16-year follow-up of the DANish Acute Myocardial Infarction 2 (DANAMI-2) trial PG Thranea, SD Kristensena, KKW Olesena, LS Mortensenb, HE Bøtkera, L.

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Presentation transcript:

16-year follow-up of the DANish Acute Myocardial Infarction 2 (DANAMI-2) trial PG Thranea, SD Kristensena, KKW Olesena, LS Mortensenb, HE Bøtkera, L Thuesenc, HS Hansend, U Abildgaarde, T Engstrømf, HR Andersena, M Maenga a: Aarhus University Hospital, b: Spange Statistics, c: Aalborg University Hospital, d: Odense University Hospital e: Copenhagen University Hospital, Gentofte, f: Copenhagen University Hospital, Copenhagen

Declaration of interest None

Background The 1990’s landmark trials (Zwolle, PAMI) showed that pPCI treatment was superior to fibrinolysis in patients admitted to invasive centres The DANAMI-2 trial (NEJM 2003) is the largest RCT to show that inter-hospital transport for pPCI is superior to fibrinolysis at 30 days of follow-up These results were confirmed in the PRAGUE-2 trial

Objective To examine the 16-year outcomes of the DANAMI-2 trial To provide a very long-term perspective on death and cardiovascular events when comparing pPCI with fibrinolysis in STEMI patients

Included 1,572 STEMI patients Invasive centres n=443 Referral hospitals n=1,129

Included 1,572 STEMI patients Invasive centres n=443 Referral hospitals n=1,129 pPCI n=223 Fibrinolysis n=220 pPCI n=567 Fibrinolysis n=562 Primary endpoint: Composite of death, reinfarction, or disabling stroke at 30 days Andersen HR et al, NEJM 2003

Included 1,572 STEMI patients Invasive centres n=443 Referral hospitals n=1,129 pPCI n=223 Fibrinolysis n=220 pPCI n=567 Fibrinolysis n=562 Primary endpoint: Composite of death, reinfarction, or disabling stroke at 30 days Andersen HR et al, NEJM 2003

Patient selection Inclusion criteria ST-elevation ≥2 mm in ≥2 contiguous leads Age ≥18 years Chest discomfort ≥30 mins and 12 hours Exclusion criteria LBBB Contraindication to fibrinolysis MI or fibrinolysis within the last 30 days Metformin-treated diabetes

Endpoints Clinical follow-up Registry-based follow-up 0-3 years 4-16 years Main endpoint: Composite of death or reinfarction Additional endpoints: Death Reinfarction Cardiac and non-cardiac death

Endpoints 0-3 years: Clinical follow-up Registry-based follow-up 0-3 years 4-16 years 0-3 years: Clinical follow-up Endpoint committee adjudication 4-16 years: Registry-based follow-up Danish Civil Registration System Danish National Patient Registry Danish Cause of Death Registry

Statistics Kaplan-Meier curves and Cox proportional hazards model: Composite endpoint and all-cause death Competing Risk Model: Reinfarction, cardiac and non-cardiac death Restricted mean model*: Difference in time to first event *Kim DH et al, JAMA 2017

Baseline characteristics Fibrinolysis (n=782) Primary PCI (n=790) P-value Age (years), median (IQR) 63 (54-73) 63 (54-72) 0.32 Male sex (%) 73.4 73.5 0.95 Previous MI (%) 11.8 11.0 0.61 Anterior index MI (%) 52.6 53.2 0.81 Diabetes (%) 7.1 7.4 0.80 Smoking (%) 58.6 58.1 0.85 Time from symptom onset to randomization (min), median (IQR) 140 (85-235) 135 (85-225) 0.23

16-year follow-up 60% of the patients reached the composite endpoint 51% died during follow-up High data completeness Vital status known for 99.7% of patients Cause of death known for 97.7% of all deaths

Composite endpoint 62.3% 58.7% Absolute difference 3.6% Hazard ratio (95% CI) 0.86 (0.76-0.98) 58.7% Thrane et al, EHJ 2019

Mean gain in time to first event (95% CI) Composite endpoint 62.3% Absolute difference 3.6% Hazard ratio (95% CI) 0.86 (0.76-0.98) Mean gain in time to first event (95% CI) 12.3 months (5.0-19.5) 58.7% Thrane et al, EHJ 2019

Reinfarction 24.5% 19.0% Absolute difference 5.5% Hazard ratio (95% CI) 0.75 (0.60-0.93) 24.5% 19.0%

Mean gain in time to first event (95% CI) Reinfarction Absolute difference 5.5% Hazard ratio (95% CI) 0.75 (0.60-0.93) Mean gain in time to first event (95% CI) 11.5 months (4.8–18.3) 24.5% 19.0%

All-cause death 51.3% 50.5% Absolute difference 0.8% Hazard ratio (95% CI) 0.95 (0.83-1.09) 51.3% 50.5%

Cardiac death 22.7% 18.3% Absolute difference 4.4% Hazard ratio (95% CI) 0.78 (0.63-0.98) 22.7% 18.3%

Referral hospitals Hazard ratio (95% CI) n = 1129 Composite endpoint 0.82 (0.71-0.96) Reinfarction 0.77 (0.60-0.98) Death 0.91 (0.77-1.07) Cardiac death 0.79 (0.61-1.01) Favours pPCI Favours fibrinolysis

Limitations Changes in management and treatment Prehospital triage Anti-thrombotic treatment Optimization of PCI devices and techniques Conservative use of rescue PCI after fibrinolysis

Conclusions: 16-year follow-up Composite endpoint Absolute reduction of 3.6% favouring pPCI >1 year gained in time to first main event with pPCI Reinfarction Absolute reduction of 5.5% favouring pPCI Cardiac death Absolute reduction of 4.4% favouring pPCI

Thank you for your attention 10.1093/eurheartj/ehz595