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. 2012 Summer;11(3):969–977.

Table 1.

Spirometric parameters of subjects before and after treatment

Patient Before treatment

After treatment
group change in methacholine solution*
FEV1 (%) PC20
(mg/ml)
AR category FEV1 (%) PC20
(mg/ml)
AR category
1 98 4 borderline 93 1 mild Placebo -2
2 90 8 borderline 90 16 normal Placebo 1
3 92 0.25 moderate to severe 88 0.125 moderate to severe Drug -1
4 112 8 borderline 109 2 mild Drug -2
5 103 4 borderline 104 4 borderline Placebo 0
6 76 1 mild 77 1 mild Drug 0
7 103 0.5 moderate to severe 98 16 normal Drug 5
8 84 4 borderline 80 0.5 moderate to severe Placebo -3
9 78 4 borderline 78 2 mild Placebo -1
10 110 4 borderline 110 4 mild Placebo 0
11 88 2 mild 89 0.25 moderate to severe Placebo -3
12 109 1 mild 88 2 mild Placebo 1
13 90 2 mild 91 4 borderline Drug 1
14 93 1 mild 94 1 mild Placebo 0
15 116 1 mild 119 1 mild Placebo 0
16 78 0.25 moderate to severe 86 1 mild Drug 2
17 81 1 mild 93 16 normal Drug 4
18 102 4 borderline 100 8 borderline Drug 2
19 109 8 borderline 103 8 borderline Drug 0
20 117 0.5 moderate to severe 110 0.5 moderate to severe Placebo 0
21 90 0.5 moderate to severe 90 8 borderline Placebo 4
22 82 2 mild 90 0.25 moderate to severe Placebo -3

AR: Airway responsiveness* Increase or decrease in solution concentration which caused more than 20% decrease in FEV1