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<title>QJM - current issue</title>
<link>http://qjmed.oxfordjournals.org</link>
<description>QJM - RSS feed of current issue</description>
<prism:eIssn>1460-2393</prism:eIssn>
<prism:coverDisplayDate>September 2008</prism:coverDisplayDate>
<prism:publicationName>QJM</prism:publicationName>
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<item rdf:about="http://qjmed.oxfordjournals.org/cgi/content/short/101/9/673?rss=1">
<title><![CDATA[Elements: In this month's issue]]></title>
<link>http://qjmed.oxfordjournals.org/cgi/content/short/101/9/673?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Bannon, M.]]></dc:creator>
<dc:date>2008-08-22</dc:date>
<dc:identifier>info:doi/10.1093/qjmed/hcn103</dc:identifier>
<dc:title><![CDATA[Elements: In this month's issue]]></dc:title>
<dc:publisher>Association of Physicians</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>101</prism:volume>
<prism:endingPage>674</prism:endingPage>
<prism:publicationDate>2008-09-01</prism:publicationDate>
<prism:startingPage>673</prism:startingPage>
<prism:section>Editorial</prism:section>
</item>

<item rdf:about="http://qjmed.oxfordjournals.org/cgi/content/short/101/9/675?rss=1">
<title><![CDATA[Advances in tumour immunotherapy]]></title>
<link>http://qjmed.oxfordjournals.org/cgi/content/short/101/9/675?rss=1</link>
<description><![CDATA[
<p>The clinical goal of tumour immunotherapy is to provide either active or passive immunity against malignancies by harnessing the immune system to target tumours. Although vaccination is an effective strategy to prevent infectious disease, it is less effective in the therapeutic setting for cancer treatment, which might be related to the low immunogenicity of tumour antigens and the reduced immunocompetence of cancer patients. Recent advances in technology have led to the development of passive immunotherapy approaches that utilize the unique specificity of antibodies and T cell receptors to target selected antigens on tumour cells. These approaches are likely to benefit patients and alter the way that clinicians treat malignant disease. In this article we review recent advances in the immunotherapy of cancer, focusing on new strategies to enhance the efficacy of passive immunotherapy with monoclonal antibodies and antigen-specific T cells.</p>
]]></description>
<dc:creator><![CDATA[King, J., Waxman, J., Stauss, H.]]></dc:creator>
<dc:date>2008-08-22</dc:date>
<dc:identifier>info:doi/10.1093/qjmed/hcn050</dc:identifier>
<dc:title><![CDATA[Advances in tumour immunotherapy]]></dc:title>
<dc:publisher>Association of Physicians</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>101</prism:volume>
<prism:endingPage>683</prism:endingPage>
<prism:publicationDate>2008-09-01</prism:publicationDate>
<prism:startingPage>675</prism:startingPage>
<prism:section>Reviews</prism:section>
</item>

<item rdf:about="http://qjmed.oxfordjournals.org/cgi/content/short/101/9/685?rss=1">
<title><![CDATA[The diabetic foot]]></title>
<link>http://qjmed.oxfordjournals.org/cgi/content/short/101/9/685?rss=1</link>
<description><![CDATA[
<p>Diabetes is reaching epidemic proportions and with it carries the risk of complications. Disease of the foot is among one of the most feared complications of diabetes. The ultimate endpoint of diabetic foot disease is amputation, which is associated with significant morbidity and mortality, besides having immense social, psychological and financial consequences. As the majority of amputations are preceded by foot ulceration, it is crucial to identify those at an increased risk. Diabetic foot ulcers may develop as a result of neuropathy, ischaemia or both and when infection complicates a foot ulcer, the combination can become limb and life threatening. Structural abnormalities such as calluses, bunions, hammer toes, claw toes, flat foot and rocker bottom foot need to be identified and managed.</p>
]]></description>
<dc:creator><![CDATA[Khanolkar, M.P., Bain, S.C., Stephens, J.W.]]></dc:creator>
<dc:date>2008-08-22</dc:date>
<dc:identifier>info:doi/10.1093/qjmed/hcn027</dc:identifier>
<dc:title><![CDATA[The diabetic foot]]></dc:title>
<dc:publisher>Association of Physicians</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>101</prism:volume>
<prism:endingPage>695</prism:endingPage>
<prism:publicationDate>2008-09-01</prism:publicationDate>
<prism:startingPage>685</prism:startingPage>
<prism:section>Reviews</prism:section>
</item>

