Prevalence of VOYAGER PAD trial exclusion criteria in unselected patients undergoing lower limb revascularization.


Journal

International angiology : a journal of the International Union of Angiology
ISSN: 1827-1839
Titre abrégé: Int Angiol
Pays: Italy
ID NLM: 8402693

Informations de publication

Date de publication:
Feb 2022
Historique:
pubmed: 17 12 2021
medline: 24 2 2022
entrez: 16 12 2021
Statut: ppublish

Résumé

The VOYAGER PAD trial investigated data on dual pathway inhibition after lower limb revascularization for peripheral arterial disease (PAD). Multiple exclusion criteria were applied. However, neither data on the prevalence of exclusion criteria nor on the total number of patients screened for inclusion was discussed. We performed a single-center prospective observational study in unselected PAD patients undergoing lower limb revascularization. Demographic and disease-specific data was collected. One hundred fifty patients were included with only 29 patients (19.3%) as potential candidates for the VOYAGER PAD study medication. Poorly controlled diabetes or severe uncontrolled hypertension (33.3%), major tissue loss (18.7%), acute limb ischaemia within prior 2 weeks (17.3%) and a history of intracranial hemorrhage, stroke or TIA (16%) were amongst the exclusion criteria most frequently met. Compared to VOYAGER PAD study patients, significant differences regarding sex (36.7% female vs. 25.8%), renal insufficiency (29.0% vs. 20.1%), previous myocardial infarction (16.7% vs. 11.1%) and known carotid artery disease (18.7% vs. 8.6%) revealed. Patients presented significantly more frequently with critical limb ischemia (56.7% vs. 30.4%) and a history of previous peripheral revascularization (72.0% vs. 35.9%). Fewer endovascular interventions (52% vs. 65.5%) and more surgeries (58% vs. 34.5%) were performed. In unselected patients undergoing revascularization for peripheral arterial disease, the majority presents with characteristics that, at present, preclude prescription of rivaroxaban in addition to aspirin. This patient cohort represents a population with higher rates of comorbidities and more complex vascular interventions, but might also benefit from dual pathway inhibition strategy.

Sections du résumé

BACKGROUND BACKGROUND
The VOYAGER PAD trial investigated data on dual pathway inhibition after lower limb revascularization for peripheral arterial disease (PAD). Multiple exclusion criteria were applied. However, neither data on the prevalence of exclusion criteria nor on the total number of patients screened for inclusion was discussed.
METHODS METHODS
We performed a single-center prospective observational study in unselected PAD patients undergoing lower limb revascularization. Demographic and disease-specific data was collected.
RESULTS RESULTS
One hundred fifty patients were included with only 29 patients (19.3%) as potential candidates for the VOYAGER PAD study medication. Poorly controlled diabetes or severe uncontrolled hypertension (33.3%), major tissue loss (18.7%), acute limb ischaemia within prior 2 weeks (17.3%) and a history of intracranial hemorrhage, stroke or TIA (16%) were amongst the exclusion criteria most frequently met. Compared to VOYAGER PAD study patients, significant differences regarding sex (36.7% female vs. 25.8%), renal insufficiency (29.0% vs. 20.1%), previous myocardial infarction (16.7% vs. 11.1%) and known carotid artery disease (18.7% vs. 8.6%) revealed. Patients presented significantly more frequently with critical limb ischemia (56.7% vs. 30.4%) and a history of previous peripheral revascularization (72.0% vs. 35.9%). Fewer endovascular interventions (52% vs. 65.5%) and more surgeries (58% vs. 34.5%) were performed.
CONCLUSIONS CONCLUSIONS
In unselected patients undergoing revascularization for peripheral arterial disease, the majority presents with characteristics that, at present, preclude prescription of rivaroxaban in addition to aspirin. This patient cohort represents a population with higher rates of comorbidities and more complex vascular interventions, but might also benefit from dual pathway inhibition strategy.

Identifiants

pubmed: 34913631
pii: S0392-9590.21.04816-1
doi: 10.23736/S0392-9590.21.04816-1
doi:

Substances chimiques

Rivaroxaban 9NDF7JZ4M3
Aspirin R16CO5Y76E

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

56-62

Auteurs

Maria A Moll (MA)

Department of Vascular Surgery, Medical University of Innsbruck, Innsbruck, Austria.

Daniela Zwerger (D)

Department of Vascular Surgery, Medical University of Innsbruck, Innsbruck, Austria.

Kristina J Grassl (KJ)

Department of Vascular Surgery, Medical University of Innsbruck, Innsbruck, Austria.

Werner Westreicher (W)

Department of Vascular Surgery, Medical University of Innsbruck, Innsbruck, Austria.

Sabrina B Neururer (SB)

Department of Clinical Epidemiology, Tyrolean Federal Institute for Integrated Care, Tirol Kliniken GmbH, Innsbruck, Austria.

Clemens W Moll (CW)

Department of Vascular Surgery, Medical University of Innsbruck, Innsbruck, Austria.

Sabine H Wipper (SH)

Department of Vascular Surgery, Medical University of Innsbruck, Innsbruck, Austria.

Josef Klocker (J)

Department of Vascular Surgery, Medical University of Innsbruck, Innsbruck, Austria - josef.klocker@i-med.ac.at.

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Classifications MeSH