Table 1. Main Features of Studies Incorporated in the Meta-Analysis.
Study | Williams et al, 2017 [15] | Supasyndh et al, 2017 [16] | Schmieder et al, 2017 [17] | Wang et al, 2017 [14] | Izzo et al, 2017 [13] |
---|---|---|---|---|---|
Type of study | Monotherapy only, drug comparison, multicenter | Monotherapy only, drug comparison, multicenter | Monotherapy or combination therapy with amlodipine, drug comparison, multicenter | Monotherapy only, drug comparison, multicenter | Monotherapy only, drug comparison, multicenter |
Blind | DB | DB | DB | DB | DB |
RCT | Yes | Yes | Yes | Yes | Yes |
Comparisons | Sacub/v vs. olmesartan | Sacub/v vs. olmesartan | Sacub/v vs. olmesartan | Sacub/v vs. valsartan | Sacub/v vs. valsartan |
Number of patients | 454 | 588 | 114 | 72 | 285 |
Study duration (weeks) | 12 - 52 | 14 | 12 - 52 | 4 | 8 |
Doses of sacubitril/valsartan per day | 200 or 400 mg | 100, 200 or 400 mg | 200 or 400 mg plus optional amlodipine, up to 10 mg QD, only if needed for BP control | 400 mg | 400 mg |
Doses of ARB per day | 20 or 40 mg (a) | 10, 20 or 40 mg (a) | 20 or 40 mg (a) plus optional amlodipine, up to 10 mg QD, only if needed for BP control | 320 mg (b) | 320 mg (b) |
(a) Olmesartan was used as a comparator drug. (b) Valsartan was used as a comparator drug. DB: double blind; RCT: randomized controlled trial; ARB: angiotensin receptor blocker; QD: every day; BP: blood pressure.