» Articles » PMID: 35168965

Biomarker Identification Using Dynamic Time Warping Analysis: a Longitudinal Cohort Study of Patients with COVID-19 in a UK Tertiary Hospital

Abstract

Objectives: COVID-19 is a heterogeneous disease, and many reports have described variations in demographic, biochemical and clinical features at presentation influencing overall hospital mortality. However, there is little information regarding longitudinal changes in laboratory prognostic variables in relation to disease progression in hospitalised patients with COVID-19.

Design And Setting: This retrospective observational report describes disease progression from symptom onset, to admission to hospital, clinical response and discharge/death among patients with COVID-19 at a tertiary centre in South East England.

Participants: Six hundred and fifty-one patients treated for SARS-CoV-2 between March and September 2020 were included in this analysis. Ethical approval was obtained from the HRA Specific Review Board (REC 20/HRA/2986) for waiver of informed consent.

Results: The majority of patients presented within 1 week of symptom onset. The lowest risk patients had low mortality (1/45, 2%), and most were discharged within 1 week after admission (30/45, 67%). The highest risk patients, as determined by the 4C mortality score predictor, had high mortality (27/29, 93%), with most dying within 1 week after admission (22/29, 76%). Consistent with previous reports, most patients presented with high levels of C reactive protein (CRP) (67% of patients >50 mg/L), D-dimer (98%>upper limit of normal (ULN)), ferritin (65%>ULN), lactate dehydrogenase (90%>ULN) and low lymphocyte counts (81%<lower limit of normal (LLN)). Increases in platelet counts and decreases in CRP, neutrophil:lymphocyte ratio (p<0.001), lactate dehydrogenase, neutrophil counts, urea and white cell counts (all p<0.01) were each associated with discharge.

Conclusions: Serial measurement of routine blood tests may be a useful prognostic tool for monitoring treatment response in hospitalised patients with COVID-19. Changes in other biochemical parameters often included in a 'COVID-19 bundle' did not show significant association with outcome, suggesting there may be limited clinical benefit of serial sampling. This may have direct clinical utility in the context of escalating healthcare costs of the pandemic.

Citing Articles

Study of Biochemical Parameters as Predictors for Need of Invasive Ventilation in Severely Ill COVID-19 Patients.

Ansari A, Pitamberwale A, Ansari S, Mahmood T, Limgaokar K, Karki G J Crit Care Med (Targu Mures). 2023; 9(4):262-270.

PMID: 37969877 PMC: 10644279. DOI: 10.2478/jccm-2023-0030.


Vascular risk factors for COVID-19 ARDS: endothelium, contact-kinin system.

Bailey M, Linden D, Guo-Parke H, Earley O, Peto T, McAuley D Front Med (Lausanne). 2023; 10:1208866.

PMID: 37448794 PMC: 10336249. DOI: 10.3389/fmed.2023.1208866.


Characterising biological mechanisms underlying ethnicity-associated outcomes in COVID-19 through biomarker trajectories: a multicentre registry analysis.

Wan Y, Puthucheary Z, Pearse R, Prowle J Br J Anaesth. 2023; 131(3):491-502.

PMID: 37198030 PMC: 10121108. DOI: 10.1016/j.bja.2023.04.008.


On-admission and dynamic trend of laboratory profiles as prognostic biomarkers in COVID-19 inpatients.

Siavoshi F, Safavi-Naini S, Shirzadeh Barough S, Azizmohammad Looha M, Hatamabadi H, Ommi D Sci Rep. 2023; 13(1):6993.

PMID: 37117397 PMC: 10144885. DOI: 10.1038/s41598-023-34166-z.


Comparison of time series clustering methods for identifying novel subphenotypes of patients with infection.

Bhavani S, Xiong L, Pius A, Semler M, Qian E, Verhoef P J Am Med Inform Assoc. 2023; 30(6):1158-1166.

PMID: 37043759 PMC: 10198539. DOI: 10.1093/jamia/ocad063.


References
1.
Burke H, Freeman A, Dushianthan A, Celinski M, Batchelor J, Phan H . Research Evaluation Alongside Clinical Treatment in COVID-19 (REACT COVID-19): an observational and biobanking study. BMJ Open. 2021; 11(1):e043012. PMC: 7830323. DOI: 10.1136/bmjopen-2020-043012. View

2.
Moutchia J, Pokharel P, Kerri A, McGaw K, Uchai S, Nji M . Clinical laboratory parameters associated with severe or critical novel coronavirus disease 2019 (COVID-19): A systematic review and meta-analysis. PLoS One. 2020; 15(10):e0239802. PMC: 7529271. DOI: 10.1371/journal.pone.0239802. View

3.
Wang Y, Zhang L, Sang L, Ye F, Ruan S, Zhong B . Kinetics of viral load and antibody response in relation to COVID-19 severity. J Clin Invest. 2020; 130(10):5235-5244. PMC: 7524490. DOI: 10.1172/JCI138759. View

4.
van Haren F, Page C, Laffey J, Artigas A, Camprubi-Rimblas M, Nunes Q . Nebulised heparin as a treatment for COVID-19: scientific rationale and a call for randomised evidence. Crit Care. 2020; 24(1):454. PMC: 7374660. DOI: 10.1186/s13054-020-03148-2. View

5.
Freeman A, Watson A, ORegan P, Wysocki O, Burke H, Freitas A . Wave comparisons of clinical characteristics and outcomes of COVID-19 admissions - Exploring the impact of treatment and strain dynamics. J Clin Virol. 2021; 146:105031. PMC: 8608665. DOI: 10.1016/j.jcv.2021.105031. View