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. 2011 Dec;49(12):4273–4278. doi: 10.1128/JCM.05026-11

Table 2.

Performances of diagnostic tests with 158 specimens of BAL fluid

Parameter for proven and probable IA vs no IAa Test result (95% CI) [no. of specimens with result/no. tested] by:
MycAssay Aspergillus PCR In-house Aspergillus PCR GM ELISA
Index cutoff, ≥1.0 Index cutoff, ≥0.5
Sensitivity (%) 94.1 (71-99) [16/17] 88.2 (63-98) [15/17] 94.1 (71-99) [16/17] 94.1 (71-99) [16/17]
Specificity (%) 98.6 (94-99) [139/141] 97.9 (93-99) [138/141] 97.9 (93-99) [138/141] 92.2 (86-96) [130/141]
Likelihood ratiob
    Positive 67.2 42.0 44.8 12.1
    Negative 0.06 0.12 0.06 0.06
PPV (%) 88.9 (65-98) [16/18] 83.3 (58-96) [15/18] 84.2 (60-96) [16/19] 59.3 (38-77) [16/27]
NPV (%) 99.3 (96-99) [139/140] 98.6 (94-99) [138/140] 99.3 (96-99) [138/139] 99.3 (95-99) [130/131]
DORc 1120.0 350.0 746.6 201.6
a

Of 158 patients studied, 17 were diagnosed with proven or probable IA according to the revised European Organization for Research and Treatment of Cancer/Mycoses Study Group criteria from 2002 (10).

b

Likelihood ratio positive, sensitivity/1 − specificity; likelihood ratio negative, 1 − sensitivity/specificity.

c

DOR, diagnostic odds ratio (likelihood ratio positive/likelihood ratio negative).