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<title>Postgraduate Medical Journal</title>
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<link>http://pmj.bmj.com</link>
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<item rdf:about="http://pmj.bmj.com/cgi/content/full/84/990/169?rss=1">
<title><![CDATA[[Editorials] Gastric cancer and Helicobacter pylori: the bug, the host or the environment?]]></title>
<link>http://pmj.bmj.com/cgi/content/full/84/990/169?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Walker, M. M, Teare, L., McNulty, C.]]></dc:creator>
<dc:date>2008-04-18</dc:date>
<dc:identifier>info:doi/10.1136/pgmj.2008.068346</dc:identifier>
<dc:title><![CDATA[[Editorials] Gastric cancer and Helicobacter pylori: the bug, the host or the environment?]]></dc:title>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<prism:number>990</prism:number>
<prism:volume>84</prism:volume>
<prism:endingPage>170</prism:endingPage>
<prism:publicationDate>2008-04-01</prism:publicationDate>
<prism:startingPage>169</prism:startingPage>
<prism:section>Editorials</prism:section>
</item>

<item rdf:about="http://pmj.bmj.com/cgi/content/full/84/990/170?rss=1">
<title><![CDATA[[Editorials] Prescribing errors by family practice residents]]></title>
<link>http://pmj.bmj.com/cgi/content/full/84/990/170?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Avery, A. J]]></dc:creator>
<dc:date>2008-04-18</dc:date>
<dc:identifier>info:doi/10.1136/pgmj.2008.067892</dc:identifier>
<dc:title><![CDATA[[Editorials] Prescribing errors by family practice residents]]></dc:title>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<prism:number>990</prism:number>
<prism:volume>84</prism:volume>
<prism:endingPage>171</prism:endingPage>
<prism:publicationDate>2008-04-01</prism:publicationDate>
<prism:startingPage>170</prism:startingPage>
<prism:section>Editorials</prism:section>
</item>

<item rdf:about="http://pmj.bmj.com/cgi/content/full/84/990/172?rss=1">
<title><![CDATA[[Reviews] Current and future management of chronic hepatitis C infection]]></title>
<link>http://pmj.bmj.com/cgi/content/full/84/990/172?rss=1</link>
<description><![CDATA[
<p>Current treatment for patients with chronic hepatitis C virus (HCV) infection consists of the combination of pegylated interferon and ribavirin. This treatment regimen achieves a sustained virological response, defined as undetectable HCV RNA 6 months after treatment cessation, in 50% of patients overall. There is therefore a need for new treatments to improve the sustained virological response rate and reduce the number of adverse effects associated with pegylated interferon and ribavirin. This review examines the current management of chronic HCV infection, including who is eligible for treatment, the optimum duration of treatment, and management of side effects. New drugs in development, such as HCV-specific protease inhibitors, polymerase inhibitors, immune modulators and ribavirin analogues, are outlined, and their role in the treatment armamentarium is discussed, whether used alone or in combination with existing treatments.</p>
]]></description>
<dc:creator><![CDATA[Cross, T J S, Antoniades, C G, Harrison, P M]]></dc:creator>
<dc:date>2008-04-18</dc:date>
<dc:identifier>info:doi/10.1136/pgmj.2008.068205</dc:identifier>
<dc:title><![CDATA[[Reviews] Current and future management of chronic hepatitis C infection]]></dc:title>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<prism:number>990</prism:number>
<prism:volume>84</prism:volume>
<prism:endingPage>176</prism:endingPage>
<prism:publicationDate>2008-04-01</prism:publicationDate>
<prism:startingPage>172</prism:startingPage>
<prism:section>Reviews</prism:section>
</item>

