AB1013 Pulse of Methylprednisolone May Reduce the Risk of Renal Involvement in Children with Henoch-Schonlein Purpura
BackgroundHenoch-Schonlein purpura (HSP) is a disease with small blood vessels inflammation. Although HSP can affect people at any age, most cases occur in children between the ages of 2 and 11. The disease involves skin, intestines, kidneys, and joints. The main symptom is a rash with numerous smal...
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description | BackgroundHenoch-Schonlein purpura (HSP) is a disease with small blood vessels inflammation. Although HSP can affect people at any age, most cases occur in children between the ages of 2 and 11. The disease involves skin, intestines, kidneys, and joints. The main symptom is a rash with numerous small bruises, which have a raised appearance, over the legs or buttocks. Almost 30-40% of children with HSP may have renal involvement. In most patients, the kidney impairment is mild and goes away without any long-term damage. However, about 5% of patients may develop progressive kidney disease and 1% may go on to end stage renal disease (ESRD).ObjectivesTo date, treatment of HSP remains primarily supportive in most cases. Hematuria at disease onset and persistence of renal manifestations during the occurrence of HSP can be significant predictors of possible development of renal sequelae. These manifestations, along with other features may predict the development of renal sequelae in most patients. Various drugs have been used to prevent renal disease from progressing. The results have been inconsistent. The aim of our study was to evaluate the efficacy of pulsed Methylprednisolone in children with HSP and renal manifestation.Methods69 children with HSP who had HSP and were admitted to Mofid Children's Hospital were evaluated; Children who had the indication of treatment were received 30mg/kg of Methylprednisolone for three consecutive days instead of traditionally oral prednisolone therapy. All of children were followed for ten years and evaluated for renal involvement.ResultsOf 69 patients with HSP, 55 children full filed the indication of therapy and were received pulsed methylprednisolone. Only 6 patients had the renal manifestation but no ESRD. Only one patient had persistent renal disease that was treated by Cyclophosphamide.ConclusionsThe previous results showed that 30-40% of children with HSP may have renal involvement and about 5% of patients may develop progressive kidney disease. Our 10 years follow up showed that only 10% of children who were admitted to Hospital and were received pulse of Methylprednisolone, had renal involvement. None of 69 patients suffered ESRD.We suggest limiting the indications of steroid therapy for children with HSP. However, if the patients need to receive steroid therapy, pulse of Methylprednisolone may reduce the latent renal complications.Disclosure of InterestNone declared |
doi_str_mv | 10.1136/annrheumdis-2015-eular.5556 |
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Although HSP can affect people at any age, most cases occur in children between the ages of 2 and 11. The disease involves skin, intestines, kidneys, and joints. The main symptom is a rash with numerous small bruises, which have a raised appearance, over the legs or buttocks. Almost 30-40% of children with HSP may have renal involvement. In most patients, the kidney impairment is mild and goes away without any long-term damage. However, about 5% of patients may develop progressive kidney disease and 1% may go on to end stage renal disease (ESRD).ObjectivesTo date, treatment of HSP remains primarily supportive in most cases. Hematuria at disease onset and persistence of renal manifestations during the occurrence of HSP can be significant predictors of possible development of renal sequelae. These manifestations, along with other features may predict the development of renal sequelae in most patients. Various drugs have been used to prevent renal disease from progressing. The results have been inconsistent. The aim of our study was to evaluate the efficacy of pulsed Methylprednisolone in children with HSP and renal manifestation.Methods69 children with HSP who had HSP and were admitted to Mofid Children's Hospital were evaluated; Children who had the indication of treatment were received 30mg/kg of Methylprednisolone for three consecutive days instead of traditionally oral prednisolone therapy. All of children were followed for ten years and evaluated for renal involvement.ResultsOf 69 patients with HSP, 55 children full filed the indication of therapy and were received pulsed methylprednisolone. Only 6 patients had the renal manifestation but no ESRD. Only one patient had