Table 3.
Treatment attributes | Estimate | 95% CI | p value |
---|---|---|---|
Efficacy | |||
Cure rate (per % change) | 0.311 | (0.267, 0.356) | < 0.001* |
Convenience | |||
Treatment duration (per week) | |||
8 weeks vs. 12 weeks | 0.255 | (0.090, 0.419) | 0.002* |
16 weeks vs. 12 weeks | − 0.061 | (− 0.219, 0.097) | 0.447 |
24 weeks vs. 12 weeks | − 0.321 | (− 0.505, − 0.138) | < 0.001* |
Once-daily tablet count and packaging | |||
1 tablet from a prescription bottle vs. 1 tablet in a single-dose blister pack | 0.090 | (− 0.035, 0.216) | 0.159 |
3 tablets in a single-dose blister pack vs. 1 tablet in a single-dose blister pack | − 0.034 | (− 0.171, 0.103) | 0.624 |
Visits during HCV treatments | |||
Simplified monitoring (no in-person visit, e.g., telephone checking in) vs. two additional office visits | 0.131 | (− 0.036, 0.298) | 0.124 |
One additional office visit vs. two additional office visits | 0.170 | (0.005, 0.336) | 0.044* |
Co-therapy management | |||
Modification of statins | |||
Temporarily reduce dose or stop taking vs. no modification | − 0.105 | (− 0.249, 0.039) | 0.152 |
Switch to a different medication vs. no modification | − 0.129 | (− 0.296, 0.038) | 0.131 |
Modification of PPIs | |||
Temporarily reduce dose/timing or stop taking vs. no modification | − 0.171 | (− 0.326, − 0.015) | 0.032* |
Switch to a different medication vs. no modification | − 0.125 | (− 0.298, 0.047) | 0.155 |
Mild common side effects | |||
Risk of adverse events (per % change) | |||
Diarrhea | − 0.033 | (− 0.040, − 0.025) | < 0.001* |
Headache | − 0.028 | (− 0.034, − 0.022) | < 0.001* |
Nausea | − 0.028 | (− 0.036, − 0.019) | < 0.001* |
aAll patients from the USA and the five European countries (UK, France, Germany, Spain, and Italy)
*p value < 0.05