Zhang 2020.
Study characteristics | |||
Patient Sampling | COVID‐19 cases: hospitalized patients from Zhongnan Hospital of Wuhan university. COVID‐19 was diagnosed based on criteria issued by the National Health Commission of China.
Controls: CAP hospitalized in Department of Respiratory and Critical Care Medicine between 22 January‐22 February 2019. 5 control patients with chronic Hepatitis B or cirrhosis were excluded |
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Patient characteristics and setting | Setting: infectious diseases department hospital; controls in pulmonary and critical care departments Site: Department of Infectious Disease, Zhongnan Hospital of Wuhan University Country: China Demographics: 4 participants < 14 years of age; of the 115 participants in the COVID‐19 group, 49 (42.60%) were male and 66 (57.40%) were female. Mean age at diagnosis was 49.52 ± 17.06 years (IQR, 35‐62; range, 20‐86 years). The CAP group included 55 (48.25%) male participants and 59 (51.75%) female participants, mean age 61.11 ± 18.84 years (IQR, 47‐76; range, 18‐89 years). Severity: 2 patients with chronic Hepatitis B were excluded, and 115 patients were included to COVID‐19 group; from the controls group, four patients with Hepatitis B or cirrhosis were excluded. |
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Index tests | Routine laboratory tests: ALT, AST, total BIL, ALP, GGT, LDH, ALB, GLB, INR, CRP | ||
Target condition and reference standard(s) | COVID‐19 was diagnosed based on criteria issued by the National Health Commission of China; includes RT‐PCR once, Clinical signs and symptoms, chest CT Controls: CAP |
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Flow and timing | Not reported | ||
Comparative | |||
Notes | |||
Methodological quality | |||
Item | Authors' judgement | Risk of bias | Applicability concerns |
DOMAIN 1: Patient Selection | |||
Was a consecutive or random sample of patients enrolled? | No | ||
Was a case‐control design avoided? | No | ||
Did the study avoid inappropriate exclusions? | No | ||
Could the selection of patients have introduced bias? | High risk | ||
Are there concerns that the included patients and setting do not match the review question? | High | ||
DOMAIN 2: Index Test (All tests) | |||
Were the index test results interpreted without knowledge of the results of the reference standard? | Unclear | ||
If a threshold was used, was it pre‐specified? | Unclear | ||
Could the conduct or interpretation of the index test have introduced bias? | Unclear risk | ||
Are there concerns that the index test, its conduct, or interpretation differ from the review question? | Low concern | ||
DOMAIN 3: Reference Standard | |||
Is the reference standards likely to correctly classify the target condition? | No | ||
Were the reference standard results interpreted without knowledge of the results of the index tests? | Unclear | ||
Could the reference standard, its conduct, or its interpretation have introduced bias? | High risk | ||
Are there concerns that the target condition as defined by the reference standard does not match the question? | Low concern | ||
DOMAIN 4: Flow and Timing | |||
Was there an appropriate interval between index test and reference standard? | Unclear | ||
Did all patients receive the same reference standard? | Unclear | ||
Were all patients included in the analysis? | Unclear | ||
Could the patient flow have introduced bias? | Unclear risk |