<item rdf:about="http://pmj.bmj.com/cgi/content/full/84/990/177?rss=1">
<title><![CDATA[[Reviews] Relevance of clotting tests in liver disease]]></title>
<link>http://pmj.bmj.com/cgi/content/full/84/990/177?rss=1</link>
<description><![CDATA[
<p>Liver disease is associated with impairment of the haemostatic function due to the abnormal and decreased synthesis of the clotting factors. It is thus only logical to have considered assessment of the clotting profile (to include prothrombin time (PT) and activated partial thromboplastin time (aPTT)) to be an integral part of the comprehensive assessment of a patient who presents with liver impairment. Laboratory abnormalities of coagulation are considered to be a predictive risk factor for bleeding, but patients with liver disease do not have bleeding pattern as those who have coagulation factor deficiencies. Recent experiments have cast doubts over the use of PT and aPTT as a marker of bleeding in liver disease and the use of such tests to decide the need for plasma replacement before interventions like liver biopsy. This article reviews the relevance of the clotting profile in liver disease, the other factors involved in the haemostatic failure associated with it, and the technical problems in the interpretation of these results. Most importantly, it stresses the need for more trials to help us guide the management of bleeding in patients with liver impairment.</p>
]]></description>
<dc:creator><![CDATA[Thachil, J]]></dc:creator>
<dc:date>2008-04-18</dc:date>
<dc:identifier>info:doi/10.1136/pgmj.2007.066415</dc:identifier>
<dc:title><![CDATA[[Reviews] Relevance of clotting tests in liver disease]]></dc:title>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<prism:number>990</prism:number>
<prism:volume>84</prism:volume>
<prism:endingPage>181</prism:endingPage>
<prism:publicationDate>2008-04-01</prism:publicationDate>
<prism:startingPage>177</prism:startingPage>
<prism:section>Reviews</prism:section>
</item>

<item rdf:about="http://pmj.bmj.com/cgi/content/full/84/990/182?rss=1">
<title><![CDATA[[Reviews] Carcinoma of the bronchus 60 years later]]></title>
<link>http://pmj.bmj.com/cgi/content/full/84/990/182?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Silvestri, G A, Spiro, S G]]></dc:creator>
<dc:date>2008-04-18</dc:date>
<dc:identifier>info:doi/10.1136/thx.2006.073106</dc:identifier>
<dc:title><![CDATA[[Reviews] Carcinoma of the bronchus 60 years later]]></dc:title>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<prism:number>990</prism:number>
<prism:volume>84</prism:volume>
<prism:endingPage>187</prism:endingPage>
<prism:publicationDate>2008-04-01</prism:publicationDate>
<prism:startingPage>182</prism:startingPage>
<prism:section>Reviews</prism:section>
</item>

<item rdf:about="http://pmj.bmj.com/cgi/content/full/84/990/188?rss=1">
<title><![CDATA[[Reviews] Diabetic heart disease]]></title>
<link>http://pmj.bmj.com/cgi/content/full/84/990/188?rss=1</link>
<description><![CDATA[
<p>Diabetes mellitus is responsible for a spectrum of cardiovascular disease. The best known complications arise from endothelial dysfunction, oxidation, inflammation, and vascular remodelling and contribute to atherogenesis. However, the effects on the heart also relate to concurrent hypertensive heart disease, as well as direct effects of diabetes on the myocardium. Diabetic heart disease, defined as myocardial disease in patients with diabetes that cannot be ascribed to hypertension, coronary artery disease, or other known cardiac disease, is reviewed.</p>
]]></description>
<dc:creator><![CDATA[Marwick, T H]]></dc:creator>
<dc:date>2008-04-18</dc:date>
<dc:identifier>info:doi/10.1136/hrt.2005.067231</dc:identifier>
<dc:title><![CDATA[[Reviews] Diabetic heart disease]]></dc:title>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<prism:number>990</prism:number>
<prism:volume>84</prism:volume>
<prism:endingPage>192</prism:endingPage>
<prism:publicationDate>2008-04-01</prism:publicationDate>
<prism:startingPage>188</prism:startingPage>
<prism:section>Reviews</prism:section>
</item>

