Analysis of English general practice level data linking medication levels, service activity and demography to levels of glycaemic control being achieved in type 2 diabetes to improve clinical practice and patient outcomes.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
06 09 2019
Historique:
entrez: 9 9 2019
pubmed: 9 9 2019
medline: 2 10 2020
Statut: epublish

Résumé

Evaluate relative clinical effectiveness of treatment options for type 2 diabetes mellitus (T2DM) using a statistical model of real-world evidence within UK general practitioner practices (GPP), to quantify the opportunities for diabetes care performance improvement. From the National Diabetes Audit in 2015-2016 and 2016-2017, GPP target glycaemic control (TGC-%HbA1c ≤58 mmol/mol) and higher glycaemic risk (HGR -%HbA1c results >86 mmol/mol) outcomes were linked using multivariate linear regression to prescribing, demographics and practice service indicators. This was carried out both cross-sectionally (XS) (within year) and longitudinally (Lo) (across years) on 35 indicators. Standardised β coefficients were used to show relative level of impact of each factor. Improvement opportunity was calculated as impact on TGC & HGR numbers. Values from 6525 GPP with 2.7 million T2DM individuals were included. The cross-sectional model accounted for up to 28% TGC variance and 35% HGR variance, and the longitudinal model accounted for up to 9% TGC and 17% HGR variance. Practice service indicators including % achieving routine checks/blood pressure/cholesterol control targets were positively correlated, while demographic indicators including % younger age/social deprivation/white ethnicity were negatively correlated. The β values for selected molecules are shown as (increased TGC; decreased HGR), canagliflozin (XS 0.07;0.145/Lo 0.04;0.07), metformin (XS 0.12;0.04/Lo -;-), sitagliptin (XS 0.06;0.02/Lo 0.10;0.06), empagliflozin (XS-;0.07/Lo 0.09;0.07), dapagliflozin (XS -;0.04/Lo -;0.4), sulphonylurea (XS -0.18;-0.12/Lo-;-) and insulin (XS-0.14;0.02/ Lo-0.09;-). Moving all GPP prescribing and interventions to the equivalent of the top performing decile of GPP could result in total patients in TGC increasing from 1.90 million to 2.14 million, and total HGR falling from 191 000 to 123 000. GPP using more legacy therapies such as sulphonylurea/insulin demonstrate poorer outcomes, while those applying holistic patient management/use of newer molecules demonstrate improved glycaemic outcomes. If all GPP moved service levels/prescribing to those of the top decile, both TGC/HGR could be substantially improved.

Identifiants

pubmed: 31494602
pii: bmjopen-2018-028278
doi: 10.1136/bmjopen-2018-028278
pmc: PMC6731821
doi:

Substances chimiques

Glycated Hemoglobin A 0
Hypoglycemic Agents 0

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e028278

Informations de copyright

© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Références

J Palliat Med. 2009 Feb;12(2):181-7
pubmed: 19207063
Diabetes Obes Metab. 2014 Feb;16(2):124-36
pubmed: 23911013
Ann Intern Med. 2013 Aug 20;159(4):262-74
pubmed: 24026259
Lipids Health Dis. 2017 Apr 13;16(1):58
pubmed: 28403877
Diabetes Obes Metab. 2018 Jan;20(1):185-194
pubmed: 28730750
Diabet Med. 2018 Jan;35(1):63-71
pubmed: 29120503
Diabetes Obes Metab. 2018 Jul;20(7):1659-1669
pubmed: 29516618
Int J Clin Pract. 2018 Apr;72(4):e13080
pubmed: 29537664

Auteurs

Adrian Heald (A)

Department of Diabetes and Endocrinology, Salford Royal NHS Foundation Trust, Salford, UK.
The School of Medicine and Manchester Academic Health Sciences Centre, The University of Manchester, Manchester, UK.

Mark Davies (M)

Res Consortium, Andover, UK.

Mike Stedman (M)

Res Consortium, Andover, UK.

Mark Livingston (M)

Clinical Biochemistry, Walsall Healthcare NHS Trust, Walsall, UK.

Mark Lunt (M)

The School of Medicine and Manchester Academic Health Sciences Centre, The University of Manchester, Manchester, UK.

Anthony Fryer (A)

Clinical Biochemistry, University Hospitals of North Midlands, Stoke on Trent, Staffordshire, UK.

Roger Gadsby (R)

Warwick Medical School, University of Warwick, Coventry, UK.

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