Type 1 diabetes

Guidelines for the management of diabetes‐related ketoacidosis (DKA) have been poorly adopted and implemented, resulting in a lack of improvement in outcomes

Diabet MedPublished Retrospective cohort study

Authors' conclusion

Our study demonstrates suboptimal adoption of guidelines. Therefore, it was perhaps unsurprising that no favourable effect on the rate of complications or outcomes in DKA episodes with reduced-rate FRIII was demonstrated. In DKA episodes where FRIII rate reduction was adopted, there was a significant delay in adjusting the FRIII when glucose levels were <14 mmol/L. Understanding the barriers and facilitators is vital in creating resources to safely implement guidelines.

Study context

Population
DKA admissions across five UK hospitals, October 2021–March 2023
Participants
753 DKA admissions
Exposure
DKA episodes with reduced-rate fixed rate intravenous insulin infusion (FRIII) vs without FRIII rate reduction
Outcome
Uptake of reduced-rate FRIII
Follow-up
Over 18 months
Methodological detailsmulticentre (five UK hospitals)
  • Multicentre (five UK hospitals)

Main finding

As reported in the abstract

Slow uptake of reduced-rate FRIII

49.7%

Observational data: associations, not effects.

Further findings

Lag between starting 10% dextrose and FRIII rate reduction when blood glucose <14 mmol/L, in episodes adopting FRIII reduction

Significant lag between starting 10% dextrose and FRIII rate reduction (median [IQR] hours)
P = 0.00001

DKA duration and LOS

No significant differences in DKA duration and LOS with vs without FRIII rate reduction

Safety

OutcomeP value
HypoglycaemiaNo significant reductionP = 0.344

Hypokalaemia and hyperkalaemia

No significant differences in frequency of hypokalaemia and hyperkalaemia with vs without FRIII rate reduction

Original publication

Guidelines for the management of diabetes‐related ketoacidosis (DKA) have been poorly adopted and implemented, resulting in a lack of improvement in outcomes. Diabet Med. Published 10 February 2025. doi:10.1111/dme.70010

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