persistent renal disease that was treated by Cyclophosphamide.ConclusionsThe previous results showed that 30-40% of children with HSP may have renal involvement and about 5% of patients may develop progressive kidney disease. Our 10 years follow up showed that only 10% of children who were admitted to Hospital and were received pulse of Methylprednisolone, had renal involvement. None of 69 patients suffered ESRD.We suggest limiting the indications of steroid therapy for children with HSP. However, if the patients need to receive steroid therapy, pulse of Methylprednisolone may reduce the latent renal complications.Disclosure of InterestNone declared</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/annrheumdis-2015-eular.5556</identifier><identifier>CODEN: ARDIAO</identifier><language>eng</language><publisher>Kidlington: Elsevier Limited</publisher><ispartof>Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.1237</ispartof><rights>2015, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>Copyright: 2015 (c) 2015, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://ard.bmj.com/content/74/Suppl_2/1237.2.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://ard.bmj.com/content/74/Suppl_2/1237.2.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,776,780,3183,23550,27901,27902,77343,77374</link.rule.ids></links><search><creatorcontrib>Javadi Parvaneh, V.</creatorcontrib><creatorcontrib>Shiari, R.</creatorcontrib><creatorcontrib>Rahmani, K.</creatorcontrib><creatorcontrib>Mehregan, F.F.</creatorcontrib><creatorcontrib>Mahboubi, L.</creatorcontrib><creatorcontrib>Salehi, S.</creatorcontrib><creatorcontrib>Yeganeh, M.H.</creatorcontrib><title>AB1013 Pulse of Methylprednisolone May Reduce the Risk of Renal Involvement in Children with Henoch-Schonlein Purpura</title><title>Annals of the rheumatic diseases</title><description>BackgroundHenoch-Schonlein purpura (HSP) is a disease with small blood vessels inflammation. Although HSP can affect people at any age, most cases occur in children between the ages of 2 and 11. The disease involves skin, intestines, kidneys, and joints. The main symptom is a rash with numerous small bruises, which have a raised appearance, over the legs or buttocks. Almost 30-40% of children with HSP may have renal involvement. In most patients, the kidney impairment is mild and goes away without any long-term damage. However, about 5% of patients may develop progressive kidney disease and 1% may go on to end stage renal disease (ESRD).ObjectivesTo date, treatment of HSP remains primarily supportive in most cases. Hematuria at disease onset and persistence of renal manifestations during the occurrence of HSP can be significant predictors of possible development of renal sequelae. These manifestations, along with other features may predict the development of renal sequelae in most patients. Various drugs have been used to prevent renal disease from progressing. The results have been inconsistent. The aim of our study was to evaluate the efficacy of pulsed Methylprednisolone in children with HSP and renal manifestation.Methods69 children with HSP who had HSP and were admitted to Mofid Children's Hospital were evaluated; Children who had the indication of treatment were received 30mg/kg of Methylprednisolone for three consecutive days instead of traditionally oral prednisolone therapy. All of children were followed for ten years and evaluated for renal involvement.ResultsOf 69 patients with HSP, 55 children full filed the indication of therapy and were received pulsed methylprednisolone. Only 6 patients had the renal manifestation but no ESRD. Only one patient had persistent renal disease that was treated by Cyclophosphamide.ConclusionsThe previous results showed that 30-40% of children with HSP may have renal involvement and about 5% of patients may develop progressive kidney disease. Our 10 years follow up showed that only 10% of children who were admitted to Hospital and were received pulse of Methylprednisolone, had renal involvement. None of 69 patients suffered ESRD.We suggest limiting the indications of steroid therapy for children with HSP. However, if the patients need to receive steroid therapy, pulse of Methylprednisolone may reduce the latent renal complications.Disclosure of InterestNone declared</description><issn>0003-4967</issn><issn>1468-2060</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNqVkE1P3DAQhq2qSN1C_4MlzqGefDixeqKrlkUCgZb2bPljrGSbtbd2wmpvvfSP8ktIWA5cOY1m5n3nHT2EnAO7ACj4V-V9bHHc2i5lOYMqw7FX8aKqKv6BLKDkzTTm7CNZMMaKrBS8_kQ-p7SZWtZAsyD7y-_AoHj69_9-7BPS4OgtDu2h30W0vkuhDx7prTrQNdrRIB1apOsu_ZmVa_Sqp9f-MfSPuEU_0M7TZdv1NqKn-25o6Qp9MG32YNrge5zW92PcjVGdkROnpsAvr_WU_P7549dyld3cXV0vL28yDXnNM6ebxnB0YI0urXLMKQAwIBxarXMUui5KhahFaXMNTKE1Shiel5UQ1hXFKTk_3t3F8HfENMhNGOP0dpIgGNSiLgo-qb4dVSaGlCI6uYvdVsWDBCZn0vINaTmTli-k5Ux6cvOjW2837zI-AxzijW8</recordid><startdate>201506</startdate><enddate>201506</enddate><creator>Javadi Parvaneh, V.