A case of long QT syndrome: challenges on a bumpy road
Key Clinical Message Beta‐agonist treatment during pregnancy may unmask the diagnosis of long QT syndrome. The QT prolongation can result in functional AV block. A history of seizure and/or sudden death in a family member should raise suspicion of ventricular tachycardia. More than one mutation may...
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| Veröffentlicht in: | CLINICAL CASE REPORTS 2017-06, Vol.5 (6), p.954-960 |
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| container_title | CLINICAL CASE REPORTS |
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| creator | Magnusson, Peter Gustafsson, Per‐Erik |
| description | Key Clinical Message
Beta‐agonist treatment during pregnancy may unmask the diagnosis of long QT syndrome. The QT prolongation can result in functional AV block. A history of seizure and/or sudden death in a family member should raise suspicion of ventricular tachycardia. More than one mutation may coexist. Refusal of beta‐blocker therapy complicates risk stratification.
Beta‐agonist treatment during pregnancy may unmask the diagnosis of Long QT syndrome. The QT prolongation can result in functional AV block. A history of seizure and/or sudden death in a family member should raise suspicion of ventricular tachycardia. More than one mutation may coexist. Refusal of beta‐blocker therapy complicates risk stratification. |
| doi_str_mv | 10.1002/ccr3.985 |
| format | Article |
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Beta‐agonist treatment during pregnancy may unmask the diagnosis of Long QT syndrome. The QT prolongation can result in functional AV block. A history of seizure and/or sudden death in a family member should raise suspicion of ventricular tachycardia. More than one mutation may coexist. Refusal of beta‐blocker therapy complicates risk stratification.</description><identifier>ISSN: 2050-0904</identifier><identifier>EISSN: 2050-0904</identifier><identifier>DOI: 10.1002/ccr3.985</identifier><identifier>PMID: 28588847</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Cardiac arrhythmia ; Case Report ; Case Reports ; Electrocardiography ; Genetic ; implantable cardioverter – defibrillator ; Long QT syndrome ; long QT syndrome, pregnancy ; Medicin och hälsovetenskap ; pregnancy ; premature ventricular complex ; risk stratification ; sudden cardiac death</subject><ispartof>CLINICAL CASE REPORTS, 2017-06, Vol.5 (6), p.954-960</ispartof><rights>2017 The Authors. published by John Wiley & Sons Ltd.</rights><rights>2017. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4605-7fa970a005085224bbdaa7178c76decce4618f21259c4572367cf43db2c983ec3</citedby><cites>FETCH-LOGICAL-c4605-7fa970a005085224bbdaa7178c76decce4618f21259c4572367cf43db2c983ec3</cites><orcidid>0000-0001-7906-7782</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458049/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458049/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,552,727,780,784,864,885,1417,11562,27924,27925,45574,45575,46052,46476,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28588847$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-327233$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:228588847$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Magnusson, Peter</creatorcontrib><creatorcontrib>Gustafsson, Per‐Erik</creatorcontrib><title>A case of long QT syndrome: challenges on a bumpy road</title><title>CLINICAL CASE REPORTS</title><addtitle>Clin Case Rep</addtitle><description>Key Clinical Message
Beta‐agonist treatment during pregnancy may unmask the diagnosis of long QT syndrome. The QT prolongation can result in functional AV block. A history of seizure and/or sudden death in a family member should raise suspicion of ventricular tachycardia. More than one mutation may coexist. Refusal of beta‐blocker therapy complicates risk stratification.
