S'abonner

Dual antiplatelet therapy duration and stent type in patients with high bleeding risk: A systematic review and network meta-analysis - 02/12/24

Doi : 10.1016/j.ahj.2024.10.004 
Tetsuya Saito, MD a, Toshiki Kuno, MD, PhD b, c, d, , Tomohiro Fujisaki, MD e, f, Rahul Gupta, MD g, Kaveh Hosseini, MD-MPH h, Hisato Takagi, MD, PhD i, Jose Wiley, MD, MPH j, Sripal Bangalore, MD, MHA k,
a Department of Cardiology, Edogawa Hospital, Tokyo, Japan 
b Division of Cardiology, Montefiore Medical Center, Albert Einstein College of Medicine, New York, NY 
c Division of Cardiology, Jacobi Medical Center, Albert Einstein College of Medicine, New York, NY 
d Cardiology Division, Massachusetts General Hospital, Harvard Medical School, Boston, MA 
e Department of Cardiovascular Medicine, Graduate School of Medical Science, Kumamoto University, Kumamoto, Japan 
f Department of Cardiovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan 
g Department of Cardiovascular Medicine, Yale School of Medicine, New Haven, CT 
h Tehran Heart Center, Cardiovascular Disease Research Institute, Tehran University of Medical Sciences, Tehran, Iran 
i Department of Cardiovascular Surgery, Shizuoka Medical Center, Shizuoka, Japan 
j Section of Cardiology, Department of Medicine, Tulane University School of Medicine, New Orleans, LA 
k Division of Cardiovascular Medicine, New York University Grossman School of Medicine, New York, NY 

Reprint requests: Toshiki Kuno, MD, PhD, Cardiology Division, Massachusetts General Hospital, Harvard Medical School, 55 Fruit Street, GRB 800, Boston, MA, 02114, USA.Cardiology Division, Massachusetts General HospitalHarvard Medical School55 Fruit Street, GRB 800BostonMA02114USA

Résumé

Background

It is uncertain whether the efficacy and safety of dual antiplatelet therapy (DAPT) in patients with high bleeding risk (HBR) vary according to DAPT duration and stent type (eg, durable polymer drug-eluting stents (DP-DESs), biodegradable polymer DESs (BP-DESs), or polymer-free drug-coated stents (PF-DCSs)). We aimed to study the stent type and DAPT duration appropriate for patients with HBR.

Methods

PubMed and EMBASE were searched until October 2023. Randomized controlled trials (RCTs) involving patients with HBR that compared standard DAPT (6-12 months) with DP- or BP-DES versus short DAPT (≤3 months) with DP- or BP-DES or PF-DCS or bare-metal stent (BMS) were identified. The primary efficacy outcome was major adverse cardiovascular events (MACEs), defined as cardiovascular death, myocardial infarction (MI), and stroke. The primary safety outcome was major bleeding. Secondary outcomes included MI and stent thrombosis (ST). We performed a network meta-analysis using a random effects model.

Results

Thirteen RCTs with a total of 19,418 patients with HBR were included. Compared to standard DAPT with DP-DES, short DAPT with BMS was associated with a higher risk of MACE and MI. For major bleeding, short DAPT strategies were associated with a lower risk than standard DAPT strategies (e.g. short DAPT with DP-DES vs standard DAPT with DP-DES; HR[95% CI]: 0.48[0.28-0.82]). Interestingly, the use of BP-DES was associated with a higher risk of ST than DP-DES (e.g. standard DAPT with BP-DES vs short DAPT with DP-DES; HR[95% CI]: 2.65[1.03-6.79]).

Conclusions

In patients with HBR who underwent percutaneous coronary intervention, a short DAPT strategy with DP-DES should be used since it offers the best combination of efficacy and safety.

Le texte complet de cet article est disponible en PDF.

Plan


 All authors take responsibility for all aspects of the reliability and freedom from bias of the data presented and their discussed interpretation.
 Brief title: DAPT duration and stent type in HBR patients.


© 2024  Elsevier Inc. Tous droits réservés.
Ajouter à ma bibliothèque Retirer de ma bibliothèque Imprimer
Export

    Export citations

  • Fichier

  • Contenu

Vol 279

P. 9-19 - janvier 2025 Retour au numéro
Article précédent Article précédent
  • Rationale and design of the multicentric randomized EVAOLD trial: Evaluation of a strategy guided by imaging versus routine invasive strategy in elderly patients with ischemia
  • Gilles Barone-Rochette, Gerald Vanzetto, Nicolas Danchin, Philippe Gabriel Steg, Olivier Hanon, Clemence Charlon, Sandra David-Tchouda, Gaetan Gavazzi, Tabassome Simon, Jean-Luc Bosson, EVAOLD study investigator
| Article suivant Article suivant
  • Effects of fortified eggs and time-restricted eating on cardiometabolic health: The prosperity trial
  • Nina Nouhravesh, Josephine Harrington, Laura H. Aberle, Cynthia L. Green, Kathleen Voss, Dave Holdsworth, Kurt Misialek, Bartel T. Slaugh, Mandee Wieand, William S. Yancy, Neha Pagidipati, Robert J. Mentz

Bienvenue sur EM-consulte, la référence des professionnels de santé.
L’accès au texte intégral de cet article nécessite un abonnement.

Déjà abonné à cette revue ?

Mon compte


Plateformes Elsevier Masson

Déclaration CNIL

EM-CONSULTE.COM est déclaré à la CNIL, déclaration n° 1286925.

En application de la loi nº78-17 du 6 janvier 1978 relative à l'informatique, aux fichiers et aux libertés, vous disposez des droits d'opposition (art.26 de la loi), d'accès (art.34 à 38 de la loi), et de rectification (art.36 de la loi) des données vous concernant. Ainsi, vous pouvez exiger que soient rectifiées, complétées, clarifiées, mises à jour ou effacées les informations vous concernant qui sont inexactes, incomplètes, équivoques, périmées ou dont la collecte ou l'utilisation ou la conservation est interdite.
Les informations personnelles concernant les visiteurs de notre site, y compris leur identité, sont confidentielles.
Le responsable du site s'engage sur l'honneur à respecter les conditions légales de confidentialité applicables en France et à ne pas divulguer ces informations à des tiers.


Tout le contenu de ce site: Copyright © 2024 Elsevier, ses concédants de licence et ses contributeurs. Tout les droits sont réservés, y compris ceux relatifs à l'exploration de textes et de données, a la formation en IA et aux technologies similaires. Pour tout contenu en libre accès, les conditions de licence Creative Commons s'appliquent.