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<title>Postgraduate Medical Journal</title>
<url>http://pmj.bmj.com/site/homepage/PMJ_95x60.gif</url>
<link>http://pmj.bmj.com</link>
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<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130652v1?rss=1">
<title><![CDATA[Dissemination of systematic reviews in a hospital setting: a comparative survey for spreading use of the Cochrane Library]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130652v1?rss=1</link>
<description><![CDATA[<sec><st>Introduction</st><p>The Cochrane Library is the most important online evidence retrieval database of systematic reviews. Since 2007, the National Health Research Institutes has offered Taiwan's regional hospitals free access to the Cochrane Library. This study investigated how these hospitals disseminate its utilisation.</p></sec><sec><st>Methods</st><p>The usage rate of Cochrane reviews was measured in the participating hospitals from January 2008 to December 2009. Thereafter, a questionnaire survey was conducted for each regional hospital disseminator at the beginning of 2010 to analyse their methods of disseminating Cochrane reviews.</p></sec><sec><st>Results</st><p>The hospitals were stratified into three groups according to the relative rate of access: high (n=15), medium (n=16) and low (n=13). In comparison with the low-usage hospitals, the high-usage hospitals tended to assign a disseminator of evidence-based medicine to take charge of the dissemination of Cochrane reviews (p&lt;0.001). In addition, the high-usage hospitals more often used the following six methods: providing relevant information via email (p&lt;0.05), investing in early adopters (p&lt;0.05), using assistance from designated personnel (p&lt;0.05), highlighting the activity of early adopters (p&lt;0.05), conducting workshops (p=0.001), and inviting experts to speak (p&lt;0.001). There was no significant difference between high- and low-usage hospitals in organisational barriers.</p></sec><sec><st>Conclusion</st><p>This study has identified several helpful strategies used by Taiwan's hospitals to enhance dissemination of the Cochrane Library, including raising of awareness, active delivery of information, mentoring relationships, and educational training. The data suggest that disseminating evidence-based medicine simultaneously is a key element.</p></sec>]]></description>
<dc:creator><![CDATA[Weng, Y.-H., Hsu, C.-C., Shih, Y.-H., Lo, H.-L., Chiu, Y.-W., Kuo, K. N.]]></dc:creator>
<dc:date>2012-05-12T02:01:27-07:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130652</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130652</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:title><![CDATA[Dissemination of systematic reviews in a hospital setting: a comparative survey for spreading use of the Cochrane Library]]></dc:title>
<prism:publicationDate>2012-05-12</prism:publicationDate>
<prism:section>Original article</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130602v1?rss=1">
<title><![CDATA[Who makes prescribing decisions in hospital inpatients? An observational study]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130602v1?rss=1</link>
<description><![CDATA[<sec><st>Purpose of the study</st><p>Errors involving drug prescriptions are a key target for patient safety initiatives. Recent studies have focused on error rates across different grades of doctors in order to target interventions. However, many prescriptions are not instigated by the doctor who writes them. It is important to clarify how often this occurs in order to interpret these studies and create interventions. This study aimed to provisionally quantify and describe prescriptions where the identity of the decision maker and prescription writer differed.</p></sec><sec><st>Design of the study</st><p>Observational data was collected in six wards, 2&nbsp;weeks per ward, at a single large UK teaching hospital over a 12-week period from January to April 2011.</p></sec><sec><st>Results</st><p>In 112/183 (61%) cases where a new medicine was prescribed, the decision maker was not the prescription writer.</p></sec><sec><st>Conclusions</st><p>Decision making and the writing of prescriptions are generally not undertaken by the same doctor. Moreover, communication about prescriptions is poor. Further research in a larger sample of hospitals is required to confirm generalisability of the results, and to inform educational interventions to reduce error rates.</p></sec>]]></description>
<dc:creator><![CDATA[Ross, S., Hamilton, L., Ryan, C., Bond, C.]]></dc:creator>
<dc:date>2012-05-12T02:01:26-07:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130602</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130602</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:subject><![CDATA[Medical management, Patients]]></dc:subject>
<dc:title><![CDATA[Who makes prescribing decisions in hospital inpatients? An observational study]]></dc:title>
<prism:publicationDate>2012-05-12</prism:publicationDate>
<prism:section>Original article</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130620v1?rss=1">
<title><![CDATA[Pulmonary alveolar proteinosis treatment by whole-lung lavage]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130620v1?rss=1</link>
<description><![CDATA[<p>Pulmonary alveolar proteinosis (PAP) is a rare condition which is characterised by the abnormal accumulation of proteinaceous material in the alveolar spaces, with resulting impairment in oxygen exchange across the involved alveoli. The diagnosis of PAP can be established by the classic &lsquo;milky&rsquo; effluent bronchoalveolar lavage fluid (BALF). The current effective treatment for PAP is whole-lung lavage (WLL). We offer one case of PAP with apparent presentations and the clinical course. This report provides some information about the diagnosis and treatment of PAP (see PAP video online).</p><p>A 39-year-old man, an ex-smoker, was brought to our respiratory department due to dry cough and progressive exertional dyspnoea for 7&nbsp;months. He had been an antimonial worker for 6&nbsp;years. Physical examination was significant for perioral cyanosis, mild clubbing and diffuse rales. Arterial blood gas analysis on room air showed oxygen partial pressure (PaO<SUB>2</SUB>) 71.5&nbsp;mm&nbsp;Hg. The serum lactate dehydrogenase level was elevated at 301&nbsp;U/l (normal...]]></description>
