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	<title>Rheumatic Disease : Article and Solution</title>
	<link>http://rawanbrotorheumatic.com</link>
	<description>Rheumatic Information by rawan broto</description>
	<pubDate>Fri, 07 Nov 2008 18:08:05 +0000</pubDate>
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	<language>en</language>
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		<title>EULAR evidence based recommendations for the management of fibromyalgia</title>
		<link>http://rawanbrotorheumatic.com/eular-evidence-based-recommendations-for-the-management-of-fibromyalgia/</link>
		<comments>http://rawanbrotorheumatic.com/eular-evidence-based-recommendations-for-the-management-of-fibromyalgia/#comments</comments>
		<pubDate>Fri, 07 Nov 2008 18:01:54 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
		<category><![CDATA[Fibromyalgia]]></category>

		<guid isPermaLink="false">http://rawanbrotorheumatic.com/eular-evidence-based-recommendations-for-the-management-of-fibromyalgia/</guid>
		<description><![CDATA[S. F. Carville1, L. Arendt-Neilson2, H. Bliddal3, F. Blotman4, J. C. Branco5, D. Buskila6, J. A. P. Da Silva7, B. Danneskiold-Samsøe3, F. Dincer8, C. Henriksson9, K. G. Henriksson10, E. Kosek11, K. Longley12, G. M. McCarthy13, S. Perrot14, M. Puszczewicz15, W. Samborski16, P. Sarzi-Puttini17, A. Silman18, M. Späth19, S. Wessely20, E. H. Choy1 1Academic Rheumatology, King&#8217;s [...]]]></description>
			<content:encoded><![CDATA[<p>S. F. Carville1, L. Arendt-Neilson2, H. Bliddal3, F. Blotman4, J. C. Branco5, D. Buskila6, J. A. P. Da Silva7, B. Danneskiold-Samsøe3, F. Dincer8, C. Henriksson9, K. G. Henriksson10, E. Kosek11, K. Longley12, G. M. McCarthy13, S. Perrot14, M. Puszczewicz15, W. Samborski16, P. Sarzi-Puttini17, A. Silman18, M. Späth19, S. Wessely20, E. H. Choy1 1Academic Rheumatology, King&#8217;s College London, London, United Kingdom, 2Centre for Sensory-Motor<br />
Interaction, Aalborg University, Aalborg, 3The Parker Institute, Frederiksberg Hospital, Copenhagen, Denmark, 4Rheumatology Department, Hospital Lapyeronie, Montpellier, France, 5Serviço de Reumatologia, Hospital Egas Moniz, Centro Hospitalar Lisboa Ocidental, Lisbon, Portugal, 6Department of Medicine, Soroka Medical Center, Beer Sheva, Israel, 7Reumatologia, Hopitais Da Universidade, Coimbra, Pakistan, 8Department of Physical and Rehabilitation Medicine, Hacettepe Medical School, Ankara, Turkey, 9INR, Section of Occupational Therapy,<br />
10Neuromuscular Unit, University Hospital, Linkoping, 11Pain Centre, Department of Neurosurgery, KarolinskaUniversity Hospital, Stockholm, Sweden, 12 -, -, Bath, United Kingdom, 13Rheumatology, Mater Misericordiae University Hospital, Dublin, Ireland, 14Pain Clinic, Hospital Cochin, Paris, France, 15Department of Rheumatology, Rheumatology and Internal Medicine University of Medical Sciences, 16Akademia Medyczna im. Karola Marcinkowskiego Poznaniu, Klinika Fizjoterapil Reumatologli I Rehabilitacji, Poznan, Poland, 17Rheumatology Unit, L. Sacco University Hospital, Milan, Italy, 18Faculty of Medical and Human Sciences ARC Epidemiology Unit, The University of Manchester, Manchester, United Kingdom, 19Friedrich-Baur-Institute, University of Munich, Munich, Germany, 20Psychological Medicine, Institute of Psychiatry, London, United Kingdom</p>
<p>Objective: To develop evidence based recommendations for the management of fibromyalgia syndrome (FMS). Methods: A multidisciplinary fibromyalgia task force was formed consisting of rheumatologists, pain specialists, experts in rehabilitation, a neurologist, an occupational therapist, a bio-scientist, psychiatrist, epidemiologist and a patient representing eleven European Countries: UK, Ireland, Portugal, Sweden, Germany, Italy, Turkey, Israel, Denmark, Poland and France.  <a href="http://rawanbrotorheumatic.com/eular-evidence-based-recommendations-for-the-management-of-fibromyalgia/#more-81" class="more-link">(more&#8230;)</a></p>
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		<item>
		<title>B Cell Depletion for Systemic Lupus Erythematosus</title>
		<link>http://rawanbrotorheumatic.com/b-cell-depletion-for-systemic-lupus-erythematosus/</link>
		<comments>http://rawanbrotorheumatic.com/b-cell-depletion-for-systemic-lupus-erythematosus/#comments</comments>
		<pubDate>Fri, 07 Nov 2008 18:00:45 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
		<category><![CDATA[Lupus]]></category>

