All studies were independently reviewed by two investigators. Any disagreement concerning the study selection and data extraction were resolved by consensus. As recommended by the Cochrane Collaboration, to evaluate the risk of bias in DTA, the Quality Assessment of Diagnostic Accuracy Studies (QUADAS)-2 tool was used [23]. Disagreements were resolved by discussion with the third independent author. The QUADAS-2 assesses four domains for bias and applicability as follows: (1) patient selection: risk of bias is considered high if there is no consecutive patient enrollment and avoidance of case-control design or inappropriate exclusion; (2) index test: risk of bias is considered high if the index test results were interpreted without blinding to the reference standard; (3) reference standard: risk of bias is considered high if the reference standard could classify the target condition incorrectly; (4) flow and timing: risk of bias is considered high if not all patients were included with the same criteria or if there was an inappropriate time interval between the index test and reference standard.
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