Basal Insulin Initiation and Maintenance in Adults with Type 2 Diabetes Mellitus in the United States.

basal insulin medication persistence patient survey type 2 diabetes mellitus

Journal

Diabetes, metabolic syndrome and obesity : targets and therapy
ISSN: 1178-7007
Titre abrégé: Diabetes Metab Syndr Obes
Pays: New Zealand
ID NLM: 101515585

Informations de publication

Date de publication:
2020
Historique:
received: 09 11 2019
accepted: 09 02 2020
entrez: 21 4 2020
pubmed: 21 4 2020
medline: 21 4 2020
Statut: epublish

Résumé

A survey of US adults with type 2 diabetes mellitus was conducted to better understand patients' insulin initiation experiences and treatment persistence behaviors. Participants were recruited from consumer panels and grouped by basal insulin treatment pattern: continuers (no gap of ≥7 days within 6 months of initiation); interrupters (gap ≥7 days, resumed treatment); discontinuers (stopped for ≥7 days, not resumed). A quota of approximately 50 respondents per persistence category was set. A total of 154 respondents (52 continuers, 52 interrupters, 50 discontinuers) completed the survey. Mean age was 51.4 years; 51.9% male. Continuers were more likely to report their views being considered during initiation, and less likely to report a sense of failure. Concerns included insulin dependence (64.3% agree/strongly agree), frequent blood glucose monitoring (55.2%), costs/ability to pay (53.9%), fears of or mistakes during self-injection (52.6%), and weight gain (52.6%). Continuers were motivated by benefits of insulin therapy; experienced or potential side effects were notable factors for interruption/discontinuation. Healthcare provider instruction was indicated as a reason for continuing, stopping, and restarting therapy. Benefits of basal insulin therapy motivated continuers while side effects impacted interruption/discontinuation. Persistence on basal insulin is often influenced by provider actions. Earlier provider intervention upon signs of treatment discontinuation may promote persistence.

Identifiants

pubmed: 32308452
doi: 10.2147/DMSO.S237948
pii: 237948
pmc: PMC7140903
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1023-1033

Informations de copyright

© 2020 Kalirai et al.

Déclaration de conflit d'intérêts

Kalirai was an employee of Eli Lilly and Company at the time the study was conducted. Perez-Nieves, Hadjiyianni, Pollom, and Reed are employees and stock holders of Eli Lilly and Company. Stephenson and Grabner are employees of HealthCore, Inc. Geremakis was an employee of HealthCore, Inc. at the time the study was conducted. Ivanova was an employee of Analysis Group, Inc. at the time the study was conducted. Fisher is a consultant to Eli Lilly and Company. The authors report no other conflicts of interest in this work.

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Auteurs

Samaneh Kalirai (S)

Eli Lilly and Company, Indianapolis, IN, USA.

Jasmina I Ivanova (JI)

Analysis Group Inc., New York, NY, USA.

Magaly Perez-Nieves (M)

Eli Lilly and Company, Indianapolis, IN, USA.

Judith J Stephenson (JJ)

HealthCore Inc., Wilmington, DE, USA.

Irene Hadjiyianni (I)

Eli Lilly and Company, Indianapolis, IN, USA.

Michael Grabner (M)

HealthCore Inc., Wilmington, DE, USA.

Roy Daniel Pollom (RD)

Eli Lilly and Company, Indianapolis, IN, USA.

Caroline Geremakis (C)

HealthCore Inc., Wilmington, DE, USA.

Beverly L Reed (BL)

Eli Lilly and Company, Indianapolis, IN, USA.

Lawrence Fisher (L)

Department of Family and Community Medicine, UC San Francisco, San Francisco, CA, USA.

Classifications MeSH