<dc:creator><![CDATA[Cai, C., Ye, M., Xu, H., Li, Y.]]></dc:creator>
<dc:date>2012-04-29T02:01:27-07:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130620</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130620</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:subject><![CDATA[Unlocked, Immunology (including allergy), Histopathology, Radiology, Surgical diagnostic tests, Cardiothoracic surgery, General surgery, Radiology (diagnostics)]]></dc:subject>
<dc:title><![CDATA[Pulmonary alveolar proteinosis treatment by whole-lung lavage]]></dc:title>
<prism:publicationDate>2012-04-29</prism:publicationDate>
<prism:section>Images in medicine</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130363v1?rss=1">
<title><![CDATA[Genetics and epigenetics of Alzheimer's disease]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130363v1?rss=1</link>
<description><![CDATA[<p>Alzheimer's disease (AD) is a highly prevalent condition that predominantly affects older adults. AD is a complex multifactorial disorder with a number of genetic, epigenetic and environmental factors which ultimately lead to premature neuronal death. Predictive and susceptibility genes play a role in AD. Early-onset familial AD is a rare autosomal dominant disorder. Genome-wide association studies have identified many potential susceptibility genes for late-onset AD, but the clinical relevance of many of these susceptibility genes is unclear. The genetic variation by susceptibility genes plays a crucial role in determining the risk of late-onset AD, as well as the onset of the disease, the course of the AD and the therapeutic response of patients to conventional drugs for AD. The newer understanding of the epigenetics in AD has also been highlighted. Recent advances in genetics, epigenetics and pharmacogenetics of AD pose new challenges to the future management of AD.</p>]]></description>
<dc:creator><![CDATA[Alagiakrishnan, K., Gill, S. S., Fagarasanu, A.]]></dc:creator>
<dc:date>2012-04-29T02:01:27-07:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130363</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130363</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:title><![CDATA[Genetics and epigenetics of Alzheimer's disease]]></dc:title>
<prism:publicationDate>2012-04-29</prism:publicationDate>
<prism:section>Reviews</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130466v1?rss=1">
<title><![CDATA[Early and late mortality in hospitalised patients with raised cardiac troponin T]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130466v1?rss=1</link>
<description><![CDATA[<sec><st>Aims</st><p>Cardiac troponins are measured in acute coronary syndrome (ACS) and other conditions. The authors investigate the prognostic significance of cardiac troponin T (TnT) test and comorbid medical conditions.</p></sec><sec><st>Methods</st><p>Consecutive patients admitted to the Aintree University Hospital, Liverpool, between 2 January 2004 and 29 February 2004 who had TnT measurement were included. Patients were separated into normal (&lt;0.01&nbsp;&mu;g/l) or raised TnT levels (&ge;0.01&nbsp;&mu;g/l), and further categorised into: (1) normal TnT with unstable angina; (2) normal TnT with non-ACS; (3) raised TnT with ACS; and (4) raised TnT with non-ACS. Cox regression was used to identify prognostic variables, and logrank test to compare 7-year survival.</p></sec><sec><st>Results</st><p>Of 1021 patients, 313 had raised TnT (195 ACS, 118 non-ACS) and 708 normal TnT (80 ACS, 628 non-ACS). Age (HR 1.06; 95% CI 1.05 to 1.07), congestive cardiac failure (HR 1.37; 95% CI 1.11 to 1.69), cerebrovascular disease (HR 1.37; 95% CI 1.10 to 1.71), chronic obstructive airway disease (HR 1.44; 95% CI 1.19 to 1.75), liver disease (HR 4.16; 95% CI 2.37 to 7.31), renal disease (HR 1.83; 95% CI 1.27 to 2.64), tumour (HR 1.39; 95% CI 1.07 to 1.79), lymphoma (HR 4.81; 95% CI 2.07 to 11.16), metastatic cancer (HR 3.55; 95% CI 2.32 to 5.45) and a higher Charlson's comorbidity score (HR 1.20, 95% CI 1.13 to 1.26) were adverse predictors. Both raised TnT with ACS (HR 1.92, 95% CI 1.54 to 2.39) and raised TnT with non-ACS (HR 2.37, 95% CI 1.87 to 3.00) were associated with worse survival. Raised TnT with non-ACS had a worse survival than raised TnT with ACS (p=0.001).</p></sec><sec><st>Conclusion</st><p>Hospitalised patients with raised TnT levels from any cause predicted a higher mortality than normal TnT, with worst survival in those without an obvious ACS.</p></sec>]]></description>
<dc:creator><![CDATA[Wong, P. S. C., Jones, J. D., Ashrafi, R., Khanzada, O., Wickramarachchi, U., Keen, T. H., Robinson, D. R.]]></dc:creator>
<dc:date>2012-04-27T02:01:31-07:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130466</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130466</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:subject><![CDATA[Liver disease, Immunology (including allergy), Drugs: cardiovascular system, Heart failure, Ischaemic heart disease, Epidemiology]]></dc:subject>
<dc:title><![CDATA[Early and late mortality in hospitalised patients with raised cardiac troponin T]]></dc:title>
<prism:publicationDate>2012-04-27</prism:publicationDate>
<prism:section>Original article</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130087v1?rss=1">
<title><![CDATA[Imaging in children presenting with acute neurological deficit: stroke]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130087v1?rss=1</link>
