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Acute coronary syndromes
Early glycoprotein IIb–IIIa inhibitors in primary angioplasty (EGYPT) cooperation: an individual patient data meta-analysis
  1. G De Luca1,2,
  2. C M Gibson3,
  3. F Bellandi4,
  4. S Murphy3,
  5. M Maioli4,
  6. M Noc5,
  7. U Zeymer6,
  8. D Dudek7,
  9. H-R Arntz8,
  10. S Zorman5,
  11. H M Gabriel9,
  12. A Emre10,
  13. D Cutlip11,
  14. G Biondi-Zoccai12,
  15. T Rakowski7,
  16. M Gyongyosi13,
  17. P Marino1,
  18. K Huber14,
  19. A W J van’t Hof15
  1. 1
    Division of Cardiology, “Maggiore della Carità” Hospital, Eastern Piedmont University, Novara, Italy
  2. 2
    Centro di Biotecnologie per la Ricerca Medica Applicata (BRMA), Eastern Piedmont University, Novara, Italy
  3. 3
    TIMI Study Group, Cardiovascular Division, Brigham and Women’s Hospital, Boston, Massachusetts, USA
  4. 4
    Division of Cardiology, Prato Hospital, Prato, Italy
  5. 5
    Center for Intensive Internal Medicine, University Medical Center, Ljubljana, Slovenia
  6. 6
    Division of Cardiology, Herzzentrum Ludwigshafen, Ludwigshafen, Germany
  7. 7
    II Department of Cardiology, Institute of Cardiology, Jagiellonian University, Krakow, Poland
  8. 8
    Medizinische Klinik II, Kardiologie/Pulmologie, Charité, Campus Benjamin Franklin, Berlin, Germany
  9. 9
    Division of Cardiology, Hospital de Santa Maria, Lisboa, Portugal
  10. 10
    Siyami Ersek Thoracic and Cardiovascular Surgery Center, Istanbul, Turkey
  11. 11
    Interventional Cardiology Section, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA
  12. 12
    Division of Cardiology, University of Turin, Turin, Italy
  13. 13
    Department of Cardiology, Medical University of Vienna, Vienna, Austria
  14. 14
    3rd Department of Medicine (Cardiology and Emergency Medicine) Wilhelminen Hospital, Vienna, Austria
  15. 15
    Division of Cardiology, Hospital “De Weezenlanden”, Zwolle, The Netherlands
  1. Dr G De Luca, Division of Cardiology, “Maggiore della Carità” Hospital, Eastern Piedmont University, Novara, Italy; giuseppe.deluca{at}maggioreosp.novara.it

Abstract

Background: Even though time-to-treatment has been shown to be a determinant of mortality in primary angioplasty, the potential benefits from early pharmacological reperfusion by glycoprotein (Gp) IIb–IIIa inhibitors are still unclear. The aim of this meta-analysis was to combine individual data from all randomised trials conducted on facilitated primary angioplasty by the use of early Gp IIb–IIIa inhibitors.

Methods and results: The literature was scanned by formal searches of electronic databases (MEDLINE, EMBASE) from January 1990 to October 2007. All randomised trials on facilitation by the early administration of Gp IIb–IIIa inhibitors in ST-segment elevation myocardial infarction (STEMI) were examined. No language restrictions were enforced. Individual patient data were obtained from 11 out of 13 trials, including 1662 patients (840 patients (50.5%) randomly assigned to early and 822 patients (49.5%) to late Gp IIb–IIIa inhibitor administration). Preprocedural Thrombolysis in Myocardial Infarction Study (TIMI) grade 3 flow was more frequent with early Gp IIb–IIIa inhibitors. Postprocedural TIMI 3 flow and myocardial blush grade 3 were higher with early Gp IIb–IIIa inhibitors but did not reach statistical significance except for abciximab, whereas the rate of complete ST-segment resolution was significantly higher with early Gp IIb–IIIa inhibitors. Mortality was not significantly different between groups, although early abciximab demonstrated improved survival compared with late administration, even after adjustment for clinical and angiographic confounding factors.

Conclusions: This meta-analysis shows that pharmacological facilitation with the early administration of Gp IIb–IIIa inhibitors in patients undergoing primary angioplasty for STEMI is associated with significant benefits in terms of preprocedural epicardial recanalisation and ST-segment resolution, which translated into non-significant mortality benefits except for abciximab.

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Footnotes

  • Competing interests: GDL received lecture fees from Merck Sharp & Dohme and Eli Lilly; MG received lecture fees from Schering Plough; UZ received research grants and lecture fees from ESSEX Pharma, GSK and Eli Lilly; DD received lecture fees from Eli Lilly; H-RA received an unrestricted grant from Eli Lilly and lecture fees from Boerhinger Ingelheim and Sanofi Aventis; GB-Z is a consultant to Boston Scientific, Cordis and Mediolanum Cardio Research and received lecture fees from Bristol Myers Squibb; AWJvH received lecture fees from Merck Sharp & Dohme.

  • Contributors: GDL: Conception and design; acquisition of data; analysis and interpretation of data; drafting of the manuscript; statistical analysis. AWJvH: Conception and design; analysis and interpretation of data; drafting of the manuscript; statistical analysis. GB-Z: statistical analysis; critical revision of the manuscript; supervision. CMG, FB, SM, MM, MN, UZ, DD, H-RA, SZ, HMG, AE, DC, GB-Z, TR, MG, PM, KH: administrative, technical or material support; critical revision of the manuscript; supervision. All authors declare that they participated in the study and that they have seen and approved the final version.