Risk Factors Associated With Six-Month Mortality in Hospitalized COVID-19 Patients: A Single-Institution Study.

6-month mortality covid-19 mortality elevated d-dimer elevated ldh lactate dehydrogenase

Journal

Cureus
ISSN: 2168-8184
Titre abrégé: Cureus
Pays: United States
ID NLM: 101596737

Informations de publication

Date de publication:
Nov 2022
Historique:
accepted: 05 11 2022
entrez: 12 12 2022
pubmed: 13 12 2022
medline: 13 12 2022
Statut: epublish

Résumé

Background Coronavirus disease 2019 (COVID-19) infection can vary from asymptomatic infection to multi-organ dysfunction. The most serious complication of infection with COVID-19 is death. Various comorbid conditions and inflammatory markers have been associated with an increased risk of mortality, specifically within the immediate post-infection period; however, less is known about long-term mortality outcomes. Objectives Our objective is to determine risk factors associated with six-month mortality in hospitalized COVID-19 patients. Methods This is a single-institution, retrospective study. We included patients hospitalized with COVID-19 from the University of Toledo Medical Center in Toledo, Ohio, who were admitted from March 20, 2020, to June 30, 2021. This study was approved by a biomedical institutional review board at the University of Toledo. Patients with available pre-stored blood samples for laboratory testing were included, and hospital charts were assessed up to six months from the date of a positive COVID-19 test result. Two groups were created based on the mortality outcome at six months from COVID-19 positive test results: survivors and non-survivors. The clinical variables or outcomes and laboratory values were compared between the two groups using non-parametric methods due to the small sample size and non-normality of the data. Either the Mann-Whitney U-test for continuous variables or Fisher's exact test for categorical variables was used for statistical analysis. Results Lactate dehydrogenase (LDH) and D-dimer levels on admission were found to be significantly higher in non-survivors than in survivors. The median high D-dimer level in non-survivors was 5.96 micrograms/milliliter (μg/mL) (interquartile range (IQR): 3.95-11.29 μg/mL) vs 1.82 μg/mL (IQR 1.13-5.55 μg/mL) in survivors (p = 0.019). Median LDH levels were also higher in non-survivors vs survivors, i.e., 621.00 international units per liter (IU/L) (IQR 440.00-849.00 IU/L) vs 328.00 IU/L (IQR 274.00-529.00 IU/L), respectively (p = 0.032). The demographic profile, comorbidity profile, and laboratory data (typically associated with short-term mortality, inflammation, and organ dysfunction) were similar between survivors and non-survivors, except for LDH and D-dimer. Conclusion Higher LDH and D-dimer levels on admission were found to be associated with an increased six-month mortality rate in hospitalized COVID-19 patients. These hematologic data can serve as risk stratification tools to prevent long-term mortality outcomes and provide proactive clinical care in hospitalized COVID-19 patients.

Identifiants

pubmed: 36505139
doi: 10.7759/cureus.31206
pmc: PMC9728985
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e31206

Informations de copyright

Copyright © 2022, Kahlon et al.

Déclaration de conflit d'intérêts

Separate study data from this study has been published from the same project in this journal. https://www.cureus.com/articles/104450-prevalence-and-clinical-significance-of-antiphospholipid-antibodies-in-hospitalized-patients-with-covid-19-infection.

Références

Sci Rep. 2021 Jun 21;11(1):12997
pubmed: 34155288
Diagn Interv Imaging. 2021 Dec;102(12):717-725
pubmed: 34312110
Platelets. 2020 May 18;31(4):490-496
pubmed: 32297540
PLoS One. 2021 Aug 5;16(8):e0255427
pubmed: 34351975
PLoS One. 2021 Oct 28;16(10):e0258351
pubmed: 34710097
J Intensive Care. 2020 Jul 10;8:49
pubmed: 32665858
Nat Med. 2020 Jul;26(7):1017-1032
pubmed: 32651579
Int J Lab Hematol. 2021 Apr;43(2):160-168
pubmed: 33264492
J Med Virol. 2021 Apr;93(4):2307-2320
pubmed: 33247599
Hamostaseologie. 2021 Oct;41(5):379-385
pubmed: 34695854
Rev Med Virol. 2021 Jul;31(4):e2199
pubmed: 34260778
Lancet Reg Health Eur. 2022 Jul;18:100394
pubmed: 35505834
Acad Emerg Med. 2020 Jul;27(7):612-613
pubmed: 32506683
JAMA. 2020 Aug 25;324(8):782-793
pubmed: 32648899
Lancet. 2020 Mar 28;395(10229):1054-1062
pubmed: 32171076
J Med Virol. 2020 Oct;92(10):1875-1883
pubmed: 32441789
World J Clin Cases. 2020 Nov 26;8(22):5535-5546
pubmed: 33344544
Am J Hematol. 2020 Jun;95(6):E131-E134
pubmed: 32129508

Auteurs

Navkirat Kahlon (N)

Hematology and Medical Oncology, The University of Toledo College of Medicine and Life Sciences, Toledo, USA.

Jasskiran Kaur (J)

Internal Medicine, The University of Toledo College of Medicine and Life Sciences, Toledo, USA.

Sishir Doddi (S)

Internal Medicine, The University of Toledo College of Medicine and Life Sciences, Toledo, USA.

Cameron Burmeister (C)

Internal Medicine, The University of Toledo College of Medicine and Life Sciences, Toledo, USA.

Taha Sheikh (T)

Internal Medicine, The University of Toledo College of Medicine and Life Sciences, Toledo, USA.

Ziad Abuhelwa (Z)

Internal Medicine, The University of Toledo College of Medicine and Life Sciences, Toledo, USA.

Aya Abugharbyeh (A)

Rheumatology, The University of Toledo College of Medicine and Life Sciences, Toledo, USA.

Ragheb Assaly (R)

Pulmonary/Critical Care Medicine, The University of Toledo College of Medicine and Life Sciences, Toledo, USA.

William Barnett (W)

Biostatistics and Epidemiology, The University of Toledo Medical Center, Toledo, USA.

Danae Hamouda (D)

Hematology and Medical Oncology, The University of Toledo College of Medicine and Life Sciences, Toledo, USA.

Classifications MeSH