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	<title>Virtual Journal Club &#187; Ann Rheum Dis</title>
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	<description>Division of Hospital Medicine Virtual Journal Club</description>
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		<title>Nephrogenic systemic fibrosis: a gadolinium-associated fibrosing disorder in patients with renal dysfunction.</title>
		<link>http://beckerinfo.net/JClub/2008/12/30/nephrogenic-systemic-fibrosis-a-gadolinium-associated-fibrosing-disorder-in-patients-with-renal-dysfunction/</link>
		<comments>http://beckerinfo.net/JClub/2008/12/30/nephrogenic-systemic-fibrosis-a-gadolinium-associated-fibrosing-disorder-in-patients-with-renal-dysfunction/#comments</comments>
		<pubDate>Tue, 30 Dec 2008 15:21:24 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Ann Rheum Dis]]></category>

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		<description><![CDATA[<table border="0" width="100%"><tr><td align="left"><a href="http://ard.bmj.com/cgi/pmidlookup?view=long&#38;pmid=19022818"><img src="http://www.ncbi.nlm.nih.gov/entrez/query/egifs/http:--highwire.stanford.edu-icons-externalservices-pubmed-standard-annrheumdis_final.gif" border="0"></a> </td><td align="right"><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&#38;cmd=Display&#38;dopt=PubMed_PubMed&#38;from_uid=19022818">Related Articles</a></td></tr></table>
        <p><b>Nephrogenic systemic fibrosis: a gadolinium-associated fibrosing disorder in patients with renal dysfunction.</b></p>
        <p>Ann Rheum Dis. 2008 Dec;67 Suppl 3:iii66-9</p>
        <p>Authors:  Kay J</p>
        <p>Nephrogenic systemic fibrosis (NSF) is a debilitating fibrosing disorder that develops in patients with underlying kidney disease following exposure to gadolinium-containing contrast agents. NSF presents with cutaneous hyperpigmentation and induration and joint contractures, but fibrosis may also develop in other organs. NSF has been observed in up to 18% of patients receiving chronic haemodialysis and also may occur in individuals with stages 3 and 4 chronic kidney disease and, occasionally, in individuals who had experienced acute renal failure. Mortality is increased significantly among individuals with NSF. Although no medical treatment has been proved to be universally effective in patients with NSF, imatinib mesylate shows potential as a therapeutic agent and is currently being studied in these patients.</p>
        <p>PMID: 19022818 [PubMed - indexed for MEDLINE]</p>]]></description>
			<content:encoded><![CDATA[<table border="0" width="100%"><tr><td align="left"><a href="http://ard.bmj.com/cgi/pmidlookup?view=long&amp;pmid=19022818"><img src="http://www.ncbi.nlm.nih.gov/entrez/query/egifs/http:--highwire.stanford.edu-icons-externalservices-pubmed-standard-annrheumdis_final.gif" border="0"></a> </td><td align="right"><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&amp;cmd=Display&amp;dopt=PubMed_PubMed&amp;from_uid=19022818">Related Articles</a></td></tr></table>
        <p><b>Nephrogenic systemic fibrosis: a gadolinium-associated fibrosing disorder in patients with renal dysfunction.</b></p>
        <p>Ann Rheum Dis. 2008 Dec;67 Suppl 3:iii66-9</p>
        <p>Authors:  Kay J</p>
        <p>Nephrogenic systemic fibrosis (NSF) is a debilitating fibrosing disorder that develops in patients with underlying kidney disease following exposure to gadolinium-containing contrast agents. NSF presents with cutaneous hyperpigmentation and induration and joint contractures, but fibrosis may also develop in other organs. NSF has been observed in up to 18% of patients receiving chronic haemodialysis and also may occur in individuals with stages 3 and 4 chronic kidney disease and, occasionally, in individuals who had experienced acute renal failure. Mortality is increased significantly among individuals with NSF. Although no medical treatment has been proved to be universally effective in patients with NSF, imatinib mesylate shows potential as a therapeutic agent and is currently being studied in these patients.</p>
        <p>PMID: 19022818 [PubMed - indexed for MEDLINE]</p>]]></content:encoded>
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		<title>A double-blind placebo controlled trial of etanercept in patients with giant cell arteritis and corticosteroid side effects.</title>
		<link>http://beckerinfo.net/JClub/2008/11/17/a-double-blind-placebo-controlled-trial-of-etanercept-in-patients-with-giant-cell-arteritis-and-corticosteroid-side-effects/</link>
		<comments>http://beckerinfo.net/JClub/2008/11/17/a-double-blind-placebo-controlled-trial-of-etanercept-in-patients-with-giant-cell-arteritis-and-corticosteroid-side-effects/#comments</comments>
		<pubDate>Mon, 17 Nov 2008 15:01:41 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Ann Rheum Dis]]></category>