<description><![CDATA[<p>Neurological deficits in the paediatric age group are much rarer than in adults; however, it is an urgent condition that relies heavily on imaging for a prompt accurate diagnosis. Neurological deficits caused by cerebrovascular diseases are defined as stroke, whereas conditions manifesting with neurological deficits without underlying cerebrovascular diseases are referred to as stroke mimics. To the best of the authors' knowledge, there is a lack of systematic pictorial review that collectively describes the imaging of neurological deficit in children. The purpose of the present series is to discuss the causes and imaging appearance of neurological deficits in childhood, based on the experience of a tertiary paediatric referral centre These are broadly categorised into stroke, infection, inflammation, metabolic disorder, cerebral neoplasms and drug poisoning. Different entities of stroke and their respective imaging findings are discussed. Paediatric stroke can further be divided into arterial ischaemic stroke, sino-venous stroke, haemorrhagic stroke and hypoxic&ndash;ischaemic encephalopathy.</p>]]></description>
<dc:creator><![CDATA[Rasalkar, D. D., Chu, W. C. W.]]></dc:creator>
<dc:date>2012-04-13T02:04:00-07:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130087</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130087</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:title><![CDATA[Imaging in children presenting with acute neurological deficit: stroke]]></dc:title>
<prism:publicationDate>2012-04-13</prism:publicationDate>
<prism:section>Reviews</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130088v1?rss=1">
<title><![CDATA[Imaging in children presenting with acute neurological deficit: paediatric stroke mimics]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130088v1?rss=1</link>
<description><![CDATA[<p>Stroke mimics refer to conditions manifesting with neurologic deficits without underlying cerebrovascular diseases. Major causes in the paediatric population under this category include infections, inflammation, demyelination, neoplasm, drug related, phacomatosis, and miscellaneous disorders. These conditions and their respective imaging findings are briefly discussed here.</p>]]></description>
<dc:creator><![CDATA[Rasalkar, D. D., Chu, W. C. W.]]></dc:creator>
<dc:date>2012-03-30T02:01:34-07:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130088</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130088</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:title><![CDATA[Imaging in children presenting with acute neurological deficit: paediatric stroke mimics]]></dc:title>
<prism:publicationDate>2012-03-30</prism:publicationDate>
<prism:section>Reviews</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130634v1?rss=1">
<title><![CDATA[Anaphylaxis: current state of knowledge for the modern physician]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130634v1?rss=1</link>
<description><![CDATA[<p>Anaphylaxis is a severe, potentially fatal, hypersensitivity reaction of rapid onset. It may trigger life-threatening cardiopulmonary compromise, often with skin and mucosal changes such as urticaria and angioedema. The prevalence of anaphylaxis is increasing and the number of cases of fatal anaphylaxis appears to be rising. Food, insect stings, and drugs are the most common triggers. Novel triggers are increasingly seen and include delayed anaphylaxis to red meat, food-dependent exercise-induced reactions and anaphylaxis to monoclonal antibodies. Anaphylaxis is usually IgE mediated, but other mechanisms also play a role for example direct mast cells activation. Differential diagnosis is discussed including asthma, syncope and shock; excessive endogenous histamine, food related syndromes, and some rare diagnoses. Intramuscular epinephrine is first line treatment. The role of other drugs is reviewed. Timed and serial serum tryptase measurements help to confirm the diagnosis. Long-term management is necessary to minimise the risk of recurrence and includes identification of the trigger(s), management of risk factors, education on avoidance and a formalised treatment plan with an epinephrine auto-injector if appropriate. Every patient who has experienced anaphylaxis should be referred to an allergy clinic for appropriate management. This is endorsed by many national guidelines (eg, UK NICE). Anaphylaxis is often misdiagnosed or miscoded as, for example, asthma or food allergy. Most doctors will encounter a patient with anaphylaxis in their career and should to be familiar with the clinical features, management and mechanisms of this potentially fatal condition.</p>]]></description>
<dc:creator><![CDATA[Rutkowski, K., Dua, S., Nasser, S.]]></dc:creator>
<dc:date>2012-03-30T02:01:33-07:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130634</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130634</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:title><![CDATA[Anaphylaxis: current state of knowledge for the modern physician]]></dc:title>
<prism:publicationDate>2012-03-30</prism:publicationDate>
<prism:section>Reviews</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130594v1?rss=1">
<title><![CDATA[Fibrates and estimated glomerular filtration rate: observations from an outpatient clinic setting and clinical implications]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130594v1?rss=1</link>
<description><![CDATA[<sec><st>Background</st><p>Previous studies have demonstrated that fibrates have an effect on creatinine concentrations. The pattern of change with fibrates in estimated glomerular filtration rate (eGFR), widely used in clinical practice, has not been previously described.</p></sec><sec><st>Methods</st><p>Data was retrospectively collected from 132 consecutive case notes of patients started on fibrates in a lipid clinic between 2002 and 2008. Pre- and post-fibrate creatinine concentrations were measured and eGFR measurements were obtained.</p></sec><sec><st>Results</st><p>Of the 79 patients with both pre and post-treatment eGFR values &lt;90&nbsp;ml/min/1.73&nbsp;m<sup>2</sup>, a significant mean eGFR reduction of 8.2&nbsp;ml/min/1.73&nbsp;m<sup>2</sup> was noted. Of these patients, 50% demonstrated a reduction in eGFR &gt;8&nbsp;ml/min/1.73&nbsp;m<sup>2</sup>, 25% demonstrated a reduction &gt;16&nbsp;ml/min/1.73&nbsp;m<sup>2</sup>, and 10% demonstrated a reduction &gt;21&nbsp;ml/min/1.73&nbsp;m<sup>2</sup>.</p></sec><sec><st>Conclusions</st><p>The authors demonstrate a significant effect of fibrates on eGFR in clinical practice. Awareness of the pattern of eGFR change is important for decisions regarding the continued use of fibrate therapy and/or commonly co-prescribed diabetic drugs and renal specialist referrals.</p></sec>]]></description>