<item rdf:about="http://qjmed.oxfordjournals.org/cgi/content/short/101/9/697?rss=1">
<title><![CDATA[Advanced chronic obstructive pulmonary disease: rethinking models of care]]></title>
<link>http://qjmed.oxfordjournals.org/cgi/content/short/101/9/697?rss=1</link>
<description><![CDATA[
<p>Chronic obstructive pulmonary disease (COPD) is unique among leading causes of death in western society. Prevalence, associated morbidity and attributable mortality continue to rise. The resultant cost in quality of life to patients, families and to the health care system in general, demands improvements in the prevention and treatment of this common and ultimately debilitating condition. Traditional healthcare approaches to COPD, based on the biomedical model, have focused on the underlying pathophysiology of <I>disease</I> within which patients receive episodic care aimed at treating and preventing acute exacerbations. In contrast, patients living with COPD interpret it from an individually experienced <I>illness</I> perspective impacted by unique contextual factors that influence personal meaning. The psychosocial ramifications that follow the inexorable decline in capacity and independence are powerful forces shaping the experience of patients living with advancing COPD. The dominant role and impact of psychosocial effects on quality of life in advancing COPD require us to rethink our approach to care to more effectively address these more elusive yet chronically troublesome issues.</p>
]]></description>
<dc:creator><![CDATA[Simpson, A.C., Rocker, G.M.]]></dc:creator>
<dc:date>2008-08-22</dc:date>
<dc:identifier>info:doi/10.1093/qjmed/hcn087</dc:identifier>
<dc:title><![CDATA[Advanced chronic obstructive pulmonary disease: rethinking models of care]]></dc:title>
<dc:publisher>Association of Physicians</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>101</prism:volume>
<prism:endingPage>704</prism:endingPage>
<prism:publicationDate>2008-09-01</prism:publicationDate>
<prism:startingPage>697</prism:startingPage>
<prism:section>Reviews</prism:section>
</item>

<item rdf:about="http://qjmed.oxfordjournals.org/cgi/content/short/101/9/705?rss=1">
<title><![CDATA[Prevalence trends for myocardial infarction and conventional risk factors among Greek adults (2002-06)]]></title>
<link>http://qjmed.oxfordjournals.org/cgi/content/short/101/9/705?rss=1</link>
<description><![CDATA[
<p><b>Aim:</b> To examine trends in the prevalence of myocardial infarction (MI) and conventional risk factors in Greek adults between 2002 and 2006.</p>
<p><b>Design:</b> Repeated cross-sectional study.</p>
<p><b>Methods:</b> Self-reported data from surveys given in Salamis during two election days in 2002 and 2006 were analysed. The same sampling method and procedures were used on both surveys. The study sample included 2805 and 3478 subjects (&gt;=20 years) in 2002 and 2006, respectively, with similar age and sex distribution to the target population.</p>
<p><b>Results:</b> The prevalence of MI increased from 4.1% (men, 6.3%; women, 1.9%) in 2002 to 4.8% (men, 7.3%; women, 2.2%) in 2006 (<I>P</I> = 0.18). At the same time, prevalence rates of major risk factors were as follows: diabetes increased from 8.7% to 10.3% (<I>P</I> = 0.037), hypertension from 20.1% to 25.7% (<I>P</I> &lt; 0.001) and hypercholesterolemia (cholesterol &gt;240 mg/dl or the use of cholesterol-lowering medication) increased from 17.5% to 22.3% (<I>P</I> &lt; 0.001). Prevalence of current smokers in 2002 (defined as persons who smoked &gt;=5 cigarettes/day) was 37.0% and in 2006 (defined as those who smoked &gt;=1 cigarettes/day) was 40.1%. Logistic regression analysis showed that the aforementioned risk factors were significantly associated with MI in both surveys; the factor that showed the greatest magnitude of association with MI was hypercholesterolemia, followed by diabetes, hypertension and smoking.</p>
<p><b>Conclusions:</b> These findings show that, in the Greek population, prevalence of MI continues to rise (at ~4% per year). This trend seems to be driven by a persistently high prevalence of smoking and the rapidly increasing burden of diabetes, hypertension and hypercholesterolemia.</p>
]]></description>
<dc:creator><![CDATA[Gikas, A., Sotiropoulos, A., Panagiotakos, D., Pastromas, V., Papazafiropoulou, A., Pappas, S.]]></dc:creator>
<dc:date>2008-08-22</dc:date>
<dc:identifier>info:doi/10.1093/qjmed/hcn076</dc:identifier>
<dc:title><![CDATA[Prevalence trends for myocardial infarction and conventional risk factors among Greek adults (2002-06)]]></dc:title>
<dc:publisher>Association of Physicians</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>101</prism:volume>
<prism:endingPage>712</prism:endingPage>
<prism:publicationDate>2008-09-01</prism:publicationDate>
<prism:startingPage>705</prism:startingPage>
<prism:section>Original Papers</prism:section>
</item>

