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A deprescribing programme aimed to optimise blood glucose-lowering medication in older people with type 2 diabetes mellitus, the OMED2-study: the study protocol for a randomised controlled trial.
Andriessen, Charlotte; Blom, Marieke T; van Hoek, Beryl A C E; de Boer, Anna W; Denig, Petra; de Wit, G Ardine; Swart, Karin; de Rooij-Peek, Angela; van Marum, Rob J; Hugtenburg, Jacqueline G; Slottje, Pauline; van Raalte, Daniël; van Bloemendaal, Liselotte; Herings, Ron; Nijpels, Giel; Vos, Rimke C; Elders, Petra J M.
Afiliação
  • Andriessen C; Department of General Practice, Amsterdam UMC, Location Vrije Universiteit, Meibergdreef 15, Amsterdam, 1105AZ, the Netherlands.
  • Blom MT; Amsterdam Public Health Research Institute, Amsterdam, the Netherlands.
  • van Hoek BACE; Department of General Practice, Amsterdam UMC, Location Vrije Universiteit, Meibergdreef 15, Amsterdam, 1105AZ, the Netherlands.
  • de Boer AW; Amsterdam Public Health Research Institute, Amsterdam, the Netherlands.
  • Denig P; Department of General Practice, Amsterdam UMC, Location Vrije Universiteit, Meibergdreef 15, Amsterdam, 1105AZ, the Netherlands.
  • de Wit GA; Amsterdam Public Health Research Institute, Amsterdam, the Netherlands.
  • Swart K; Department of Public Health and Primary Care / Health Campus The Hague, LUMC, Leiden, The Netherlands.
  • de Rooij-Peek A; Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, Netherlands.
  • van Marum RJ; Department of Health Sciences, Faculty of Beta Sciences, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.
  • Hugtenburg JG; Centre for Public Health, Healthcare and Society, National Institute of Public Health and the Environment, Bilthoven, the Netherlands.
  • Slottje P; PHARMO Institute for Drug Outcomes Studies, Utrecht, The Netherlands.
  • van Raalte D; Diabetesvereniging Nederland, Leusden, Netherlands.
  • van Bloemendaal L; Department of Geriatric Medicine, Jeroen Bosch Hospital, 's-Hertogenbosch, the Netherlands.
  • Herings R; Department of Clinical Pharmacology, Jeroen Bosch Hospital, 's-Hertogenbosch, the Netherlands.
  • Nijpels G; Department of Elderly Care Medicine, Amsterdam University Medical Center, Amsterdam, the Netherlands.
  • Vos RC; Department of General Practice, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
  • Elders PJM; Department of General Practice, Amsterdam UMC, Location Vrije Universiteit, Meibergdreef 15, Amsterdam, 1105AZ, the Netherlands.
Trials ; 25(1): 505, 2024 Jul 25.
Article em En | MEDLINE | ID: mdl-39049109
ABSTRACT

BACKGROUND:

Older patients with type 2 diabetes mellitus (T2D) have an increased risk of hypoglycaemic episodes when using sulphonylureas or insulin. In the Netherlands, guidelines exist for reducing glucose-lowering medication in older patients. However, evidence is lacking that a medication reduction in older patients can be safely pursued. Here, we will examine if promoting the deprescribing of insulin/sulphonylureas with a deprescribing programme (DPP) in general practice affects T2D-complications in older overtreated patients.

METHODS:

We will perform a 11 cluster randomised controlled trial in 86 general practices in the Netherlands. The DPP will consist of education sessions with general practitioners and practice nurses about reducing glucose-lowering medication in older patients (≥ 70 years). Topics of the sessions include the necessity of deprescribing, tools to initiate deprescribing and strategies to discuss deprescribing with patients (shared decision making). The DPP further includes a support programme with practice visits. The study will employ a selection tool to identify possibly overtreated older patients from the electronic medical records of the general practitioner. Eligibility for enrolment in the study will be based on HbA1c targets indicated by the Dutch guidelines, which depend on age, diabetes duration, presence of frailty, and life expectancy. The control group will provide usual care. We aim to include 406 patients. The follow-up period will be 2 years. For the primary outcome, the effect of the DPP on T2D-complications will be assessed by counting the cumulative incidence of events related to under- and overtreatment in T2D as registered in the electronic medical records. We shall perform an intention-to-treat analysis and an analysis including only patients for whom deprescribing was initiated. The implementation of the DPP in general practice will be evaluated quantitatively and qualitatively using the Extended Normalisation Process Theory (ENPT) and the Reach, Efficacy - Adoption, Implementation and Maintenance (RE-AIM) model. Other secondary outcomes include quality of life, cognitive functioning, events related to overtreatment or undertreatment, biomarkers of health, amount of blood glucose-lowering medication prescriptions, and cost-effectiveness.

DISCUSSION:

This study will provide insight into the safety and feasibility of a programme aimed at deprescribing sulphonylureas/insulin in older people with T2D who are treated in general practice. TRIAL REGISTRATION ISRCTN Registry, ISRCTN50008265 , registered 09 March, 2023.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Compostos de Sulfonilureia / Glicemia / Ensaios Clínicos Controlados Aleatórios como Assunto / Diabetes Mellitus Tipo 2 / Desprescrições / Controle Glicêmico / Hipoglicemiantes Limite: Aged / Humans País/Região como assunto: Europa Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Compostos de Sulfonilureia / Glicemia / Ensaios Clínicos Controlados Aleatórios como Assunto / Diabetes Mellitus Tipo 2 / Desprescrições / Controle Glicêmico / Hipoglicemiantes Limite: Aged / Humans País/Região como assunto: Europa Idioma: En Ano de publicação: 2024 Tipo de documento: Article