<item rdf:about="http://pmj.bmj.com/cgi/content/full/84/990/193?rss=1">
<title><![CDATA[[Original articles] Prognostic significance of genotyping Helicobacter pylori infection in patients in younger age groups with gastric cancer]]></title>
<link>http://pmj.bmj.com/cgi/content/full/84/990/193?rss=1</link>
<description><![CDATA[
<sec><st>Background:</st>
<p>Malignant tumours of the stomach are common, but the incidence of stomach cancer varies from country to country, probably a result of genetic, epigenetic and environmental factors. Stomach cancer often occurs in older people whose stomachs produce only small quantities of acid. Although infection with <I>Helicobacter pylori</I> has been proven beyond doubt in the aetiopathogenesis of various gastric disorders, not much is known about the genotypes of <I>H pylori</I> infection in early-onset gastric cancer.</p>
</sec>
<sec><st>Aim:</st>
<p>To ascertain the genotypes of <I>H pylori</I> in gastric cancer.</p>
</sec>
<sec><st>Methods:</st>
<p>Ninety-two patients were separated into three groups on the basis of their endoscopic findings: group 1, gastric cancer; group 2, gastric ulcer; group 3, non-ulcer dyspepsia. Gastric biopsy specimens were obtained for culture and DNA isolation; additional specimens were taken from subjects with gastric cancer for histopathological analysis. Amplification was performed using specific oligonucleotide primers to obtain genotypic data. Four samples from each group were randomly selected for sequence analysis.</p>
</sec>
<sec><st>Results:</st>
<p>Genotypic analysis showed <I>cag</I>T+ve/<I>hrg</I>A+ve/<I>cag</I>A+ve/<I>cag</I>E+ve/<I>vac</I>As1+ve to be highly prevalent in 79% of cases of <I>H pylori</I> infection. This genotype was found in 88% of subjects in group 1 and 78% in group 2. Intestinal-type adenocarcinoma was found in 35 subjects (83%), 32 (9%) of which harboured this genotype. Sequence analysis showed no significant strain-specific variations.</p>
</sec>
<sec><st>Conclusions:</st>
<p>Certain genotypes of <I>H pylori</I> have higher predictive value for the development of intestinal-type carcinoma at an early age. Genotyping of <I>H pylori</I> may well be a useful tool for screening people at increased risk of developing malignancy.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Tiwari, S K, Manoj, G, Kumar, G V., Sivaram, G, Hassan, S I, Prabhakar, B, Devi, U, Jalaluddin, S, Kumar, K, Ahmed, S, Abid, Z, Habeeb, M A, Khan, A A, Habibullah, C M]]></dc:creator>
<dc:date>2008-04-18</dc:date>
<dc:identifier>info:doi/10.1136/pgmj.2007.065060</dc:identifier>
<dc:title><![CDATA[[Original articles] Prognostic significance of genotyping Helicobacter pylori infection in patients in younger age groups with gastric cancer]]></dc:title>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<prism:number>990</prism:number>
<prism:volume>84</prism:volume>
<prism:endingPage>197</prism:endingPage>
<prism:publicationDate>2008-04-01</prism:publicationDate>
<prism:startingPage>193</prism:startingPage>
<prism:section>Original articles</prism:section>
</item>

<item rdf:about="http://pmj.bmj.com/cgi/content/full/84/990/198?rss=1">
<title><![CDATA[[Original articles] Prescription writing skills of residents in a family practice residency programme in Bahrain]]></title>
<link>http://pmj.bmj.com/cgi/content/full/84/990/198?rss=1</link>
<description><![CDATA[
<sec><st>Purpose of the study:</st>
<p>To evaluate the prescription writing skill of final year residents in a family practice residency programme (FPRP) in Bahrain, and to compare skill of residents who have graduated from medical schools with problem based learning (PBL) versus traditional (non-PBL) curricula.</p>
</sec>
<sec><st>Study design:</st>
<p>Prescriptions issued by the residents were prospectively collected for two consecutive cohorts in May 2004 and May 2005. Prescription errors were classified as errors of omission (minor and major), commission (incorrect information) and integration (drug&ndash;drug interactions).</p>
</sec>
<sec><st>Results:</st>
<p>In 69.6% of medications with major omission errors, dosage form (39.4%) and length of treatment (18.5%) were not specified. In 24.7% of medications with commission errors, dosing frequency (19.9%) and incorrect strength/dose (2.2%) were the most common errors. Integration errors comprised 5.7% of all prescribing errors. No significant differences were observed between PBL and non-PBL graduates with regard to the total number of prescriptions with errors, drugs per prescription, polypharmacy, and the total number of drugs with errors. The proportion of prescriptions with a potential for drug&ndash;drug interactions was comparable between PBL and non-PBL graduates. PBL graduates prescribed medications using brand names at a rate greater than non-PBL, whereas non-PBL graduates prescribed medications on inappropriate "as required" basis, and injections at a rate greater than PBL residents.</p>
</sec>
<sec><st>Conclusions:</st>
<p>Prescription writing skill of the final year residents in an FPRP programme was suboptimal for both PBL and non-PBL graduates. Integration of prescription writing skill and a rational pharmacotherapeutic programme into the FPRP curriculum is recommended.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Khaja, K A J A., Sequeira, R P, Al-Ansari, T M, Damanhori, A H H]]></dc:creator>
<dc:date>2008-04-18</dc:date>
<dc:identifier>info:doi/10.1136/pgmj.2007.062547</dc:identifier>
<dc:title><![CDATA[[Original articles] Prescription writing skills of residents in a family practice residency programme in Bahrain]]></dc:title>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<prism:number>990</prism:number>
<prism:volume>84</prism:volume>
<prism:endingPage>204</prism:endingPage>
<prism:publicationDate>2008-04-01</prism:publicationDate>
<prism:startingPage>198</prism:startingPage>
<prism:section>Original articles</prism:section>
</item>

