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Real-World Effectiveness and Safety of Insulin Glargine 300 U/mL in Patients with T2D Uncontrolled on NPH or Premixed Insulins as Part of Routine Clinical Practice in Bulgaria: ToUPGRADE Study.
Kamenov, Zdravko; Pehlivanova, Veselina; Kuneva, Tsvetodara; Kirilov, Kiril; Bobeva, Roza; Stoykova, Julija; Mihalevska, Svetla.
Afiliação
  • Kamenov Z; University Hospital "Aleksandrovska", Medical University of Sofia, Sofia, Bulgaria. zkamenov@hotmail.com.
  • Pehlivanova V; Sanofi, Sofia, Bulgaria.
  • Kuneva T; Diagnostic-Consultative Centre 1, Ruse, Bulgaria.
  • Kirilov K; Medical Ambulatory Centre "Asklepii", Dupnitsa, Bulgaria.
  • Bobeva R; Multiprofile Hospital for Active Treatment "Dr. Ivan Seliminski", Sliven, Bulgaria.
  • Stoykova J; Multiprofile Hospital for Active Treatment, Pleven, Bulgaria.
  • Mihalevska S; Sanofi, Sofia, Bulgaria.
Diabetes Ther ; 12(3): 913-930, 2021 Mar.
Article em En | MEDLINE | ID: mdl-33604804
ABSTRACT

INTRODUCTION:

The aim of this study is to demonstrate the real-life effectiveness and safety of insulin glargine 300 U/mL (Gla-300) in patients with type 2 diabetes (T2D) previously uncontrolled on NPH ± prandial insulin or premixed insulins in routine clinical practice in Bulgaria.

METHODS:

This was a 24-week prospective, observational study performed in 40 inpatient and outpatient sites across the country.

RESULTS:

A total of 286 patients were included in the study. The mean age (± SD) was 61.2 ± 10.0 years with duration of diabetes of 11.64 ± 7.5 years and body mass index (BMI) of 32.1 ± 5.7 kg/m2. HbA1c before Gla-300 initiation was 9.8 ± 1.0%, and fasting plasma glucose (FPG) was 13.1 ± 3.4 mmol/L. HbA1c and FPG change from baseline to week 24 was - 1.86% (p < 0.001) and - 4.8 mmol/L (p < 0.001), respectively. The proportion of patients reaching their individualized HbA1c at week 24 was 39.1% (95% CI 33.3-45.1%), while the proportion of patients reaching their individualized HbA1c target without confirmed and/or severe hypoglycaemia was 34.8% (95% CI 29.2-40.7%). At study end, 19.0% (95% CI 14.6-24.1%) achieved HbA1c < 7%. Body weight decreased from 88.3 to 87.0 kg from baseline to week 24 with mean change of - 1.3 kg (p < 0.001). The incidence and event rates of anytime confirmed (≤ 3.9 mmol/L) and/or severe hypoglycaemia were low 7.7% and 0.42 events per patient-year, respectively. The overall Insulin Treatment Satisfaction Questionnaire (ITSQ) score increased from 53.2 to 78.2 from baseline to week 24 and the difference of 25.1 ± 21.5 points was significant (p < 0.001).

CONCLUSIONS:

In real-life settings, Gla-300 significantly improved glycaemic control and insulin treatment satisfaction in people with T2D who were inadequately controlled with NPH ± prandial insulin or premixed insulin analogues. Improvement of glycaemic control was associated with a very low risk of hypoglycaemia and with significant weight loss irrespective of the previous insulin regimen.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Evaluation_studies / Observational_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Evaluation_studies / Observational_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article