Glucose dysregulation and its association with COVID-19 mortality and hospital length of stay.


Journal

Diabetes & metabolic syndrome
ISSN: 1878-0334
Titre abrégé: Diabetes Metab Syndr
Pays: Netherlands
ID NLM: 101462250

Informations de publication

Date de publication:
Mar 2022
Historique:
received: 24 12 2021
revised: 09 02 2022
accepted: 21 02 2022
pubmed: 8 3 2022
medline: 1 4 2022
entrez: 7 3 2022
Statut: ppublish

Résumé

We investigate the impact of blood glucose on mortality and hospital length of stay (HLOS) among COVID-19 patients. Retrospective study of 456 patients with confirmed COVID-19 and glycemic dysregulation in the New York City area. We found that impaired glucose adjusted for other organs systems involved (OR:1.87; 95% CI:1.36-2.57, p < 0.001), increased glucose nadir (OR:34.28; 95% CI:3.97-296.05, p < 0.01) and abnormal blood glucose levels at discharge (OR:5.07; 95% CI:2.31-11.14, p < 0.001) were each significantly associated with increased odds for mortality. New or higher from baseline insulin requirement during hospitalization (OR:0.34; 95% CI:0.15-0.78; p < 0.05) was significantly associated with decreased odds for mortality. Increased glucose peak (B = 0.001, SE=<0.001, p < 0.001), new or higher from baseline insulin requirement during hospitalization (B = 0.11, SE = 0.03, p < 0.001), and increased days to dysglycemia (B = 0.15, SE = 0.04, p < 0.001) were each significantly associated with increased HLOS. Increased glucose nadir (B = -0.67, SE = 0.07, p < 0.001), insulin intravenous drip (B = -0.10, SE = 0.05, p < 0.05), and increased proportion days endocrine system involved (B = -0.25, SE = 0.06, p < 0.001) were each significantly associated with decreased HLOS. Glucose dysregulation adversely affects mortality and HLOS in COVID-19. These data can help clinicians to guide patient treatment and management in COVID-19 patients.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
We investigate the impact of blood glucose on mortality and hospital length of stay (HLOS) among COVID-19 patients.
METHODS METHODS
Retrospective study of 456 patients with confirmed COVID-19 and glycemic dysregulation in the New York City area.
RESULTS RESULTS
We found that impaired glucose adjusted for other organs systems involved (OR:1.87; 95% CI:1.36-2.57, p < 0.001), increased glucose nadir (OR:34.28; 95% CI:3.97-296.05, p < 0.01) and abnormal blood glucose levels at discharge (OR:5.07; 95% CI:2.31-11.14, p < 0.001) were each significantly associated with increased odds for mortality. New or higher from baseline insulin requirement during hospitalization (OR:0.34; 95% CI:0.15-0.78; p < 0.05) was significantly associated with decreased odds for mortality. Increased glucose peak (B = 0.001, SE=<0.001, p < 0.001), new or higher from baseline insulin requirement during hospitalization (B = 0.11, SE = 0.03, p < 0.001), and increased days to dysglycemia (B = 0.15, SE = 0.04, p < 0.001) were each significantly associated with increased HLOS. Increased glucose nadir (B = -0.67, SE = 0.07, p < 0.001), insulin intravenous drip (B = -0.10, SE = 0.05, p < 0.05), and increased proportion days endocrine system involved (B = -0.25, SE = 0.06, p < 0.001) were each significantly associated with decreased HLOS.
CONCLUSION CONCLUSIONS
Glucose dysregulation adversely affects mortality and HLOS in COVID-19. These data can help clinicians to guide patient treatment and management in COVID-19 patients.

Identifiants

pubmed: 35255293
pii: S1871-4021(22)00053-4
doi: 10.1016/j.dsx.2022.102439
pmc: PMC8867960
pii:
doi:

Substances chimiques

Blood Glucose 0
Glucose IY9XDZ35W2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

102439

Informations de copyright

Copyright © 2022 Diabetes India. Published by Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest All authors have no conflicts of interest to report for the manuscript “Glucose Dysregulation and its Association with COVID-19 Mortality and Hospital Length of Stay”.

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Auteurs

Steven Mirabella (S)

Department of Internal Medicine, Nassau University Medical Center, East Meadow, NY, USA. Electronic address: smirabel@numc.edu.

Sandra Gomez-Paz (S)

Department of Internal Medicine, Nassau University Medical Center, East Meadow, NY, USA. Electronic address: sgomezpa@numc.edu.

Eric Lam (E)

Department of Internal Medicine, Nassau University Medical Center, East Meadow, NY, USA. Electronic address: elam@numc.edu.

Luis Gonzalez-Mosquera (L)

Department of Internal Medicine, Nassau University Medical Center, East Meadow, NY, USA. Electronic address: lgonzal2@numc.edu.

Joshua Fogel (J)

Department of Business Management, Brooklyn College, Brooklyn, NY, USA. Electronic address: jfogel@brooklyn.cuny.edu.

Sofia Rubinstein (S)

Department of Internal Medicine, Division of Nephrology & Hypertension, Nassau University Medical Center, East Meadow, NY, USA. Electronic address: srubinst@numc.edu.

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