Glycaemic outcomes in hospital with IDegAsp versus BIAsp30 premixed insulins

Author:

Walt Joshua R.12ORCID,Loughran Julie3,Fourlanos Spiros145ORCID,Barmanray Rahul D.145ORCID,Zhu Jasmine3,Varadarajan Suresh3,Kyi Mervyn1345ORCID

Affiliation:

1. Department of Diabetes and Endocrinology The Royal Melbourne Hospital Melbourne Victoria Australia

2. Royal Melbourne Clinical School The University of Melbourne Melbourne Victoria Australia

3. Endocrinology Unit Northern Hospital Epping Victoria Australia

4. Department of Medicine at Royal Melbourne Hospital The University of Melbourne Parkville Victoria Australia

5. Australian Centre for Accelerating Diabetes Innovations The University of Melbourne Parkville Victoria Australia

Abstract

AbstractBackground and AimsIDegAsp (Ryzodeg 70/30), a unique premixed formulation of long‐acting insulin degludec and rapid‐acting insulin aspart, is increasing in use. Management of IDegAsp during hospitalisation is challenging because of degludec's ultra‐long duration of action. We investigated inpatient glycaemia in patients treated with IDegAsp compared to biphasic insulin aspart (BIAsp30; Novomix30).MethodsWe performed a retrospective observational study at two hospitals assessing inpatients with type 2 diabetes treated with IDegAsp or BIAsp30 prior to and during hospital admission. Standard inpatient glycaemic outcomes were analysed based on capillary blood glucose (BG) measurements.ResultsWe assessed 88 individuals treated with IDegAsp and 88 HbA1c‐matched individuals treated with BIAsp30. Patient characteristics, including insulin dose at admission, were well matched, but the IDegAsp group had less frequent twice‐daily insulin dosing than the BIAsp30 group (49% vs 87%, P < 0.001). Patient‐days with BG <4 mmol/L were not different (10.6% vs 9.9%, P = 0.7); however, the IDegAsp group had a higher patient‐day mean BG (10.4 (SD 3.4) vs 10.0 (3.4) mmol/L, P < 0.001), and more patient‐days with mean BG >10 mmol/L (48% vs 38%, P < 0.001) compared to the BIAsp30 group. Glucose was higher in the IDegAsp group in the evening (4 PM to midnight) (11.6 (SD 4.0) vs 10.9 (4.6) mmol/L, P = 0.004), but not different at other times during the day.ConclusionsInpatients treated with IDegAsp compared to BIAsp30 had similar hypoglycaemia incidence, but higher hyperglycaemia incidence, potentially related to less frequent twice‐daily dosing. With the increasing use of IDegAsp in the community, development of hospital management guidelines for this insulin formulation is needed.

Publisher

Wiley

Reference31 articles.

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