		<guid isPermaLink="false">http://rawanbrotorheumatic.com/b-cell-depletion-for-systemic-lupus-erythematosus/</guid>
		<description><![CDATA[David Isenberg
United Kingdom
B lymphocytes are an essential component of the adaptive immune response. The surface antigen CD20 is expressed throughout B cell differentiation except at the very earliest and plasma cell stages. It is thought to act as a cross membrane calcium ion channel and to play a key role in B cell activation. In [...]]]></description>
			<content:encoded><![CDATA[<p>David Isenberg<br />
United Kingdom</p>
<p>B lymphocytes are an essential component of the adaptive immune response. The surface antigen CD20 is expressed throughout B cell differentiation except at the very earliest and plasma cell stages. It is thought to act as a cross membrane calcium ion channel and to play a key role in B cell activation. In consequence it has been hypothesised that targeting CD20 may prove therapeutic in the management of diseases like lupus that are largely B cell mediated. B cell depletion using rituximab, a chimeric human-mouse monoclonal antibody, was first utilized for the treatment of non-Hodgkin&#8217;s lymphoma in 1997. For the past six years my colleagues and I have been treating patients with severe SLE who have failed conventional immunosuppressive therapy (N=40) and although our studies remain open label the results have been extremely encouraging. Our preferred therapeutic regime is 1g rituximab IV, 750mg of cyclophosphamide IV and 250mg of Methylprednisolone IV - each infusion is given on two occasions two weeks<br />
apart. Our results (1,2) have indicated that this combination of drugs will achieve B cell depletion in virtually every case and that mean period of B cell depletion is approximately six months.  <a href="http://rawanbrotorheumatic.com/b-cell-depletion-for-systemic-lupus-erythematosus/#more-80" class="more-link">(more&#8230;)</a></p>
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		</item>
		<item>
		<title>Update on the treatment of lupus nephritis</title>
		<link>http://rawanbrotorheumatic.com/update-on-the-treatment-of-lupus-nephritis/</link>
		<comments>http://rawanbrotorheumatic.com/update-on-the-treatment-of-lupus-nephritis/#comments</comments>
		<pubDate>Fri, 07 Nov 2008 17:58:43 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
		<category><![CDATA[Lupus]]></category>

		<guid isPermaLink="false">http://rawanbrotorheumatic.com/update-on-the-treatment-of-lupus-nephritis/</guid>
		<description><![CDATA[CC Mok (MD, FRCP, FHKCP, FHKAM)
Department of Medicine, Tuen Mun Hospital
Hong Kong SAR, China
Therapy of lupus nephritis can be divided into an induction phase and a maintenance phase. Initial treatment is usually more aggressive and aims at inducing remission of nephritis while maintenance therapy is needed to prevent renal flares. Mycophenolate mofetil (MMF) has been [...]]]></description>
			<content:encoded><![CDATA[<p>CC Mok (MD, FRCP, FHKCP, FHKAM)<br />
Department of Medicine, Tuen Mun Hospital<br />
Hong Kong SAR, China</p>
<p>Therapy of lupus nephritis can be divided into an induction phase and a maintenance phase. Initial treatment is usually more aggressive and aims at inducing remission of nephritis while maintenance therapy is needed to prevent renal flares. Mycophenolate mofetil (MMF) has been shown by randomized controlled trials to be superior to, or at least as effective as, oral or intravenous pulse cyclophosphamide (CYC) as induction therapy for severe lupus nephritis. Adverse effects such as amenorrhoea and major infections are less frequent with MMF than CYC.  <a href="http://rawanbrotorheumatic.com/update-on-the-treatment-of-lupus-nephritis/#more-79" class="more-link">(more&#8230;)</a></p>
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		</item>
		<item>
		<title>Systemic Lupus Erythematosus - Outcome and Origins</title>
		<link>http://rawanbrotorheumatic.com/systemic-lupus-erythematosus-outcome-and-origins/</link>
		<comments>http://rawanbrotorheumatic.com/systemic-lupus-erythematosus-outcome-and-origins/#comments</comments>
		<pubDate>Fri, 07 Nov 2008 17:57:44 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
		<category><![CDATA[Lupus]]></category>

