Restenosis Intra-Stent of Drug-Eluting Stents: Drug-Eluting Balloon vs Everolimus-Eluting Stent | Clinical Trial - RIBS IV


The optimal treatment of drug-eluting stent (DES)–in-stent restenosis (ISR) remains challenging. The current trial sought to investigate outcomes after drug-eluting balloon (DEB) versus DES implantation for patients with DES-ISR.

Contribution to the Literature: The RIBS IV trial showed that everolimus-eluting stents are superior to drug-coated balloon for the treatment of DES-ISR. 

Study Design

  • Randomized
  • Parallel

Patient Populations:

  • Mean patient age: 66 years old
  • Percentage female: 17%
  • Number of enrollees: 309
  • Duration of follow-up: 1 year

  • DES-ISR (>50% stenosis)
  • Angina or silent ischemia
  • ISR amenable for both modalities


  • Stent related:
  • Stent location undefined
  • Unknown stent type
  • ISR <1 month
  • Thrombus
  • Vessel diameter <2 mm
  • ISR length >30 mm
  • ISR outside the stent

  • General:
  • Life expectancy <1 year
  • Female in childbearing age
  • Problems with follow-up angiography
  • Intolerance to aspirin/clopidogrel
  • Left ventricular ejection fraction <25%

Primary Endpoints:

  • MLD at 6-9 months

Secondary Endpoints:

  • Combined clinical and angiographic endpoints at 6-9 months, 1 year, and 3 years
  • Efficacy outcomes:
    - Angiographic: 1) restenosis rate, 2) % diameter stenosis, 3) acute gain, 4) late loss, 5) net gain
    - Composite of death, MI, target vessel revascularization, and analysis of individual events
  • Safety outcomes: stent thrombosis, bleeding episodes

Drug/Procedures Used:

Patients were randomized in a 1:1 ratio to either percutaneous transluminal coronary angioplasty (PTCA) with DEB (SeQuent Please B) or percutaneous coronary intervention (PCI) with everolimus-eluting stent (EES) (Xience Prime).

Principal Findings:

A total of 309 patients were randomized, 154 to DEB and 155 to DES. Baseline characteristics were fairly similar between the two arms. Diabetes was present in 46%. Presenting feature was stable angina or silent ischemia in 49%. >1 stent intervention in the target lesion was noted in 12% of patients. The median time to ISR was 535 days, with left anterior descending artery (LAD) being the target vessel in 48% and right coronary artery in 29%. Prior DES was PES in 25% and limus-type in the remainder.

On quantitative coronary angiography (QCA) analysis at baseline, in-segment reference vessel diameter (2.59 mm vs. 2.67 mm, p = 0.21) and lesion length (10.4 mm vs. 10.7 mm, p = 0.56) were similar between the DEB and DES arms. Post-procedure minimum lesion diameter (MLD) (2.2 vs. 2.49 mm, p < 0.0001) and acute gain (1.31 vs. 1.48 mm, p = 0.006) were lower in the DEB arm.

On 6- to 9-month QCA analysis, the in-segment MLD (1.8 mm vs. 2.03 mm, p = 0.004) and in-lesion MLD (1.89 mm vs. 2.2 mm, p < 0.0001) were significantly lower in the DEB arm. Correspondingly, there was a trend toward greater late lumen loss with DEB use (0.14 mm vs. 0.06 mm, p = 0.06).

Clinical endpoints at 1 year including the composite major adverse cardiac event (MACE) endpoint (16% vs. 7%, p = 0.009) and freedom from target lesion revascularization were significantly lower in the DEB arm (87% vs. 95.5%, p = 0.007). Rates of myocardial infarction (MI) were numerically higher (3.2% vs. 1.3%), with two stent thrombosis events in the DEB and one in the EES arm.


The results of the RIBS IV trial indicate that PTCA with a DEB is inferior to EES PCI in patients with DES-ISR. Although rare, DES-ISR remains a challenging lesion subset, with no clear consensus from clinical trials. For BMS-ISR, the late lumen loss was lower in RIBS V with DEB PTCA (0.14 mm) than observed in this trial (0.3 mm), consistent with the observation made by some investigators that DES-ISR is more diffuse and prolific than BMS-ISR. Further data on the optimal treatment of this lesion subset are awaited.


Alfonso F, Pérez-Vizcayno MJ, Cárdenas A, et al. A Prospective Randomized Trial of Drug-Eluting Balloons Versus Everolimus-Eluting Stents in Patients With In-Stent Restenosis of Drug-Eluting Stents: The RIBS IV Randomized Clinical Trial. J Am Coll Cardiol 2015;66:23-33.

Presented by Dr. Fernando Alfonso at the Transcatheter Cardiovascular Therapeutics meeting (TCT 2014), Washington, DC, September 14, 2014.

Clinical Topics: Invasive Cardiovascular Angiography and Intervention, Noninvasive Imaging, Interventions and Imaging, Angiography, Nuclear Imaging

Keywords: Myocardial Infarction, Coronary Angiography, Thrombosis, Drug-Eluting Stents, Sirolimus, Angioplasty, Balloon, Coronary, Stents, Percutaneous Coronary Intervention, Transcatheter Cardiovascular Therapeutics

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