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Polyvascular disease: A narrative review of current evidence and a consideration of the role of antithrombotic therapy

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Polyvascular disease: A narrative review of current evidence and a consideration of the role of antithrombotic therapy. / Hoffnung Weissler, E; Schuyler Jones, W; Desormais, Ileana; Debus, Sebastian; Mazzolai, Lucia; Espinola-Klein, Christine; Nicol, Sigrid; Mark R, Nehler; Sillesen, Henrik; Aboyans, Victor; Patel, Manesh R .

In: ATHEROSCLEROSIS, Vol. 2020, No. 315, 10.1016/j.atherosclerosis.2020.11.001, 06.11.2020, p. 10-17.

Research output: SCORING: Contribution to journal › Other (editorial matter etc.) › Research

Harvard

Hoffnung Weissler, E, Schuyler Jones, W, Desormais, I, Debus, S, Mazzolai, L, Espinola-Klein, C, Nicol, S, Mark R, N, Sillesen, H, Aboyans, V & Patel, MR 2020, 'Polyvascular disease: A narrative review of current evidence and a consideration of the role of antithrombotic therapy', ATHEROSCLEROSIS, vol. 2020, no. 315, 10.1016/j.atherosclerosis.2020.11.001, pp. 10-17. https://doi.org/10.1016/j.atherosclerosis.2020.11.001

APA

Hoffnung Weissler, E., Schuyler Jones, W., Desormais, I., Debus, S., Mazzolai, L., Espinola-Klein, C., Nicol, S., Mark R, N., Sillesen, H., Aboyans, V., & Patel, M. R. (2020). Polyvascular disease: A narrative review of current evidence and a consideration of the role of antithrombotic therapy. ATHEROSCLEROSIS, 2020(315), 10-17. [10.1016/j.atherosclerosis.2020.11.001]. https://doi.org/10.1016/j.atherosclerosis.2020.11.001

Vancouver

Hoffnung Weissler E, Schuyler Jones W, Desormais I, Debus S, Mazzolai L, Espinola-Klein C et al. Polyvascular disease: A narrative review of current evidence and a consideration of the role of antithrombotic therapy. ATHEROSCLEROSIS. 2020 Nov 6;2020(315):10-17. 10.1016/j.atherosclerosis.2020.11.001. https://doi.org/10.1016/j.atherosclerosis.2020.11.001

Bibtex

@article{3018bee9f3e440ba9d7e99d4c06b418e,
title = "Polyvascular disease: A narrative review of current evidence and a consideration of the role of antithrombotic therapy",
abstract = "Background and aims: Polyvascular disease (PVD) affects approximately 20% of patients with atherosclerosis and is a strong independent risk factor for ischemic outcomes. However, guidelines do not address screening or treatment for PVD, and there have been no PVD-specific trials. We reviewed subgroup analyses of large randomized controlled trials of more intense antithrombotic therapy to determine whether increased intensity of therapy improved ischemic outcomes in patients with PVD.Methods: MEDLINE, MEDLINE in-Process, EMBASE, and the Cochrane Library were queried for randomized controlled trials larger than 5000 patients evaluating secondary prevention therapies in patients with coronary artery disease or lower extremity peripheral artery disease.Results: Thirteen trials were included ranging in size from 7243 to 27,395 patients. In 9 trials (CHARISMA, TRA 2°P-TIMI 50, PEGASUS-TIMI 54, VOYAGER PAD, TRACER, EUCLID, TRILOGY ACS, PLATO, and COMPASS), patients in the PVD subgroup treated with increased-intensity antithrombotic therapy had similar or greater relative risk reductions for ischemic events in comparison with the general trial cohorts. In four trials (DAPT, THEMIS, APPRAISE-2, and ATLAS ACS 2 TIMI 51), the PVD subgroup had an increased hazard of ischemic events with increased-intensity therapy compared with the general trial cohorts.Conclusions: More intense antithrombotic therapy in patients with PVD was associated with a similar relative risk reduction for ischemic events compared with patients without PVD. Therefore, patients with PVD benefit from a larger absolute risk reduction because of their higher baseline risk. Future trials in patients with atherosclerotic cardiovascular disease should intentionally include PVD patients to adequately assess treatment options for this under-studied, under-treated population.",
author = "{Hoffnung Weissler}, E and {Schuyler Jones}, W and Ileana Desormais and Sebastian Debus and Lucia Mazzolai and Christine Espinola-Klein and Sigrid Nicol and {Mark R}, Nehler and Henrik Sillesen and Victor Aboyans and Patel, {Manesh R}",
year = "2020",
month = nov,
day = "6",
doi = "10.1016/j.atherosclerosis.2020.11.001",
language = "English",
volume = "2020",
pages = "10--17",
journal = "ATHEROSCLEROSIS",
issn = "0021-9150",
publisher = "Elsevier Ireland Ltd",
number = "315",