		<guid isPermaLink="false">http://rawanbrotorheumatic.com/systemic-lupus-erythematosus-outcome-and-origins/</guid>
		<description><![CDATA[David Isenberg
United Kingdom
Systemic lupus erythematosus (SLE) is a complex autoimmune rheumatic disease whose outlook has improved significantly from the 1950&#8217;s when 50%, 4 year survival was noted, to the present when around 80%, 15 year survival is generally recorded. However significant numbers of patients continue to die early from lupus and its morbidity is also [...]]]></description>
			<content:encoded><![CDATA[<p>David Isenberg<br />
United Kingdom</p>
<p>Systemic lupus erythematosus (SLE) is a complex autoimmune rheumatic disease whose outlook has improved significantly from the 1950&#8217;s when 50%, 4 year survival was noted, to the present when around 80%, 15 year survival is generally recorded. However significant numbers of patients continue to die early from lupus and its morbidity is also significant in some patients. In a cohort of 442 patients with lupus followed up in the Centre for Rheumatology at University College London between 1978 and 2005, 65 patients died with an average age of 47.1 years. The major causes of death were infection, cancer and atherosclerosis. We have recorded deaths in several young teenagers and others in their early twenties. Thus, although the outlook for patients with lupus is much improved and newer, principally biological agents, now offer the prospect of far more focussed and appropriate treatment for this disease, there is a continuing need to understand rather better its precise aetiopathogenesis. <a href="http://rawanbrotorheumatic.com/systemic-lupus-erythematosus-outcome-and-origins/#more-78" class="more-link">(more&#8230;)</a></p>
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		<item>
		<title>Disease Activity in Rheumatoid Arthritis</title>
		<link>http://rawanbrotorheumatic.com/disease-activity-in-rheumatoid-arthritis/</link>
		<comments>http://rawanbrotorheumatic.com/disease-activity-in-rheumatoid-arthritis/#comments</comments>
		<pubDate>Fri, 07 Nov 2008 17:56:16 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
		<category><![CDATA[Rheumatoid Arthritis]]></category>

		<guid isPermaLink="false">http://rawanbrotorheumatic.com/disease-activity-in-rheumatoid-arthritis/</guid>
		<description><![CDATA[John Edmonds
Dept of Rheumatology
St George Hospital, Sydney, Australia
‘Disease Activity’ in rheumatoid arthritis is a concept that attempts to capture, in some quantitative sense, the energy of pathological processes that result in the damage of rheumatoid arthritis. Rheumatologists speak of disease that is more or less ‘active’, of persistent ‘disease activity’ resulting in ‘joint damage’. Given [...]]]></description>
			<content:encoded><![CDATA[<p>John Edmonds<br />
Dept of Rheumatology<br />
St George Hospital, Sydney, Australia</p>
<p>‘Disease Activity’ in rheumatoid arthritis is a concept that attempts to capture, in some quantitative sense, the energy of pathological processes that result in the damage of rheumatoid arthritis. Rheumatologists speak of disease that is more or less ‘active’, of persistent ‘disease activity’ resulting in ‘joint damage’. Given that the thrust of RA therapy is ‘disease control’, clinicians need some measure of ‘disease activity’. Disease activity is the target of antirheumatic<br />
therapy but how can we know whether treatment is ‘adequate’ if we cannot measure the target of our therapy? <a href="http://rawanbrotorheumatic.com/disease-activity-in-rheumatoid-arthritis/#more-77" class="more-link">(more&#8230;)</a></p>
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		<item>
		<title>Rheumatologic manifestations of renal diseases</title>
		<link>http://rawanbrotorheumatic.com/rheumatologic-manifestations-of-renal-diseases/</link>
		<comments>http://rawanbrotorheumatic.com/rheumatologic-manifestations-of-renal-diseases/#comments</comments>
		<pubDate>Tue, 04 Nov 2008 06:16:24 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
		<category><![CDATA[Artritis]]></category>

