AIR-STEMI Trial Finds 35% Lower Cardiovascular Risk With Physiology-Guided PCI

AIR-STEMI trial results presented at ESC Congress 2026 show physiology-guided complete revascularisation reduced cardiovascular events by 35% and improved procedural safety in STEMI patients with multivessel coronary disease.

Sahajanand Medical Technologies (SMT) has highlighted findings from the AIR-STEMI clinical trial, which showed that functional coronary angiography-guided complete revascularisation was associated with a 35% relative reduction in the risk of major cardiovascular events compared with conventional angiography-guided complete revascularisation in patients with ST-segment elevation myocardial infarction (STEMI) and multivessel coronary artery disease.

The investigator-initiated, multicentre, randomised trial also reported improved procedural safety with the physiology-guided approach. Its findings were presented during a Hot Line session at ESC Congress 2026 and published simultaneously in The New England Journal of Medicine.

The study addressed a critical decision faced by clinicians after urgent percutaneous coronary intervention (PCI) to treat the artery responsible for a STEMI. Following the procedure, doctors must determine which additional, non-culprit coronary lesions require treatment. Although conventional angiography reveals the anatomy of a narrowing, it does not always establish whether the narrowing restricts blood flow.

AIR-STEMI investigated whether physiology derived from angiographic images could help identify functionally important lesions that require treatment while allowing non-flow-limiting lesions to be safely deferred.

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The trial enrolled 1,823 patients with STEMI and multivessel coronary artery disease following successful culprit-lesion PCI. Participants were randomly assigned to undergo complete revascularisation guided by either functional coronary angiography or conventional angiography.

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In the physiology-guided group, eligible non-culprit lesions with an angiography-derived fractional flow reserve value of 0.80 or less were treated with PCI. Lesions with a value above 0.80 were deferred.

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Supraflex Cruz, SMT’s sirolimus-eluting, biodegradable-polymer drug-eluting stent, was the recommended stent platform within the trial.

At a median follow-up of 17.9 months, the primary composite endpoint of all-cause death, myocardial infarction, cerebrovascular accident (stroke or transient ischemic attack) or ischaemia-driven coronary revascularisation occurred in 81 patients (8.9%) in the physiology-guided group, compared with 125 patients (13.7%) in the angiography-guided group.

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