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PRE-Operative ECHOcardiograhy for prevention of cardiovascular events after non-cardiac surgery in intermediate- and high-risk patients: protocol for a low-interventional, mixed-cohort prospective study design (PREOP-ECHO)

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dc.contributor.authorKim, Eun Kyoung-
dc.contributor.authorChoi, Hong-Mi-
dc.contributor.authorChoi, Eui-Young-
dc.contributor.authorLee, Hye Sun-
dc.contributor.authorPark, Goeun-
dc.contributor.authorHan, Dong Woo-
dc.contributor.authorLee, Sang-Eun-
dc.contributor.authorPark, Chan Seok-
dc.contributor.authorHwang, Ji-won-
dc.contributor.authorChoi, Jae Hyuk-
dc.contributor.authorKim, Mi-Na-
dc.contributor.authorKim, Hyung-Kwan-
dc.contributor.authorKim, Dae-Hee-
dc.contributor.authorShin, Sung-Hee-
dc.contributor.authorSohn, Il Suk-
dc.contributor.authorShin, Mi-Seung-
dc.contributor.authorNa, Jin Oh-
dc.contributor.authorCho, Iksung-
dc.contributor.authorLee, Sun Hwa-
dc.contributor.authorPark, Yong Hyun-
dc.contributor.authorPark, Tae-Ho-
dc.contributor.authorKim, Kye Hun-
dc.contributor.authorCho, Goo-Young-
dc.contributor.authorJung, Hae Ok-
dc.contributor.authorPark, Dae-Gyun-
dc.contributor.authorHong, Ji Yeon-
dc.contributor.authorKang, Duk-Hyun-
dc.date.accessioned2022-11-18T11:40:46Z-
dc.date.available2022-11-18T11:40:46Z-
dc.date.created2022-11-17-
dc.date.issued2022-09-14-
dc.identifier.issn1745-6215-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/145752-
dc.description.abstractBackground: Cardiac evaluation using transthoracic echocardiography before noncardiac surgery is common in real-world practice. However, evidence supporting preoperative echocardiography is lacking. This study aims to evaluate the additional benefit of preoperative echocardiography in predicting postoperative cardiovascular events (CVE) in noncardiac surgery. Methods: This study is designed as a multicenter, prospective study to assess the utility of preoperative echocardiography in patients undergoing intermediate- or high-risk noncardiac surgery. This trial comprises two studies: (1) a randomized controlled trial (RCT) for patients undergoing intermediate-risk surgery with fewer than three clinical risk factors from the revised cardiac risk index (intermediate-risk group) and (2) a prospective cohort study for patients undergoing intermediate-risk surgery with three or more clinical risk factors, or who undergo high-risk surgery regardless of the number of clinical risk factors (high-risk group). We hypothesize that the use of preoperative echocardiography will reduce postoperative CVEs in patients undergoing intermediate- to high-risk surgery through discovery of and further intervention for unexpected cardiac abnormalities before elective surgery. A total of 2330 and 2184 patients will be enrolled in the two studies. The primary endpoint is a composite of all-cause death; aborted sudden cardiac arrest; type I acute myocardial infarction; clinically diagnosed unstable angina; stress-induced cardiomyopathy; lethal arrhythmia, such as sustained ventricular tachycardia or ventricular fibrillation; and/or newly diagnosed or acutely decompensated heart failure within 30 days after surgery. Discussion: This study will be the first large-scale prospective study examining the benefit of preoperative echocardiography in predicting postoperative CVE. The PREOP-ECHO trial will help doctors identify patients at risk of postoperative CVE using echocardiography and thereby reduce postoperative CVEs.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherBMC-
dc.subjectCARDIAC RISK-
dc.subject30-DAY MORTALITY-
dc.subjectAORTIC-STENOSIS-
dc.subjectTROPONIN LEVELS-
dc.subjectASSOCIATION-
dc.subjectGUIDELINES-
dc.subjectMANAGEMENT-
dc.subjectSOCIETY-
dc.subjectRECOMMENDATIONS-
dc.subjectCOMPLICATIONS-
dc.titlePRE-Operative ECHOcardiograhy for prevention of cardiovascular events after non-cardiac surgery in intermediate- and high-risk patients: protocol for a low-interventional, mixed-cohort prospective study design (PREOP-ECHO)-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Mi-Na-
dc.identifier.doi10.1186/s13063-022-06701-2-
dc.identifier.scopusid2-s2.0-85137911799-
dc.identifier.wosid000853907300001-
dc.identifier.bibliographicCitationTRIALS, v.23, no.1-
dc.relation.isPartOfTRIALS-
dc.citation.titleTRIALS-
dc.citation.volume23-
dc.citation.number1-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.subject.keywordPlusCARDIAC RISK-
dc.subject.keywordPlus30-DAY MORTALITY-
dc.subject.keywordPlusAORTIC-STENOSIS-
dc.subject.keywordPlusTROPONIN LEVELS-
dc.subject.keywordPlusASSOCIATION-
dc.subject.keywordPlusGUIDELINES-
dc.subject.keywordPlusMANAGEMENT-
dc.subject.keywordPlusSOCIETY-
dc.subject.keywordPlusRECOMMENDATIONS-
dc.subject.keywordPlusCOMPLICATIONS-
dc.subject.keywordAuthorEchocardiography-
dc.subject.keywordAuthorNoncardiac surgery-
dc.subject.keywordAuthorTrial design-
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