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. 2018 Apr 19;67(11):1705–1711. doi: 10.1093/cid/ciy326

Table 2.

Performance of the Urinary Galactofuranose-Antigen Detection Dipstick Assay

IA Diagnosis Subjects With Positive Tests, No. (%) Sensitivity, % (95% CI) Specificity, % (95% CI)
Overall cohort (n = 78)a
 Proven/probable IA (n = 30) 24 (80) 80 (61.4–92.3) 92 (74–99)
 Controls (n = 25) 2 (8)
Overall cohort, with β-d-glucan (n = 78)b
 Proven/probable (n = 40) 32 (80) 80 (64.4–90.9) 92 (74–99)
 Controls (n = 25) 2 (8)
Subgroup: hematological malignancy/BMT/neutropenia (n = 50)c
 Proven/probable IA (n = 19) 17 (89.5) 89.5 (66.7–98.7) 90.9 (58.7–99.8)
 Controls (n = 11) 1 (9.1)
Subgroup: noncancer (n = 28)c
 Proven/probable IA (n = 11) 7 (63.6) 63.6 (30.8–89.1) 92.9 (66.1–99.8)
 Controls (n = 14) 1 (7.1)

Abbreviations: BMT, bone marrow transplant; CI, confidence interval; IA, invasive aspergillosis.

aExcludes 23 subjects with possible IA. Controls include no invasive fungal infection (IFI) or non-Aspergillus IFI.

bCase definitions considering β-d-glucan results, upgrading 10 subjects with possible IA to probable. Controls include no IFI or non-Aspergillus IFI.

cCancer subgroup excludes 20 subjects with possible IA and noncancer subgroup excludes 3 subjects with possible IA. Cancer subgroup includes 2 solid organ transplant recipients who had concurrent cancer with neutropenia.