DI-015 Use of omalizumab for treatment of mast cell activation disease
BackgroundEvidence of the efficacy of omalizumab for mast cell activation disease (MCAD) has been collected from only a few case series and isolated cases. It is not approved for this indication in the USA or Europe.PurposeTo describe omalizumab’s effectiveness in a patient with MCAD.Material and me...
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Veröffentlicht in: | European journal of hospital pharmacy. Science and practice 2016-03, Vol.23 (Suppl 1), p.A124-A124 |
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creator | Fernández-Ginés, FD Rodriguez-Cuadros, TB Cañizares-Paz, S Alférez-García, I |
description | BackgroundEvidence of the efficacy of omalizumab for mast cell activation disease (MCAD) has been collected from only a few case series and isolated cases. It is not approved for this indication in the USA or Europe.PurposeTo describe omalizumab’s effectiveness in a patient with MCAD.Material and methodsA 40-year-old woman with MCAD syndrome had initial symptoms of hives, itching, angio-oedema, flushing, palpitations, diarrhoea, dizziness, dyspnoea and episodes of anaphylaxis. After a maximum dose of antihistamines, the patient presented with urticaria symptoms, to the same clinic, reporting constraint of her usual daily activities.ResultsShe had improvement in symptoms with omalizumab therapy, reducing the flushing, urticaria and tachycardias, and had better exercise tolerance. These symptoms had not improved with the maximum dose of antihistamine. For management of the disease, previous studies used the same dose of omalizumab, regardless of the levels of IgE and patient weight. The patient described generalised tingling the days prior to the next dose and in the days after administration. She continues to receive omalizumab 300 mg subcutaneously every 4 weeks, showing a good clinical response.ConclusionThis case supports the potential efficacy of omalizumab as a mast cell stabiliser for MCAS in adults not responding to maximal antihistamine therapy.References and/or AcknowledgementsTo my pharmacists colleagues.No conflict of interest. |
doi_str_mv | 10.1136/ejhpharm-2016-000875.282 |
format | Article |
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It is not approved for this indication in the USA or Europe.PurposeTo describe omalizumab’s effectiveness in a patient with MCAD.Material and methodsA 40-year-old woman with MCAD syndrome had initial symptoms of hives, itching, angio-oedema, flushing, palpitations, diarrhoea, dizziness, dyspnoea and episodes of anaphylaxis. After a maximum dose of antihistamines, the patient presented with urticaria symptoms, to the same clinic, reporting constraint of her usual daily activities.ResultsShe had improvement in symptoms with omalizumab therapy, reducing the flushing, urticaria and tachycardias, and had better exercise tolerance. These symptoms had not improved with the maximum dose of antihistamine. For management of the disease, previous studies used the same dose of omalizumab, regardless of the levels of IgE and patient weight. The patient described generalised tingling the days prior to the next dose and in the days after administration. She continues to receive omalizumab 300 mg subcutaneously every 4 weeks, showing a good clinical response.ConclusionThis case supports the potential efficacy of omalizumab as a mast cell stabiliser for MCAS in adults not responding to maximal antihistamine therapy.References and/or AcknowledgementsTo my pharmacists colleagues.No conflict of interest.</description><identifier>ISSN: 2047-9956</identifier><identifier>EISSN: 2047-9964</identifier><identifier>DOI: 10.1136/ejhpharm-2016-000875.282</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><subject>Histamine ; Monoclonal antibodies ; Urticaria</subject><ispartof>European journal of hospital pharmacy. Science and practice, 2016-03, Vol.23 (Suppl 1), p.A124-A124</ispartof><rights>2016, 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: 2016 (c) 2016, 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>2016 2016, 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><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Fernández-Ginés, FD</creatorcontrib><creatorcontrib>Rodriguez-Cuadros, TB</creatorcontrib><creatorcontrib>Cañizares-Paz, S</creatorcontrib><creatorcontrib>Alférez-García, I</creatorcontrib><title>DI-015 Use of omalizumab for treatment of mast cell activation disease</title><title>European journal of hospital pharmacy. Science and practice</title><description>BackgroundEvidence of the efficacy of omalizumab for mast cell activation disease (MCAD) has been collected from only a few case series and isolated cases. It is not approved for this indication in the USA or Europe.PurposeTo describe omalizumab’s effectiveness in a patient with MCAD.Material and methodsA 40-year-old woman with MCAD syndrome had initial symptoms of hives, itching, angio-oedema, flushing, palpitations, diarrhoea, dizziness, dyspnoea and episodes of anaphylaxis. After