Abbonarsi

A randomized trial comparing clopidogrel versus ticlopidine therapy in patients undergoing infarct artery stenting for acute myocardial infarction with abciximab as adjunctive therapy - 21/08/11

Doi : 10.1016/j.ahj.2005.04.010 
Guido Parodi, MD, PhD, FESC a, , Roberto Sciagrà, MD b, Angela Migliorini, MD a, Gentian Memisha, MD a, Guia Moschi, MD a, Renato Valenti, MD a, Alberto Pupi, MD b, David Antoniucci, MD a
a Division of Cardiology, Careggi Hospital, Florence, Italy 
b Nuclear Medicine Unit, Department of Clinical Physiopathology, University of Florence, Florence, Italy 

Reprint requests: Guido Parodi, MD, PhD, FESC, Division of Cardiology, Careggi Hospital, Viale Morgagni 85, I-50134, Florence, Italy.

Riassunto

Aim

To evaluate the impact of a clopidogrel therapy on the effectiveness of myocardial reperfusion in patients with ST-segment elevation acute myocardial infarction (AMI) undergoing routine infarct-related artery (IRA) stent implantation and receiving routine abciximab therapy.

Background

Inflammatory processes after mechanical restoration of flow in AMI play a central role in decreasing the effectiveness of reperfusion at microcirculatory level. Several studies suggest that clopidogrel may exert a protective effect against adverse cardiovascular events by virtue of its anti-inflammatory properties.

Methods

A total of 133 patients with a first ST-elevation AMI were randomized to clopidogrel (600-mg loading dose before IRA stenting followed by 75 mg daily, n = 66) or ticlopidine (500 mg before IRA stenting followed by 250 mg twice daily, n = 67). The primary end point was scintigraphic infarct size at 1 month. The secondary end points were ST-segment elevation resolution within 3 hours of procedure and 1-month clinical outcome, as a composite of death, reinfarction, target vessel revascularization, and stroke within 1 month of the index procedure.

Results

The 1-month technetium 99m sestamibi scintigraphy revealed similar infarct size (16.2% ± 14.6% vs 15.0% ± 14.1%, P = .703) and severity (0.48 ± 0.18 vs 0.49 ± 0.15, P = .592) in the clopidogrel group as compared with the ticlopidine group. Three-hour ST-segment resolution rate was similar in the 2 study groups (86% vs 89%, P = .642). At 1 month, there was no difference in major cardiovascular adverse event rate (3% vs 3%, P = .988). Discontinuation of thienopiridine therapy within the first month occurred in no patient randomized to clopidogrel and in 3 (4.5%) patients randomized to ticlopidine (P = .082).

Conclusion

Clopidogrel has no impact on the effectiveness of myocardial reperfusion in patients with AMI treated routinely with stenting and abciximab. However, clopidogrel, administered as a 600-mg loading dose followed by 75 mg daily, is safe and at least as effective as the standard ticlopidine therapy in this subgroup of patients.

Il testo completo di questo articolo è disponibile in PDF.

Mappa


 This study was supported by a research grant from the ARCARD ONLUS Foundation, Florence, Italy.


© 2005  Mosby, Inc. Tutti i diritti riservati.
Aggiungere alla mia biblioteca Togliere dalla mia biblioteca Stampare
Esportazione

    Citazioni Export

  • File

  • Contenuto

Vol 150 - N° 2

P. 220.e1-220.e5 - agosto 2005 Ritorno al numero
Articolo precedente Articolo precedente
  • Left ventricular ejection fraction to predict early mortality in patients with non–ST-segment elevation acute coronary syndromes
  • Xavier Bosch, Pierre Théroux
| Articolo seguente Articolo seguente
  • Heart disease epidemic in Pakistan: Women and men at equal risk
  • Tazeen H. Jafar, Fahim H. Jafary, Saleem Jessani, Nish Chaturvedi

Benvenuto su EM|consulte, il riferimento dei professionisti della salute.
L'accesso al testo integrale di questo articolo richiede un abbonamento.

Già abbonato a @@106933@@ rivista ?

@@150455@@ Voir plus

Il mio account


Dichiarazione CNIL

EM-CONSULTE.COM è registrato presso la CNIL, dichiarazione n. 1286925.

Ai sensi della legge n. 78-17 del 6 gennaio 1978 sull'informatica, sui file e sulle libertà, Lei puo' esercitare i diritti di opposizione (art.26 della legge), di accesso (art.34 a 38 Legge), e di rettifica (art.36 della legge) per i dati che La riguardano. Lei puo' cosi chiedere che siano rettificati, compeltati, chiariti, aggiornati o cancellati i suoi dati personali inesati, incompleti, equivoci, obsoleti o la cui raccolta o di uso o di conservazione sono vietati.
Le informazioni relative ai visitatori del nostro sito, compresa la loro identità, sono confidenziali.
Il responsabile del sito si impegna sull'onore a rispettare le condizioni legali di confidenzialità applicabili in Francia e a non divulgare tali informazioni a terzi.


Tutto il contenuto di questo sito: Copyright © 2026 Elsevier, i suoi licenziatari e contributori. Tutti i diritti sono riservati. Inclusi diritti per estrazione di testo e di dati, addestramento dell’intelligenza artificiale, e tecnologie simili. Per tutto il contenuto ‘open access’ sono applicati i termini della licenza Creative Commons.