The impact of the extent of side branch disease on outcomes following bifurcation stenting.


Journal

Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions
ISSN: 1522-726X
Titre abrégé: Catheter Cardiovasc Interv
Pays: United States
ID NLM: 100884139

Informations de publication

Date de publication:
07 2020
Historique:
received: 12 10 2019
revised: 25 01 2020
accepted: 25 02 2020
pubmed: 10 3 2020
medline: 9 2 2021
entrez: 10 3 2020
Statut: ppublish

Résumé

To define the impact of side branch (SB) lesion length on clinical outcomes after percutaneous coronary intervention (PCI) on bifurcation lesions. The role of the SB lesion length remains questionable in PCI planning and its implication on clinical outcome is controversial. Data from the retrospective multicenter EBC-P2BiTO registry were analyzed. The primary endpoint was the occurrence of major adverse cardiac events (MACE), defined as the composite of cardiac death, myocardial infarction excluding periprocedural, or stent thrombosis at 13 months median follow-up (IQR 11-28). By using propensity scores for inverse probability of treatment weighting (IPTW), the comparison of treatment groups was adjusted to correct for potential confounding. Among 1,252 patients, SB was normal in 489 (39%), diseased in 763 (61%) cases. MACE occurred in 68 patients (5.4%). The optimal discriminant SB lesion length for MACE was ≥10 mm, with an area under the curve of 0.71 (p < .01). The incidence of MACE was higher among patients with SB lesions ≥10 mm (8%) than with normal SB (4.1%) (hazard ratio [HR], 2.8; 95% confidence interval [CI], 1.5-5.3; p = .001, IPTW-adjusted) or SB lesions <10 mm (5.1%) (HR, 1.5; 95% CI, 1.1-3.3; p = .048, IPTW-adjusted), being similar between these last two groups. In bifurcation PCI, SB lesion length ≥ 10 mm identifies patients at higher risk of MACE than those with <10 mm SB lesions and those without SB disease, considering that no differences were observed among these last two groups. Careful planning is mandatory when approaching bifurcations with long SB lesions.

Sections du résumé

OBJECTIVES
To define the impact of side branch (SB) lesion length on clinical outcomes after percutaneous coronary intervention (PCI) on bifurcation lesions.
BACKGROUND
The role of the SB lesion length remains questionable in PCI planning and its implication on clinical outcome is controversial.
METHODS
Data from the retrospective multicenter EBC-P2BiTO registry were analyzed. The primary endpoint was the occurrence of major adverse cardiac events (MACE), defined as the composite of cardiac death, myocardial infarction excluding periprocedural, or stent thrombosis at 13 months median follow-up (IQR 11-28). By using propensity scores for inverse probability of treatment weighting (IPTW), the comparison of treatment groups was adjusted to correct for potential confounding.
RESULTS
Among 1,252 patients, SB was normal in 489 (39%), diseased in 763 (61%) cases. MACE occurred in 68 patients (5.4%). The optimal discriminant SB lesion length for MACE was ≥10 mm, with an area under the curve of 0.71 (p < .01). The incidence of MACE was higher among patients with SB lesions ≥10 mm (8%) than with normal SB (4.1%) (hazard ratio [HR], 2.8; 95% confidence interval [CI], 1.5-5.3; p = .001, IPTW-adjusted) or SB lesions <10 mm (5.1%) (HR, 1.5; 95% CI, 1.1-3.3; p = .048, IPTW-adjusted), being similar between these last two groups.
CONCLUSIONS
In bifurcation PCI, SB lesion length ≥ 10 mm identifies patients at higher risk of MACE than those with <10 mm SB lesions and those without SB disease, considering that no differences were observed among these last two groups. Careful planning is mandatory when approaching bifurcations with long SB lesions.

Identifiants

pubmed: 32150341
doi: 10.1002/ccd.28842
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

E84-E92

Informations de copyright

© 2020 Wiley Periodicals, Inc.

Références

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Auteurs

Marco Zimarino (M)

Institute of Cardiology "G. d'Annunzio" University Chieti-Pescara, Chieti, Italy.
Interventional Cath Lab, ASL 2 Abruzzo, Chieti, Italy.

Emanuele Barbato (E)

Division of Cardiology, Department of Advanced Biomedical Sciences, Federico II University of Naples, Naples, Italy.

Sunao Nakamura (S)

Department of Cardiology, New Tokyo Hospital, Chiba, Japan.

Francesco Radico (F)

Institute of Cardiology "G. d'Annunzio" University Chieti-Pescara, Chieti, Italy.

Marta Di Nicola (M)

Department of Medical, Oral and Biotechnological Sciences, Laboratory of Biostatistics "G. d'Annunzio", Chieti, Italy.

Carlo Briguori (C)

Interventional Cardiology Unit, Mediterranea Cardiocentro, Naples, Italy.

Robert J Gil (RJ)

Department of Invasive Cardiology, Central Clinical Hospital of the Ministry of Interior, Warsaw, Poland.

Vojko Kanic (V)

Department of Cardiology and Angiology, University Medical Centre, Maribor, Slovenia.

Matteo Perfetti (M)

Interventional Cath Lab, ASL 2 Abruzzo, Chieti, Italy.

Mariano Pellicano (M)

Division of Cardiology, Department of Advanced Biomedical Sciences, Federico II University of Naples, Naples, Italy.
Cardiovascular Center Aalst, OLV Clinic, Aalst, Belgium.

Kristina Mairic (K)

Department of Cardiovascular Medicine, University Hospital Centre, Zagreb, Croatia.

Goran Stankovic (G)

Department of Cardiology, Clinical Center of Serbia, University of Belgrade, Belgrade, Serbia.

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