Effect of underlying comorbidities on the infection and severity of COVID-19 in South Korea
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Abstract
Background
The coronavirus disease (COVID-19) pandemic is an emerging threat worldwide. It is still unclear how comorbidities affect the risk of infection and severity of COVID-19.
Methods
A nationwide retrospective case-control study of 65,149 individuals, aged 18 years or older, whose medical cost for COVID-19 testing were claimed until April 8, 2020. The diagnosis of COVID-19 and severity of COVID-19 infection were identified from the reimbursement data using diagnosis codes and based on whether respiratory support was used, respectively. Odds ratios were estimated using multiple logistic regression, after adjusting for age, sex, region, healthcare utilization, and insurance status.
Results
The COVID-19 group (5,172 of 65,149) was younger and showed higher proportion of females. 5.6% (293 of 5,172) of COVID-19 cases were severe. The severe COVID-19 group had older patients and a higher male ratio than the non-severe group. Cushing syndrome (Odds ratio range (ORR) 2.059-2.358), chronic renal disease (ORR 1.292-1.604), anemia (OR 1.132), bone marrow dysfunction (ORR 1.471-1.645), and schizophrenia (ORR 1.287-1.556) showed significant association with infection of COVID-19. In terms of severity, diabetes (OR 1.417, 95% CI 1.047-1.917), hypertension (OR 1.378, 95% CI 1.008-1.883), heart failure (ORR 1.562-1.730), chronic lower respiratory disease (ORR 1.361-1.413), non-infectious lower digestive system disease (ORR 1.361-1.418), rheumatoid arthritis (ORR 1.865-1.908), substance use (ORR 2.790-2.848), and schizophrenia (ORR 3.434-3.833) were related with severe COVID-19.
Conclusions
We identified several comorbidities associated with COVID-19. Health care workers should be more careful when diagnosing and treating COVID-19 when the patient has the above-mentioned comorbidities.
Take Home message
Comorbidities that might be associated with COVID-19 infection and severe clinical course were identified, which could assist in formulating public health measures to mitigate the risk in groups with increased risk.
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SciScore for 10.1101/2020.05.08.20095174: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement not detected. Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Table 2: Resources
No key resources detected.
Results from OddPub: We did not detect open data. We also did not detect open code. Researchers are encouraged to share open data when possible (see Nature blog).
Results from LimitationRecognizer: We detected the following sentences addressing limitations in the study:This study had a few limitations. Firstly, this study was limited to data from the nationwide claim database of subjects who received laboratory test of COVID-19. Thus, the database including those who were tested via “Drive …
SciScore for 10.1101/2020.05.08.20095174: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement not detected. Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Table 2: Resources
No key resources detected.
Results from OddPub: We did not detect open data. We also did not detect open code. Researchers are encouraged to share open data when possible (see Nature blog).
Results from LimitationRecognizer: We detected the following sentences addressing limitations in the study:This study had a few limitations. Firstly, this study was limited to data from the nationwide claim database of subjects who received laboratory test of COVID-19. Thus, the database including those who were tested via “Drive Through” or local health centers and treated in non-medical facility was not included in this study. Therefore, the number of officially announced population was different from that of the analyzed population, which was used in this study. Despite this limitation, this study was conducted only for those who performed the laboratory test for COVID-19 on insurance claims database. Therefore, the negative control group had a confirmed a negative result of SARS-CoV-2 infection. Thus, the comparison between this negative control group and case group helped in proper evaluation of the risk factors for COVID 19 occurrence. Another limitation was the inability of the data source to provide the information on the severity of the comorbidities. Finally, we could not evaluate the detailed mechanism of the relationship between comorbidities and the diagnosis or severity of COVID-19. However, most comorbidities identified in each individual’s health insurance claim data could be used for this study. It could be possible to discover previously unknown or unexpected risk factors based on a data driven approach.
Results from TrialIdentifier: No clinical trial numbers were referenced.
Results from Barzooka: We did not find any issues relating to the usage of bar graphs.
Results from JetFighter: We did not find any issues relating to colormaps.
Results from rtransparent:- Thank you for including a conflict of interest statement. Authors are encouraged to include this statement when submitting to a journal.
- Thank you for including a funding statement. Authors are encouraged to include this statement when submitting to a journal.
- No protocol registration statement was detected.
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