Condition P07A
Heart failure with left ventricular ejection fraction above 40 percent
Adults with heart failure and LVEF above 40 percent (mildly reduced or preserved).
4 randomized trials; 0 fitted analyses across 7 outcomes.
All outcomes
Each outcome is analyzed per time window and estimand, with doses kept apart (each dose) and pooled (each medicine). Analyses with too few connected trials are shown as descriptive.
Cardiovascular death or heart failure eventsprimary
| Time window | Estimand | Treatments | Trials | Nodes | Analysis |
|---|---|---|---|---|---|
| longest follow-up | Cause specific hazards | Each dose separately | 1 | 2 | Descriptive only |
| longest follow-up | Cause specific hazards | Doses of a drug pooled | 1 | 2 | Descriptive only |
KCCQ clinical summary score changeprimary
| Time window | Estimand | Treatments | Trials | Nodes | Analysis |
|---|---|---|---|---|---|
| weeks 36 to 64 (target week 52) | Hypothetical (as if everyone stayed on treatment) | Doses of a drug pooled | 1 | 2 | Descriptive only |
| weeks 36 to 64 (target week 52) | Hypothetical (as if everyone stayed on treatment) | Each dose separately | 1 | 2 | Descriptive only |
| weeks 36 to 64 (target week 52) | Treatment policy | Doses of a drug pooled | 1 | 2 | Descriptive only |
| weeks 36 to 64 (target week 52) | Treatment policy | Each dose separately | 1 | 2 | Descriptive only |
Heart failure events
| Time window | Estimand | Treatments | Trials | Nodes | Analysis |
|---|---|---|---|---|---|
| longest follow-up | Cause specific hazards | Doses of a drug pooled | 1 | 2 | Descriptive only |
| longest follow-up | Cause specific hazards | Each dose separately | 1 | 2 | Descriptive only |
Serious adverse events
| Time window | Estimand | Treatments | Trials | Nodes | Analysis |
|---|---|---|---|---|---|
| longest follow-up | Recorded harms | Each dose separately | 1 | 2 | Descriptive only |
| longest follow-up | Recorded harms | Doses of a drug pooled | 1 | 2 | Descriptive only |
Discontinuation due to adverse events
| Time window | Estimand | Treatments | Trials | Nodes | Analysis |
|---|---|---|---|---|---|
| longest follow-up | Recorded harms | Each dose separately | 1 | 2 | Descriptive only |
| longest follow-up | Recorded harms | Doses of a drug pooled | 1 | 2 | Descriptive only |
Discontinuation due to gastrointestinal adverse events
| Time window | Estimand | Treatments | Trials | Nodes | Analysis |
|---|---|---|---|---|---|
| longest follow-up | Recorded harms | Each dose separately | 1 | 2 | Descriptive only |
| longest follow-up | Recorded harms | Doses of a drug pooled | 1 | 2 | Descriptive only |
Acute pancreatitis
| Time window | Estimand | Treatments | Trials | Nodes | Analysis |
|---|---|---|---|---|---|
| longest follow-up | Recorded harms | Doses of a drug pooled | 1 | 2 | Descriptive only |
| longest follow-up | Recorded harms | Each dose separately | 1 | 2 | Descriptive only |