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      ASSOCIATION OF HYPERGLYCAEMIA WITH HOSPITAL MORTALITY IN NONDIABETIC COVID-19 PATIENTS: A COHORT STUDY

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          Abstract

          Objective

          Diabetes is a known risk factor for mortality in Coronavirus disease 2019 (COVID-19) patients. Our objective was to identify prevalence of hyperglycaemia in COVID-19 patients with and without prior diabetes and quantify its association with COVID-19 disease course.

          Research Design and Methods

          This observational cohort study included all consecutive COVID-19 patients admitted to John H Stroger Jr. Hospital, Chicago, IL from March 15, 2020 to May 3, 2020 and followed till May 15, 2020. The primary outcome was hospital mortality, and the studied predictor was hyperglycaemia [any blood glucose ≥ 7.78 mmol/L (140 mg/dL) during hospitalization].

          Results

          Of the 403 COVID-19 patients studied, 51 (12.7%) died; 335 (83.1%) were discharged while 17 (4%) were still in hospital. Hyperglycaemia occurred in 228 (56.6%) patients; 83 of these hyperglycaemic patients (36.4%) had no prior history of diabetes. Compared to the reference group no-diabetes / no-hyperglycaemia patients the no-diabetes / hyperglycaemia patients showed higher mortality [1.8% versus 20.5%, adjusted odds ratio 21.94 (95% confidence interval 4.04-119.0), P <  0.001]; improved prediction of death ( P =  0.01) and faster progression to death ( P <  0.01). Hyperglycaemia within the first 24 and 48 hours was also significantly associated with mortality (odds ratio 2.15 and 3.31, respectively).

          Conclusions

          Hyperglycaemia without prior diabetes was common (20.6% of hospitalized COVID-19 patients) and was associated with an increased risk of and faster progression to death. Development of hyperglycaemia in COVID-19 patients who do not have diabetes is an early indicator of progressive disease.

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          Author and article information

          Journal
          Diabetes Metab
          Diabetes Metab
          Diabetes & Metabolism
          Published by Elsevier Masson SAS.
          1262-3636
          1878-1780
          26 March 2021
          26 March 2021
          : 101254
          Affiliations
          [a ]M&H Research, LLC, San Antonio, Texas, USA
          [b ]Division of Nephrology, Department of Medicine, Cook County Health, Chicago, Illinois, USA
          [c ]Rush Medical College, Chicago, Illinois, USA
          [d ]Cerner Corporation, Kansas City, Missouri, USA
          [e ]Department of Emergency Medicine, Wayne State University School of Medicine, Detroit, Michigan, USA
          Author notes
          [* ]Corresponding author at: M&H Research, LLC, 12023 Waterway Rdg, San Antonio, Texas, 78249, USA.
          [1]

          Equal contribution as first author.

          Article
          S1262-3636(21)00037-9 101254
          10.1016/j.diabet.2021.101254
          7994287
          33781926
          d6fc0cbb-bbc5-41b3-9db0-2c2356f100d6
          © 2021 Published by Elsevier Masson SAS.

          Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

          History
          : 18 November 2020
          : 26 February 2021
          : 16 March 2021
          Categories
          Original Article

          covid-19,diabetes,hospital mortality,hyperglycaemia
          covid-19, diabetes, hospital mortality, hyperglycaemia

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