Key result
Pre-hospital abciximab linked to ~4-fold higher rate of aborted MI vs. in-hospital administration in STEMI.
Why the study?
The incidence, patient characteristics, and predictors of aborted myocardial infarction in STEMI patients undergoing primary PCI were not well defined.
Does pre-hospital abciximab administration increase the incidence of aborted myocardial infarction in patients with STEMI undergoing primary PCI?
Cohort (n=179)
Does pre-hospital abciximab administration increase the incidence of aborted myocardial infarction in patients with STEMI undergoing primary PCI?
Odds Ratio: 4.2 (95% CI 1.7–10.3)
Pre-hospital administration of abciximab in STEMI patients undergoing primary PCI significantly increases the likelihood of aborted myocardial infarction compared to in-hospital administration.
Pre-hospital abciximab may increase aborted MI rates in STEMI; hypothesis-generating and should not yet change practice.
AIMS: This study was performed to assess the incidence, patient characteristics and predictors of aborted myocardial infarction (MI) in patients with ST-segment elevation MI (STEMI) undergoing primary percutaneous coronary intervention (PPCI). METHODS AND RESULTS: We enrolled 179 consecutive patients with STEMI within a fixed protocol for PPCI (Leiden MISSION! project); 90 patients received abciximab bolus in the hospital (in-hospital group) and 89 patients received abciximab bolus in the ambulance (pre-hospital group). Thirty-two patients (18%) fulfilled the criteria for an aborted MI. The incidence of aborted MI was four times higher in the pre-hospital abciximab group compared to the in-hospital group (OR = 4.2, 95% CI = 1.7-10.3). The median time between symptoms onset and abciximab bolus administration was significantly shorter in the aborted MI compared to established MI patients (70 vs. 115 min, p = 0.005). Multivariable analysis identified prehospital abciximab administration as the main predictor of aborted MI (OR = 2.86, 95% CI = 1.1-7.5). CONCLUSIONS: In patients with STEMI treated with PPCI, the incidence of aborted MI was 18%. Pre-hospital abciximab administration was the main predictor of aborted MI, and this effect was related to the initiation of treatment within the first two hours after symptoms onset and to the higher infarct related artery patency at presentation.
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Hassan et al. (2009) conducted a cohort in ST-segment elevation myocardial infarction (STEMI) (n=179). Pre-hospital abciximab bolus vs. In-hospital abciximab bolus was evaluated on Aborted myocardial infarction (MI) (OR 4.2, 95% CI 1.7-10.3). Pre-hospital abciximab administration in STEMI patients undergoing primary PCI was associated with a four-fold higher incidence of aborted MI compared to in-hospital administration (OR 4.2; 95% CI 1.7-10.3).
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