Table 3.
First author, year (ref #) |
Inclusion criteria |
Intervention | Duration, years |
Composite fatal and non-fatal cardiovascular events |
All-cause mortality (%) | Cardiovascular mortality (%) |
||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Intervention | Placebo | HR (95%CI) |
Intervention | Placebo | HR (95%CI) |
Intervention | Placebo | HR (95%CI) |
||||
FOSIDIAL, 2006 (95). | HD, LVH (n=397) | Fosinopril titrated up to 20 mg/day | 2 | NA | NA | 0.80 (0.59–1.1) | - | - | - | - | - | - |
Takahashi et al., 2006 (96). | HD (n=80) | Candesartan 4–8 mg/day | 19.4 mo | 16.3 | 45.9 | 0.29 (0.12–0.70) | - | 18.9 | NA | - | - | - |
Suzuki et al., 2008 (97). | HD, SBP >160 mmHg or >150 mmHg if receiving anti-HT drugs (n=366) | Losartan up to 100 mg, or candesartan up to 12 mg/day or valsartan up to 160 mg/day | 3 | 19 | 33 | 0.51 (0.33–0.79) | 14 | 21 | 0.64 (0.39–1.06) | - | - | - |
OCTOPUS, 2013 (98). | HD, BP≥140/90 mmHg (n=469) | Olmesartan 10–40 mg/day until achieved target BP of <140/90 mmHg | 3.5 | 35.3 | 34 | 1.00 (0.71–1.40) | 24 | 22.2 | 0.97 (0.62–1.52) | - | - | - |
DOHAS, 2014 (101). | HD, serum K <6.5 mEq/L (n=309) | Spironolactone 25 mg/day | 3 | 5.7 | 15.1 | 0.40 (0.20–0.81) | 6.4 | 19.7 | 0.36 (0.19–0.66) | 2.5 | 4.6 | 0.57 (.18–1.87) |
4D, 2005 (6). | HD, type 2 DM, LDL 90–180 mg/dL (n=1255) | Atorvastatin 20 mg/day | 4 | 37 | 38 | 0.92 (0.77–1.10) | 48 | 50 | 0.93 (0.79–1.08) | 20 | 23 | 0.81 (0.64–1.03) |
AURORA, 2009 (26). | HD (n=2776) | Rosuvastatin 10 mg/day | 3.8 | 28.5 | 29.5 | 0.96 (0.84–1.11) | 45.8 | 47.7 | 0.96 (0.86–1.07) | 23.3 | 23.4 | 1.00 (0.85–1.16) |
SHARP, 2011 (8). | CKD Cr≥1.7 mg/dL in men or 1.5 mg/dL in women (n = 9270) | Simvastatin 20 mg/day plus ezetimibe 10 mg/day | 4.9 | 11.3 | 13.4 | 0.83 (0.74–0.94) | 24.6 | 24.1 | 1.02 (0.94–1.1) | 5.4 | 5.9 | 0.93 (0.78–1.10) |
Dialysis subgroup (n=3023; HD=2527, PD=496) | Simvastatin 20 mg/day plus ezetimibe 10 mg/day | 4.9 | 15 | 16.5 | 0.90 (0.75–1.08) | - | - | - | - | - | - |