<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Glastras SJ</submitter><funding>Novo Nordisk</funding><pagination>E1091</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7230791</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(4)</volume><pubmed_abstract>Treatment intensification in people with type 2 diabetes following failure of basal insulin commonly involves the addition of a rapid-acting insulin analogue (basal plus one or more prandial doses; multiple daily injections) or by a switch to premixed insulin. Insulin degludec/insulin aspart (IDegAsp), comprising rapid-acting insulin aspart and ultra-long-acting insulin degludec in solution, enables both fasting and post-prandial glucose control, with some advantages over other treatment intensification options. These include straightforward dose titration, flexibility in dose timing, low injection burden, simplicity of switching and a lower risk of hypoglycaemia. In Australia, where insulin degludec on its own is not available, IDegAsp enables patients to still benefit from its ultra-long-acting properties. This review aims to provide guidance on where and how to use IDegAsp. Specifically, guidance is included on the initiation of IDegAsp in insulin-naïve patients, treatment intensification from basal insulin, switching from premixed or basal-bolus insulin to IDegAsp, up-titration from once- to twice-daily IDegAsp and the use of IDegAsp in special populations or situations.</pubmed_abstract><journal>Journal of clinical medicine</journal><pubmed_title>The Clinical Role of Insulin Degludec/Insulin Aspart in Type 2 Diabetes: An Empirical Perspective from Experience in Australia.</pubmed_title><pmcid>PMC7230791</pmcid><funding_grant_id>-</funding_grant_id><pubmed_authors>McGill M</pubmed_authors><pubmed_authors>Fulcher GR</pubmed_authors><pubmed_authors>Glastras SJ</pubmed_authors><pubmed_authors>Cohen N</pubmed_authors><pubmed_authors>Kilov G</pubmed_authors><pubmed_authors>Dover T</pubmed_authors><pubmed_authors>MacIsaac RJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Clinical Role of Insulin Degludec/Insulin Aspart in Type 2 Diabetes: An Empirical Perspective from Experience in Australia.</name><description>Treatment intensification in people with type 2 diabetes following failure of basal insulin commonly involves the addition of a rapid-acting insulin analogue (basal plus one or more prandial doses; multiple daily injections) or by a switch to premixed insulin. Insulin degludec/insulin aspart (IDegAsp), comprising rapid-acting insulin aspart and ultra-long-acting insulin degludec in solution, enables both fasting and post-prandial glucose control, with some advantages over other treatment intensification options. These include straightforward dose titration, flexibility in dose timing, low injection burden, simplicity of switching and a lower risk of hypoglycaemia. In Australia, where insulin degludec on its own is not available, IDegAsp enables patients to still benefit from its ultra-long-acting properties. This review aims to provide guidance on where and how to use IDegAsp. Specifically, guidance is included on the initiation of IDegAsp in insulin-naïve patients, treatment intensification from basal insulin, switching from premixed or basal-bolus insulin to IDegAsp, up-titration from once- to twice-daily IDegAsp and the use of IDegAsp in special populations or situations.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Apr</publication><modification>2024-11-13T11:57:56.203Z</modification><creation>2020-05-26T07:09:44Z</creation></dates><accession>S-EPMC7230791</accession><cross_references><pubmed>32290465</pubmed><doi>10.3390/jcm9041091</doi></cross_references></HashMap>