Therapeutic strategies after coronary stenting in chronically anticoagulated patients: the MUSICA study
- A Sambola1,
- I Ferreira-González1,11,
- J Angel1,
- F Alfonso2,
- J Maristany3,
- O Rodríguez4,
- H Bueno5,
- J R López-Minguez6,
- J Zueco7,
- F Fernández-Avilés5,
- A San Román8,
- B Prendergast9,
- V Mainar10,
- D García-Dorado1,
- P Tornos1
- 1Area del Cor Hospital, Universitari Vall d’Hebron, Barcelona, Spain
- 2Hospital Clínico de Madrid, Madrid, Spain
- 3Hospital de Bellvitge, Barcelona, Spain
- 4Hospital Germans Trias i Pujol, Barcelona, Spain
- 5Hospital Gregorio Marañón, Madrid, Spain
- 6Hospital Infanta Cristina, Badajoz, Spain
- 7Hospital de Valdecilla, Santander, Spain
- 8ICICOR Valladolid, Spain
- 9The John Radcliffe Hospital, Oxford, UK
- 10Hospital Universitario de Alicante, Alicant, Spain
- 11CIBER de Epidemiología y Salud Pública (CIBERESP), Barcelona, Spain
- Correspondence to Dr A Sambola, Servei de Cardiologia, Hospital Universitari Vall d’ Hebron, P Vall d’Hebron 119–129, 08035 Barcelona, Spain; asambola{at}vhebron.net
- Accepted 5 May 2009
- Published Online First 17 May 2009
Abstract
Objectives: To identify the therapeutic regimens used at discharge in patients receiving oral anticoagulant therapy (OAT) who undergo stenting percutaneous coronary intervention and stent implantation (PCI-S), and to assess the safety and efficacy associated with different therapeutic regimens according to thromboembolic risk.
Design: A prospective multicentre registry.
Setting: In hospital, after discharge and follow-up by telephone call.
Patients and methods: 405 patients (328 male/77 female; mean (SD) age 71 (9) years) receiving OAT who underwent PCI-S between November 2003 and June 2006 from nine catheterisation laboratories of tertiary care teaching hospitals in Spain and one in the United Kingdom were included.
Results: Three therapeutic regimens were identified at discharge: triple therapy (TT)—that is, any anticoagulant (AC) plus double antiplatelet therapy (DAT; 278 patients (68.6%); AC and a single antiplatelet (AC+AT; 46 (11.4%)) and DAT only (81 (20%)). At 6 months, patients receiving TT showed the greatest rate of bleeding events. No patients receiving DAT at low thromboembolic risk presented a bleeding event (14.8% receiving TT, 11.8% receiving AC+AT and 0% receiving DAT, p = 0.033) or cardiovascular event (6.7% receiving TT, 0% receiving AC+AT and 0% receiving DAT, p = 0.126). The combination of AC+AT showed the worst rate of adverse events in the whole cohort, especially in patients at moderate–high thromboembolic risk.
Conclusions: In patients receiving OAT, TT was the most commonly used regimen after PCI-S. DAT was associated with the lowest rate of bleeding events and a similar efficacy to TT in patients at low thromboembolic risk. TT should probably be restricted to patients at moderate–high thromboembolic risk.
Footnotes
-
Funding The Spanish Network for Research in Cardiovascular diseases REIPI RD 06/0014/0025.
-
Competing interests None.
-
Ethics approval Approval from the ethics committee of each participant hospital.
-
Provenance and peer review Not commissioned; externally peer reviewed.