}

RIS

TY - JOUR

T1 - Polyvascular disease: A narrative review of current evidence and a consideration of the role of antithrombotic therapy

AU - Hoffnung Weissler, E

AU - Schuyler Jones, W

AU - Desormais, Ileana

AU - Debus, Sebastian

AU - Mazzolai, Lucia

AU - Espinola-Klein, Christine

AU - Nicol, Sigrid

AU - Mark R, Nehler

AU - Sillesen, Henrik

AU - Aboyans, Victor

AU - Patel, Manesh R

PY - 2020/11/6

Y1 - 2020/11/6

N2 - Background and aims: Polyvascular disease (PVD) affects approximately 20% of patients with atherosclerosis and is a strong independent risk factor for ischemic outcomes. However, guidelines do not address screening or treatment for PVD, and there have been no PVD-specific trials. We reviewed subgroup analyses of large randomized controlled trials of more intense antithrombotic therapy to determine whether increased intensity of therapy improved ischemic outcomes in patients with PVD.Methods: MEDLINE, MEDLINE in-Process, EMBASE, and the Cochrane Library were queried for randomized controlled trials larger than 5000 patients evaluating secondary prevention therapies in patients with coronary artery disease or lower extremity peripheral artery disease.Results: Thirteen trials were included ranging in size from 7243 to 27,395 patients. In 9 trials (CHARISMA, TRA 2°P-TIMI 50, PEGASUS-TIMI 54, VOYAGER PAD, TRACER, EUCLID, TRILOGY ACS, PLATO, and COMPASS), patients in the PVD subgroup treated with increased-intensity antithrombotic therapy had similar or greater relative risk reductions for ischemic events in comparison with the general trial cohorts. In four trials (DAPT, THEMIS, APPRAISE-2, and ATLAS ACS 2 TIMI 51), the PVD subgroup had an increased hazard of ischemic events with increased-intensity therapy compared with the general trial cohorts.Conclusions: More intense antithrombotic therapy in patients with PVD was associated with a similar relative risk reduction for ischemic events compared with patients without PVD. Therefore, patients with PVD benefit from a larger absolute risk reduction because of their higher baseline risk. Future trials in patients with atherosclerotic cardiovascular disease should intentionally include PVD patients to adequately assess treatment options for this under-studied, under-treated population.

AB - Background and aims: Polyvascular disease (PVD) affects approximately 20% of patients with atherosclerosis and is a strong independent risk factor for ischemic outcomes. However, guidelines do not address screening or treatment for PVD, and there have been no PVD-specific trials. We reviewed subgroup analyses of large randomized controlled trials of more intense antithrombotic therapy to determine whether increased intensity of therapy improved ischemic outcomes in patients with PVD.Methods: MEDLINE, MEDLINE in-Process, EMBASE, and the Cochrane Library were queried for randomized controlled trials larger than 5000 patients evaluating secondary prevention therapies in patients with coronary artery disease or lower extremity peripheral artery disease.Results: Thirteen trials were included ranging in size from 7243 to 27,395 patients. In 9 trials (CHARISMA, TRA 2°P-TIMI 50, PEGASUS-TIMI 54, VOYAGER PAD, TRACER, EUCLID, TRILOGY ACS, PLATO, and COMPASS), patients in the PVD subgroup treated with increased-intensity antithrombotic therapy had similar or greater relative risk reductions for ischemic events in comparison with the general trial cohorts. In four trials (DAPT, THEMIS, APPRAISE-2, and ATLAS ACS 2 TIMI 51), the PVD subgroup had an increased hazard of ischemic events with increased-intensity therapy compared with the general trial cohorts.Conclusions: More intense antithrombotic therapy in patients with PVD was associated with a similar relative risk reduction for ischemic events compared with patients without PVD. Therefore, patients with PVD benefit from a larger absolute risk reduction because of their higher baseline risk. Future trials in patients with atherosclerotic cardiovascular disease should intentionally include PVD patients to adequately assess treatment options for this under-studied, under-treated population.

UR - https://pubmed.ncbi.nlm.nih.gov/33190107/

U2 - 10.1016/j.atherosclerosis.2020.11.001

DO - 10.1016/j.atherosclerosis.2020.11.001

M3 - Other (editorial matter etc.)

VL - 2020

SP - 10

EP - 17

JO - ATHEROSCLEROSIS

JF - ATHEROSCLEROSIS

SN - 0021-9150

IS - 315

M1 - 10.1016/j.atherosclerosis.2020.11.001

ER -