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