Breaking Therapeutic Inertia in Type 2 Diabetes: Active Detection of In-Patient Cases Allows Improvement of Metabolic Control at Midterm

Author:

Lucas Martín Anna M.1,Guanyabens Elena1,Zavala-Arauco R.1,Chamorro Joaquín1,Granada Maria Luisa2,Mauricio Didac1,Puig-Domingo Manuel1

Affiliation:

1. Endocrinology and Nutrition Service, Germans Trias i Pujol Research Institute and Hospital, Department of Medicine, Autonomous University of Barcelona, Can Ruti Campus, Ctra. Canyet s/n, Badalona, 08916 Barcelona, Spain

2. Hormone Laboratory, Germans Trias i Pujol Research Institute and Hospital, Department of Medicine, Autonomous University of Barcelona, Can Ruti Campus, Ctra. Canyet s/n, Badalona, 08916 Barcelona, Spain

Abstract

Type 2 diabetes (T2D) exists in 25–40% of hospitalized patients. Therapeutic inertia is the delay in the intensification of a treatment and it is frequent in T2D. The objectives of this study were to detect patients admitted to surgical wards with hyperglycaemia (HH; fasting glycaemia > 140 mg/dL) as well as those with T2D and suboptimal chronic glycaemic control (SCGC) and to assess the midterm impact of treatment modifications indicated at discharge. A total of 412 HH patients were detected in a period of 18 months; 86.6% (357) had a diagnosed T2D. Their preadmittanceHbA1cwas 7.7 ± 1.5%; 47% (189) hadHbA1c≥ 7.4% (SCGC) and were moved to the upper step in the therapeutic algorithm at discharge. Another 15 subjects (3.6% of the cohort) had T2D according to their currentHbA1c. Ninety-four of the 189 SCGC patients were evaluated 3–6 months later. TheirHbA1cbefore in-hospital-intervention was 8.6 ± 1.2% and 7.5 ± 1.2% at follow-up (P<0.004). Active detection of hyperglycaemia in patients admitted in conventional surgical beds permits the identification of T2D patients with SCGC as well as previously unknown cases. A shift to the upper step in the therapeutic algorithm at discharge improves this control. Hospitalization is an opportunity to break therapeutic inertia.

Funder

Novo Nordisk

Publisher

Hindawi Limited

Subject

Endocrine and Autonomic Systems,Endocrinology,Endocrinology, Diabetes and Metabolism

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