<dc:creator><![CDATA[Abbas, A., Saraf, S., Ramachandran, S., Raju, J., Ramachandran, S.]]></dc:creator>
<dc:date>2012-03-29T02:02:12-07:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130594</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130594</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:title><![CDATA[Fibrates and estimated glomerular filtration rate: observations from an outpatient clinic setting and clinical implications]]></dc:title>
<prism:publicationDate>2012-03-29</prism:publicationDate>
<prism:section>Original article</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130494v1?rss=1">
<title><![CDATA[Coronary artery spasm and ventricular arrhythmias]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130494v1?rss=1</link>
<description><![CDATA[<p>Coronary artery spasm (CAS) is characterised by chest pain at rest and transient ST segment elevation on the ECG. The natural history of variant angina is not fully understood. Patients with CAS are younger, mostly female subjects and usually do not have traditional cardiovascular risk factors other than cigarette smoking. Cardiac arrhythmias are known to be associated with CAS. Ventricular arrhythmia is a well-recognised complication and sudden cardiac death has also been documented. The most important diagnostic tool in CAS is coronary angiography. 24&nbsp;h ECG Holter monitoring can be very useful in the diagnosis of ventricular arrhythmias caused by CAS. The mainstay therapy for CAS is calcium channel blockers and nitrates. The use of &beta;-blockers, especially the non-selective group, can promote attacks or prolong vasospastic state. The indication for implantable cardioverter defibrillator (ICD) implantation in a patient with CAS is still not clearly established. The role of primary prevention with the use of ICD is controversial; however, ICD implantation should be considered in high risk patients despite optimal medical treatment.</p>]]></description>
<dc:creator><![CDATA[Looi, K. L., Grace, A., Agarwal, S.]]></dc:creator>
<dc:date>2012-03-21T02:01:09-07:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130494</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130494</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:title><![CDATA[Coronary artery spasm and ventricular arrhythmias]]></dc:title>
<prism:publicationDate>2012-03-21</prism:publicationDate>
<prism:section>Reviews</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130375v1?rss=1">
<title><![CDATA[Outcome and relapse risks of thrombotic thrombocytopaenic purpura: an Egyptian experience]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130375v1?rss=1</link>
<description><![CDATA[<sec><st>Background</st><p>Thrombotic thrombocytopaenic purpura (TTP) is a rare life-threatening disease. Plasma exchange has significantly decreased the mortality from this disease, which still tends to recur in a substantial proportion of patients. This study describes the clinical spectrum and response to treatment and explores the risks of relapse in a cohort of patients.</p></sec><sec><st>Methods</st><p>Patients treated for TTP at the Clinical Haematology Unit, Cairo University, Egypt, between 2000 and 2008 were identified. Complete demographic, clinical history and full clinical examination, laboratory, treatment modalities and duration, and outcome data were collected and analysed. The follow-up duration was 24 months.</p></sec><sec><st>Results</st><p>30 patients; 13 men (43%) and 17 women (57%) with a median age of 42 years were treated for 46 episodes of TTP. The median duration of disease onset to diagnosis for the first episode was 7 days. Twenty-three patients (76.66%) were diagnosed as idiopathic primary and seven patients (23.33%) were secondary TTP. Four patients died during the first 24 h. Of the 26 patients, 22 (85.6%) achieved remission with an average of 7.55 plasma exchange sessions, Another nine patients had 25 relapses (mean 2.7). Splenectomy was performed in three patients (11.5%). The 24-month overall survival was 80%. The initial low platelet count and high LDH were the only two statistically significant relapse predictors.</p></sec><sec><st>Conclusions</st><p>The current results conform to the reported literature on the outcome of TTP. The very early mortality due to late referral highlights the need of education about the disease among primary healthcare providers.</p></sec>]]></description>
<dc:creator><![CDATA[El-Husseiny, N. M., Goubran, H., Fahmy, H. M., Tawfik, N. M., Moustafa, H., Amin, S. N., El-Ekiaby, M.]]></dc:creator>
<dc:date>2012-03-20T02:01:44-07:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130375</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130375</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:subject><![CDATA[General practice / family medicine, Haematology (incl blood transfusion), Epidemiology]]></dc:subject>
<dc:title><![CDATA[Outcome and relapse risks of thrombotic thrombocytopaenic purpura: an Egyptian experience]]></dc:title>
<prism:publicationDate>2012-03-20</prism:publicationDate>
<prism:section>Original article</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130590v1?rss=1">
<title><![CDATA[Ventricular septal rupture and intraseptal pseudo-aneurysm complicating acute myocardial infarction: management in the multimodality imaging era]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130590v1?rss=1</link>
