Direct Stenting versus Conventional Stenting in Patients with ST-Segment Elevation Myocardial Infarction—A COMPARE CRUSH Sub-Study

Author:

Vogel Rosanne F.12,Delewi Ronak2,Wilschut Jeroen M.3,Lemmert Miguel E.34,Diletti Roberto3,van Vliet Ria5,van der Waarden Nancy W. P. L.6,Nuis Rutger-Jan3,Paradies Valeria5,Alexopoulos Dimitrios7,Zijlstra Felix3,Montalescot Gilles8,Angiolillo Dominick J.9,Krucoff Mitchell W.10,Van Mieghem Nicolas M.3,Smits Pieter C.5,Vlachojannis Georgios J.1511ORCID

Affiliation:

1. Department of Cardiology, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands

2. Department of Cardiology, Amsterdam UMC Location AMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands

3. Department of Cardiology, Erasmus University Medical Center, 3000 CA Rotterdam, The Netherlands

4. Department of Cardiology, Isala Hospital, 8025 AB Zwolle, The Netherlands

5. Department of Cardiology, Maasstad Hospital, 3079 DZ Rotterdam, The Netherlands

6. AmbulanceZorg Rotterdam-Rijnmond, 2993 LT Barendrecht, The Netherlands

7. Department of Cardiology, Attikon University Hospital, 12462 Athens, Greece

8. ACTION Group, Groupe Hospitalier Pitie-Salpetriere Hospital (AP-HP), Sorbonne University, 75013 Paris, France

9. Division of Cardiology, University of Florida College of Medicine, Jacksonville, FL 32610, USA

10. Department of Cardiology, Duke University Medical Center, Durham, NC 27710, USA

11. Department of Cardiology, Euroclinic Athens, 11521 Athens, Greece

Abstract

Background: Direct stenting (DS) compared with conventional stenting (CS) after balloon predilatation may reduce distal embolization during percutaneous coronary intervention (PCI), thereby improving tissue reperfusion. In contrast, DS may increase the risk of stent underexpansion and target lesion failure. Methods: In this sub-study of the randomized COMPARE CRUSH trial (NCT03296540), we reviewed the efficacy of DS versus CS in a cohort of contemporary, pretreated ST-segment elevation myocardial infarction (STEMI) patients undergoing primary PCI. We compared DS versus CS, assessing (1) stent diameter in the culprit lesion, (2) thrombolysis in myocardial infarction (TIMI) flow in the infarct-related artery post-PCI and complete ST-segment resolution (STR) one-hour post-PCI, and (3) target lesion failure at one year. For proportional variables, propensity score weighting was applied to account for potential treatment selection bias. Results: This prespecified sub-study included 446 patients, of whom 189 (42%) were treated with DS. Stent diameters were comparable between groups (3.2 ± 0.5 vs. 3.2 ± 0.5 mm, p = 0.17). Post-PCI TIMI 3 flow and complete STR post-PCI rates were similar between groups (DS 93% vs. CS 90%, adjusted OR 1.16 [95% CI, 0.56–2.39], p = 0.69, and DS 72% vs. CS 58%, adjusted OR 1.29 [95% CI 0.77–2.16], p = 0.34, respectively). Moreover, target lesion failure rates at one year were comparable (DS 2% vs. 1%, adjusted OR 2.93 [95% CI 0.52–16.49], p = 0.22). Conclusion: In this contemporary pretreated STEMI cohort, we found no difference in early myocardial reperfusion outcomes between DS and CS. Moreover, DS seemed comparable to CS in terms of stent diameter and one-year vessel patency.

Funder

Maasstad research B.V.

Publisher

MDPI AG

Subject

General Medicine

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