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Browsing by Author "Westerhout, Cynthia M. (6506479036)"

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    Publication
    Impact of a pharmacoinvasive strategy when delays to primary PCI are prolonged
    (2015)
    Gershlick, Anthony H. (7005330722)
    ;
    Westerhout, Cynthia M. (6506479036)
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    Armstrong, Paul W. (35380325200)
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    Huber, Kurt (35376715600)
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    Halvorsen, Sigrun (9039942100)
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    Steg, Philippe Gabriel (56212505300)
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    Ostojic, Miodrag (34572650500)
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    Goldstein, Patrick (7103144663)
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    Carvalho, Antonio C. (55426495300)
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    Van De Werf, Frans (36048879600)
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    Wilcox, Robert G. (36658310600)
    Objectives Primary percutaneous coronary intervention (P-PCI) is the preferred reperfusion option in ST-elevation myocardial infarction, but its benefits become attenuated as time to its potential delivery becomes prolonged. Based on the STrategic Reperfusion Early After Myocardial Infarction trial, we assessed the impact of increasing time delay on outcomes in patients randomised to a pharmacoinvasive strategy (PI) or P-PCI. Methods Thirty-day clinical outcomes were examined according to PCI-related delay (P-RD). Data from hospitals that enrolled >10 randomised patients were used and P-RD categorised as ≤55 min, >55-97 min and >97 min. Results Composite of death/congestive heart failure/ cardiogenic shock/myocardial infarction in PI and P-PCI arms occurred in 10.6% versus 10.3% (≤55 min, p=0.910); 13.9% versus 17.9% (>55-97 min, p=0.148) and 13.5% versus 16.2% (>97 min, p=0.470), respectively. While there was no worsening of outcomes for PI across the P-RD spectrum, this occurred in the P-PCI arm ( p(trend)=0.038). For P-RD ≤55 min, fewer events tended to occur with P-PCI than PI. Conversely, as P-RD increased to >55 min, PI-assigned patients had better outcomes than P-PCI, suggesting an event-free advantage with PI as P-RD increased (p (interaction)=0.094). Analysing P-RD continuously showed that for every 10-min increment there was an increasing trend towards bene fit among PI-assigned patients ( p(interaction)=0.073). Conclusions As P-RD increased, PI outcomes became superior to P-PCI when P-RD is prolonged and exceeds guideline-mandated times. In such circumstances, a PI strategy may provide an alternative reperfusion option. Adverse time delays for delivery of P-PCI should be considered when evaluating reperfusion strategies.
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    Implications of ischaemic area at risk and mode of reperfusion in ST-elevation myocardial infarction
    (2016)
    Bainey, Kevin R. (8064642600)
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    Fresco, Claudio (7003822117)
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    Zheng, Yinggan (56120094700)
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    Halvorsen, Sigrun (9039942100)
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    Carvalho, Antonio (55426495300)
    ;
    Ostojic, Miodrag (34572650500)
    ;
    Goldstein, Patrick (7103144663)
    ;
    Gershlick, Anthony H. (7005330722)
    ;
    Westerhout, Cynthia M. (6506479036)
    ;
    Van De Werf, Frans (36048879600)
    ;
    Armstrong, Paul W. (35380325200)
    Objective Uncertainty exists concerning the relative merits of pharmacological versus mechanical coronary reperfusion in patients presenting early with ST-elevation myocardial infarction (STEMI) with extensive myocardium at risk. Accordingly, we investigated whether the extent of baseline ST-segment shift was related to the response of either reperfusion modality in patients with STEMI presenting within 3 h of symptoms. Methods We analysed baseline ECGs from 1859 patients enrolled in the STrategic Reperfusion Early After Myocardial Infarction (STREAM) trial. The sum of ST-segment elevation (ΣSTE) and ST-segment deviation (ΣSTD) was categorised into quartiles and associations with the primary endpoint (30-day death/shock/congestive heart failure/re-myocardial infarction) for each reperfusion strategy (early fibrinolysis vs primary percutaneous coronary intervention) were explored. Results Overall, there was a progressive rise in the 30-day primary endpoint according to quartiles of baseline ΣSTE (10.3% (0-5 mm), 12.4% (5.5-8.5 mm), 12.1% (9-13.5 mm), 17.6% (>14.0 mm), p=0.008) and ΣSTD (9.0% (0-9 mm), 13.5% (9.5-14 mm), 14.7% (14.5-20 mm), 15.3% (>20 mm), p=0.019). Both ΣSTE and ΣSTD were associated with the primary endpoint (ΣSTE: p=0.071; ΣSTD: p=0.024). However, there was no interaction between quartiles of baseline ΣSTE or ΣSTD and efficacy of either reperfusion strategy on the 30-day clinical outcomes (ΣSTE: p (interaction)=0.696; ΣSTD: p (interaction)=0.542). Conclusions These data demonstrate an association between ΣSTE or ΣSTD on the baseline ECG and clinical events at 30 days following reperfusion therapy in STEMI. More importantly, the response to different reperfusion strategies was not influenced by the extent of jeopardised myocardium. Trial registration number NCT00623623; Post-results.

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