NSAIDs hypersensitivity: questions not resolved
PURPOSE OF REVIEWNSAIDs are the drugs most frequently involved in hypersensitivity reactions (HSR). These are frequently prescribed at all ages. HSR are of great concern and can affect people at any age. These drugs can induce reactions by stimulating the adaptive immune system (IgE or T cell), know...
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Veröffentlicht in: | Current opinion in allergy and clinical immunology 2018-08, Vol.18 (4), p.291-301 |
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description | PURPOSE OF REVIEWNSAIDs are the drugs most frequently involved in hypersensitivity reactions (HSR). These are frequently prescribed at all ages. HSR are of great concern and can affect people at any age. These drugs can induce reactions by stimulating the adaptive immune system (IgE or T cell), known as selective responders or more frequently by abnormalities in biochemical pathways related with prostaglandin metabolism. These are known as cross-intolerant. With some exceptions, skin testing and in-vitro studies are of little value in selective responders.
RECENT FINDINGSIn the last years, several classifications have been provided based on clinical symptoms, time interval between drug intake and appearance of symptoms, response to other nonchemically related NSAIDs and the diseases. Based on this classification, several well differentiated categories within each group of entities cross-intolerant and selective responders are now recognized. The most complex groups for evaluation are cross-intolerant in which three major groups existNSAIDs exacerbated respiratory disease, NSAIDs exacerbated cutaneous disease and NSAIDs-induced urticaria/angioedema in the absence of chronic spontaneous urticaria. Within the selective responders, there are two mechanisms involveddrug-specific IgE or T-cell effector responses. New entities have been added to this classification like mixed reactions within the cross-intolerant category, that must manifest as anaphylaxis and multiple immediate selective reactions.
SUMMARYThe precise evaluation of patients with NSAIDs hypersensitivity following established guidelines will improve not only our understanding but also the management of these entices. As the number of patients affected with NSAIDs is important, further studies are warranted. |
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RECENT FINDINGSIn the last years, several classifications have been provided based on clinical symptoms, time interval between drug intake and appearance of symptoms, response to other nonchemically related NSAIDs and the diseases. Based on this classification, several well differentiated categories within each group of entities cross-intolerant and selective responders are now recognized. The most complex groups for evaluation are cross-intolerant in which three major groups existNSAIDs exacerbated respiratory disease, NSAIDs exacerbated cutaneous disease and NSAIDs-induced urticaria/angioedema in the absence of chronic spontaneous urticaria. Within the selective responders, there are two mechanisms involveddrug-specific IgE or T-cell effector responses. New entities have been added to this classification like mixed reactions within the cross-intolerant category, that must manifest as anaphylaxis and multiple immediate selective reactions.