</creator><creator>Shiari, R.</creator><creator>Rahmani, K.</creator><creator>Mehregan, F.F.</creator><creator>Mahboubi, L.</creator><creator>Salehi, S.</creator><creator>Yeganeh, M.H.</creator><general>Elsevier Limited</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>201506</creationdate><title>AB1013 Pulse of Methylprednisolone May Reduce the Risk of Renal Involvement in Children with Henoch-Schonlein Purpura</title><author>Javadi Parvaneh, V. ; Shiari, R. ; Rahmani, K. ; Mehregan, F.F. ; Mahboubi, L. ; Salehi, S. ; Yeganeh, M.H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1276-fb88c6ef1dcb4daf0fa111c19fedbb2e9b734aeeb94d2b10aedca9c624599df33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Javadi Parvaneh, V.</creatorcontrib><creatorcontrib>Shiari, R.</creatorcontrib><creatorcontrib>Rahmani, K.</creatorcontrib><creatorcontrib>Mehregan, F.F.</creatorcontrib><creatorcontrib>Mahboubi, L.</creatorcontrib><creatorcontrib>Salehi, S.</creatorcontrib><creatorcontrib>Yeganeh, M.H.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><jtitle>Annals of the rheumatic diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Javadi Parvaneh, V.</au><au>Shiari, R.</au><au>Rahmani, K.</au><au>Mehregan, F.F.</au><au>Mahboubi, L.</au><au>Salehi, S.</au><au>Yeganeh, M.H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>AB1013 Pulse of Methylprednisolone May Reduce the Risk of Renal Involvement in Children with Henoch-Schonlein Purpura</atitle><jtitle>Annals of the rheumatic diseases</jtitle><date>2015-06</date><risdate>2015</risdate><volume>74</volume><issue>Suppl 2</issue><spage>1237</spage><pages>1237-</pages><issn>0003-4967</issn><eissn>1468-2060</eissn><coden>ARDIAO</coden><abstract>BackgroundHenoch-Schonlein purpura (HSP) is a disease with small blood vessels inflammation. Although HSP can affect people at any age, most cases occur in children between the ages of 2 and 11. The disease involves skin, intestines, kidneys, and joints. The main symptom is a rash with numerous small bruises, which have a raised appearance, over the legs or buttocks. Almost 30-40% of children with HSP may have renal involvement. In most patients, the kidney impairment is mild and goes away without any long-term damage. However, about 5% of patients may develop progressive kidney disease and 1% may go on to end stage renal disease (ESRD).ObjectivesTo date, treatment of HSP remains primarily supportive in most cases. Hematuria at disease onset and persistence of renal manifestations during the occurrence of HSP can be significant predictors of possible development of renal sequelae. These manifestations, along with other features may predict the development of renal sequelae in most patients. Various drugs have been used to prevent renal disease from progressing. The results have been inconsistent. The aim of our study was to evaluate the efficacy of pulsed Methylprednisolone in children with HSP and renal manifestation.Methods69 children with HSP who had HSP and were admitted to Mofid Children's Hospital were evaluated; Children who had the indication of treatment were received 30mg/kg of Methylprednisolone for three consecutive days instead of traditionally oral prednisolone therapy. All of children were followed for ten years and evaluated for renal involvement.ResultsOf 69 patients with HSP, 55 children full filed the indication of therapy and were received pulsed methylprednisolone. Only 6 patients had the renal manifestation but no ESRD. Only one patient had persistent renal disease that was treated by Cyclophosphamide.ConclusionsThe previous results showed that 30-40% of children with HSP may have renal involvement and about 5% of patients may develop progressive kidney disease. Our 10 years follow up showed that only 10% of children who were admitted to Hospital and were received pulse of Methylprednisolone, had renal involvement. None of 69 patients suffered ESRD.We suggest limiting the indications of steroid therapy for children with HSP. However, if the patients need to receive steroid therapy, pulse of Methylprednisolone may reduce the latent renal complications.Disclosure of InterestNone declared</abstract><cop>Kidlington</cop><pub>Elsevier Limited</pub><doi>10.1136/annrheumdis-2015-eular.5556</doi></addata></record> |
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title | AB1013 Pulse of Methylprednisolone May Reduce the Risk of Renal Involvement in Children with Henoch-Schonlein Purpura |
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