TY - JOUR
T1 - Clinical features and risk predictor markers in COVID-19 patients in correlation with disease severity and comorbidities- A data-based retrospective study
AU - Suvarna, Renuka
AU - Biswas, Monalisa
AU - Belle, Vijetha Shenoy
AU - Shanbhag, Vishal
N1 - Funding Information:
The authors acknowledge Manipal Academy of Higher Education for providing a congenial and supportive platform for carrying out the research study.
Publisher Copyright:
© 2022 University of Stockholm. All rights reserved.
PY - 2022/4
Y1 - 2022/4
N2 - Background: COVID-19 infection displays a highly heterogeneous spectrum of severities. Laboratory findings are pivotal cues to assess disease severity and aid in retarding/ reversing disease progression. This study aims to identify the haematological, biochemical, and immunological specifics of COVID-19 patients with varying severity and associated comorbidities. Methods: This retrospective study recruited a total of 192 RT PCR confirmed COVID-19 patients. Data on laboratory findings, clinical characteristics, treatment, and hospital stay were obtained and analysed. Results: The patients were grouped into mild, moderate, and severe categories based on disease severity. 96 patients had mild disease, 31 were classified as having moderate COVID-19, and 67 patients had severe COVID-19. 39.58% of the patients were females. The overall death rate among admitted COVID-19 patients is observed to be 19.02%, sepsis and multi-organ failure as the most common cause. The variation in laboratory variables and comorbidities as CAD, CKD, HTN, DM strongly correlate with the severity and increases with the age factor. Pre-existing chronic liver disease emerged to be a comorbidity of significance for acquiring severe COVID-19. Conclusion: Presence of comorbidities, advanced age and male sex emerged as important risk factors while derangements in thrombo-inflammatory markers and haematological indices might be crucial predictors of disease progression. Thromboembolism or superinfection induced sepsis, and multi-organ failure emerged as leading contributors to mortality. High-risk patterns in thrombo inflammatory and immunohematological markers allow for early detection of the disease progression and aid in the institution of personalized intensive therapeutic interventions and monitoring to avoid further deaths.
AB - Background: COVID-19 infection displays a highly heterogeneous spectrum of severities. Laboratory findings are pivotal cues to assess disease severity and aid in retarding/ reversing disease progression. This study aims to identify the haematological, biochemical, and immunological specifics of COVID-19 patients with varying severity and associated comorbidities. Methods: This retrospective study recruited a total of 192 RT PCR confirmed COVID-19 patients. Data on laboratory findings, clinical characteristics, treatment, and hospital stay were obtained and analysed. Results: The patients were grouped into mild, moderate, and severe categories based on disease severity. 96 patients had mild disease, 31 were classified as having moderate COVID-19, and 67 patients had severe COVID-19. 39.58% of the patients were females. The overall death rate among admitted COVID-19 patients is observed to be 19.02%, sepsis and multi-organ failure as the most common cause. The variation in laboratory variables and comorbidities as CAD, CKD, HTN, DM strongly correlate with the severity and increases with the age factor. Pre-existing chronic liver disease emerged to be a comorbidity of significance for acquiring severe COVID-19. Conclusion: Presence of comorbidities, advanced age and male sex emerged as important risk factors while derangements in thrombo-inflammatory markers and haematological indices might be crucial predictors of disease progression. Thromboembolism or superinfection induced sepsis, and multi-organ failure emerged as leading contributors to mortality. High-risk patterns in thrombo inflammatory and immunohematological markers allow for early detection of the disease progression and aid in the institution of personalized intensive therapeutic interventions and monitoring to avoid further deaths.
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U2 - 10.37896/YMER21.04/15
DO - 10.37896/YMER21.04/15
M3 - Article
AN - SCOPUS:85138140971
SN - 0044-0477
VL - 21
SP - 160
EP - 184
JO - Ymer
JF - Ymer
IS - 4
ER -