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		<description><![CDATA[Julie T. Li-Yu, MD, FPCP, FPRA
University of Santo Tomas Hospital
Manila, Philippines
Musculoskeletal complaints among patients undergoing hemodialysis are commonly encountered. These appear to be major limiting factors in the quality of life in long term survivors. It might be considered a trade off for prolonged lifespan of patients kept on chronic hemodialysis that bone abnormalities are [...]]]></description>
			<content:encoded><![CDATA[<p>Julie T. Li-Yu, MD, FPCP, FPRA<br />
University of Santo Tomas Hospital<br />
Manila, Philippines</p>
<p>Musculoskeletal complaints among patients undergoing hemodialysis are commonly encountered. These appear to be major limiting factors in the quality of life in long term survivors. It might be considered a trade off for prolonged lifespan of patients kept on chronic hemodialysis that bone abnormalities are considered important in clinical management of these patients.<br />
The variation as to the nature and type of bone disease is related to patient’s age, duration of renal disease, variation of the pathogenic processes involved, type of therapy, differences in diet, and type and duration of dialysis therapy.Abnormal metabolism or action of vitamin D is responsible for defective mineralization of bone in renal failure. <a href="http://rawanbrotorheumatic.com/rheumatologic-manifestations-of-renal-diseases/#more-76" class="more-link">(more&#8230;)</a></p>
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		<item>
		<title>Hyperuricemia and gout in Taiwan Aborigines - Prevalence, risk factors, and prevention</title>
		<link>http://rawanbrotorheumatic.com/hyperuricemia-and-gout-in-taiwan-aborigines-prevalence-risk-factors-and-prevention/</link>
		<comments>http://rawanbrotorheumatic.com/hyperuricemia-and-gout-in-taiwan-aborigines-prevalence-risk-factors-and-prevention/#comments</comments>
		<pubDate>Tue, 04 Nov 2008 06:09:39 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
		<category><![CDATA[Gout and Hiperuricemia]]></category>

		<guid isPermaLink="false">http://rawanbrotorheumatic.com/hyperuricemia-and-gout-in-taiwan-aborigines-prevalence-risk-factors-and-prevention/</guid>
		<description><![CDATA[Chung-Tei Chou
Division of Allergy-Immunology-Rheumatology, Department of Medicine
Veterans General Hospital, Taipei, Taiwan
Prevalence of hyperuricemia and gout among Taiwan Aborigines. Two major studies have been conducted on gout in Taiwan Aborigines. Chou et al. spent one year examining 342 indigenous people of the Atayal tribe in aboriginal villages in central Taiwan. Gout was confirmed in 40 subjects, [...]]]></description>
			<content:encoded><![CDATA[<p>Chung-Tei Chou<br />
Division of Allergy-Immunology-Rheumatology, Department of Medicine<br />
Veterans General Hospital, Taipei, Taiwan</p>
<p>Prevalence of hyperuricemia and gout among Taiwan Aborigines. Two major studies have been conducted on gout in Taiwan Aborigines. Chou et al. spent one year examining 342 indigenous people of the Atayal tribe in aboriginal villages in central Taiwan. Gout was confirmed in 40 subjects, 95% of whom were male. We found the prevalence of hyperuricemia and gout in Atayal Aborigines to be 41.4% and 11.7%, respectively. Of the 40 gouty patients, 54% had tophi and 35% of their first-degree relatives had gout. The other epidemiological study focusing on the prevalence and risk factors of gout was completed by Chang et al. Unlike Chou&#8217;s study, the sample Aborigines in Chang&#8217;s study were older than 40 years and originated from 3 different tribes (Atayal, Paiwan, Bunun, and mixed). The findings showed 15.2% of males and 4.8% of females had gout, did not differ much from Chou&#8217;s study. Of the 3 tribes studied by Chang et al, prevalence was highest in Bunun men (28.1%), followed by Atayals (12.5%) and Paiwans (5.5%). In this study, no data regarding the hyperuricemia of different tribes was collected. However, in a previous study, Chang et al. showed 27% to 45% of aboriginal boys and 13% to 41% of aboriginal girls had hyperuricemia. Taken together, Chou and Chang confirmed the hypothesis that hyperuricemia and gout were frequent among indigenous people. <a href="http://rawanbrotorheumatic.com/hyperuricemia-and-gout-in-taiwan-aborigines-prevalence-risk-factors-and-prevention/#more-75" class="more-link">(more&#8230;)</a></p>
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		<item>
		<title>Differential diagnosis of common forms of arthritis</title>
		<link>http://rawanbrotorheumatic.com/differential-diagnosis-of-common-forms-of-arthritis/</link>
		<comments>http://rawanbrotorheumatic.com/differential-diagnosis-of-common-forms-of-arthritis/#comments</comments>
		<pubDate>Tue, 04 Nov 2008 06:08:15 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
		<category><![CDATA[Artritis]]></category>

