Table 2.
Intervention participants n = 776 |
Control patients n = 776 |
p value | |
---|---|---|---|
Total symptoms collected by IVR system | 997 | NA | |
Total symptoms discussed by pharmacist | 1018 | NA | |
Related to target medication—probable | 188 (18.5%) | NA | |
Related to target medication—possible | 479 (47.1%) | NA | |
Related to target medication—unlikely | 351 (34.5%) | NA | |
Severity of pharmacist-confirmed possible and probable symptoms (N = 668) | |||
Mild | 266 (39.8%) | NA | |
Significant | 400 (59.9%) | NA | |
Life-threatening | 1 (0.15%) | NA | |
Total symptoms documented by MD in notes | 277 | 164 | < 0.0001 |
Number of symptoms per 100 patients | 36 | 21 | < 0.0001 |
Number of patients with symptoms documented by MD | 177 | 122 | < 0.0001 |
Total unique symptoms documented (including IVR documented and MD notes) | 1303 | 164 | < 0.0001 |
Total unique patients with symptoms documented (including IVR documented) | 448 | 120 | < 0.0001 |
Total unique symptoms documented by MD or RPh as probably or possibly related to the drug | 753 | 164 | < 0.0001 |
Total unique patients with symptoms documented by MD or RPh as probably or possibly related to the drug | 425 | 120 | < 0.0001 |
Drug discontinuations (CPOE d/c code reason) |
N = 5106* No. (%) |
N = 5897† No. (%) |
|
Discontinuations 1 year from prescription | 1694 (33.2) | 1977 (33.5) | 0.70 |
Discontinuations due to adverse event‡ | 254 (15.0) | 217 (11.0) | 0.0003 |
*Missing data on target medication discontinuations for 37 patients
†Missing data on target medication discontinuations for 88 patients
‡Discontinuation due to an adverse event as a coded justification in the EHR