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. 2016 Jul 5;10(7):e0004812. doi: 10.1371/journal.pntd.0004812

Table 5. Evaluation of the intrinsic parameters of the combo RT-qPCR assay for the diagnosis of human rabies, using the RT-hnPCR as the referent method.

Type of sample Total numbera Combo RT-qPCR result Mean Cq value ± SD Sensitivity Specificity Positive predicted value Negative predicted value
No. pos. samples/Total no. of samples (%)
From all patients From pos. patients
Sample Skin biopsy 67 43/67 (64.2) 43/47 (91.5) 31.53 ± 4.38 102b 100 100 96.3
Saliva 120 20/120 (16.7) 20/37 (54) 33. 93 ± 3.00 74c 100 100 93.4
CSF 12 3/12 (25) 3/7 (42.9) 25.3 ± 0.14 100 100 100 100
Brain biopsy 12 10/12 (83.3) 10/10 (100) 21.4 ± 5.56 100 100 100 100
Total 211 76/211 (36) 76/101 (75.2) 30.70 ± 5.7 92.7 100 100 95.6
Patientd   65 41/65 (63.1) 41/41 (100) 41/65 (61.5) 100 100 100 100

a Total number includes samples tested in Cambodia, France and Morocco from all patients (negative and positive for rabies).

b One additional skin biopsy sample was detected with the pan-RABV RT-qPCR (n = 43) compared to the RT-hnPCR (n = 42).

c 8 saliva samples from a same patient were not detected and one saliva sample from another patient was detected with the pan-RABV RT-qPCR compared to the RT-hnPCR, leading to a total of n = 20 and n = 27 saliva samples detected for the pan-RABV RT-qPCR and the RT-hnPCR, respectively.

d Including all patients, with rabies-confirmed and negative patients.