Clinical features and management of severe COVID-19: A retrospective study in Wuxi, Jiangsu Province, China
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Abstract
Objective
We aimed to investigate clinical features and management of 55 COVID-19 patients in Wuxi, especially severe COVID-19.
Methods
Epidemiological, demographic, clinical, laboratory, imaging, treatment, and outcome data of patients were collected. Follow-up lasted until April 6, 2020.
Results
All 55 patients included 47 (85.5%) non-severe patients and 8 (14.5%) severe patients. Common comorbidities were hypertension and diabetes. Common symptoms were fever, cough and sputum. Lymphopenia was a common laboratory finding, and ground-glass opacity was a common chest CT feature. All patients received antiviral therapy of α-interferon inhalation and lopinavir-ritonavir tablets. Common complications included acute liver injury and respiratory failure. All patients were discharged. No death was occurred and no medical staff got infected. Patients with severe COVID-19 showed significantly older age, decreased lymphocytes, increased C reactive protein, and higher frequency of bilateral lung infiltration compared to non-severe patients. Significantly more treatments including antibiotic therapy and mechanical ventilation, longer hospitalization stay and higher cost were shown on severe patients.
Conclusions
Our study suggested that patients with severe COVID-19 may be more likely to have an older age, present with lymphopenia and bilateral lung infiltration, receive multiple treatments and stay longer in hospital.
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SciScore for 10.1101/2020.04.10.20060335: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement IRB: This study was approved by the Ethics Commission of Wuxi Fifth People’s Hospital (2020-007-1), a designated infectious diseases hospital of COVID-19 and informed consent from participants was also waived by the Ethics Commission.
Consent: This study was approved by the Ethics Commission of Wuxi Fifth People’s Hospital (2020-007-1), a designated infectious diseases hospital of COVID-19 and informed consent from participants was also waived by the Ethics Commission.Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Table 2: Resources
Software and Algorithms Sentences Resources Statistical analyses … SciScore for 10.1101/2020.04.10.20060335: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement IRB: This study was approved by the Ethics Commission of Wuxi Fifth People’s Hospital (2020-007-1), a designated infectious diseases hospital of COVID-19 and informed consent from participants was also waived by the Ethics Commission.
Consent: This study was approved by the Ethics Commission of Wuxi Fifth People’s Hospital (2020-007-1), a designated infectious diseases hospital of COVID-19 and informed consent from participants was also waived by the Ethics Commission.Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Table 2: Resources
Software and Algorithms Sentences Resources Statistical analyses were done using SPSS (version 26.0) or Graphpad Prism (version 8.0). SPSSsuggested: (SPSS, RRID:SCR_002865)Graphpad Prismsuggested: (GraphPad Prism, RRID:SCR_002798)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:Several limitations do exist in our study. First, this study included only 55 cases thanks to good monitoring and screening in Wuxi, which may cause some statistical and selective bias of our results. Second, no immune function test like serum T cells or cytokines and some other tests like serum lactate dehydrogenase were involved in the laboratory test. As such their role might be underestimated in causing severe disease. Third, this study was limited to the local investigation, and the findings may be inconsistent with nationwide or worldwide studies, which may decrease its credibility.
Results from TrialIdentifier: We found the following clinical trial numbers in your paper:
Identifier Status Title NCT04257656 Terminated A Trial of Remdesivir in Adults With Severe COVID-19 NCT04252664 Suspended A Trial of Remdesivir in Adults With Mild and Moderate COVID… NCT04292899 Completed Study to Evaluate the Safety and Antiviral Activity of Remde… 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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