Catheter-directed interventions for pulmonary embolism.


Journal

European heart journal. Acute cardiovascular care
ISSN: 2048-8734
Titre abrégé: Eur Heart J Acute Cardiovasc Care
Pays: England
ID NLM: 101591369

Informations de publication

Date de publication:
29 Sep 2022
Historique:
received: 11 07 2022
accepted: 12 07 2022
pubmed: 30 7 2022
medline: 4 10 2022
entrez: 29 7 2022
Statut: ppublish

Résumé

Pulmonary embolism (PE) is common, life-threatening, and often recurrent among survivors. The clinical manifestations of PE range from incidental detection to sudden death, with approximately one-third of PE deaths occurring suddenly. State-of-the-art management of acute PE relies on early detection, risk stratification based on clinical, imaging, and biomarker criteria, and multidisciplinary decision-making. The primary goal of catheter-directed interventions for acute PE is to interrupt the cycle of right ventricular failure, hypoperfusion, and oxygen supply/demand imbalance by increasing the cross-sectional area of the patent pulmonary vasculature, thereby lowering resistance and alleviating V/Q mismatch. Innovations in percutaneous interventions have led to several approaches described in this review: rheolytic thrombectomy, catheter-directed thrombolysis, and aspiration or mechanical thrombectomy. The central challenge moving forward will be integrating growing clinical trial evidence into multidisciplinary, individualized care pathways meeting the diverse clinical needs of patients presenting with acute PE.

Identifiants

pubmed: 35905304
pii: 6651959
doi: 10.1093/ehjacc/zuac089
doi:

Substances chimiques

Biomarkers 0
Fibrinolytic Agents 0
Oxygen S88TT14065

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

721-727

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Déclaration de conflit d'intérêts

Conflict of interest: A.K. has no pertinent disclosures. B.A.B. received grant support through Brigham and Women’s Hospital: Pfizer, Ionis, AstraZeneca, and Abbott Vascular; consulting/personal fees: Abiomed, SpectraWAVE, Endovascular Engineering, CSI, Philips, Abbott Vascular, Servier, Daiichi-Sankyo, Janssen, and Quark. B.A.B. is a member of the TIMI Study Group, which has received institutional grant support through the Brigham and Women’s Hospital from: Abbott, Amgen, Anthos Therapeutics, AstraZeneca, Bayer HealthCare Pharmaceuticals, Inc., Daiichi-Sankyo, Eisai, Intarcia, MedImmune, Merck, Novartis, Pfizer, Quark Pharmaceuticals, Regeneron Pharmaceuticals, Inc., Roche, Siemens Healthcare Diagnostics, Inc., The Medicines Company, and Zora Biosciences.

Auteurs

Ajar Kochar (A)

Cardiovascular Division, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA.
Harvard Medical School, 25 Shattuck Street, Boston, MA 02115, USA.

Brian A Bergmark (BA)

Cardiovascular Division, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA.
Harvard Medical School, 25 Shattuck Street, Boston, MA 02115, USA.
Thrombolysis in Myocardial Infarction (TIMI) Study Group, Hale Building for Transformative Medicine, 60 Fenwood Road, Suite 7022, Boston, MA 02115, USA.

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Classifications MeSH