Affiliation:
1. Department of Diabetes and Endocrinology Prince of Wales Hospital Randwick New South Wales Australia
2. School of Clinical Medicine UNSW Randwick New South Wales Australia
3. Centre for Health Systems and Safety Research, Australian Institute of Health Innovation, Faculty of Medicine, Health and Human Sciences Macquarie University Ryde New South Wales Australia
4. Clinical Insights and Analytics South East Sydney Local Health District Caringbah New South Wales Australia
Abstract
AbstractAimsThe safety of continuing metformin during a hospital admission has not been robustly demonstrated. We evaluated the association of continuing metformin in hospital with the risk for a hospital‐acquired complication (HAC).MethodsThis is a retrospective observational study of patients admitted to a medical or surgical ward. We considered those with diabetes who continued metformin (DM/MET group), those who discontinued metformin upon admission (DM/MET‐STOP), and those with diabetes not on metformin just prior to and during admission (DM/NoMET). We prepared propensity score‐matched (PSM) control groups from admitted patients without diabetes. The likelihood of a HAC was determined using a Kaplan–Meier survival analysis. A Cox proportional hazards model was employed to calculate the hazard ratio, adjusted for covariates.ResultsOf the 4446 (14%) patients with diabetes, 3331 (10%) were prescribed metformin on admission, and it was continued in 2557 patients. HAC occurred in 5.5% of DM/MET group and 6.4% of the PSM control group. Continuation of metformin was associated with a lower likelihood of HAC, adjusted hazard ratio 0.85 (95% CI 0.69, 1.04), p = 0.117 compared to a PSM‐matched control group without diabetes. The DM/NoMET and DM/MET‐STOP groups had an increased risk for HAC, adjusted HR 1.77 (1.44, 2.18), p < 0.001 and 2.57 (2.10, 3.13), p < 0.001, as compared to their respective PSM control groups.ConclusionAn individualized assessment to continue metformin during hospital admission was associated with a reduced likelihood of HAC, with the caveat that there was limited matching to non‐diabetes controls. This finding warrants further exploration.
Funder
Diabetes Australia Research Trust
National Health and Medical Research Council
South Eastern Sydney Local Health District