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		<description><![CDATA[<table border="0" width="100%"><tr><td align="left"><a href="http://ard.bmj.com/cgi/pmidlookup?view=long&#38;pmid=18086726"><img src="http://www.ncbi.nlm.nih.gov/entrez/query/egifs/http:--highwire.stanford.edu-icons-externalservices-pubmed-standard-annrheumdis_final.gif" border="0"></a> </td><td align="right"><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&#38;cmd=Display&#38;dopt=PubMed_PubMed&#38;from_uid=18086726">Related Articles</a></td></tr></table>
        <p><b>A double-blind placebo controlled trial of etanercept in patients with giant cell arteritis and corticosteroid side effects.</b></p>
        <p>Ann Rheum Dis. 2008 May;67(5):625-30</p>
        <p>Authors:  Martínez-Taboada VM, Rodríguez-Valverde V, Carreño L, López-Longo J, Figueroa M, Belzunegui J, Mola EM, Bonilla G</p>
        <p>OBJECTIVE: Open label studies have suggested that tumour necrosis factor (TNF) antagonists led to sustained improvement and corticosteroid sparing effect in patients with giant cell arteritis (GCA). To confirm these observations, we conducted a randomised, double-blind, placebo controlled trial with etanercept in patients with biopsy-proven GCA with side effects secondary to corticosteroids. METHODS: We randomly assigned patients with GCA to receive etanercept (n = 8) or placebo (n = 9) over 1 year together with corticosteroids that were reduced according to a predefined schedule. The primary outcome was the ability to withdraw the corticosteroid therapy and control the disease activity at 12 months. RESULTS: Baseline characteristics were similar in the two groups, although patients in the etanercept group showed higher levels of basal glycaemia (p = 0.02) and a higher erythrocyte sedimentation rate (ESR) (p = 0.01). After 12 months, 50% of the patients in the etanercept group and 22.2% in the placebo group were able to control the disease without corticosteroid therapy (p value not significant). Patients in the etanercept group had a significant lower dose of accumulated prednisone during the first year of treatment (p = 0.03). There were no differences in the number and type of adverse events. CONCLUSION: The limited number of patients included in this study does not allow us to draw definitive conclusions. Etanercept therapy was well tolerated in this aged population. The therapeutic role of etanercept in patients with GCA should be evaluated in studies with a larger number of patients.</p>
        <p>PMID: 18086726 [PubMed - indexed for MEDLINE]</p>]]></description>
			<content:encoded><![CDATA[<table border="0" width="100%"><tr><td align="left"><a href="http://ard.bmj.com/cgi/pmidlookup?view=long&amp;pmid=18086726"><img src="http://www.ncbi.nlm.nih.gov/entrez/query/egifs/http:--highwire.stanford.edu-icons-externalservices-pubmed-standard-annrheumdis_final.gif" border="0"></a> </td><td align="right"><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&amp;cmd=Display&amp;dopt=PubMed_PubMed&amp;from_uid=18086726">Related Articles</a></td></tr></table>
        <p><b>A double-blind placebo controlled trial of etanercept in patients with giant cell arteritis and corticosteroid side effects.</b></p>
        <p>Ann Rheum Dis. 2008 May;67(5):625-30</p>
        <p>Authors:  Martínez-Taboada VM, Rodríguez-Valverde V, Carreño L, López-Longo J, Figueroa M, Belzunegui J, Mola EM, Bonilla G</p>
        <p>OBJECTIVE: Open label studies have suggested that tumour necrosis factor (TNF) antagonists led to sustained improvement and corticosteroid sparing effect in patients with giant cell arteritis (GCA). To confirm these observations, we conducted a randomised, double-blind, placebo controlled trial with etanercept in patients with biopsy-proven GCA with side effects secondary to corticosteroids. METHODS: We randomly assigned patients with GCA to receive etanercept (n = 8) or placebo (n = 9) over 1 year together with corticosteroids that were reduced according to a predefined schedule. The primary outcome was the ability to withdraw the corticosteroid therapy and control the disease activity at 12 months. RESULTS: Baseline characteristics were similar in the two groups, although patients in the etanercept group showed higher levels of basal glycaemia (p = 0.02) and a higher erythrocyte sedimentation rate (ESR) (p = 0.01). After 12 months, 50% of the patients in the etanercept group and 22.2% in the placebo group were able to control the disease without corticosteroid therapy (p value not significant). Patients in the etanercept group had a significant lower dose of accumulated prednisone during the first year of treatment (p = 0.03). There were no differences in the number and type of adverse events. CONCLUSION: The limited number of patients included in this study does not allow us to draw definitive conclusions. Etanercept therapy was well tolerated in this aged population. The therapeutic role of etanercept in patients with GCA should be evaluated in studies with a larger number of patients.</p>
        <p>PMID: 18086726 [PubMed - indexed for MEDLINE]</p>]]></content:encoded>
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