<description><![CDATA[<p>Ventricular septal rupture is a rare but important complication occurring in around 1%&ndash;3% of cases of acute myocardial infarction and carries a high mortality.<cross-ref type="bib" refid="b1">1</cross-ref> We report a patient in whom a ventricular septal rupture was better tolerated due to a serpiginous course of the rupture, combined with an unusual pseudoaneurysm of the septum.</p><p>A 69-year-old male subject was admitted to our emergency department with a 2-week history of exertional breathlessness, which was preceded by an acute episode of precordial discomfort for which the patient did not seek medical attention. On clinical examination, the resting heart rate was regular at 100 beats per minute. The supine blood pressure was 95/75&nbsp;mm&nbsp;Hg. There were signs of moderate biventricular failure and a loud pan-systolic murmur loudest at the lower-left sternal edge.</p><p>The ECG confirmed the presence of an inferior myocardial infarct. Transthoracic echocardiography showed a defect in the posterior-basal part of the inter-ventricular septum...]]></description>
<dc:creator><![CDATA[Amin, F. R., Mandal, A. K. J., Al-Obaidi, M., Missouris, C. G.]]></dc:creator>
<dc:date>2012-03-16T02:01:46-07:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130590</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130590</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:subject><![CDATA[Genetics, Congenital heart disease, Drugs: cardiovascular system, Echocardiography, Hypertension, Reproductive medicine, Interventional cardiology, Ischaemic heart disease, Radiology, Clinical diagnostic tests, Cardiothoracic surgery, Radiology (diagnostics), Epidemiology]]></dc:subject>
<dc:title><![CDATA[Ventricular septal rupture and intraseptal pseudo-aneurysm complicating acute myocardial infarction: management in the multimodality imaging era]]></dc:title>
<prism:publicationDate>2012-03-16</prism:publicationDate>
<prism:section>Images in medicine</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130727v1?rss=1">
<title><![CDATA[Care of the patient with an autism spectrum disorder by the general physician]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130727v1?rss=1</link>
<description><![CDATA[<p>Autism spectrum disorders (ASD), comprising classic autism, Asperger syndrome, Rett syndrome, childhood disintegrative disorder and pervasive development disorder-not otherwise specified, represent complex neurodevelopmental conditions characterised by impaired social interactions, difficulties with communication and repetitive, stereotyped behaviours. It is estimated that up to 1% of the general population may be affected by an ASD. Whether due to improved diagnostic techniques or a true rise in incidence, the prevalence of patients with ASD is rising, and these individuals are increasingly encountered in a variety of healthcare settings. Care givers of patients with an ASD report frequently that lack of awareness of the complications of these disorders and the method of appropriately assessing these individuals impair the effective delivery of healthcare to this patient population. It is now clear that patients with an ASD, in addition to the defining characteristics of these disorders, can present to the outpatient, emergency department and inpatient settings with a variety of psychiatric, neurological, gastrointestinal, nutritional/metabolic, dental, ophthalmological, cardiovascular, gynaecological, traumatic and musculoskeletal conditions that can require acute intervention. In addition, the common treatments given to patients with an ASD may result in side effects and complications that may require acute intervention. For physicians who encounter patients with an ASD, the combination of impaired social interactions, difficulties with communication and stereotyped behaviours creates an additional barrier to diagnosis and treatment of these individuals. Careful preparation of the examination environment, direct engagement of care givers and the patient and the use of communication techniques and pharmacological adjuncts can aid physicians in treating the patient with an ASD in the outpatient, emergency department and inpatient settings.</p>]]></description>
<dc:creator><![CDATA[Venkat, A., Jauch, E., Russell, W. S., Crist, C. R., Farrell, R.]]></dc:creator>
<dc:date>2012-03-16T02:01:45-07:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130727</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130727</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:title><![CDATA[Care of the patient with an autism spectrum disorder by the general physician]]></dc:title>
<prism:publicationDate>2012-03-16</prism:publicationDate>
<prism:section>Reviews</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130293v1?rss=1">
<title><![CDATA[Muscle weakness, health status and frequency of exacerbations in chronic obstructive pulmonary disease]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130293v1?rss=1</link>
<description><![CDATA[<sec><st>Background</st><p>Multiple factors contribute to muscle weakness and reduced muscle mass in chronic obstructive pulmonary disease (COPD) and this impacts patients' quality of life. One factor implicated in this process is systemic inflammation, an accompaniment of acute exacerbations. Recurrent exacerbations are associated with lower health status. This study examines the relationship between muscle weaknesses, health status and exacerbation frequency in a cohort of patients with COPD.</p></sec><sec><st>Methods</st><p>This is an observational study of 188 (95 female) patients with COPD attending two hospital clinics in the northeast of England between 2004 and 2007. We measured spirometry, body mass index, health status (St George's Respiratory Questionnaire) and grip strength and recorded Medical Research Council dyspnoea scores and the frequency of exacerbations in the previous year.</p></sec><sec><st>Results</st><p>Patients were aged 72.5&plusmn;8.3&nbsp;years (data expressed as mean&plusmn;SD) with Medical Research Council score of 3.6&plusmn;0.8, forced expiratory volume in one second (FEV<SUB>1</SUB>) of 49.2&plusmn;21.5 per cent predicted and a total St George's Respiratory Questionnaire score of 72.2&plusmn;15.5. Grip strength, expressed as per cent predicted, was 72.0&plusmn;21.8 in men and 81.0&plusmn;18.2 in women. Exacerbations ranged from zero to five in the previous year and there were associations of reduced grip strength with exacerbation frequency (<sup>2</sup>=9.634; p=0.0019) and lower health status (<sup>2</sup>=34.00; p&lt;0.001).</p></sec><sec><st>Conclusion</st><p>Our data clearly demonstrate that reduction in grip strength occurs more frequently and to a greater extent in patients with a history of frequent exacerbations and is associated with reduced health status.</p></sec>]]></description>