<item rdf:about="http://qjmed.oxfordjournals.org/cgi/content/short/101/9/713?rss=1">
<title><![CDATA[Physical activity is negatively associated with the metabolic syndrome in the elderly]]></title>
<link>http://qjmed.oxfordjournals.org/cgi/content/short/101/9/713?rss=1</link>
<description><![CDATA[
<p><b>Background:</b> An inverse association between physical activity and metabolic syndrome has been reported in several cohorts, but very few specific studies are available in the elderly, in whom neurological and musculo-skeletal diseases are expected to lead to a remarkable age-related decline of physical activity.</p>
<p><b>Aim and Design:</b> The relationships among physical activity, insulin resistance and metabolic syndrome were assessed in a cross-sectional study concerning 1144 subjects aged 65&ndash;91 years resident in Pianoro (northern Italy). Household and leisure-time activities were assessed by a self-administered questionnaire (Physical Activity Scale for Elderly&mdash;PASE). Routine clinical and biochemical data (including fasting insulin) were used to assess insulin resistance [Homeostasis Model Assessment (HOMA) method] and the prevalence of metabolic syndrome.</p>
<p><b>Results:</b> All PASE scores were inversely correlated with waist circumference, triglycerides and HOMA index, with highest significance for leisure-time activities (<I>P</I> &lt;= 0.005). The PASE score for household activities was also correlated inversely with blood glucose (<I>P</I> &lt; 0.05), and directly with HDL cholesterol (<I>P</I> &lt; 0.001). In logistic regression analysis, the metabolic syndrome was more prevalent among sedentary subjects (corresponding to the low tertile of leisure-time activities) than in the remaining more active population (odds ratio 1.51, 95% confidence interval 1.12&ndash;2.03, <I>P</I> = 0.007), independently of possible confounders.</p>
<p><b>Conclusion:</b> Physical activity is inversely associated with insulin resistance and the metabolic syndrome even in the elderly. Community programs favoring physical activity are expected to significantly improve the health status in these subjects.</p>
]]></description>
<dc:creator><![CDATA[Bianchi, G., Rossi, V., Muscari, A., Magalotti, D., Zoli, M., the Pianoro Study Group]]></dc:creator>
<dc:date>2008-08-22</dc:date>
<dc:identifier>info:doi/10.1093/qjmed/hcn084</dc:identifier>
<dc:title><![CDATA[Physical activity is negatively associated with the metabolic syndrome in the elderly]]></dc:title>
<dc:publisher>Association of Physicians</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>101</prism:volume>
<prism:endingPage>721</prism:endingPage>
<prism:publicationDate>2008-09-01</prism:publicationDate>
<prism:startingPage>713</prism:startingPage>
<prism:section>Original Papers</prism:section>
</item>

