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. 2015 Dec 10;2015(12):CD011134. doi: 10.1002/14651858.CD011134.pub2

Koizumi 1992.

Study characteristics
Patient sampling Country
Japan
Study design
Cross‐sectional with follow‐up of cases
Setting
Hospital
Dates of data collection
1986 ‐ 1990
Population (n)
194
Inclusion criteria
Unclear
Exclusion criteria
Cases undergoing operation later, benign colorectal disease.
Participants Included (n)
77
Patient characteristics and setting Age range
32 ‐ 83
Smoking status
Unknown
Site of primary tumour
Colorectal
Stage of primary tumour
Unknown
Perioperative investigations done to ensure no residual disease
N/R
Chemotherapy/radiotherapy?
N/R
Follow‐up schedule
N/R
Recurrences (n)
34
Site of recurrences
N/R
Index tests CEA timing
N/R
CEA technique
N/R
CEA threshold
5 µg/L
Definition of positive
N/R
Which CEA value (s) used?
At time of recurrence
Target condition and reference standard(s) Reference standard
Unclear
Flow and timing Timing of CEA vs reference standard (days)
N/R
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? Unclear    
Did the study avoid inappropriate exclusions? Unclear    
    Unclear Unclear
DOMAIN 2: Index Test All CEA thresholds
If a threshold was used, was it pre‐specified? Yes    
Is the same method and instrument used for all CEA measurements? Unclear    
Is there an estimation of reproducibility of the method, for example the % coefficient of variation at specific concentrations? No    
Is there an indication of method accuracy, for example, is there evidence of participation in an external quality assessment and proficiency testing scheme? No    
    Unclear Low
DOMAIN 3: Reference Standard
Is the reference standards likely to correctly classify the target condition? Unclear    
Were the reference standard results interpreted without knowledge of the results of the index tests? Unclear    
    Unclear Unclear
DOMAIN 4: Flow and Timing
Did all patients receive the same reference standard? Unclear    
Were all patients included in the analysis? Yes    
Was the index test repeated prior to the reference standard? Unclear    
Was the the timing between index test(s) and reference standard ascertainable? Yes    
Did all patients receive a reference standard? Unclear    
    Unclear