<dc:creator><![CDATA[Ansari, K., Keaney, N., Taylor, I., Burns, G., Farrow, M.]]></dc:creator>
<dc:date>2012-03-02T02:02:01-08:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130293</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130293</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:subject><![CDATA[Immunology (including allergy)]]></dc:subject>
<dc:title><![CDATA[Muscle weakness, health status and frequency of exacerbations in chronic obstructive pulmonary disease]]></dc:title>
<prism:publicationDate>2012-03-02</prism:publicationDate>
<prism:section>Original article</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130306v1?rss=1">
<title><![CDATA[Inadvertent prescription of gelatin-containing oral medication: its acceptability to patients]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130306v1?rss=1</link>
<description><![CDATA[<p>When prescribing, doctors usually only consider the &lsquo;active&rsquo; component of any drug's formulation ignoring the majority of the agents which make up the bulk of the tablet or capsule, collectively known as excipients. Many urological drugs contain the excipient gelatin which is, universally, of animal origin; this may conflict with the dietetic ideals of patients. A questionnaire-based study, undertaken between January and June 2010 in a mixed ethnicity inner-city population presenting with urological symptoms, asked which patients preferred not to ingest animal-based products, who would ask about the content of their prescribed treatment and who would refuse to take that medication if alternatives were available. Ultimately, the authors sought to find out how many patients had been inadvertently prescribed gelatin-containing oral medications and to suggest ways in which prescriptions might be more congruous with an individual patient's dietetic wishes. This study demonstrated that 43.2% of the study population would prefer not to take animal product-containing medication even if no alternative were available. 51% of men with lower urinary tract symptoms were also found to have inadvertently been prescribed gelatin-containing products against their preferred dietary restriction. Education of healthcare professionals about excipients and getting them to ask about a patient's dietetic preferences may help avoid inadvertent prescription of the excipient gelatin in oral medications. Substitution of gelatin with vegetable-based alternatives and clearer labelling on drug packaging are alternative strategies to help minimise the risks of inadvertently contravening a patient's dietetic beliefs when prescribing oral medication.</p>]]></description>
<dc:creator><![CDATA[Vissamsetti, B., Payne, M., Payne, S.]]></dc:creator>
<dc:date>2012-02-28T06:10:59-08:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130306</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130306</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:subject><![CDATA[Press releases, Diet]]></dc:subject>
<dc:title><![CDATA[Inadvertent prescription of gelatin-containing oral medication: its acceptability to patients]]></dc:title>
<prism:publicationDate>2012-02-28</prism:publicationDate>
<prism:section>Ethics and law</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130355v1?rss=1">
<title><![CDATA[Outpatient parenteral antibiotic therapy for infective endocarditis: a review of 4 years' experience at a UK centre]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130355v1?rss=1</link>
<description><![CDATA[<sec><st>Objectives</st><p>To review the role of outpatient parenteral antibiotic therapy (OPAT) in the management of infective endocarditis (IE) with the aim to guide further development of the service modality both locally and at other centres, in light of the evolving recommendations on patient suitability in international guidelines.</p></sec><sec><st>Methods</st><p>A retrospective case review of all patients receiving OPAT for IE in Sheffield between January 2006 and October 2010 was conducted. Data were collected on site and microbiology of infection, antibiotic regimens, adverse events during OPAT therapy and outcomes were studied.</p></sec><sec><st>Results</st><p>A total of 36 episodes of IE were treated in 34 patients. All patients received initial treatment as inpatients. Treatment was successful in 34/36 episodes (94.4%) with no evidence of recurrence at a median of 30&nbsp;months follow-up. One patient had a relapse 2&nbsp;months after completion of OPAT for enterococcal endocarditis and was found to have concurrent chronic prostatitis. One patient died of a ruptured pulmonary root abscess while receiving OPAT. Adverse events occurred in 12 episodes (33.3%), of which seven were line associated. In four cases adverse events resulted in re-hospitalisation. A successful outcome was achieved in 22/24 episodes (91.7%) deemed to be less suitable for OPAT due to higher risk of complications by Infectious Diseases Society of America guidelines.</p></sec><sec><st>Conclusions</st><p>OPAT is a safe and effective means of completing therapy for IE, including prosthetic valve endocarditis and other cases at a higher risk of complicated disease. However, the relatively high rate of adverse events highlights the need for well-developed protocols and policies for patient selection and follow-up within the context of a formal OPAT service.</p></sec>]]></description>
