Table 2.
Medication duration and adverse reactions of treatment in the BTM monitoring group and the control group
| Monitoring group (n = 28) |
Control group (n = 29) |
p value | |
|---|---|---|---|
| Alendronate duration (days) | 236 ± 71 | 90 ± 0 | 0.000 |
| Calcitriol + Ca duration (days) | 214 ± 72 | 90 ± 0 | 0.000 |
| Total medication duration (days) | 259 ± 72 | 90 ± 0 | 0.000 |
| Adverse reaction | 5 (17.9%)a | 2 (6.9%)b | 0.392 |
Ca calcium
aThree patients had gastrointestinal reaction and two patients had muscular soreness
bOne patient had gastrointestinal reaction and one patient had headache