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. 2022 May 20;2022(5):CD013665. doi: 10.1002/14651858.CD013665.pub3

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
  • Fever

  • Dyspnoea

  • Weakness

  • Shivering

  • Fatigue

  • Dry cough

  • Anorexia

  • Anosmia

  • Ageusia

  • Dizziness

  • Sweating

Target condition and reference standard(s)
  • TC: COVID‐19 pneumonia

  • RS: thin‐slice high‐resolution multi‐slice spiral CT scan in a supine position, and high‐resolution CT images of all patients were reviewed by a radiologist with > 14 years of experience in chest imaging

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