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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)

  • Eun Kyoung Kim
  • , Hong Mi Choi
  • , Eui Young Choi*
  • , Hye Sun Lee
  • , Goeun Park
  • , Dong Woo Han
  • , Sang Eun Lee
  • , Chan Seok Park
  • , Ji won Hwang
  • , Jae Hyuk Choi
  • , Mi Na Kim
  • , Hyung Kwan Kim
  • , Dae Hee Kim
  • , Sung Hee Shin
  • , Il Suk Sohn
  • , Mi Seung Shin
  • , Jin Oh Na
  • , Iksung Cho
  • , Sun Hwa Lee
  • , Yong Hyun Park
  • Tae Ho Park, Kye Hun Kim, Goo Young Cho, Hae Ok Jung, Dae Gyun Park, Ji Yeon Hong, Duk Hyun Kang
*Corresponding author for this work
  • Sungkyunkwan University
  • Seoul National University
  • Yonsei University
  • Ewha Womans University
  • The Catholic University of Korea
  • Inje University
  • Hallym University
  • Korea University
  • University of Ulsan
  • Inha University
  • Kyung Hee University
  • Gachon University
  • Pusan National University
  • Dong-A University
  • Chonnam National University

Research output: Contribution to journalJournal articlepeer-review

Abstract

Background: 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. Trial registration: The Clinical Research Information Service KCT0006279 for RCT and KCT0006280 for prospective cohort study. Registered on June 21, 2021.

Original languageEnglish
Article number776
JournalTrials
Volume23
Issue number1
DOIs
StatePublished - 2022.12

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Echocardiography
  • Noncardiac surgery
  • Trial design

Quacquarelli Symonds(QS) Subject Topics

  • Medicine
  • Pharmacy & Pharmacology

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