SUMMARYThe precise evaluation of patients with NSAIDs hypersensitivity following established guidelines will improve not only our understanding but also the management of these entices. As the number of patients affected with NSAIDs is important, further studies are warranted.</description><identifier>ISSN: 1528-4050</identifier><identifier>EISSN: 1473-6322</identifier><identifier>DOI: 10.1097/ACI.0000000000000454</identifier><identifier>PMID: 29878898</identifier><language>eng</language><publisher>United States: Copyright Wolters Kluwer Health, Inc. All rights reserved</publisher><subject>Angioedema - blood ; Angioedema - diagnosis ; Angioedema - epidemiology ; Angioedema - immunology ; Anti-Inflammatory Agents, Non-Steroidal - adverse effects ; Drug Hypersensitivity - blood ; Drug Hypersensitivity - diagnosis ; Drug Hypersensitivity - epidemiology ; Drug Hypersensitivity - immunology ; Humans ; Hypersensitivity, Immediate - blood ; Hypersensitivity, Immediate - diagnosis ; Hypersensitivity, Immediate - epidemiology ; Hypersensitivity, Immediate - immunology ; Immunoglobulin E - blood ; Immunoglobulin E - immunology ; Immunologic Tests - methods ; Immunologic Tests - standards ; Pharmacogenomic Testing - methods ; Pharmacogenomic Variants - immunology ; Prevalence ; Respiratory Tract Diseases - blood ; Respiratory Tract Diseases - diagnosis ; Respiratory Tract Diseases - epidemiology ; Respiratory Tract Diseases - immunology ; Symptom Flare Up ; T-Lymphocyte Subsets - drug effects ; T-Lymphocyte Subsets - immunology</subject><ispartof>Current opinion in allergy and clinical immunology, 2018-08, Vol.18 (4), p.291-301</ispartof><rights>Copyright © 2018 Wolters Kluwer Health, Inc. All rights reserved.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3564-7dc0cf51c639b94b72a68bc9606b7590a9a871262c8b1888a92a1cf4959d620a3</citedby><cites>FETCH-LOGICAL-c3564-7dc0cf51c639b94b72a68bc9606b7590a9a871262c8b1888a92a1cf4959d620a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29878898$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Blanca-Lopez, Natalia</creatorcontrib><creatorcontrib>Somoza-Alvarez, Maria L</creatorcontrib><creatorcontrib>Bellon, Teresa</creatorcontrib><creatorcontrib>Amo, Gemma</creatorcontrib><creatorcontrib>Canto, Gabriela</creatorcontrib><creatorcontrib>Blanca, Miguel</creatorcontrib><title>NSAIDs hypersensitivity: questions not resolved</title><title>Current opinion in allergy and clinical immunology</title><addtitle>Curr Opin Allergy Clin Immunol</addtitle><description>PURPOSE OF REVIEWNSAIDs are the drugs most frequently involved in hypersensitivity reactions (HSR). These are frequently prescribed at all ages. HSR are of great concern and can affect people at any age. These drugs can induce reactions by stimulating the adaptive immune system (IgE or T cell), known as selective responders or more frequently by abnormalities in biochemical pathways related with prostaglandin metabolism. These are known as cross-intolerant. With some exceptions, skin testing and in-vitro studies are of little value in selective responders.
RECENT FINDINGSIn the last years, several classifications have been provided based on clinical symptoms, time interval between drug intake and appearance of symptoms, response to other nonchemically related NSAIDs and the diseases. Based on this classification, several well differentiated categories within each group of entities cross-intolerant and selective responders are now recognized. The most complex groups for evaluation are cross-intolerant in which three major groups existNSAIDs exacerbated respiratory disease, NSAIDs exacerbated cutaneous disease and NSAIDs-induced urticaria/angioedema in the absence of chronic spontaneous urticaria. Within the selective responders, there are two mechanisms involveddrug-specific IgE or T-cell effector responses. New entities have been added to this classification like mixed reactions within the cross-intolerant category, that must manifest as anaphylaxis and multiple immediate selective reactions.
