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Table 1 Study characteristics of laboratory-based immunoassays against laboratory reference standard [EIA vs EIA]s

From: Diagnostic accuracy of tests to detect hepatitis B surface antigen: a systematic review of the literature and meta-analysis

Study [author, year]

Location [country, city]

Sample size

Study design

Setting

Sample type

Assay under evaluation [type, brand]

Reference standard [type, brand]

Liu, 2014 [14]

China

250

CC

Hospital patients; outpatients

(Preselected based on CMIA quantitative results)

Serum

ECLIA, Cobas

ELISA, Wantai

CMIA, Architect HBsAg

Peng, 2011 [49]

China

498

CC

Hospital patients

(Preselected based on S/CO from KHB screen)

Serum

ELISA, KHB

CMIA, Architect HBsAg

Geretti, 2010 [47]

Ghana, Kumasi

838

CS – CSQ

HIV clinic (1/3 on lamivudine)

Serum

CMIA, Architect HBsAg

CMIA, Liaison Ultra

EIA, Murex v3

CMIA, Architect/ Liaison

EIA, Murex v3a

Ol, 2009 [48]

Cambodia

120

CS – CSQ

Blood donors (rural community)

Serum

ELISA, Monolisa

CMIA, Architect HBsAg

Viet, 2012 [50]

Vietnam

119

CS – CSQ

Blood donors (rural community)

Serum

EIA, Monolisa Ultra

CMIA, Architect HBsAg

  1. aReactive all three assays OR reactive in one assay with neutralisation
  2. CC case control, CMIA chemiluminescent microparticle enzyme immunoassay, CS cross-sectional, CSQ consecutive patients, ECLIA electrochemiluminescent immunoassay, EIA enzyme immunoassay, ELISA enzyme linked immunosorbent assay, KHB KHB Ltd., Shanghai, S/CO signal cut-off ratio