Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 May-Jun;155(5&6):554-564.
doi: 10.4103/ijmr.ijmr_2605_21.

Association of hyperglycaemia at-admission & diabetes mellitus with 28 day mortality in patients admitted with moderate-severe SARS-CoV-2 infection: A retrospective study

Affiliations

Association of hyperglycaemia at-admission & diabetes mellitus with 28 day mortality in patients admitted with moderate-severe SARS-CoV-2 infection: A retrospective study

Navya Mary Kurian et al. Indian J Med Res. 2022 May-Jun.

Abstract

Background & objectives: The association between hyperglycaemia at admission, diabetes mellitus (DM) status and mortality in hospitalized SARS-CoV-2 infected patients is not clear. The purpose of this study was to determine the relationship between DM, at-admission hyperglycaemia and 28 day mortality in patients admitted with moderate-severe SARS-CoV-2 infection requiring intensive care.

Methods: All consecutive moderate-to-severe patients with SARS-CoV-2 infection admitted to the intensive care units (ICUs) over six months were enrolled in this single-centre, retrospective study. The predicators for 28 day mortality were analysed from the independent variables including DM status and hyperglycaemia at-admission.

Results: Four hundred and fifty two patients with SARS-CoV-2 were admitted to the ICU, with a mean age of 58.5±13.4 yr, 78.5 per cent being male, HbA1c of 7.2 per cent (6.3-8.8) and 63.7 per cent having DM. Overall, 28 day mortality was 48.9 per cent. In univariate analysis, mortality in diabetes patients was comparable with non-diabetes (47.9 vs. 50.6%, P=0.58), while it was significantly higher in hyperglycaemic group (60.4 vs. 35.8%, P<0.001). In multivariate Cox regression analysis, after adjusting for age, sex and comorbidities, hyperglycaemia at-admission was an independent risk factor of mortality [hazard ratio (HR) 1.45, 95% confidence interval (CI) (1.06-1.99), P<0.05].

Interpretation & conclusions: This study showed that the presence of hyperglycaemia at-admission in critically ill SARS-CoV-2 patients was an independent predictor of 28 day mortality. However, the findings may be susceptible to unmeasured confounding, and more research from prospective studies is required.

Keywords: COVID-19; Critical illness; SARS-CoV-2; diabetes mellitus; hyperglycaemia; intensive care units; mortality.

PubMed Disclaimer

Conflict of interest statement

Conflicts of Interest: None.

Figures

Figure
Figure
Kaplan-Meier analysis showing survival from severe disease (SARS-CoV-2) infection through 28 days in ICU for patients with hyperglycaemia (HG) and no diabetes mellitus (HG+No DM), HG and diabetes (HG+DM), no HG but with diabetes (No HG+DM), and no HG and no diabetes (No HG+No DM), log rank (Mantel-Cox) Chi-Square 33.7, P<0.001.

References

    1. Cucinotta D, Vanelli M. WHO declares COVID-19 a pandemic. Acta Biomed. 2020;91:157–60. - PMC - PubMed
    1. Ministry of Health and Family Welfare, Government of India. [accessed on June 30, 2022];COVID-19 India. Available from: https://www.mohfw.gov.in/
    1. Matarese A, Gambardella J, Sardu C, Santulli G. miR-98 Regulates TMPRSS2 expression in human endothelial cells:Key implications for COVID-19. Biomedicines. 2020;8:462. - PMC - PubMed
    1. Onder G, Rezza G, Brusaferro S. Case-fatality rate and characteristics of patients dying in relation to COVID-19 in Italy. JAMA. 2020;323:1775–6. - PubMed
    1. Seiglie J, Platt J, Cromer SJ, Bunda B, Foulkes AS, Bassett IV, et al. Diabetes as a risk factor for poor early outcomes in patients hospitalized with COVID-19. Diabetes Care. 2020;43:2938–44. - PMC - PubMed