SUMMARYThe precise evaluation of patients with NSAIDs hypersensitivity following established guidelines will improve not only our understanding but also the management of these entices. As the number of patients affected with NSAIDs is important, further studies are warranted.</description><subject>Angioedema - blood</subject><subject>Angioedema - diagnosis</subject><subject>Angioedema - epidemiology</subject><subject>Angioedema - immunology</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - adverse effects</subject><subject>Drug Hypersensitivity - blood</subject><subject>Drug Hypersensitivity - diagnosis</subject><subject>Drug Hypersensitivity - epidemiology</subject><subject>Drug Hypersensitivity - immunology</subject><subject>Humans</subject><subject>Hypersensitivity, Immediate - blood</subject><subject>Hypersensitivity, Immediate - diagnosis</subject><subject>Hypersensitivity, Immediate - epidemiology</subject><subject>Hypersensitivity, Immediate - immunology</subject><subject>Immunoglobulin E - blood</subject><subject>Immunoglobulin E - immunology</subject><subject>Immunologic Tests - methods</subject><subject>Immunologic Tests - standards</subject><subject>Pharmacogenomic Testing - methods</subject><subject>Pharmacogenomic Variants - immunology</subject><subject>Prevalence</subject><subject>Respiratory Tract Diseases - blood</subject><subject>Respiratory Tract Diseases - diagnosis</subject><subject>Respiratory Tract Diseases - epidemiology</subject><subject>Respiratory Tract Diseases - immunology</subject><subject>Symptom Flare Up</subject><subject>T-Lymphocyte Subsets - drug effects</subject><subject>T-Lymphocyte Subsets - immunology</subject><issn>1528-4050</issn><issn>1473-6322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kD9PwzAQxS0EoqXwDRDKyJL27NiOzVaVf5UqGIDZchxHDbhJsZNW-fYEWhBi4Ja74b13dz-EzjGMMch0Mp3Nx_C7KKMHaIhpmsQ8IeSwnxkRMQUGA3QSwisAJhLIMRoQKVIhpBiiycPTdH4domW3tj7YKpRNuSmb7ip6b21oyroKUVU3kbehdhubn6KjQrtgz_Z9hF5ub55n9_Hi8W4-my5ikzBO4zQ3YAqGDU9kJmmWEs1FZiQHnqVMgpZapJhwYkSGhRBaEo1NQSWTOSegkxG63OWuff11iVqVwVjndGXrNigC_W8YKIFeSndS4-sQvC3U2pcr7TuFQX2iUj0q9RdVb7vYb2izlc1_TN9seoHYCba1a3o4b67dWq-WVrtm-X_2B57wc0U</recordid><startdate>20180801</startdate><enddate>20180801</enddate><creator>Blanca-Lopez, Natalia</creator><creator>Somoza-Alvarez, Maria L</creator><creator>Bellon, Teresa</creator><creator>Amo, Gemma</creator><creator>Canto, Gabriela</creator><creator>Blanca, Miguel</creator><general>Copyright Wolters Kluwer Health, Inc. All rights reserved</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20180801</creationdate><title>NSAIDs hypersensitivity: questions not resolved</title><author>Blanca-Lopez, Natalia ; Somoza-Alvarez, Maria L ; Bellon, Teresa ; Amo, Gemma ; Canto, Gabriela ; Blanca, Miguel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3564-7dc0cf51c639b94b72a68bc9606b7590a9a871262c8b1888a92a1cf4959d620a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Angioedema - blood</topic><topic>Angioedema - diagnosis</topic><topic>Angioedema - epidemiology</topic><topic>Angioedema - immunology</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - adverse effects</topic><topic>Drug Hypersensitivity - blood</topic><topic>Drug Hypersensitivity - diagnosis</topic><topic>Drug Hypersensitivity - epidemiology</topic><topic>Drug Hypersensitivity - immunology</topic><topic>Humans</topic><topic>Hypersensitivity, Immediate - blood</topic><topic>Hypersensitivity, Immediate - diagnosis</topic><topic>Hypersensitivity, Immediate - epidemiology</topic><topic>Hypersensitivity, Immediate - immunology</topic><topic>Immunoglobulin E - blood</topic><topic>Immunoglobulin E - immunology</topic><topic>Immunologic Tests - methods</topic><topic>Immunologic Tests - standards</topic><topic>Pharmacogenomic Testing - methods</topic><topic>Pharmacogenomic Variants - immunology</topic><topic>Prevalence</topic><topic>Respiratory Tract Diseases - blood</topic><topic>Respiratory Tract Diseases - diagnosis</topic><topic>Respiratory Tract Diseases - epidemiology</topic><topic>Respiratory Tract Diseases - immunology</topic><topic>Symptom Flare Up</topic><topic>T-Lymphocyte Subsets - drug