Strategies for overcoming therapeutic inertia in type 2 diabetes: A systematic review and meta-analysis.


Journal

Diabetes, obesity & metabolism
ISSN: 1463-1326
Titre abrégé: Diabetes Obes Metab
Pays: England
ID NLM: 100883645

Informations de publication

Date de publication:
09 2021
Historique:
revised: 17 05 2021
received: 08 02 2021
accepted: 25 05 2021
pubmed: 29 6 2021
medline: 12 8 2021
entrez: 28 6 2021
Statut: ppublish

Résumé

To systematically investigate the effect of interventions to overcome therapeutic inertia on glycaemic control in individuals with type 2 diabetes. We electronically searched for randomized controlled trials or quasi-experimental studies published between January 1, 2004 and December 31, 2019 evaluating the effect of interventions on glycated haemoglobin (HbA1c) control. Characteristics of included studies and HbA1c difference between intervention and control arms (main outcome) were extracted. Interventions were grouped as: care management and patient education; nurse or certified diabetes educator (CDE); pharmacist; or physician-based. Thirty-six studies including 22 243 individuals were combined in nonlinear random-effects meta-regressions; the median (range) duration of intervention was 1 year (0.9 to 36 months). Compared to the control arm, HbA1c reduction ranged from: -17.7 mmol/mol (-1.62%) to -4.4 mmol/mol (-0.40%) for nurse- or CDE-based interventions; -13.1 mmol/mol (-1.20%) to 3.3 mmol/mol (0.30%) for care management and patient education interventions; -9.8 mmol/mol (-0.90%) to -6.6 mmol/mol (-0.60%) for pharmacist-based interventions; and -4.4 mmol/mol (-0.40%) to 2.8 mmol/mol (0.26%) for physician-based interventions. Across the included studies, a reduction in HbA1c was observed only during the first year (6 months: -4.2 mmol/mol, 95% confidence interval [CI] -6.2, -2.2 [-0.38%, 95% CI -0.56, -0.20]; 1 year: -1.6 mmol/mol, 95% CI -3.3, 0.1 [-0.15%, 95% CI -0.30, 0.01]) and in individuals with preintervention HbA1c >75 mmol/mol (9%). The most effective approaches to mitigating therapeutic inertia and improving HbA1c were those that empower nonphysician providers such as pharmacists, nurses and diabetes educators to initiate and intensify treatment independently, supported by appropriate guidelines.

Identifiants

pubmed: 34180129
doi: 10.1111/dom.14455
doi:

Substances chimiques

Glycated Hemoglobin A 0

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2137-2154

Informations de copyright

© 2021 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.

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Auteurs

Rhea E Powell (RE)

Mathematica, Princeton, New Jersey, USA.

Francesco Zaccardi (F)

Leicester Real World Evidence Unit, Leicester Diabetes Research Centre, University of Leicester, Leicester, UK.

Christine Beebe (C)

Quantumed Consulting, San Diego, California, USA.

Xin Mei Chen (XM)

American Diabetes Association, Arlington, Virginia, USA.

Alyssa Crawford (A)

Mathematica, Princeton, New Jersey, USA.

John Cuddeback (J)

AMGA (American Medical Group Association), Alexandria, Virginia, USA.

Robert A Gabbay (RA)

American Diabetes Association, Arlington, Virginia, USA.
Harvard Medical School, Boston, Massachusetts, USA.

Lauren Kissela (L)

American Diabetes Association, Arlington, Virginia, USA.

Michelle L Litchman (ML)

University of Utah College of Nursing, Salt Lake City, Utah, USA.

Rajesh Mehta (R)

Healthagen, a CVS Health Company, Scottsdale, Arizona, USA.

Luigi Meneghini (L)

UT Southwestern Medical Center, Parkland Health and Hospital System, Dallas, Texas, USA.

Kevin M Pantalone (KM)

Endocrinology and Metabolism Institute, Cleveland Clinic, Cleveland, Ohio, USA.

Swapnil Rajpathak (S)

Merck & Co., Inc., Kenilworth, New Jersey, USA.

Paul Scribner (P)

American Diabetes Association, Arlington, Virginia, USA.

Jessica W Skelley (JW)

Samford University, Department of Pharmacy Practice, Birmingham, Alabama, USA.

Kamlesh Khunti (K)

Leicester Real World Evidence Unit, Leicester Diabetes Research Centre, University of Leicester, Leicester, UK.

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