Table III.
Efficacy, dose change requirements, and side effects of BTX injections.
| Group 1 | Group 2 | p- value | |
|---|---|---|---|
| Efficacy | |||
| Effective injections | 204 (93%) | 180 (94%) | 0.6895 |
| Ineffective injections | 15 (7%) | 11 (6%) | |
| Breathiness | |||
| No breathiness | 170 (78%) | 137 (71%) | 0.1732 |
| Breathiness | 49 (22%) | 54 (29%) | |
| Dysphagia | |||
| No dysphagia | 217 (99%) | 191 (99%) | |
| Dysphagia | 2 (1%) | 2 (1%) | |
| Dose change | |||
| Injection dose unchanged | 117 (60%) | 95 (59%) | 0.8367 |
| Injection dose changed | 78 (40%) | 65 (41%) | |
Group 1 = point-touch technique; Group 2 = EMG guided technique.
There were no statistical differences noted between groups and rate of effective injection, need to change dose, or breathiness. (all p>0.05). There was no difference between groups and the rate of dysphagia, though this was not statistically analyzed as there were too few events. The dose effect, presence of breathiness, and presence of dysphagia were not described in the hospital charts of 7, 7, and 5 subjects, respectively. These few were pair-wise dropped and the total number statistically analyzed are reflected in the table.
Total subjects in each subgroup have different totals (n) reflecting analysis of quantifiable data for the statistical model. For instance, even though 417 injections were available for analysis, only 355 (195 injections and 160 injections, Groups 1 & 2 respectively) were analyzed for dose change, as the final injection for each subject was not included because a subsequent dose change could not be determined.