Tissue characterisation and primary percutaneous coronary intervention guidance using intravascular ultrasound: rationale and design of the SPECTRUM study

Author:

Groenland Frederik T W,Mahmoud Karim DORCID,Neleman Tara,Ziedses des Plantes Annemieke C,Scoccia Alessandra,Ligthart Jurgen,Witberg Karen T,Nuis Rutger-Jan,den Dekker Wijnand K,Wilschut Jeroen M,Diletti Roberto,Zijlstra Felix,Kardys Isabella,Cummins Paul,Van Mieghem Nicolas M,Daemen JoostORCID

Abstract

IntroductionIntravascular ultrasound (IVUS) improves clinical outcome in patients undergoing percutaneous coronary intervention (PCI) but dedicated prospective studies assessing the safety and efficacy of IVUS guidance during primary PCI are lacking.Methods and analysisThe SPECTRUM study is a prospective investigator-initiated single-centre single-arm observational cohort study aiming to enrol 200 patients presenting with ST-segment elevation myocardial infarct undergoing IVUS-guided primary PCI. IVUS will be performed at baseline, postintervention and postoptimisation (if applicable), using a 40–60 MHz high-definition (HD) system. Baseline tissue characterisation includes the morphological description of culprit lesion plaque characteristics and thrombus as assessed with HD-IVUS. The primary endpoint is target vessel failure at 12 months (defined as a composite of cardiac death, target vessel myocardial infarction and clinically driven target vessel revascularisation). The secondary outcome of interest is IVUS-guided optimisation, defined as IVUS-guided additional balloon dilatation or stent placement. Other endpoints include clinical and procedural outcomes along with post-PCI IVUS findings.Ethics and disseminationThe protocol of this study was approved by the Ethics Committee of the Erasmus University Medical Center, Rotterdam, the Netherlands. Written informed consent is obtained from all patients. Study findings will be submitted to international peer-reviewed journals in the field of cardiovascular imaging and interventions and will be presented at international scientific meetings.Trial registration numberNCT05007535.

Funder

Microport, Shanghai, China

ACIST Medical Systems, Inc., Eden Prairie, Minnesota, USA

Publisher

BMJ

Subject

Cardiology and Cardiovascular Medicine

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