<dc:creator><![CDATA[Partridge, D. G., O'Brien, E., Chapman, A. L. N.]]></dc:creator>
<dc:date>2012-02-25T02:01:18-08:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130355</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130355</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:subject><![CDATA[Drugs: infectious diseases, Drugs: cardiovascular system, Chemotherapy]]></dc:subject>
<dc:title><![CDATA[Outpatient parenteral antibiotic therapy for infective endocarditis: a review of 4 years' experience at a UK centre]]></dc:title>
<prism:publicationDate>2012-02-25</prism:publicationDate>
<prism:section>Original article</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130215v1?rss=1">
<title><![CDATA[Sudden cardiac death among competitive adult athletes: a review]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130215v1?rss=1</link>
<description><![CDATA[<p>Sudden cardiac death is the leading cause of mortality among young athletes with an incidence of 1&ndash;2 per 100 000 athletes per annum. It is described as &lsquo;an event that is non-traumatic, non-violent, unexpected, and resulting from sudden cardiac arrest within six hours of previously witnessed normal health&rsquo;. Most predisposed athletes have no symptoms and there is no warning for the impending tragic event. The majority of cases are caused by an underlying structural cardiac abnormality, most commonly hypertrophic cardiomyopathy. More recently, the understanding of non-structural causes such as long QT syndrome and Brugada syndrome has grown and diagnostic criteria have been developed. This review presents the known aetiologies of sudden cardiac death among athletes and outlines their identification and management including implications for future sporting participation as laid out in the consensus documents produced by the European Society of Cardiology and the 36th Bethesda Conference.</p>]]></description>
<dc:creator><![CDATA[Pugh, A., Bourke, J. P., Kunadian, V.]]></dc:creator>
<dc:date>2012-02-23T02:03:07-08:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130215</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130215</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:title><![CDATA[Sudden cardiac death among competitive adult athletes: a review]]></dc:title>
<prism:publicationDate>2012-02-23</prism:publicationDate>
<prism:section>Reviews</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130539v1?rss=1">
<title><![CDATA[Advances in antiplatelet therapy for acute coronary syndromes]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130539v1?rss=1</link>
<description><![CDATA[<p>Admissions to emergency care centres with acute coronary syndromes remain one of the principal burdens on healthcare systems in the Western world. Early pharmacological treatment in these patients is crucial, lessening the impact on both morbidity and mortality, with the cornerstone of management being antiplatelet agents. While aspirin and clopidogrel have been the drugs of choice for nearly a decade, an array of newer, more potent antiplatelet agents are now available or in late stage development. Data are rapidly gathering suggesting these agents have superior anti-ischaemic properties, improving patient outcomes, but that for some agents increased vigilance and appropriate patient selection may be necessary to guard against bleeding complications. In this review, the authors aim to deliver an overview of the changing field of antiplatelet therapy and provide information about the relative risks and benefits of these newer agents, many of which will be entering widespread clinical use imminently.</p>]]></description>
<dc:creator><![CDATA[Contractor, H., Ruparelia, N.]]></dc:creator>
<dc:date>2012-02-22T02:01:22-08:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130539</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130539</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:title><![CDATA[Advances in antiplatelet therapy for acute coronary syndromes]]></dc:title>
<prism:publicationDate>2012-02-22</prism:publicationDate>
<prism:section>Reviews</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130276v1?rss=1">
<title><![CDATA[Imaging in pulmonary hypertension, part 3: small vessel diseases]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130276v1?rss=1</link>
<description><![CDATA[<p>Pulmonary hypertension is a significant cause of morbidity and mortality. Unfortunately, non-specific presentation and lack of awareness of the disease frequently lead to significant delay in diagnosis, often with the onset of right heart failure, when prognosis is poor and therapy is of limited effectiveness. The classification of pulmonary hypertension is a clinical one grouping diseases into categories with similar patho-physiological mechanism and therapeutic options. Pulmonary biopsy can provide a definitive diagnosis but is hazardous in patients with pulmonary hypertension. Imaging has emerged as an invaluable tool in differentiating the aetiology, assessing disease severity and directing further management. One of the most important roles of imaging is to differentiate diseases resulting from obstruction of the large pulmonary arteries from those secondary to diffuse small vessel disease, as these have very different prognosis and are also treated differently. Small vessel diseases causing pulmonary arterial hypertension most commonly result from diffuse remodelling of the pulmonary arterioles. There are multiple causes of arteriolar remodelling which share similar histopathological, clinical and imaging features. In a subgroup of small vessel diseases causing pulmonary hypertension the predominant site of increased vascular resistance is at the level of the capillaries or venules. Correct diagnosis of pulmonary veno-occlusive disease and pulmonary capillary haemangiomatosis is essential since poor prognosis and inadvertent administration of vasodilators (conventional therapy for arteriolar predominant disease) can result in fatal pulmonary oedema. Multimodality imaging plays an important role in suggesting a diagnosis, guiding further investigation and directing treatment.</p>]]></description>