<item rdf:about="http://pmj.bmj.com/cgi/content/full/84/990/205?rss=1">
<title><![CDATA[[Original articles] Cardiac autonomic neuropathy in diabetes mellitus: prevalence, risk factors and utility of corrected QT interval in the ECG for its diagnosis]]></title>
<link>http://pmj.bmj.com/cgi/content/full/84/990/205?rss=1</link>
<description><![CDATA[
<sec><st>Objectives:</st>
<p>To study the prevalence and risk factors for cardiac autonomic neuropathy (CAN) and the utility of prolongation of corrected QT interval (QTc) in the ECG to diagnose CAN in patients with diabetes mellitus.</p>
</sec>
<sec><st>Design and setting:</st>
<p>Cross-sectional study conducted among patients attending the diabetic clinic of a teaching hospital.</p>
</sec>
<sec><st>Methods:</st>
<p>The prevalence of CAN among 100 patients with type 1 and type 2 diabetes mellitus was assessed by the five autonomic function tests by Eving&rsquo;s methodology. The CAN score in each patient and its relationship to the QTc interval were analysed. Possible influences of age, duration of diabetes and coexistent peripheral neuropathy on the occurrence of CAN also were studied.</p>
</sec>
<sec><st>Results:</st>
<p>The prevalence of CAN was 60%. Univariate analysis showed a significant association between CAN and higher age (odds ratio (OR) 15.75), prolongation of QTc (OR 5.55), duration of disease over 10 years (OR 2) and peripheral neuropathy (p&lt;0.001) in patients with type 1 diabetes. Significant risks for CAN among patients with type 2 diabetes were coexistent peripheral neuropathy (OR 14), prolonged QTc (OR 9.75), higher age (OR 7.2) and disease duration over 10 years (OR 1.92) in univariate analysis, but none of them showed independent risk in multivariate analysis. Disease duration over 10 years resulted in QTc prolongation in a significant numbers of cases with type 1 (p&lt;0.001) and type 2 (p = 0.006) diabetes. The sensitivity, specificity and positive predictive value of QTc prolongation for the diagnosis of CAN were 77%, 62.5% and 77% in type 1 and 76.5%, 75% and 81.3% in type 2, respectively. Higher CAN scores correlated with longer QTc intervals (coefficient of correlation 0.73; p&lt;0.001).</p>
</sec>
<sec><st>Conclusions:</st>
<p>The prevalence of CAN in diabetes mellitus is high. Higher age, longer duration of diabetes and peripheral neuropathy are significant risk factors. QTc interval in the ECG can be used to diagnose CAN with reasonable sensitivity, specificity and positive predictive value.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Pappachan, J M, Sebastian, J, Bino, B C, Jayaprakash, K, Vijayakumar, K, Sujathan, P, Adinegara, L A]]></dc:creator>
<dc:date>2008-04-18</dc:date>
<dc:identifier>info:doi/10.1136/pgmj.2007.064048</dc:identifier>
<dc:title><![CDATA[[Original articles] Cardiac autonomic neuropathy in diabetes mellitus: prevalence, risk factors and utility of corrected QT interval in the ECG for its diagnosis]]></dc:title>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<prism:number>990</prism:number>
<prism:volume>84</prism:volume>
<prism:endingPage>210</prism:endingPage>
<prism:publicationDate>2008-04-01</prism:publicationDate>
<prism:startingPage>205</prism:startingPage>
<prism:section>Original articles</prism:section>
</item>

