Table 1

Comparison between DAPA-MI, DECLARE-TIMI 58, and DAPA-HF trials4–7

TrialsDAPA-MIDECLARE-TIMI 58DAPA-HF
Target populationAMIASCVD + DMHF
SubgroupPlaceboPrevious MIIschaemic origin
Number of patents in the subgroup199835842674
Demographics
 Age (year)636268
 Male sex (%)7976.479.9
 Europe (%)10049.852.5
 Weight (kg)85.591NA
 eGFR (mL/min/1.73 m2)83.48863.7
 HbA1c (%)5.78NA
Medical history
 Myocardial infarction (%)9.510072.5
 Stroke (%)2.56.110.7
 Diabetes (%)NA10049.9
 Heart failure (%)NA21.546.1
Baseline medication
 ACE inhibitor/ARB use (%)91.884.184.6
 Beta-blockers use (%)89.982.296
 Statins use (%)94.991.183.5
Outcomesa
 Follow-up duration (year)14.21.5
 CV death/hospitalization for HF (%)2.610.520.9
 MACE (%)3.617.8NA
 CV death (%)1.25.312.5
 All cause death (%)1.710.315.2
 Hospitalization for HF1.66.312.7
TrialsDAPA-MIDECLARE-TIMI 58DAPA-HF
Target populationAMIASCVD + DMHF
SubgroupPlaceboPrevious MIIschaemic origin
Number of patents in the subgroup199835842674
Demographics
 Age (year)636268
 Male sex (%)7976.479.9
 Europe (%)10049.852.5
 Weight (kg)85.591NA
 eGFR (mL/min/1.73 m2)83.48863.7
 HbA1c (%)5.78NA
Medical history
 Myocardial infarction (%)9.510072.5
 Stroke (%)2.56.110.7
 Diabetes (%)NA10049.9
 Heart failure (%)NA21.546.1
Baseline medication
 ACE inhibitor/ARB use (%)91.884.184.6
 Beta-blockers use (%)89.982.296
 Statins use (%)94.991.183.5
Outcomesa
 Follow-up duration (year)14.21.5
 CV death/hospitalization for HF (%)2.610.520.9
 MACE (%)3.617.8NA
 CV death (%)1.25.312.5
 All cause death (%)1.710.315.2
 Hospitalization for HF1.66.312.7

aTo ensure maximum comparability with the DAPA-MI placebo group, the event rates reported above in the DECLARE-TIMI 58 and DAPA-HF are derived from the placebo groups of each respective subgroup.

Table 1

Comparison between DAPA-MI, DECLARE-TIMI 58, and DAPA-HF trials4–7

TrialsDAPA-MIDECLARE-TIMI 58DAPA-HF
Target populationAMIASCVD + DMHF
SubgroupPlaceboPrevious MIIschaemic origin
Number of patents in the subgroup199835842674
Demographics
 Age (year)636268
 Male sex (%)7976.479.9
 Europe (%)10049.852.5
 Weight (kg)85.591NA
 eGFR (mL/min/1.73 m2)83.48863.7
 HbA1c (%)5.78NA
Medical history
 Myocardial infarction (%)9.510072.5
 Stroke (%)2.56.110.7
 Diabetes (%)NA10049.9
 Heart failure (%)NA21.546.1
Baseline medication
 ACE inhibitor/ARB use (%)91.884.184.6
 Beta-blockers use (%)89.982.296
 Statins use (%)94.991.183.5
Outcomesa
 Follow-up duration (year)14.21.5
 CV death/hospitalization for HF (%)2.610.520.9
 MACE (%)3.617.8NA
 CV death (%)1.25.312.5
 All cause death (%)1.710.315.2
 Hospitalization for HF1.66.312.7
TrialsDAPA-MIDECLARE-TIMI 58DAPA-HF
Target populationAMIASCVD + DMHF
SubgroupPlaceboPrevious MIIschaemic origin
Number of patents in the subgroup199835842674
Demographics
 Age (year)636268
 Male sex (%)7976.479.9
 Europe (%)10049.852.5
 Weight (kg)85.591NA
 eGFR (mL/min/1.73 m2)83.48863.7
 HbA1c (%)5.78NA
Medical history
 Myocardial infarction (%)9.510072.5
 Stroke (%)2.56.110.7
 Diabetes (%)NA10049.9
 Heart failure (%)NA21.546.1
Baseline medication
 ACE inhibitor/ARB use (%)91.884.184.6
 Beta-blockers use (%)89.982.296
 Statins use (%)94.991.183.5
Outcomesa
 Follow-up duration (year)14.21.5
 CV death/hospitalization for HF (%)2.610.520.9
 MACE (%)3.617.8NA
 CV death (%)1.25.312.5
 All cause death (%)1.710.315.2
 Hospitalization for HF1.66.312.7

aTo ensure maximum comparability with the DAPA-MI placebo group, the event rates reported above in the DECLARE-TIMI 58 and DAPA-HF are derived from the placebo groups of each respective subgroup.

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