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Treatment of non-culprit lesions in STEMI: An incomplete journey

Treatment of non-culprit lesions in STEMI: An incomplete journey
Treatment of non-culprit lesions in STEMI: An incomplete journey

Approximately 50% of patients presenting with an acute ST-segment elevation myocardial infarction (STEMI) have multivessel coronary artery disease (CAD). A number of randomized studies (Table 1) have all shown that complete revascularization (CR), either at the time of primary percutaneous coronary revascularization (PPCI) or within 45 days of the index admission, is safe and reduces the risk of repeat coronary revascularization and myocardial infarction (MI), particularly in the non-infarct related artery (NIRA). Despite consistently showing clinical benefit for CR, the results from the trials show variations in what drives this effect. Specifically, no study to date has provided a mechanistic insight as to how complete revascularization of chronic bystander disease may lead to the observed clinical benefit. Indeed, the randomized studies, through the variable nature of their results (reduction in MI versus revascularization etc.), have suggested the possibility that there are differing mechanisms for the observed benefit. In this review, we summarize the evidence base, highlight the limitations, and make the case that we need to understand the mechanism(s) underpinning the advantage of revascularization of NIRA in order to establish which patients are most likely to benefit. Without this insight, the current "one size fits all" approach may lead us in the wrong direction.

Complete revascularization, ST-elevation myocardial infarction
1553-8389
Mahmoudi, Michael
f6a55246-399e-4f81-944e-a4b169786e8a
Curzen, Nick
70f3ea49-51b1-418f-8e56-8210aef1abf4
Mahmoudi, Michael
f6a55246-399e-4f81-944e-a4b169786e8a
Curzen, Nick
70f3ea49-51b1-418f-8e56-8210aef1abf4

Mahmoudi, Michael and Curzen, Nick (2021) Treatment of non-culprit lesions in STEMI: An incomplete journey. Cardiovascular Revascularization Medicine : including molecular interventions. (doi:10.1016/j.carrev.2021.09.001).

Record type: Review

Abstract

Approximately 50% of patients presenting with an acute ST-segment elevation myocardial infarction (STEMI) have multivessel coronary artery disease (CAD). A number of randomized studies (Table 1) have all shown that complete revascularization (CR), either at the time of primary percutaneous coronary revascularization (PPCI) or within 45 days of the index admission, is safe and reduces the risk of repeat coronary revascularization and myocardial infarction (MI), particularly in the non-infarct related artery (NIRA). Despite consistently showing clinical benefit for CR, the results from the trials show variations in what drives this effect. Specifically, no study to date has provided a mechanistic insight as to how complete revascularization of chronic bystander disease may lead to the observed clinical benefit. Indeed, the randomized studies, through the variable nature of their results (reduction in MI versus revascularization etc.), have suggested the possibility that there are differing mechanisms for the observed benefit. In this review, we summarize the evidence base, highlight the limitations, and make the case that we need to understand the mechanism(s) underpinning the advantage of revascularization of NIRA in order to establish which patients are most likely to benefit. Without this insight, the current "one size fits all" approach may lead us in the wrong direction.

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More information

Accepted/In Press date: 9 September 2021
e-pub ahead of print date: 11 September 2021
Published date: 11 September 2021
Additional Information: Publisher Copyright: © 2021 Elsevier Inc.
Keywords: Complete revascularization, ST-elevation myocardial infarction

Identifiers

Local EPrints ID: 452963
URI: http://eprints.soton.ac.uk/id/eprint/452963
ISSN: 1553-8389
PURE UUID: fbfbfe5d-8342-4cf6-a3c7-787cbfcc4c3d
ORCID for Michael Mahmoudi: ORCID iD orcid.org/0000-0003-1293-8461
ORCID for Nick Curzen: ORCID iD orcid.org/0000-0001-9651-7829

Catalogue record

Date deposited: 07 Jan 2022 11:48
Last modified: 17 Mar 2024 03:41

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