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Literature reviews and special ar tides. Generally they are solicited by the editor and are 4, 000 to 7, 000 words excluding references. Persons interested in submitting such material should consult the editor. Reviews should focus on the literature of the last two to three years and should include an abstract. Brief reports. The maximum length is 1, 200 words, plus no more than ten references and one table or figure. Reports of unusual cases. Such re ports, describing highly unusual or dif ficult patients and their management, should not exceed 1, 200 words and ten references. They should consist of a brief literature review, an account of the case and its treatment, and a dis cussion. Open Forum, letters. The Open Fo rum section contains letters to the editor plus other short comment and opinion. Letters published at the dis cretion of the editor ; can be no more than 500 words plus a maximum of five references, and must be double and plendil. PLAVIX indication expanded to include patients with any acute coronary syndromes ACS ; PARIS, France, and PRINCETON, New Jersey - September 7, 2006 Sanofi-aventis EURONEXT: SAN and NYSE: SNY ; and Bristol-Myers Squibb Company NYSE: BMY ; announced today that the European Commission has granted a new indication for the antiplatelet agent PLAVIX clopidogrel bisulfate ; to include patients with ST-segment Elevation acute Myocardial Infarction STEMI ; who are eligible for thrombolytic therapy. STEMI is a severe heart attack in which an artery supplying the heart with blood is generally blocked completely.1 These blockages are caused by clot formation in the coronary arteries, which is associated with an underlying disease known as atherothrombosis.2 PLAVIX is a prescription antiplatelet medicine taken once a day that helps keep platelets in the blood from sticking together and forming clots. PLAVIX is approved for early and long term risk reduction in patients at risk for atherothrombotic events. The new indication is based on the findings of two clinical trials that treated patients who had STEMI with PLAVIX administered on a background of standard therapy, including ASA. "PLAVIX taken with ASA has previously been shown to reduce the risk of death, recurrent heart attacks or stroke in patients with unstable angina or less severe heart attacks, " said Keith A.A. Fox, Professor of Cardiology, University of Edinburgh, Scotland. "Now, based on the results of two clinical trials, CLARITY-TIMI 28 and COMMIT CCS-2, clopidogrel has been approved by the European Commission as showing benefit, together with ASA acetyl salicylic acid ; , in patients with the most severe types of heart attacks. With this new guidance from the European Commission, clopidogrel shows benefit in patients across the spectrum of acute coronary syndrome." There are approximately 10 million heart attacks per year worldwide; 3 and 3 million are STEMI events.4 In 2005, for the United Kingdom, France, Germany, Italy and Spain, there were more than 1 million acute coronary syndrome events, of which 25% were STEMI.13 Patients who have experienced STEMI are also at high risk of another heart attack, stroke or death.5. Nations imposes a pharmacy as instructions plavix to buy become more and potassium.
Workshop themes contents presentations ; Generally there was a similar good satisfaction with all the presentations and the identified subthemes. The health issues in schools were particularly well received and commented upon as an area where a lot of effort should be placed, based on the KEDAHR generated knowledge. Many of the other themes were also observed as bringing lots of useful information to the participants, with a few critics of some being too brief on the subject. Group work The central aim of the workshop was the interaction between researchers and users of health knowledge, enabling action-oriented research to be identified and health policy recommendations to evolve. In order to succeed in this, high commitment from all the participants to involve themselves in the group process was needed. This was unfortunately not accomplished to a fully satisfactory level. The tendency of some group members to not join the groups resulted in variation of group competency and resulted in a need to merge two groups in order to secure competency in discussions. Although the group process did not succeed exactly as intended, important linkages between KEDAHR competences and the Ministry of Health and the Ministry of Education were established in connection with the health education focus. The group works' contribution to the final discussion and conclusion was both comprehensive and targeted. Among the participants the group work was rated as acceptable as ranking was influenced by the observations on lack of commitment from other group members, but also acknowledged the inspiration occurring when researchers and users meet. Overall relevance and quality of the workshop process and results The participants were very satisfied with the workshop, finding it extremely relevant and of high quality. The intention of bringing users and researchers together, in order to learn from and supplement each other, was found to be an important experience needed for future health achievements. Identified workshop weaknesses were mostly of practical character, for instance concerning poor time keeping. The relatively little time spent on the health systems theme was also identified as a workshop shortcoming. Among strengths of the workshop, the ability to identify research gaps, and the need to involve stakeholders in the research process was pointed out.