Evidence map›Paper›PMID 38496128›Full record

ArticleCureus2024

Diabetes and COVID-19 Outcomes: An Analysis of Freeman Health System Patients.

Timothy Wiant, Logan Schmidt, SaiBhavana Srikakolapu, Nova Beyersdorfer, Mariam Akhtar, Kerry Johnson, Greg Stahl, Darrin S Goade, Robert D Arnce

Abstract read
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Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Timothy WiantCollege of Medicine, Kansas City University, Kansas City, USA.
Logan SchmidtCollege of Medicine, Kansas City University, Kansas City, USA.
SaiBhavana SrikakolapuCollege of Medicine, Kansas City University, Joplin, USA.
Nova BeyersdorferCollege of Medicine, Kansas City University, Joplin, USA.
Mariam AkhtarCollege of Medicine, Kansas City University, Joplin, USA.
Kerry JohnsonMathematics, Missouri Southern State University, Joplin, USA.
Greg StahlCollege of Medicine, Kansas City University, Joplin, USA.
Darrin S GoadePharmacy, Freeman Health System, Joplin, USA.
Robert D ArnceCollege of Medicine, Kansas City University, Joplin, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs COVID-19 continues to affect millions of people around the world, it has become vital to understand how comorbidities such as diabetes affect the health outcomes of these patients. While earlier studies have focused on major metropolitan areas, rural settings have been comparatively understudied. The goal of this study is to understand the effect on mortality that these two diseases have in the inpatient setting of a rural population.

methodsThe electronic medical records of all adult patients admitted to Freeman Health System, Joplin, Missouri, United States, between April 1, 2020, and December 31, 2021, were reviewed for the presence of COVID-19 infection and/or diabetes (type I and type II). Freeman Health is a major health system headquartered in Southwest Missouri. Diagnoses were obtained through the use of standard International Classification of Disease, 10

resultsThe all-cause mortality rate was 19.94% (137/687, with a 95% confidence interval (CI) of 16.95%-22.93%) in patients admitted with both diabetes (the combined type I and type II subsets) and COVID-19 (P1). The mortality rate was 16.03% (167/1042, with 95% CI of 13.80%-18.25%) in patients admitted with COVID-19 who did not have diabetes (P2). Patients admitted with a comorbid diagnosis of diabetes but without COVID-19 (P5) had a much lower mortality rate of 5.98% (249/4164, with a 95% CI of 5.26%-6.70%). The combination of both COVID-19 and diabetes together was associated with a higher mortality rate than either of the two separately. The mortality rate was additionally elevated in patients with both type II diabetes and COVID-19 (P4) (134/663, mortality rate of 20.21% with 95% CI of 17.15%-23.27%) versus those with COVID-19 without diabetes (P2) (167/1042, 16.03% with 95% CI of 13.80%-18.25%), an overall difference of 4.18% (95% CI of 0.40%-7.94%). The subset of patients with type I diabetes with COVID-19 (P3) and type I diabetes without COVID-19 (P6) were too small to accurately power individual analysis. The subset of patients with diabetes (type I and type II) and without COVID-19 (P5) had the lowest mortality rate of any subset adequately powered for analysis at 5.98% (249/41464, CI of 5.26%-6.70%).  Conclusions: The results of this study show that type II diabetes is a significant risk factor for mortality in admitted COVID-19 patients. P4 had the highest overall mortality of any subset studied. The study was underpowered to show if type I diabetes patients, with and without COVID-19, had an increased mortality when analyzed separately. COVID-19 significantly increased mortality in all subsets adequately powered for full analysis.

Indexed as

covid-19diabetesmortalityrural populationtype 1 and type 2 diabetes mellitus

Identifiers

PMID38496128
PMCPMC10944295

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.