Scoring balloon predilation before bioresorbable vascular scaffold implantation in patients with in-stent restenosis: the RIBS VI 'scoring' study. Issue 2 (16th June 2020)
- Record Type:
- Journal Article
- Title:
- Scoring balloon predilation before bioresorbable vascular scaffold implantation in patients with in-stent restenosis: the RIBS VI 'scoring' study. Issue 2 (16th June 2020)
- Main Title:
- Scoring balloon predilation before bioresorbable vascular scaffold implantation in patients with in-stent restenosis: the RIBS VI 'scoring' study
- Authors:
- Alfonso, Fernando
Cuesta, Javier
García del Blanco, Bruno
Bosa, Francisco
Pérez de Prado, Armando
Masotti, Mónica
Trillo, Ramiro
Rumoroso, José Ramón
Moreno, Raul
Cequier, Angel
Gutiérrez, Hipólito
García Touchard, Arturo
López-Mínguez, José Ramón
Zueco, Javier
Serra, Antonio
Velázquez, Maite
Morís, César
Bastante, Teresa
García-Guimaraes, Marcos
Rivero, Fernando
Fernández-Pérez, Cristina - Other Names:
- other.
- Abstract:
- Abstract : Supplemental Digital Content is available in the text. Abstract : Background: Currently drug-eluting stents (DES) and drug-eluting balloons are recommended in patients with in-stent restenosis (ISR). However, the efficacy of bioresorbable vascular scaffolds (BVS) after scoring balloon (SCB) predilation in these patients is unknown. Methods: RIBS VI (NCT02672878) and RIBS VI 'Scoring' (NCT03069066) are prospective multicentre studies assessing the value of BVS in patients with ISR. Inclusion and exclusion criteria were identical in both studies. Results of conventional BVS implantation (112 patients) were compared with those obtained with systematic SCB therapy before BVS (108 patients). Angiographic follow-up was scheduled for all patients. Results: On late angiography (93% of eligible patients) the in-segment minimal lumen diameter (primary end-point) (1.88 ± 0.5 vs. 1.90 ± 0.4 mm, P = 0.81), % diameter stenosis (28 ± 17 vs. 29 ± 15%), late lumen loss (0.23 ± 0.4 vs. 0.22 ± 0.4 mm) and binary restenosis rate (8.5 vs. 9.3%) were similar in the conventional BVS and SCB + BVS groups, respectively. At 1-year follow-up (100% of patients) target lesion revascularization (TLR) requirement (9.8 vs. 11.1%) was similar with the two strategies. Freedom from cardiac death, myocardial infarction and TLR was 88% and 87%, respectively. Results remained unchanged after adjusting for potential baseline confounders and were consistent in 10 prespecified subgroups. Conclusion: ThisAbstract : Supplemental Digital Content is available in the text. Abstract : Background: Currently drug-eluting stents (DES) and drug-eluting balloons are recommended in patients with in-stent restenosis (ISR). However, the efficacy of bioresorbable vascular scaffolds (BVS) after scoring balloon (SCB) predilation in these patients is unknown. Methods: RIBS VI (NCT02672878) and RIBS VI 'Scoring' (NCT03069066) are prospective multicentre studies assessing the value of BVS in patients with ISR. Inclusion and exclusion criteria were identical in both studies. Results of conventional BVS implantation (112 patients) were compared with those obtained with systematic SCB therapy before BVS (108 patients). Angiographic follow-up was scheduled for all patients. Results: On late angiography (93% of eligible patients) the in-segment minimal lumen diameter (primary end-point) (1.88 ± 0.5 vs. 1.90 ± 0.4 mm, P = 0.81), % diameter stenosis (28 ± 17 vs. 29 ± 15%), late lumen loss (0.23 ± 0.4 vs. 0.22 ± 0.4 mm) and binary restenosis rate (8.5 vs. 9.3%) were similar in the conventional BVS and SCB + BVS groups, respectively. At 1-year follow-up (100% of patients) target lesion revascularization (TLR) requirement (9.8 vs. 11.1%) was similar with the two strategies. Freedom from cardiac death, myocardial infarction and TLR was 88% and 87%, respectively. Results remained unchanged after adjusting for potential baseline confounders and were consistent in 10 prespecified subgroups. Conclusion: This study suggests that results of conventional BVS implantation in patients with ISR are not improved by systematic predilation with SCB. ClinicalTrials.gov ID: NCT02672878 (RIBS VI) and NCT03069066 (RIBS VI 'Scoring'). … (more)
- Is Part Of:
- Coronary artery disease. Volume 32:Issue 2(2021)
- Journal:
- Coronary artery disease
- Issue:
- Volume 32:Issue 2(2021)
- Issue Display:
- Volume 32, Issue 2 (2021)
- Year:
- 2021
- Volume:
- 32
- Issue:
- 2
- Issue Sort Value:
- 2021-0032-0002-0000
- Page Start:
- 96
- Page End:
- 104
- Publication Date:
- 2020-06-16
- Subjects:
- drug-eluting balloons -- rug-eluting stents -- in-stent restenosis
Coronary heart disease -- Periodicals
Coronary Disease -- Indexes
Coronary Disease -- Periodicals
616.123005 - Journal URLs:
- http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=00019501-000000000-00000 ↗
http://www.coronary-artery.com/ ↗
http://journals.lww.com/pages/default.aspx ↗
http://firstsearch.oclc.org ↗ - DOI:
- 10.1097/MCA.0000000000000904 ↗
- Languages:
- English
- ISSNs:
- 0954-6928
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3472.049000
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