a maximum dose of antihistamines, the patient presented with urticaria symptoms, to the same clinic, reporting constraint of her usual daily activities.ResultsShe had improvement in symptoms with omalizumab therapy, reducing the flushing, urticaria and tachycardias, and had better exercise tolerance. These symptoms had not improved with the maximum dose of antihistamine. For management of the disease, previous studies used the same dose of omalizumab, regardless of the levels of IgE and patient weight. The patient described generalised tingling the days prior to the next dose and in the days after administration. She continues to receive omalizumab 300 mg subcutaneously every 4 weeks, showing a good clinical response.ConclusionThis case supports the potential efficacy of omalizumab as a mast cell stabiliser for MCAS in adults not responding to maximal antihistamine therapy.References and/or AcknowledgementsTo my pharmacists colleagues.No conflict of interest.</description><subject>Histamine</subject><subject>Monoclonal antibodies</subject><subject>Urticaria</subject><issn>2047-9956</issn><issn>2047-9964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kMtKAzEUhoMoWGrfIeB6au6TLKVeWii4seuQZBI6ZdKpSSroyo0v6pM4Q9Wlq3PgfPyH_wMAYjTHmIobv9setibFiiAsKoSQrPmcSHIGJgSxulJKsPO_nYtLMMu5tYhTKhWjagKWd6sKYf718bnJHvYB9tF07fsxGgtDn2BJ3pTo92W8RZMLdL7roHGlfTWl7fewabM32V-Bi2C67Gc_cwo2D_fPi2W1fnpcLW7XlcUIscp5ii0xUtXGIt9YZT0xOGDssCfBBMlZCI2rnR2qSEKUIFZyK4MgDrHQ0Cm4PuUeUv9y9LnoXX9M--GlJpyTmpOh7X8UriVjQlFJB4qeKBt3-pDaaNKbxkiPbvWvWz261Se3enBLvwEq8W6L</recordid><startdate>201603</startdate><enddate>201603</enddate><creator>Fernández-Ginés, FD</creator><creator>Rodriguez-Cuadros, TB</creator><creator>Cañizares-Paz, S</creator><creator>Alférez-García, I</creator><general>BMJ Publishing Group LTD</general><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>201603</creationdate><title>DI-015 Use of omalizumab for treatment of mast cell activation disease</title><author>Fernández-Ginés, FD ; Rodriguez-Cuadros, TB ; Cañizares-Paz, S ; Alférez-García, I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1004-ce31b2a897ab0edb9be2a1f11c1e2faf854ffdc7cb875822962b85b8f62c04fd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Histamine</topic><topic>Monoclonal antibodies</topic><topic>Urticaria</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fernández-Ginés, FD</creatorcontrib><creatorcontrib>Rodriguez-Cuadros, TB</creatorcontrib><creatorcontrib>Cañizares-Paz, S</creatorcontrib><creatorcontrib>Alférez-García, I</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</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><jtitle>European journal of hospital pharmacy. Science and practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fernández-Ginés, FD</au><au>Rodriguez-Cuadros, TB</au><au>Cañizares-Paz, S</au><au>Alférez-García, I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DI-015 Use of omalizumab for treatment of mast cell activation disease</atitle><jtitle>European journal of hospital pharmacy. Science and practice</jtitle><date>2016-03</date><risdate>2016</risdate><volume>23</volume><issue>Suppl 1</issue><spage>A124</spage><epage>A124</epage><pages>A124-A124</pages><issn>2047-9956</issn><eissn>2047-9964</eissn><abstract>BackgroundEvidence of the efficacy of omalizumab for mast cell activation disease (MCAD) has been collected from only a few case series and isolated cases. It is not approved for this indication in the USA or Europe.PurposeTo describe omalizumab’s effectiveness in a patient with MCAD.Material and methodsA 40-year-old woman with MCAD syndrome had initial symptoms of hives, itching, angio-oedema, flushing, palpitations, diarrhoea, dizziness, dyspnoea and episodes of anaphylaxis. After a maximum dose of antihistamines, the patient presented with urticaria symptoms, to the same clinic, reporting constraint of her usual daily activities.ResultsShe had improvement in symptoms with omalizumab therapy, reducing the flushing, urticaria and tachycardias, and had better exercise tolerance. These symptoms had not improved with the maximum dose of antihistamine. For management of the disease, previous studies used the same dose of omalizumab, regardless of the levels of IgE and patient weight. The patient described generalised tingling the days prior to the next dose and in the days after administration. She continues to receive omalizumab 300 mg subcutaneously every 4 weeks, showing a good clinical response.ConclusionThis case supports the potential efficacy of omalizumab as a mast cell stabiliser for MCAS in adults not responding to maximal antihistamine therapy.References and/or AcknowledgementsTo my pharmacists colleagues.No conflict of interest.</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/ejhpharm-2016-000875.282</doi></addata></record> |
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subjects | Histamine Monoclonal antibodies Urticaria |
title | DI-015 Use of omalizumab for treatment of mast cell activation disease |
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