PMID- 16387830 OWN - NLM STAT- MEDLINE DCOM- 20060814 LR - 20181113 IS - 1468-201X (Electronic) IS - 1355-6037 (Print) IS - 1355-6037 (Linking) VI - 92 IP - 8 DP - 2006 Aug TI - Impact of chronic oral anticoagulation on management and outcomes of patients with acute myocardial infarction: data from the RICO survey. PG - 1077-83 AB - OBJECTIVE: To determine the prevalence of chronic oral anticoagulant drug treatment (COA) among patients with acute myocardial infarction (AMI) and its impact on management and outcome. METHODS: All patients with ST segment elevation AMI on the RICO (a French regional survey for AMI) database were included in this analysis. COA was defined as continuous use >or= 48 hours before AMI. RESULTS: Among the 2112 patients with ST elevation myocardial infarction (STEMI), 93 (4%) patients were receiving COA. These patients were older and more likely to have a history of hypertension, diabetes and prior myocardial infarction than patients without COA. In addition, fewer patients who received COA underwent reperfusion therapy or received an antiplatelet agent (aspirin/thienopyridines). Moreover, patients receiving COA experienced a higher incidence of in-hospital major adverse events (death, recurrent myocardial infarction or major bleeding, p = 0.005). Multivariate analysis showed that only ejection fraction, current smoking and multiple vessel disease, but not COA, were independent predictive factors for major adverse events. In contrast, COA was an independent predictive factor for heart failure when adjusted for age, diabetes, creatinine clearance, reperfusion, heparin and glycoprotein IIb/IIIa inhibitors (odds ratio 2.06, CI 95% 1.23 to 3.43, p = 0.005). CONCLUSION: In this population based registry, patients with STEMI with prior use of COA constituted a fairly large group (4%) with an overall higher baseline risk profile than that of patients without COA. Fewer in the COA group received reperfusion therapy or aggressive antithrombotic treatment and they experienced more adverse in-hospital outcomes. Thus, further studies are warranted to develop specific management strategies for this high risk group. FAU - Oudot, A AU - Oudot A AD - Service de Cardiologie, CHU Bocage, Dijon, France. FAU - Steg, P G AU - Steg PG FAU - Danchin, N AU - Danchin N FAU - Dentan, G AU - Dentan G FAU - Zeller, M AU - Zeller M FAU - Sicard, P AU - Sicard P FAU - Buffet, P AU - Buffet P FAU - Laurent, Y AU - Laurent Y FAU - Janin-Manificat, L AU - Janin-Manificat L FAU - L'Huillier, I AU - L'Huillier I FAU - Beer, J C AU - Beer JC FAU - Makki, H AU - Makki H FAU - Morel, P AU - Morel P FAU - Cottin, Y AU - Cottin Y LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20051230 PL - England TA - Heart JT - Heart (British Cardiac Society) JID - 9602087 RN - 0 (Anticoagulants) RN - 0 (Fibrinolytic Agents) RN - 0 (Platelet Aggregation Inhibitors) SB - IM CIN - Heart. 2006 Aug;92(8):1011-2. PMID: 16844847 MH - Administration, Oral MH - Aged MH - Anticoagulants/administration & dosage/*adverse effects MH - Drug Interactions MH - Female MH - Fibrinolytic Agents/*therapeutic use MH - France/epidemiology MH - Humans MH - Male MH - Middle Aged MH - Multivariate Analysis MH - Myocardial Infarction/*drug therapy/epidemiology MH - Myocardial Reperfusion/statistics & numerical data MH - Platelet Aggregation Inhibitors/*therapeutic use MH - Prevalence MH - Prognosis MH - Recurrence MH - Risk Factors PMC - PMC1861111 EDAT- 2006/01/03 09:00 MHDA- 2006/08/15 09:00 PMCR- 2009/08/01 CRDT- 2006/01/03 09:00 PHST- 2006/01/03 09:00 [pubmed] PHST- 2006/08/15 09:00 [medline] PHST- 2006/01/03 09:00 [entrez] PHST- 2009/08/01 00:00 [pmc-release] AID - hrt.2005.074070 [pii] AID - ht74070 [pii] AID - 10.1136/hrt.2005.074070 [doi] PST - ppublish SO - Heart. 2006 Aug;92(8):1077-83. doi: 10.1136/hrt.2005.074070. Epub 2005 Dec 30.