.6) school holiday days and 117.1 (13.4) weekend/public holiday days). Adherence reduced during school holidays (adjusted OR (aOR) 0.81; 95% CI 0.72 to 0.91; p<0.001) and during weekends/public holidays (aOR 0.74; 95% CI 0.69 to 0.80; p<0.001). Adverse effects to the intervention did not affect overall adherence (aOR 0.77; 95% CI 0.3 to 2.01; p=0.6). Age, gender, body mass index, diabetes duration, insulin dose, HbA1c (Haemoglobin A1c) or socioeconomic status did not predict adherence. Medication adherence was reduced during school holidays and on weekends in children with T1D. Clinical characteristics including socioeconomic status and the presence of adverse effects did not predict adherence. ACTRN12611000148976.

Sections du résumé

BACKGROUND
Non-adherence to treatment in childhood chronic illness has serious consequences for health and healthcare costs. Accurate detailed objective data on adherence are minimal in this age group.
OBJECTIVE
To evaluate medication adherence using electronic monitoring systems in children with type 1 diabetes (T1D).
DESIGN
A cohort study of 90 T1D children (aged 13.6±2.5 years, 41 males) from two paediatric diabetes clinics, participated in a 12-month double-blind, randomised, placebo-controlled trial (1:1 allocation). This cohort provided 28 336 days of study observations; 7138 school holiday and 8875 weekend/public holiday days.
METHOD
Adherence to intervention (metformin (n=45) or placebo (n=45)) was measured objectively by Medication Event Monitoring Systems (MEMS) including proportion of medication doses taken and daily adherence patterns and by tablet count at 3, 6 and 12 months. The trial was completed in June 2015.
RESULTS
There was an average (SD) of 363.3 (42) days of MEMS observations available for each study participant (94.1 (12.6) school holiday days and 117.1 (13.4) weekend/public holiday days). Adherence reduced during school holidays (adjusted OR (aOR) 0.81; 95% CI 0.72 to 0.91; p<0.001) and during weekends/public holidays (aOR 0.74; 95% CI 0.69 to 0.80; p<0.001). Adverse effects to the intervention did not affect overall adherence (aOR 0.77; 95% CI 0.3 to 2.01; p=0.6). Age, gender, body mass index, diabetes duration, insulin dose, HbA1c (Haemoglobin A1c) or socioeconomic status did not predict adherence.
CONCLUSION
Medication adherence was reduced during school holidays and on weekends in children with T1D. Clinical characteristics including socioeconomic status and the presence of adverse effects did not predict adherence.
TRIAL REGISTRATION NUMBER
ACTRN12611000148976.

Identifiants

pubmed: 31079072
pii: archdischild-2018-316303
doi: 10.1136/archdischild-2018-316303
doi:

Substances chimiques

Glycated Hemoglobin A 0
Hypoglycemic Agents 0
hemoglobin A1c protein, human 0
Metformin 9100L32L2N

Banques de données

ANZCTR
['ACTRN12611000148976']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

890-894

Informations de copyright

© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Catherine Leggett (C)

SA Pharmacy, Women's and Children's Hospital, North Adelaide, South Australia, Australia.

Lynne Giles (L)

School of Public Health, University of Adelaide, Robinson Institute, Adelaide, South Australia, Australia.

Jemma Jay Angela Anderson (JJA)

Endocrinology and Diabetes Department, Women's and Children's Hospital, North Adelaide, South Australia, Australia.
Discipline of Paediatrics, University of Adelaide, Robinson Research Institute, Adelaide, South Australia, Australia.

Matthew Doogue (M)

Department of Medicine, University of Otago, Christchurch, New Zealand.

Jennifer Couper (J)

Endocrinology and Diabetes Department, Women's and Children's Hospital, North Adelaide, South Australia, Australia.
Discipline of Paediatrics, University of Adelaide, Robinson Research Institute, Adelaide, South Australia, Australia.

Alexia Sophie Pena (AS)

Endocrinology and Diabetes Department, Women's and Children's Hospital, North Adelaide, South Australia, Australia.
Discipline of Paediatrics, University of Adelaide, Robinson Research Institute, Adelaide, South Australia, Australia.

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