<item rdf:about="http://qjmed.oxfordjournals.org/cgi/content/short/101/9/723?rss=1">
<title><![CDATA[Evidence and consequences of spectrum bias in studies of criteria for liver transplant in paracetamol hepatotoxicity]]></title>
<link>http://qjmed.oxfordjournals.org/cgi/content/short/101/9/723?rss=1</link>
<description><![CDATA[
<p><b>Objective:</b> In severe paracetamol hepatotoxicity, orthotopic liver transplant (OLT) is a standard treatment in patients judged to have a hopeless prognosis. The most commonly used criteria to make this decision are the King's College Criteria (KCC). We aimed to compare the expected survival for patients who meet the KCC and do not receive transplant and those who receive OLT.</p>
<p><b>Methods:</b> A systematic review of studies of survival in patients who met the KCC according to whether they were transplanted. Data from these studies was extrapolated to compare long-term survival with and without adjustment for Quality of Life.</p>
<p><b>Results:</b> The survival of patients meeting KCC and undergoing transplant has not been specifically studied. UK data on transplants for acute liver failure indicate 1 and 10 year survival rates of 65 and 44%, respectively. Survival in those without transplant was documented in 15 studies. The average long-term survival rate was 24.9%. Survival was worse in studies originating in the King's unit (13.8 vs. 30.0%). It was apparent that this may be due to spectrum bias occurring in this much larger unit. There was clear evidence that those with the best prognosis were preferentially transplanted at the Kings liver unit, indicating the criteria may perform significantly worse at predicting death without transplant than previously estimated. Even so, for a 20-year-old meeting KCC, the best estimate of life expectancy with transplant (13.5 years) is no better than without (13.4 years). Adjustment for quality of life made OLT clearly a worse option.</p>
<p><b>Conclusion:</b> Criteria for OLT that have a much higher positive predictive value (for death without transplant) are required. Such studies must be conducted only on those who would be considered suitable for transplant. Non-orthotopic liver transplant may be a preferred option in such circumstances, although much more data on survival after this procedure are required.</p>
]]></description>
<dc:creator><![CDATA[Ding, G.K.A., Buckley, N.A.]]></dc:creator>
<dc:date>2008-08-22</dc:date>
<dc:identifier>info:doi/10.1093/qjmed/hcn077</dc:identifier>
<dc:title><![CDATA[Evidence and consequences of spectrum bias in studies of criteria for liver transplant in paracetamol hepatotoxicity]]></dc:title>
<dc:publisher>Association of Physicians</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>101</prism:volume>
<prism:endingPage>729</prism:endingPage>
<prism:publicationDate>2008-09-01</prism:publicationDate>
<prism:startingPage>723</prism:startingPage>
<prism:section>Original Papers</prism:section>
</item>

<item rdf:about="http://qjmed.oxfordjournals.org/cgi/content/short/101/9/731?rss=1">
<title><![CDATA[Factors that affect longevity of intravenous cannulas: a prospective study]]></title>
<link>http://qjmed.oxfordjournals.org/cgi/content/short/101/9/731?rss=1</link>
<description><![CDATA[
<p><b>Background:</b> Few guidelines exist to guide medical personnel on the most successful means of achieving sustained intravenous cannulation. This study examines the impact of gauge and site of intravenous cannulas (IC) on the longevity of ICs in hospitalized patients.</p>
<p><b>Methods:</b> A prospective study was conducted on 500 ICs inserted into patients of St Vincent's Private hospital from December 2005 to June 2006. Patients were followed until the IC had been removed or changed. Statistical analysis was performed using Cox proportional hazards.</p>
<p><b>Results:</b> Of the 500 ICs inserted, 37% were 18 g, 46% were 20 g and 18% were 22 g. Gauge of IC was the most significant predictor of increased longevity of IC (<I>P</I> = 0.0002, RR = 1.17, 95% CI 1.08&ndash;1.27). The median survival of 18, 20 and 22 g were 57 h (95% CI 49&ndash;72), 43 h (95% CI 36&ndash;48.5) and 29 h (95% CI 24&ndash;40.5), respectively. The site of IC placement influenced the longevity of ICs (<I>P</I> = 0.005, RR= 0.7, 95% CI 0.55&ndash;0.9), as did male gender (<I>P</I> = 0.03, RR = 0.76, 95% CI 0.6&ndash;0.97). However in subgroup analysis, the most marked effect on IC longevity was evident in those patients with 18 g placed in the forearm/wrist (median 72 h) with less marked changes in other site/gauge combinations. In contrast, 22 g ICs placed in the hand had a median lifespan of 29 h.</p>
<p><b>Conclusion:</b> IC gauge and site of placement are important factors in determining IC longevity. 18 g ICs placed in the forearm/wrist can considerably increase the longevity of ICs and should be attempted in patients who require sustained cannulation.</p>
]]></description>
<dc:creator><![CDATA[Dillon, M.F., Curran, J., Martos, R., Walsh, C., Walsh, J., Al-Azawi, D., Lee, C.S., O'shea, D.]]></dc:creator>
<dc:date>2008-08-22</dc:date>
<dc:identifier>info:doi/10.1093/qjmed/hcn078</dc:identifier>
<dc:title><![CDATA[Factors that affect longevity of intravenous cannulas: a prospective study]]></dc:title>
<dc:publisher>Association of Physicians</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>101</prism:volume>
<prism:endingPage>735</prism:endingPage>
<prism:publicationDate>2008-09-01</prism:publicationDate>
<prism:startingPage>731</prism:startingPage>
<prism:section>Original Papers</prism:section>
</item>