effects</topic><topic>T-Lymphocyte Subsets - immunology</topic><toplevel>online_resources</toplevel><creatorcontrib>Blanca-Lopez, Natalia</creatorcontrib><creatorcontrib>Somoza-Alvarez, Maria L</creatorcontrib><creatorcontrib>Bellon, Teresa</creatorcontrib><creatorcontrib>Amo, Gemma</creatorcontrib><creatorcontrib>Canto, Gabriela</creatorcontrib><creatorcontrib>Blanca, Miguel</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Current opinion in allergy and clinical immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Blanca-Lopez, Natalia</au><au>Somoza-Alvarez, Maria L</au><au>Bellon, Teresa</au><au>Amo, Gemma</au><au>Canto, Gabriela</au><au>Blanca, Miguel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>NSAIDs hypersensitivity: questions not resolved</atitle><jtitle>Current opinion in allergy and clinical immunology</jtitle><addtitle>Curr Opin Allergy Clin Immunol</addtitle><date>2018-08-01</date><risdate>2018</risdate><volume>18</volume><issue>4</issue><spage>291</spage><epage>301</epage><pages>291-301</pages><issn>1528-4050</issn><eissn>1473-6322</eissn><abstract>PURPOSE OF REVIEWNSAIDs are the drugs most frequently involved in hypersensitivity reactions (HSR). These are frequently prescribed at all ages. HSR are of great concern and can affect people at any age. These drugs can induce reactions by stimulating the adaptive immune system (IgE or T cell), known as selective responders or more frequently by abnormalities in biochemical pathways related with prostaglandin metabolism. These are known as cross-intolerant. With some exceptions, skin testing and in-vitro studies are of little value in selective responders.
RECENT FINDINGSIn the last years, several classifications have been provided based on clinical symptoms, time interval between drug intake and appearance of symptoms, response to other nonchemically related NSAIDs and the diseases. Based on this classification, several well differentiated categories within each group of entities cross-intolerant and selective responders are now recognized. The most complex groups for evaluation are cross-intolerant in which three major groups existNSAIDs exacerbated respiratory disease, NSAIDs exacerbated cutaneous disease and NSAIDs-induced urticaria/angioedema in the absence of chronic spontaneous urticaria. Within the selective responders, there are two mechanisms involveddrug-specific IgE or T-cell effector responses. New entities have been added to this classification like mixed reactions within the cross-intolerant category, that must manifest as anaphylaxis and multiple immediate selective reactions.
SUMMARYThe precise evaluation of patients with NSAIDs hypersensitivity following established guidelines will improve not only our understanding but also the management of these entices. As the number of patients affected with NSAIDs is important, further studies are warranted.</abstract><cop>United States</cop><pub>Copyright Wolters Kluwer Health, Inc. All rights reserved</pub><pmid>29878898</pmid><doi>10.1097/ACI.0000000000000454</doi><tpages>11</tpages></addata></record> |
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subjects | Angioedema - blood Angioedema - diagnosis Angioedema - epidemiology Angioedema - immunology Anti-Inflammatory Agents, Non-Steroidal - adverse effects Drug Hypersensitivity - blood Drug Hypersensitivity - diagnosis Drug Hypersensitivity - epidemiology Drug Hypersensitivity - immunology Humans Hypersensitivity, Immediate - blood Hypersensitivity, Immediate - diagnosis Hypersensitivity, Immediate - epidemiology Hypersensitivity, Immediate - immunology Immunoglobulin E - blood Immunoglobulin E - immunology Immunologic Tests - methods Immunologic Tests - standards Pharmacogenomic Testing - methods Pharmacogenomic Variants - immunology Prevalence Respiratory Tract Diseases - blood Respiratory Tract Diseases - diagnosis Respiratory Tract Diseases - epidemiology Respiratory Tract Diseases - immunology Symptom Flare Up T-Lymphocyte Subsets - drug effects T-Lymphocyte Subsets - immunology |
title | NSAIDs hypersensitivity: questions not resolved |
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