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		<description><![CDATA[Richard Travers
Senior Rheumatologist and Head of Rheumatology Unit
Western Hospital, Footscray, Australia
This brief talk is aimed at the general physician whose opinion has been sought about a patient with joint pains. Rheumatology is a clinical specialty. There are a limited number of ways that a joint can react to noxious stimuli, and the answers to questions [...]]]></description>
			<content:encoded><![CDATA[<p>Richard Travers<br />
Senior Rheumatologist and Head of Rheumatology Unit<br />
Western Hospital, Footscray, Australia</p>
<p>This brief talk is aimed at the general physician whose opinion has been sought about a patient with joint pains. Rheumatology is a clinical specialty. There are a limited number of ways that a joint can react to noxious stimuli, and the answers to questions generated by the history and physical examination will nearly always point you in the right direction, and examples of the common entities will be given. The exceptions are those rare periodic syndromes (palindromic rheumatism and FMF, for example) where the joints and back movements may look normal at the first visit. The joints will also look normal in the common, but distressing, fibromyalgia, in some viral syndromes and in statin-related myalgia. <a href="http://rawanbrotorheumatic.com/differential-diagnosis-of-common-forms-of-arthritis/#more-74" class="more-link">(more&#8230;)</a></p>
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		<title>Vibe Technologies Vibrational Integrated Bio-photonic Energizer Machine Multi-Frequency Field Generator</title>
		<link>http://rawanbrotorheumatic.com/vibe-technologies-vibrational-integrated-bio-photonic-energizer-machine-multi-frequency-field-generator/</link>
		<comments>http://rawanbrotorheumatic.com/vibe-technologies-vibrational-integrated-bio-photonic-energizer-machine-multi-frequency-field-generator/#comments</comments>
		<pubDate>Tue, 04 Nov 2008 04:33:02 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
		<category><![CDATA[Reumatik]]></category>

		<guid isPermaLink="false">http://rawanbrotorheumatic.com/vibe-technologies-vibrational-integrated-bio-photonic-energizer-machine-multi-frequency-field-generator/</guid>
		<description><![CDATA[Audience: Healthcare professionals
    FDA notified healthcare professionals of a Class I Recall of the Vibe Technologies Vibrational Integrated Bio-photonic Energizer Machine Multi-Frequency Field Generator. This device has not been approved by FDA, lacks safety and effectiveness data, and is not manufactured under current good manufacturing practices. The manufacturer has submitted no evidence [...]]]></description>
			<content:encoded><![CDATA[<p>Audience: Healthcare professionals<br />
    FDA notified healthcare professionals of a Class I Recall of the Vibe Technologies Vibrational Integrated Bio-photonic Energizer Machine Multi-Frequency Field Generator. This device has not been approved by FDA, lacks safety and effectiveness data, and is not manufactured under current good manufacturing practices. The manufacturer has submitted no evidence to FDA to support any of their claims that the product could treat or cure such diseases as cancer, depression, infection and pain. Individuals with the device should stop using it immediately and contact the manufacturer to make arrangements to return the device.</p>
<p>Read the entire 2008 MedWatch Safety Summary, including a link to the FDA Recall notice regarding this issue at:</p>
<p>http://www.fda.gov/medwatch/safety/2008/safety08.htm#Vibe</p>
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		<title>Fluoroquinolone increased risk of tendinitis and tendon rupture</title>
		<link>http://rawanbrotorheumatic.com/fluoroquinolone-increased-risk-of-tendinitis-and-tendon-rupture/</link>
		<comments>http://rawanbrotorheumatic.com/fluoroquinolone-increased-risk-of-tendinitis-and-tendon-rupture/#comments</comments>
		<pubDate>Mon, 13 Oct 2008 16:41:30 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
		<category><![CDATA[Reumatik]]></category>

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		<description><![CDATA[FDA has asked that a boxed warning be added to the prescribing information for fluoroquinolone antibiotics. The warning will remind healthcare professionals that patients taking these drugs may experience an increased risk of tendinitis and tendon rupture. Fluoroquinolones include Cipro (ciprofloxacin), Factive (gemifloxacin), Levaquin (levofloxacin), Avelox (moxifloxacin), Noroxin (norfloxacin), Floxin (ofloxacin) and Proquin (ciprofloxacin hydrochloride).
]]></description>
			<content:encoded><![CDATA[<p>FDA has asked that a boxed warning be added to the prescribing information for fluoroquinolone antibiotics. The warning will remind healthcare professionals that patients taking these drugs may experience an increased risk of tendinitis and tendon rupture. Fluoroquinolones include Cipro (ciprofloxacin), Factive (gemifloxacin), Levaquin (levofloxacin), Avelox (moxifloxacin), Noroxin (norfloxacin), Floxin (ofloxacin) and Proquin (ciprofloxacin hydrochloride). <a href="http://rawanbrotorheumatic.com/fluoroquinolone-increased-risk-of-tendinitis-and-tendon-rupture/#more-70" class="more-link">(more&#8230;)</a></p>
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