Evaluates HBsAg detection methods in low-level reactive samples, indicating the need for improved specificity.
significantly with the widespread adoption of automated chemiluminescent immunoassays, which offer high sensitivity and rapid turnaround times suitable for high-volume testing in clinical laboratories [2, 3].However, the increased sensitivity of these automated platforms can compromise specificity, particularly in low-prevalence populations, such as asymptomatic individuals undergoing routine health checkups [4].A persistent challenge in laboratory medicine is the detection of samples with low-level reactivity-typically defined as a signal-to-cutoff (S/CO) ratio between 1.0 and 10.0.Within this range, a significant proportion of reactive results are biological false positives caused by non-specific interference, heterophilic antibodies, or sample matrix effects rather than true viral infection [5, 6].To mitigate the risk of misdiagnosis and unnecessary medical Hepatitis B surface antigen (HBsAg) is the principal serological marker for the diagnosis of acute and chronic hepatitis B virus (HBV) infection [1].Detection methods for HBsAg have evolved 저수준 반응성 검체에서 Abbott Architect와 Roche Elecsys 자동화 HBsAg 확인 중화 검사법의 비교 평가
No takes yet. Share an insight, caveat, or question.
Jaeeun Yoo (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: