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Outcomes of drug-coated balloon angioplasty in patients with dyslipidemia in the BIOLUX P-III registry: A subgroup analysis.
Dodd, James Evan; Hanna, Joseph; Brodmann, Marianne; Golledge, Jonathan; Zeller, Thomas; Moscovic, Matej; Dahm, Johannes; Troisi, Nicola; Tepe, Gunnar; Wong, Jacqueline; Ward, Natalie C; Mwipatayi, Bibombe Patrice.
  • Dodd JE; Department of Vascular Surgery, Royal Perth Hospital, Perth, Australia.
  • Hanna J; Department of Vascular Surgery, Royal Perth Hospital, Perth, Australia.
  • Brodmann M; Department of Angiology, Medical University Graz, Graz, Austria.
  • Golledge J; Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, Australia.
  • Zeller T; The Department of Vascular and Endovascular Surgery, Townsville University Hospital, Townsville, Australia.
  • Moscovic M; Clinic Cardiology and Angiology II, Universitäts-Herzzentrum Freiburg, Freiburg, Germany.
  • Dahm J; Department of Angiology, Institute of Cardiovascular Diseases, Kosice, Slovakia.
  • Troisi N; Department of Angiology and Cardiology, Herz- und Gefäßzentrum Neu-Bethlehem, Göttingen, Germany.
  • Tepe G; Unit of Vascular and Endovascular Surgery, Department of Surgery, San Giovanni di Dio Hospital, Florence, Italy.
  • Wong J; Department of Diagnostic and Interventional Radiology, Klinikum Rosenheim, Rosenheim, Germany.
  • Ward NC; Department of Vascular Surgery, Royal Perth Hospital, Perth, Australia.
  • Mwipatayi BP; Dobney Hypertension Centre, Medical School, University of Western Australia, Perth, Australia.
Vascular ; : 17085381241275795, 2024 Aug 19.
Article en En | MEDLINE | ID: mdl-39158589
ABSTRACT

OBJECTIVES:

The aim of this study was to assess the mid-term outcomes of the use of drug-coated balloons (DCBs) to treat infrainguinal peripheral arterial disease (PAD) in patients with dyslipidemia.

METHODS:

BIOLUX P-III is a prospective, international, multicenter, all-comers registry-based study that was conducted at 44 sites with follow-ups at 6, 12 and 24 months. The present study is a subgroup analysis comparing the outcomes associated with endovascular revascularization with those associated with Passeo-18 lux DCBs in patients with and without dyslipidemia. The proportions of patients free from major adverse events (defined as device- or procedure-related mortality within 30 days, clinically driven target lesion revascularization (CD-TLR) and major target limb amputation), target vessel revascularization, and patient-reported outcomes within 24 months postintervention were compared between the two groups.

RESULTS:

A total of 876 patients with symptomatic PAD who underwent peripheral revascularization with DCBs and had information on their dyslipidemia status were included; 588 of those patients had dyslipidemia. There was no difference in the proportion of patients free from MAEs between the groups. The percentages of patients who were 6, 12 and 24 months free from CD-TLR were significantly lower in the dyslipidemia group than in the nondyslipidemia group (86.3% vs 91.9% at 2 years, p = .0183). Similarly, the percentage of patients free from target vessel revascularization was lower in the dyslipidemia group at all timepoints (83.3% vs 89.3% at 2 years, p = .0203). There was no difference in mortality or major or minor limb amputation rates. Other secondary outcomes were similar between the groups.

CONCLUSIONS:

Compared to those without dyslipidemia, patients with symptomatic PAD and dyslipidemia who underwent revascularization with a Passeo-18 lux DCB had greater rates of CD-TLR and TVR. However, having dyslipidemia did not increase the risk of mortality or limb amputation. CLINICAL TRIAL REGISTRATION NCT02276313.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article