030 IMPACT OF INTER-HOSPITAL TRANSFER FOR PRIMARY PERCUTANEOUS CORONARY INTERVENTION ON SURVIVAL (10 108 STEMI PATIENTS FROM THE LONDON HEART ATTACK GROUP)
Background Primary percutaneous coronary intervention (PCI) is the preferred reperfusion strategy in patients with ST-segment elevation myocardial infarction (STEMI). We evaluated whether direct transfer to a cardiac centre performing primary percutaneous coronary intervention (PPCI) leads to improv...
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Published in | Heart (British Cardiac Society) Vol. 99; no. suppl 2; pp. A22 - A23 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BMJ Publishing Group Ltd and British Cardiovascular Society
01.05.2013
BMJ Publishing Group LTD |
Online Access | Get full text |
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Summary: | Background Primary percutaneous coronary intervention (PCI) is the preferred reperfusion strategy in patients with ST-segment elevation myocardial infarction (STEMI). We evaluated whether direct transfer to a cardiac centre performing primary percutaneous coronary intervention (PPCI) leads to improved survival compared with transfer via a non-PPCI performing hospital in STEMI patients in a regional network. Table 1 Variable Direct Indirect p Value Age 64.92±13.33 61.96±13.25 0.296 Previous MI 929 (14.3%) 640 (17.7%) p<0.0001 Previous CABG 161 (2.5%) 136 (3.8%) p<0.0001 Diabetes mellitus 993 (15.3%) 537 (14.9%) 0.683 Cardiogenic shock 384 (5.9%) 208 (5.8%) 0.724 Poor LV function (<30%) 397 (6.1%) 177 (4.9%) p<0.0001 Call to door (PCI centre) 60 min IQR (45–78) 118 IQR (71–199) p<0.0001 Door to balloon 47 min IQR (28–117) 43 min IQR (25–120) 0.590 IRA TIMI 0 3532 (62.9%) 1679 (54.5%) p<0.0001 Methods This was an observational cohort study of 10 108 patients with STEMI treated with PPCI between 2004 and 2011 at eight tertiary cardiac centres across London, UK. Patient's details were recorded at the time of the procedure into the British Cardiac Intervention Society (BCIS) database. Outcome was assessed by all-cause mortality. Anonymous datasets from the eight centres were merged for analysis. The primary end-point was all-cause mortality at a median follow-up of 3.0 years (IQR range 1.2–4.6 years). Results 6492 patients (64.2%) were transferred directly to a PCI performing centre (direct) and 3616, (35.8%) were transferred via a non-PCI performing centre (indirect). There were higher rates of previous MI and previous CABG in the indirect group, with higher rates of poor LV function in the direct group (table 1). Median time to reperfusion (symptom to balloon) in transferred patients was 58 min longer compared to patients admitted directly (p<0.001). However, symptom to first hospital door times were similar. Transferred patients had significantly lower rates of infarct-related artery (IRA) TIMI 0 flow (54.5% vs 62.9%, p<0.0001) and higher rates of IRA TIMI 3 flow (17% vs 10.7%, p>0.0001) at presentation compared to those transferred directly. Kaplan-Meier analysis demonstrated no significant difference in mortality rates between patients with and without transfer (12.3% direct vs 14.3% indirect, p=0.060). Age-adjusted Cox analysis revealed inter-hospital transfer for PPCI was associated with all cause mortality (HR 0.89 (95% CI 0.79 to 0.99)), however this was not maintained after multivariate adjustment (HR 0.84 (95% CI 0.62 to 1.14)). Figure 1 Kaplan-Meier curves showing cumulative probability of all-cause mortality after PPCI according to transfer strategy. Conclusions In this large registry survival appear comparable in patients with STEMI admitted directly versus transferred for primary PCI. This is despite longer symptom to balloon times. This unexpected finding may reflect the earlier initiation of medical therapy (eg, anti-platelets and GpIIb/IIIa receptor inhibitors) and earlier pharmacological reperfusion, reflected by lower IRA TIMI 0 rates at angiography in the patients transferred from a non-PCI hospital. |
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Bibliography: | istex:7107D54DC6F4D76A004C90376E59C931B694C1FB href:heartjnl-99-A22-2.pdf ark:/67375/NVC-ZM1L9SDP-M local:heartjnl;99/suppl_2/A22-b |
ISSN: | 1355-6037 1468-201X |
DOI: | 10.1136/heartjnl-2013-304019.30 |