<item rdf:about="http://qjmed.oxfordjournals.org/cgi/content/short/101/9/737?rss=1">
<title><![CDATA[Adding fresh frozen plasma to rituximab for the treatment of patients with refractory advanced CLL]]></title>
<link>http://qjmed.oxfordjournals.org/cgi/content/short/101/9/737?rss=1</link>
<description><![CDATA[
<p><b>Background:</b> Many patients with chronic lymphocytic leukaemia (CLL) develop progressive, treatment-resistant disease. Rituximab (RTX), a monoclonal antibody targeting CD20 on B lymphocytes and widely used in other indolent B cell neoplasms is less efficacious in CLL, possibly due to associated complement deficiencies.</p>
<p><b>Objective:</b> To examine in open trial whether providing complement by concurrent administration of fresh frozen plasma (FFP) will enhance the effect of RTX in CLL.</p>
<p><b>Setting:</b> Outpatient haematology clinics in Israel and Greece.</p>
<p><b>Patients:</b> Five patients with severe treatment-resistant CLL. All had been previously treated with fludarabine and three also failed treatment with RTX.</p>
<p><b>Intervention:</b> Two units of FFP followed with RTX 375 mg/m<sup>2</sup> as a single agent, repeated every 1&ndash;2 weeks, as needed.</p>
<p><b>Results:</b> A rapid and dramatic clinical and laboratory response was achieved in all patients. Lymphocyte counts dropped markedly followed by shrinkage of lymph nodes and spleen and improvement of the anaemia and thrombocytopenia. This could be maintained over 8 months (median) with additional cycles if necessary. Treatment was well tolerated in all cases.</p>
<p><b>Conclusion:</b> Adding FFP to RTX may provide a useful therapeutic option in patients with advanced CLL resistant to treatment.</p>
]]></description>
<dc:creator><![CDATA[Klepfish, A., Rachmilewitz, E.A., Kotsianidis, I., Patchenko, P., Schattner, A.]]></dc:creator>
<dc:date>2008-08-22</dc:date>
<dc:identifier>info:doi/10.1093/qjmed/hcn085</dc:identifier>
<dc:title><![CDATA[Adding fresh frozen plasma to rituximab for the treatment of patients with refractory advanced CLL]]></dc:title>
<dc:publisher>Association of Physicians</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>101</prism:volume>
<prism:endingPage>740</prism:endingPage>
<prism:publicationDate>2008-09-01</prism:publicationDate>
<prism:startingPage>737</prism:startingPage>
<prism:section>Original Papers</prism:section>
</item>

<item rdf:about="http://qjmed.oxfordjournals.org/cgi/content/short/101/9/741?rss=1">
<title><![CDATA[What ever happened to the Mediterranean diet?]]></title>
<link>http://qjmed.oxfordjournals.org/cgi/content/short/101/9/741?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Birtwhistle, R.]]></dc:creator>
<dc:date>2008-08-22</dc:date>
<dc:identifier>info:doi/10.1093/qjmed/hcn097</dc:identifier>
<dc:title><![CDATA[What ever happened to the Mediterranean diet?]]></dc:title>
<dc:publisher>Association of Physicians</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>101</prism:volume>
<prism:endingPage>742</prism:endingPage>
<prism:publicationDate>2008-09-01</prism:publicationDate>
<prism:startingPage>741</prism:startingPage>
<prism:section>Commentaries</prism:section>
</item>

