Alizadehsani 2021.
Study characteristics | |||
Patient Sampling |
Purpose: diagnosis of COVID‐19 pneumonia; to identify risk factors for disease and mortality Design: cross‐sectional cohort, prospective data collection Recruitment: all patients referred to the imaging department through the ED on suspicion of COVID‐19 (with flu‐like symptoms) Sample size: n = 319 (123 cases) Inclusion criteria: patients with flu‐like symptoms referred to the imaging department Exclusion criteria: none specified |
||
Patient characteristics and setting |
Facility cases: patients with positive findings on lung CT Facility controls: patients with negative lung CT Country: Iran Dates: 01 March 2020‐08 April 2020 Symptoms and severity: not specified. 1/3 had COVID‐19 pneumonia Demographics: mean age cases: 52.0 years controls: 44.1 years M%/F%: cases 40.8/59.2, controls 50.4/49.6 Exposure history: travelling in past 3 months: cases 4.9%, controls 3.1% |
||
Index tests |
|
||
Target condition and reference standard(s) |
|
||
Flow and timing | Timing not specified | ||
Comparative | |||
Notes | Funding: none declared | ||
Methodological quality | |||
Item | Authors' judgement | Risk of bias | Applicability concerns |
DOMAIN 1: Patient Selection | |||
Was a consecutive or random sample of patients enrolled? | Unclear | ||
Was a case‐control design avoided? | Yes | ||
Did the study avoid inappropriate exclusions? | Yes | ||
Did the study avoid inappropriate inclusions? | 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? | Yes | ||
If a threshold was used, was it pre‐specified? | No | ||
Could the conduct or interpretation of the index test have introduced bias? | High 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? | Yes | ||
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? | Unclear 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? | Yes | ||
Were all patients included in the analysis? | Yes | ||
Could the patient flow have introduced bias? | Unclear risk |