Karon 2008.

Study characteristics
Patient Sampling	Cross‐sectional study, consecutive sampling
Patient characteristics and setting	Sample size: 177 Gestational age: preterm (> 32 weeks) and term (> 37 weeks) Race/ethnicity: "Caucasian" (presumed white), Asian, Hispanic, African American Prior phototherapy use: no Setting: well‐infant nursery at the Mayo Clinic (Rochester, MN)
Index tests	TcB device: BiliChek Site of TcB measurement: forehead
Target condition and reference standard(s)	Target condition: neonatal hyperbilirubinaemia TSB measurement method: diazo and vitro method
Flow and timing	Time intervalbetween tests: ≤ 30 minutes Number of paired results: 177
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?	Yes
Was a case‐control design avoided?	Yes
Did the study avoid inappropriate exclusions?	Yes
Could the selection of patients have introduced bias?		Low risk
Are there concerns that the included patients and setting do not match 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?		Low 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?	Yes
Did all patients receive the same reference standard?	No
Were all patients included in the analysis?	Yes
Could the patient flow have introduced bias?		Low risk