<dc:creator><![CDATA[Gopalan, D., McCann, C., Sheares, K., Screaton, N.]]></dc:creator>
<dc:date>2012-01-19T07:35:56-08:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130276</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130276</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:title><![CDATA[Imaging in pulmonary hypertension, part 3: small vessel diseases]]></dc:title>
<prism:publicationDate>2012-01-19</prism:publicationDate>
<prism:section>Reviews</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130232v1?rss=1">
<title><![CDATA[The preparedness of UK graduates in acute care: a systematic literature review]]></title>
<link>http://pmj.bmj.com/cgi/content/short/postgradmedj-2011-130232v1?rss=1</link>
<description><![CDATA[<sec><st>Purpose of study</st><p>The ability to recognise acutely unwell patients and to instigate generic resuscitation is essential for all newly qualified doctors. The aim of this review is to synthesise recent work examining the perceived preparedness of UK medical graduates in acute care, relative to the other outcomes detailed in Tomorrow's Doctors (2009).</p></sec><sec><st>Study design</st><p>A systematic literature search was performed using five databases. It sought literature related to preparedness in acute care and other Tomorrow's Doctors outcomes from the perspectives of the graduates themselves and their professional colleagues. Two researchers undertook data extraction and quality scoring, and preparedness ratings in each outcome were mapped to a generic rating scale to allow comparison between studies.</p></sec><sec><st>Results</st><p>256 articles were recovered, with 10 included in the final analysis. The 10 articles suggested that graduates perceive themselves to be least well prepared in acute care and prescribing. Their professional colleagues perceive them to be less prepared in acute care than in any of the other outcomes and perceive preparedness in acute care to have declined since the first publication of Tomorrow's Doctors. Furthermore, there is evidence that preparedness in acute care is an area of concern for UK graduates.</p></sec><sec><st>Conclusions</st><p>The assimilation of evidence in this review suggests that recent changes in UK undergraduate training, while improving preparedness in some areas, may have neglected acute care. While not a good surrogate for actual preparedness, perceived preparedness is important in influencing the behaviour of new graduates and therefore warrants further consideration.</p></sec>]]></description>
<dc:creator><![CDATA[Tallentire, V. R., Smith, S. E., Skinner, J., Cameron, H. S.]]></dc:creator>
<dc:date>2011-12-13T03:31:03-08:00</dc:date>
<dc:identifier>info:doi/10.1136/postgradmedj-2011-130232</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;postgradmedj-2011-130232</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:subject><![CDATA[Press releases, Adult intensive care]]></dc:subject>
<dc:title><![CDATA[The preparedness of UK graduates in acute care: a systematic literature review]]></dc:title>
<prism:publicationDate>2011-12-13</prism:publicationDate>
<prism:section>Original article</prism:section>
</item>
<item rdf:about="http://pmj.bmj.com/cgi/content/short/pgmj.2008.074245v1?rss=1">
<title><![CDATA[Improving outcome in severe trauma: trauma systems and initial management--intubation, ventilation and resuscitation]]></title>
<link>http://pmj.bmj.com/cgi/content/short/pgmj.2008.074245v1?rss=1</link>
<description><![CDATA[
<p>Severe trauma is an increasing global problem mainly affecting fit and healthy younger adults. Improvements in the entire pathway of trauma care have led to improvements in outcome. Development of a regional trauma system based around a trauma centre is associated with a 15&ndash;50% reduction in mortality. Trauma teams led by senior doctors provide better care. Although intuitively advantageous, the involvement of doctors in the pre-hospital care of trauma patients currently lacks clear evidence of benefit. Poor airway management is consistently identified as a cause of avoidable morbidity and mortality. Rapid sequence induction/intubation is frequently indicated but the ideal drugs have yet to be identified. The benefits of cricoid pressure are not clear cut. Dogmas in the management of pneumothoraces have been challenged: chest x-ray has a role in the diagnosis of tension pneumothoraces, needle aspiration may be ineffective, and small pneumothoraces can be managed conservatively. Identification of significant haemorrhage can be difficult and specific early resuscitation goals are not easily definable. A hypotensive approach may limit further bleeding but could worsen significant brain injury. The ideal initial resuscitation fluid remains controversial. In appropriately selected patients early aggressive blood product resuscitation is beneficial. Hypothermia can exacerbate bleeding and the benefit in traumatic brain injury is not adequately studied for firm recommendations.</p>
]]></description>
<dc:creator><![CDATA[Harris, T., Davenport, R., Hurst, T., Jones, J.]]></dc:creator>
<dc:date>2010-11-01T13:54:16-07:00</dc:date>
<dc:identifier>info:doi/10.1136/pgmj.2008.074245</dc:identifier>
<dc:identifier>hwp:master-id:postgradmedj;pgmj.2008.074245</dc:identifier>
<dc:publisher>The Fellowship of Postgraduate Medicine</dc:publisher>
<dc:title><![CDATA[Improving outcome in severe trauma: trauma systems and initial management--intubation, ventilation and resuscitation]]></dc:title>
<prism:publicationDate>2010-11-01</prism:publicationDate>
<prism:section>Reviews</prism:section>
</item>
</rdf:RDF>
