Summary of findings 5. Angiotensin receptor neprilysin inhibitors (ARNIs) compared to usual care for chronic heart failure with preserved ejection fraction.
ARNIs compared to usual care for chronic heart failure with preserved ejection fraction | ||||||
Patient or population: patients with chronic heart failure with preserved ejection fraction Setting: secondary care Intervention: ARNI (sacubitril‐valsartan) Comparison: ARB (valsartan) | ||||||
Outcomes | Anticipated absolute effects* (95% CI) | Relative effect (95% CI) | № of participants (studies) | Certainty of the evidence (GRADE) | Comments | |
Risk with usual care | Risk with ARNI | |||||
Cardiovascular mortality (RR) Median follow‐up: 35 months |
Study population | RR 0.96 (0.79 to 1.15) | 4796 (1 study) | ⊕⊕⊕⊝ MODERATE1 | ||
89 per 1,000 | 85 per 1,000 (70 to 102) | |||||
Heart failure hospitalisation, first (RR) Range of follow‐up: 24 weeks to 35 months |
Study population | RR 0.89 (0.80 to 1.00) |
7362 (2 studies) |
⊕⊕⊕⊝ MODERATE1 | ||
142 per 1,000 | 126 per 1,000 (113 to 142) |
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Hyperkalaemia Range of follow‐up: 36 weeks to 35 months |
Study population | RR 0.88 (0.77 to 1.01) | 5054 (2 studies) | ⊕⊕⊕⊝ MODERATE1 | ||
147 per 1,000 | 129 per 1,000 (113 to 148) | |||||
All‐cause mortality (RR) Range of follow‐up: 36 weeks to 35 months |
Study population | (RR 0.97 CI 0.84 to 1.11) |
7663 (3 studies) | ⊕⊕⊕⊕ HIGH | ||
138 per 1,000 | 134 per 1,000 (117 to 153) | |||||
Quality of life Range of follow‐up: 36 weeks to 35 months |
PARAMOUNT reported change from baseline for the KCCQ overall summary score for the intervention arm (n =118) as 11.25 (2.185) and the control arm (n = 116) as 11.31 (2.183) and summarised the findings as "no difference in KCCQ score between treatment groups". PARAGON‐HF reported a difference of the clinical summary score KCCQ between treatment arms as 1.0 (0.0 to 2.1). PARALLAX reported "KCCQ improved in both treatment groups, with an early benefit of S/V that was no longer significant after 24 week". |
⊕⊕⊕⊕ HIGH | ||||
*The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI). ARB: Angiotensin receptor blocker; ARNIs: Angiotensin receptor neprilysin inhibitors; CI: Confidence interval; KCCQ: Kansas City Cardiomyopathy Questionnaire; MD: Mean difference; RCT: Randomised controlled trial; RR: Risk ratio | ||||||
GRADE Working Group grades of evidence High certainty: We are very confident that the true effect lies close to that of the estimate of the effect Moderate certainty: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different Low certainty: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect Very low certainty: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect |
1Downgraded by one level due to imprecision.