<item rdf:about="http://pmj.bmj.com/cgi/content/full/84/990/211?rss=1">
<title><![CDATA[[Original articles] Educational quality improvement report: outcomes from a revised morbidity and mortality format that emphasised patient safety]]></title>
<link>http://pmj.bmj.com/cgi/content/full/84/990/211?rss=1</link>
<description><![CDATA[
<sec><st>Problem:</st>
<p>Although Morbidity and Mortality conferences (MMC) were originally designed to promote quality care through careful analysis of adverse events, focus on individual actions or the fear of incrimination may interfere with identification of system issues contributing to the adverse outcomes.</p>
</sec>
<sec><st>Design:</st>
<p>Pre- and post-intervention assessments of participant attitudes toward patient safety and conference redesign were performed utilizing an attitudinal survey. Participants provided a unique identifier for paired-means procedure. A list of contributing factors, recommended solutions, and targeted system improvements was maintained with ongoing progress recorded.</p>
</sec>
<sec><st>Setting:</st>
<p>Department of Internal Medicine training program at University of Missouri &ndash; Columbia, an academic health care center affiliated with the University of Missouri Hospitals and Clinics and the Harry S. Truman Veteran&rsquo;s Administration Hospital.</p>
</sec>
<sec><st>Participants:</st>
<p>Residents and fellows from the Department of Internal Medicine residency program.</p>
</sec>
<sec><st>Educational Objectives:</st>
<p>(1) Distinguish between culture of blame/shame and patient safety culture, (2) Identify gaps in quality contributing to adverse outcomes, (3) Identify strategies to close gaps, (4) Participate in root cause analysis, demonstrating an ability to review an adverse event and recommend an action plan.</p>
</sec>
<sec><st>Strategies for Change:</st>
<p>An interdisciplinary team modified the internal medicine MMC to emphasize a better understanding of patient safety principles and system-based practice interventions. For each adverse event analyzed, root causes were identified, followed by discussion of system interventions that might prevent future such events.</p>
</sec>
<sec><st>Key measures for improvement:</st>
<p>(1) Attitudes of residents and fellows regarding patient safety, as measured on a 20 item, five-point ordinal scale (strongly disagree to strongly agree) survey, (2) System improvements generated from the Patient Safety M&amp;M Conferences (PSMMC), and (3) Attendance at PSMMC.</p>
</sec>
<sec><st>Effects of change:</st>
<p>Clinical outcomes: Conference participants offered 121 system improvement recommendations; 39 suggested system interventions were pursued based upon the likelihood of achieving high impact changes. These targeted changes were assigned to department/facility representatives with 23 (59%) improvements implemented, 11 (28%) partially implemented or in progress, and five (13%) abandoned due to impracticality or redundancy. Educational outcomes: Surveys were completed by 58 residents and fellows before and after modification of conference format. Six of the 20 survey items showed significant change with four of these changes occurring in the desired direction. Eleven of the remaining 14 responses changed in the desired direction, but did not reach statistical significance. Average MMC attendance increased from 41&plusmn;8 to 50&plusmn;10 (<I>p&lt;0.03</I>) participants.</p>
</sec>
<sec><st>Lessons learnt:</st>
<p>The new PSMMC initiated multiple improvements in the quality of patient care without sacrificing attendance or attitudes of the residents or fellows. The new PSMMC promotes opportunities for participants to improve quality of patient care in a safe and nurturing environment.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Bechtold, M L, Scott, S, Dellsperger, K C, Hall, L W, Nelson, K, Cox, K R]]></dc:creator>
<dc:date>2008-04-18</dc:date>
<dc:identifier>info:doi/10.1136/qshc.2006.021139</dc:identifier>
<dc:title><![CDATA[[Original articles] Educational quality improvement report: outcomes from a revised morbidity and mortality format that emphasised patient safety]]></dc:title>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<prism:number>990</prism:number>
<prism:volume>84</prism:volume>
<prism:endingPage>216</prism:endingPage>
<prism:publicationDate>2008-04-01</prism:publicationDate>
<prism:startingPage>211</prism:startingPage>
<prism:section>Original articles</prism:section>
</item>