<item rdf:about="http://qjmed.oxfordjournals.org/cgi/content/short/101/9/743?rss=1">
<title><![CDATA[Physical activity in the elderly--it is never too late!]]></title>
<link>http://qjmed.oxfordjournals.org/cgi/content/short/101/9/743?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Song, S.H.]]></dc:creator>
<dc:date>2008-08-22</dc:date>
<dc:identifier>info:doi/10.1093/qjmed/hcn095</dc:identifier>
<dc:title><![CDATA[Physical activity in the elderly--it is never too late!]]></dc:title>
<dc:publisher>Association of Physicians</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>101</prism:volume>
<prism:endingPage>744</prism:endingPage>
<prism:publicationDate>2008-09-01</prism:publicationDate>
<prism:startingPage>743</prism:startingPage>
<prism:section>Commentaries</prism:section>
</item>

<item rdf:about="http://qjmed.oxfordjournals.org/cgi/content/short/101/9/745?rss=1">
<title><![CDATA[Severe disseminated hydatid disease successfully treated medically with prolonged administration of albendazole]]></title>
<link>http://qjmed.oxfordjournals.org/cgi/content/short/101/9/745?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Ntusi, N. A., Horsfall, C.]]></dc:creator>
<dc:date>2008-08-22</dc:date>
<dc:identifier>info:doi/10.1093/qjmed/hcn058</dc:identifier>
<dc:title><![CDATA[Severe disseminated hydatid disease successfully treated medically with prolonged administration of albendazole]]></dc:title>
<dc:publisher>Association of Physicians</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>101</prism:volume>
<prism:endingPage>746</prism:endingPage>
<prism:publicationDate>2008-09-01</prism:publicationDate>
<prism:startingPage>745</prism:startingPage>
<prism:section>Clinical Pictures</prism:section>
</item>

<item rdf:about="http://qjmed.oxfordjournals.org/cgi/content/short/101/9/747?rss=1">
<title><![CDATA[Zenker's diverticulum]]></title>
<link>http://qjmed.oxfordjournals.org/cgi/content/short/101/9/747?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[McGrath, E.E., McCabe, J., Odudu, A.]]></dc:creator>
<dc:date>2008-08-22</dc:date>
<dc:identifier>info:doi/10.1093/qjmed/hcn081</dc:identifier>
<dc:title><![CDATA[Zenker's diverticulum]]></dc:title>
<dc:publisher>Association of Physicians</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>101</prism:volume>
<prism:endingPage>748</prism:endingPage>
<prism:publicationDate>2008-09-01</prism:publicationDate>
<prism:startingPage>747</prism:startingPage>
<prism:section>Clinical Pictures</prism:section>
</item>

<item rdf:about="http://qjmed.oxfordjournals.org/cgi/content/short/101/9/749?rss=1">
<title><![CDATA[Anaemia as predictor of gastrointestinal bleeding in atrial fibrillation patients undergoing percutaneous coronary artery stenting]]></title>
<link>http://qjmed.oxfordjournals.org/cgi/content/short/101/9/749?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Manzano-Fernandez, S., Marin, F., Martinez, J. A. H., Cambronero, F., Valdes, M., Ruiz-Nodar, J. M., Perez-Berbel, P., Lip, G. Y.H.]]></dc:creator>
<dc:date>2008-08-22</dc:date>
<dc:identifier>info:doi/10.1093/qjmed/hcn082</dc:identifier>
<dc:title><![CDATA[Anaemia as predictor of gastrointestinal bleeding in atrial fibrillation patients undergoing percutaneous coronary artery stenting]]></dc:title>
<dc:publisher>Association of Physicians</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>101</prism:volume>
<prism:endingPage>751</prism:endingPage>
<prism:publicationDate>2008-09-01</prism:publicationDate>
<prism:startingPage>749</prism:startingPage>
<prism:section>Correspondence</prism:section>
</item>

</rdf:RDF>