Beta‐agonist treatment during pregnancy may unmask the diagnosis of Long QT syndrome. The QT prolongation can result in functional AV block. A history of seizure and/or sudden death in a family member should raise suspicion of ventricular tachycardia. More than one mutation may coexist. Refusal of beta‐blocker therapy complicates risk stratification.</description><subject>Cardiac arrhythmia</subject><subject>Case Report</subject><subject>Case Reports</subject><subject>Electrocardiography</subject><subject>Genetic</subject><subject>implantable cardioverter – defibrillator</subject><subject>Long QT syndrome</subject><subject>long QT syndrome, pregnancy</subject><subject>Medicin och hälsovetenskap</subject><subject>pregnancy</subject><subject>premature ventricular complex</subject><subject>risk stratification</subject><subject>sudden cardiac death</subject><issn>2050-0904</issn><issn>2050-0904</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>D8T</sourceid><recordid>eNp1kU9PGzEQxS3UChCN1E9QWeqlhy6M_61tDkhRWlokJASCXi2v1xuWbtbBzhbl2-MoCQ2HnDyyf-_N8wxCnwmcEgB65lxkp1qJA3RMQUABGviHnfoIjVJ6AgACkgoCh-iIKqGU4vIYlWPsbPI4NLgL_RTf3uO07OsYZv4cu0fbdb6f-oRDjy2uhtl8iWOw9Sf0sbFd8qPNeYIeLn_eT34X1ze_ribj68LxEkQhG6slWMhRlKCUV1VtrSRSOVnW3jnPS6IaSqjQjgtJWSldw1ldUacV846doGLtm178fKjMPLYzG5cm2NZsrv7myhuuSwYi83ovP4-h_i_aCul2Fln7fa_2R_tnbEKcmmEwjOagLOMXazyzM1873y-i7d53fPfSt49mGv4ZwYUCrrPB141BDM-DTwvzFIbY53EaokEIDZKVmfq2plwMKUXfvHUgYFb7N6v9m7z_jH7ZTfQG7vxwM82XtvPLvUZmMrljK8NXPcy4-w</recordid><startdate>201706</startdate><enddate>201706</enddate><creator>Magnusson, Peter</creator><creator>Gustafsson, Per‐Erik</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><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>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><scope>ACNBI</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>DF2</scope><scope>ZZAVC</scope><scope>BZJLE</scope><scope>STUKM</scope><orcidid>https://orcid.org/0000-0001-7906-7782</orcidid></search><sort><creationdate>201706</creationdate><title>A case of long QT syndrome: challenges on a bumpy road</title><author>Magnusson, Peter ; Gustafsson, Per‐Erik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4605-7fa970a005085224bbdaa7178c76decce4618f21259c4572367cf43db2c983ec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Cardiac arrhythmia</topic><topic>Case Report</topic><topic>Case Reports</topic><topic>Electrocardiography</topic><topic>Genetic</topic><topic>implantable cardioverter – defibrillator</topic><topic>Long QT syndrome</topic><topic>long QT syndrome, pregnancy</topic><topic>Medicin och hälsovetenskap</topic><topic>pregnancy</topic><topic>premature ventricular complex</topic><topic>risk stratification</topic><topic>sudden cardiac death</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Magnusson, Peter</creatorcontrib><creatorcontrib>Gustafsson, Per‐Erik</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library Free Content</collection><collection>PubMed</collection><collection>CrossRef</collection><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 Essentials</collection><collection>ProQuest Central</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 Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content 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>PubMed Central (Full Participant titles)</collection><collection>SWEPUB Uppsala universitet full text</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Uppsala universitet</collection><collection>SwePub Articles full text</collection><collection>SwePub Other</collection><collection>SwePub Other full text</collection><jtitle>CLINICAL CASE REPORTS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Magnusson, Peter</au><au>Gustafsson, Per‐Erik</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A case of long QT syndrome: challenges on a bumpy road</atitle><jtitle>CLINICAL CASE REPORTS</jtitle><addtitle>Clin Case Rep</addtitle><date>2017-06</date><risdate>2017</risdate><volume>5</volume><issue>6</issue><spage>954</spage><epage>960</epage><pages>954-960</pages><issn>2050-0904</issn><eissn>2050-0904</eissn><abstract>Key Clinical Message
Beta‐agonist treatment during pregnancy may unmask the diagnosis of long QT syndrome. The QT prolongation can result in functional AV block. A history of seizure and/or sudden death in a family member should raise suspicion of ventricular tachycardia. More than one mutation may coexist. Refusal of beta‐blocker therapy complicates risk stratification.
Beta‐agonist treatment during pregnancy may unmask the diagnosis of Long QT syndrome. The QT prolongation can result in functional AV block. A history of seizure and/or sudden death in a family member should raise suspicion of ventricular tachycardia. More than one mutation may coexist. Refusal of beta‐blocker therapy complicates risk stratification.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>28588847</pmid><doi>10.1002/ccr3.985</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-7906-7782</orcidid><oa>free_for_read</oa></addata></record> |
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| subjects | Cardiac arrhythmia Case Report Case Reports Electrocardiography Genetic implantable cardioverter – defibrillator Long QT syndrome long QT syndrome, pregnancy Medicin och hälsovetenskap pregnancy premature ventricular complex risk stratification sudden cardiac death |
| title | A case of long QT syndrome: challenges on a bumpy road |
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