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. 2011 Aug 30;2011:0204.
Ref (type) Population Outcome, Interventions Results and statistical analysis Effect size Favours
Withdrawal
[32]
RCT
3164 people with New York Heart Association (NYHA) functional class II to IV heart failure Proportion of people withdrawing from RCT
18% with low-dose lisinopril (2.5 or 5.0 mg/day)
17% with high-dose lisinopril (32.5 or 35.0 mg/day)
Absolute numbers not reported

Significance not assessed
Adverse effects
[32]
RCT
3164 people with NYHA functional class II to IV heart failure Proportion of people with dizziness
12% with low-dose lisinopril (2.5 or 5.0 mg/day)
19% with high-dose lisinopril (32.5 or 35.0 mg/day)
Absolute numbers not reported

Significance not assessed
[32]
RCT
3164 people with NYHA functional class II to IV heart failure Proportion of people with hypotension
7% with low-dose lisinopril (2.5 or 5.0 mg/day)
11% with high-dose lisinopril (32.5 or 35.0 mg/day)
Absolute numbers not reported

Significance not assessed
[32]
RCT
3164 people with NYHA functional class II to IV heart failure Proportion of people with worsening renal function
7% with low-dose lisinopril (2.5 or 5.0 mg/day)
10% with high-dose lisinopril (32.5 or 35.0 mg/day)
Absolute numbers not reported

Significance not assessed
[32]
RCT
3164 people with NYHA functional class II to IV heart failure Proportion of people with significant change in serum potassium concentration
7% with low-dose lisinopril (2.5 or 5.0 mg/day)
7% with high-dose lisinopril (32.5 or 35.0 mg/day)
Absolute numbers not reported

Significance not assessed
[32]
RCT
3164 people with NYHA functional class II to IV heart failure Proportion of people with cough
13% with low-dose lisinopril (2.5 or 5.0 mg/day)
11% with high-dose lisinopril (32.5 or 35.0 mg/day)
Absolute numbers not reported

Significance not assessed