Randomized Trial Evaluating Percutaneous Coronary Intervention for the Treatment of Chronic Total Occlusion: The DECISION-CTO Trial

Seung Whan Lee, Pil Hyung Lee, Jung Min Ahn, Duk Woo Park, Sung Cheol Yun, Seungbong Han, Heejun Kang, Soo Jin Kang, Young Hak Kim, Cheol Whan Lee, Seong Wook Park, Seung Ho Hur, Seung Woon Rha, Sung Ho Her, Si Wan Choi, Bong Ki Lee, Nae Hee Lee, Jong Young Lee, Sang Sig Cheong, Moo Hyun KimYoung Keun Ahn, Sang Wook Lim, Sang Gon Lee, Shirish Hiremath, Teguh Santoso, Wasan Udayachalerm, Jun Jack Cheng, David J. Cohen, Toshiya Muramatsu, Etsuo Tsuchikane, Yasushi Asakura, Seung Jung Park

Research output: Contribution to journalArticlepeer-review

239 Citations (Scopus)


Background: Procedural results for percutaneous coronary intervention (PCI) in coronary vessels with chronic total occlusion (CTO) have improved in recent years, and PCI strategies have moved toward more complete revascularization with more liberal use of CTO-PCI. However, evidence evaluating CTO-PCI is limited to observational studies and small clinical trials. Methods: In this open-label, multicenter, randomized, noninferiority trial, PCI-eligible patients were assigned to receive either 1 of 2 strategies: PCI or no PCI for the qualifying de novo CTO lesion with the option for PCI of obstructive non-CTO lesions at the discretion of the operator. The primary end point was a composite of death, myocardial infarction, stroke, or any revascularization. Health-related quality of life was assessed at baseline and at 1, 6, 12, 24, and 36 months. Because of slow recruitment, the trial was stopped before completion of the 1284 planned enrollments. Results: Between March 2010 and September 2016, 834 patients were randomly assigned to the CTO-PCI (n=417) or no CTO-PCI (n=398) strategy. Among the patients assigned to the no CTO-PCI strategy, 78 (19.6%) crossed over to receive staged CTO-PCI within 3 days of randomization. The overall CTO-PCI success rate was 90.6%. Serious nonfatal complications associated with CTO-PCI occurred in 3 patients (1 stroke, 1 cardiac tamponade, and 1 patient with recurrent episodes of ventricular tachyarrhythmia induced by intracoronary thrombus). Approximately half of the patients in each group underwent PCI for an average of 1.3 non-CTO lesions, resulting in a comparable residual SYNTAX score (Synergy Between PCI With TAXUS and Cardiac Surgery; 3.7±5.4 versus 4.0±5.9, P=0.42) confined to non-CTO vessels. During a median follow-up of 4.0 years (interquartile range, 2.4 to 5.1 years), there was no significant difference between the CTO-PCI and the no CTO-PCI strategies in the incidence of the primary end point (22.3% versus 22.4%, hazard ratio, 1.03; 95% CI, 0.77 to 1.37; P=0.86). Both CTO-PCI and no CTO-PCI strategy were associated with significant improvements but without between-group differences in disease-specific health status that was sustained through 36 months. Conclusions: CTO-PCI was feasible with high success rates. There was no difference in the incidence of major adverse cardiovascular events with CTO-PCI versus no CTO-PCI, but the study was limited by low power for clinical end points and high crossover rates between groups. Clinical Trial Registration: URL: https://www.clinicaltrials.gov. Unique identifier: NCT01078051.

Original languageEnglish
Pages (from-to)1674-1683
Number of pages10
Issue number14
Publication statusPublished - 2019 Apr 2

Bibliographical note

Funding Information:
This work was supported by a grant from the CardioVascular Research Foundation Korea.

Publisher Copyright:
© 2018 American Heart Association, Inc.


  • arterial occlusive diseases
  • outcome
  • percutaneous coronary intervention
  • randomized controlled trial

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Physiology (medical)


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