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15 Years of Experience with Biphasic Insulin Aspart 30 in Type 2 Diabetes.
Liebl, Andreas; Mohan, Viswanathan; Yang, Wenying; Strojek, Krzysztof; Linjawi, Sultan.
Afiliação
  • Liebl A; Department for Internal Medicine, Center for Diabetes and Metabolism, m&i-Fachklinik Bad Heilbrunn, Woernerweg 30, 83670, Bad Heilbrunn, Germany. andreas.liebl@fachklinik-bad-heilbrunn.de.
  • Mohan V; Dr. Mohan's Diabetes Specialties Centre and Madras Diabetes Research Foundation, Chennai, India.
  • Yang W; China-Japan Friendship Hospital, Beijing, China.
  • Strojek K; Department of Internal Diseases Diabetology and Cardiometabolic Diseases, SMDZ in Zabrze, Medical University of Silesia, Katowice, Poland.
  • Linjawi S; Coffs Endocrine and Diabetes Services, Coffs Harbour, NSW, 2450, Australia.
Drugs R D ; 18(1): 27-39, 2018 Mar.
Article em En | MEDLINE | ID: mdl-29468559
Since clinical experience with biphasic insulin aspart 30 (BIAsp 30) in type 2 diabetes mellitus (T2DM) was reviewed in 2012 after 10 years of use worldwide, additional studies have been published that highlight new aspects, including use in real-world populations. Evidence from 35 new studies confirms and builds upon previous work indicating that BIAsp 30 continues to have pharmacodynamic and clinical advantages over biphasic human insulin (BHI 30), including in real-world practice with unselected populations of patients. BIAsp 30 has also been shown to be safe and efficacious as an add-on to dipeptidyl peptidase-4 (DPP-4) inhibitors. Intensification with BIAsp 30 is a safe and effective way to improve glycemic control, and titration performed by patients can achieve results that are at least comparable to those when being guided by healthcare providers. Stepwise intensification using BIAsp 30 is comparable to intensification using a basal-bolus regimen, and twice-daily BIAsp 30 provides similar glycemic control to a basal-plus regimen. Data from large observational studies, in particular, have identified patient-related characteristics that are associated with improved clinical responses, suggesting that earlier initiation and intensification of therapy is warranted. Finally, new health-economic analyses continue to confirm that BIAsp 30 is cost effective versus other therapies such as BHI 30, neutral protamine Hagedorn (NPH), or insulin glargine in both insulin-naïve and insulin-experienced patients. After 15 years of clinical use worldwide, analysis of more recent 5-year data indicates that BIAsp 30 remains a safe, effective, and simple-to-use insulin for initiation and intensification by diabetes specialists and primary care physicians in a variety of patients with T2DM.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Insulinas Bifásicas / Insulina Aspart / Insulina Isófana Tipo de estudo: Observational_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Drugs R D Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Insulinas Bifásicas / Insulina Aspart / Insulina Isófana Tipo de estudo: Observational_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Drugs R D Ano de publicação: 2018 Tipo de documento: Article