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Table 3 Evaluation of the parallel in vitro - in vivo tests in the two groups

From: A novel rapid (20-minute) IL-6 release assay using blood mononuclear cells of patients with various clinical forms of drug induced skin injuries

Parameters

" Test A" solution

%

" Test B" solution

%

Total N of parallel tests

99

 

85

 

Both negative

42

 

54

 

Both positive

41

 

12

 

Neg. IL-6, pos. in vivo*

7

 

15

 

Pos. IL-6, neg. in vivo**

9

 

5

 

Sensitivity

 

85.4

 

44.4

Specificity

 

82.4

 

93.1

Reliability

 

83.8

 

77.6

Positive predictive value

 

82.0

 

70.6

Negative predictive value

 

85.7

 

78.2

  1. *false negative.
  2. **false positive.
  3. "Test A": 100 mM NaCl, 24 mM KCl, 10 mM CaCl2, 10 mM MgCl2, 11 mM glucose; pH:7.2.
  4. "Test B": 145 mM NaCl, 21 mM KCl, 0.7 mM CaCl2, 0.7 mM MgCl2, 11 mM glucose; pH:7.2.
  5. *in vivo: "Test A": oral provocation 2, intradermal 5 tests were positive.
  6. *in vivo: "Test B": oral provocation 5, epicutaneous 2, intradermal 8 tests were positive.
  7. **in vivo: "Test A": oral provocation 5, epicutaneous 1, intradermal 3 tests were negative.
  8. **in vivo: "Test B": oral provocation 3, intradermal 2 tests were negative.