Key result
A pharmaco-invasive strategy was associated with a lower risk of 2-year all-cause mortality compared to late PCI (HR 0.433; 95% CI 0.21-0.87; P=0.02), with no difference compared to primary PCI.
Why the study?
Primary PCI within 120 minutes of first medical contact is the preferred reperfusion therapy for STEMI, but it is not always available.
Does a pharmaco-invasive strategy reduce all-cause mortality compared to late PCI in STEMI patients presenting within 12 hours of symptom onset?
Cohort (n=439)
No
Does a pharmaco-invasive strategy reduce all-cause mortality compared to late PCI in STEMI patients presenting within 12 hours of symptom onset?
Hazard Ratio: 0.433 (95% CI 0.21–0.87)
p-value: p=0.02
A pharmaco-invasive strategy provides similar long-term mortality benefits to primary PCI and is superior to late PCI in STEMI patients when timely primary PCI is unavailable.
May support pharmaco-invasive strategy when timely pPCI unavailable in developing countries; leaves open need for prospective confirmation.
Introduction Early Primary percutaneous coronary intervention (pPCI) is the preferred reperfusion therapy for most patients with ST-segment elevation myocardial infarction (STEMI), and the European guidelines recommend pPCI to occur within 120 min of first medical contact. However, this is not always available. Methods We performed a retrospective study of patients admitted for STEMI to a level I cardiac intensive care unit in a developing country, to analyze the efficacy of the pharmaco-invasive (PI) strategy versus late PCI over a 2-year follow-up. Results Four hundred and thirty-nine STEMI patients presented within the first 12 h of symptom onset, pPCI was performed in 154 patients, PI-strategy in 185 patients, and finally Late PCI in 100 patients. All-cause mortality at 2-year risk was statistically significant associated with cardiogenic shock during initial hospitalization, LM and ostio-proximal left anterior descending artery as the culprit artery, severe conductance disorders requiring the use of a temporary pacemaker, and acute kidney disease with glomerular filtration rate < 30 ml/min/1.72 m2 . For the revascularization strategy, there as a well-demonstrated benefit of the pPCI versus Late PCI strategy with (hazard ratio (HR) = 0.293; 95% confidence interval (CI) 0.11–0.737; P = 0.009), as well as a benefit of the PI-strategy versus Late PCI strategy with (HR = 0.433; 95%CI 0.21–0.87; P = 0.02). However, there was no difference between the pPCI and PI-strategy. Conclusion The PI-strategy remains a reasonable alternative for pPCI when the latter is not available, with a prognosis almost identical to pPCI in the long term whenever patients are treated early after the onset of symptoms.
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Bouyaddid et al. (2023) conducted a cohort in ST-segment elevation myocardial infarction (STEMI) (n=439). Pharmaco-invasive (PI) strategy vs. Late PCI was evaluated on All-cause mortality (HR 0.433, 95% CI 0.21-0.87, p=0.02). A pharmaco-invasive strategy was associated with a lower risk of 2-year all-cause mortality compared to late PCI (HR 0.433; 95% CI 0.21-0.87; P=0.02), with no difference compared to primary PCI.
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