<item rdf:about="http://pmj.bmj.com/cgi/content/full/84/990/217?rss=1">
<title><![CDATA[[Case reports] Drug interaction with anti-mycobacterial treatment as a cause of clopidogrel resistance]]></title>
<link>http://pmj.bmj.com/cgi/content/full/84/990/217?rss=1</link>
<description><![CDATA[
<p>The case is reported of a patient presenting with recurrent acute myocardial infarction due to stent thrombosis resulting from possible clopidogrel resistance caused by interaction between clopidogrel and anti-tuberculosis drugs. A brief overview of drug interaction as a risk factor for clopidogrel resistance is given.</p>
]]></description>
<dc:creator><![CDATA[Srinivasan, M, Smith, D]]></dc:creator>
<dc:date>2008-04-18</dc:date>
<dc:identifier>info:doi/10.1136/pgmj.2007.065193</dc:identifier>
<dc:title><![CDATA[[Case reports] Drug interaction with anti-mycobacterial treatment as a cause of clopidogrel resistance]]></dc:title>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<prism:number>990</prism:number>
<prism:volume>84</prism:volume>
<prism:endingPage>219</prism:endingPage>
<prism:publicationDate>2008-04-01</prism:publicationDate>
<prism:startingPage>217</prism:startingPage>
<prism:section>Case reports</prism:section>
</item>

<item rdf:about="http://pmj.bmj.com/cgi/content/full/84/990/220?rss=1">
<title><![CDATA[[Case reports] Importance of checking anti-glomerular basement membrane antibody status in patients with anti-neutrophil cytoplasmic antibody-positive vasculitis]]></title>
<link>http://pmj.bmj.com/cgi/content/full/84/990/220?rss=1</link>
<description><![CDATA[
<p>The case is reported of a 68-year-old man with perinuclear anti-neutrophil cytoplasmic antibody (pANCA)-associated glomerulonephritis who developed antibodies to glomerular basement membrane (anti-GBM) resulting in end stage renal failure. His pANCA titre on admission was 1:1024 IgG and he was anti-myeloperoxidase positive. A renal biopsy showed advanced sclerosing necrotising glomerulonephritis consistent with a pauci-immune ANCA-positive glomerulonephritis. He was treated with steroids and cyclophosphamide. His serum creatinine profile improved. He had a relapse of disease 16 months later, which was successfully treated. After a further 16 months, he presented with acute renal failure (creatinine 1060 &micro;mol/l). His pANCA titre on admission was 1:64 IgG. This was treated as a further relapse of ANCA-positive vasculitis. He became oliguric and his haemoglobin concentration fell. Eight days after admission, he was found to be strongly positive for anti-GBM (138 U/ml). Despite receiving cyclophosphamide, steroids and plasma exchange, he remained dialysis-dependent.</p>
]]></description>
<dc:creator><![CDATA[Gallagher, J L, Sinha, S, Reeve, R, Kalra, P A]]></dc:creator>
<dc:date>2008-04-18</dc:date>
<dc:identifier>info:doi/10.1136/pgmj.2007.062752</dc:identifier>
<dc:title><![CDATA[[Case reports] Importance of checking anti-glomerular basement membrane antibody status in patients with anti-neutrophil cytoplasmic antibody-positive vasculitis]]></dc:title>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<prism:number>990</prism:number>
<prism:volume>84</prism:volume>
<prism:endingPage>222</prism:endingPage>
<prism:publicationDate>2008-04-01</prism:publicationDate>
<prism:startingPage>220</prism:startingPage>
<prism:section>Case reports</prism:section>
</item>

<item rdf:about="http://pmj.bmj.com/cgi/content/full/84/990/223?rss=1">
<title><![CDATA[[On reflection] A day out with Darwin]]></title>
<link>http://pmj.bmj.com/cgi/content/full/84/990/223?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Launer, J.]]></dc:creator>
<dc:date>2008-04-18</dc:date>
<dc:identifier>info:doi/10.1136/pgmj.2008.069559</dc:identifier>
<dc:title><![CDATA[[On reflection] A day out with Darwin]]></dc:title>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<prism:number>990</prism:number>
<prism:volume>84</prism:volume>
<prism:endingPage>224</prism:endingPage>
<prism:publicationDate>2008-04-01</prism:publicationDate>
<prism:startingPage>223</prism:startingPage>
<prism:section>On reflection</prism:section>
</item>

<item rdf:about="http://pmj.bmj.com/cgi/content/full/84/990/224?rss=1">
<title><![CDATA[[Correction] Correction]]></title>
<link>http://pmj.bmj.com/cgi/content/full/84/990/224?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>2008-04-18</dc:date>
<dc:title><![CDATA[[Correction] Correction]]></dc:title>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<prism:number>990</prism:number>
<prism:volume>84</prism:volume>
<prism:endingPage>224</prism:endingPage>
<prism:publicationDate>2008-04-01</prism:publicationDate>
<prism:startingPage>224</prism:startingPage>
<prism:section>Correction</prism:section>
</item>

</rdf:RDF>