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<meta name="keywords" content="C0344432, disease or syndrome, polymorphic ventricular tachycardia, ventricular tachycardia, polymorphic, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="A type of ventricular tachycardia that is characterized by variable QRS complexes within each lead (i.e., QRS complexes may be different from beat to beat)." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=138002
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ConceptID=C0344432
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Polymorphic ventricular tachycardia</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>138002</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0344432</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Polymorphic Ventricular Tachycardia; polymorphic ventricular tachycardia; Ventricular tachycardia, polymorphic; ventricular tachycardia, polymorphic</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Ventricular tachycardia, polymorphic (251159007)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
||
<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0031677">HP:0031677</a></td></tr>
|
||
<tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0020575" target="_blank">MONDO:0020575</a></td></tr>
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<div class="portlet mgSection" id="ID_100">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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||
<div class="portlet_content ln">A type of ventricular tachycardia that is characterized by variable QRS complexes within each lead (i.e., QRS complexes may be different from beat to beat). [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="TLline">Polymorphic ventricular tachycardia</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/2848" ref="tree=MeSH" title="MedGen record for Disorder of cardiovascular system">Disorder of cardiovascular system</a></span><ul><li><span class="TLline"><a href="/medgen/116727" ref="tree=MeSH" title="MedGen record for Abnormality of the cardiovascular system">Abnormality of the cardiovascular system</a></span><ul><li><span class="TLline"><a href="/medgen/869166" ref="tree=MeSH" title="MedGen record for Abnormal cardiovascular system physiology">Abnormal cardiovascular system physiology</a></span><ul><li><span class="TLline"><a href="/medgen/1393551" ref="tree=MeSH" title="MedGen record for Abnormality of cardiovascular system electrophysiology">Abnormality of cardiovascular system electrophysiology</a></span><ul><li><span class="TLline"><a href="/medgen/2039" ref="tree=MeSH" title="MedGen record for Cardiac arrhythmia">Cardiac arrhythmia</a></span><ul><li><span class="TLline"><a href="/medgen/12068" ref="tree=MeSH" title="MedGen record for Ventricular tachycardia">Ventricular tachycardia</a></span><ul><li><span class="matched_ds">Polymorphic ventricular tachycardia</span><ul><li><span class="TLline"><a href="/medgen/393837" ref="tree=MeSH" title="MedGen record for Catecholaminergic polymorphic ventricular tachycardia 2">Catecholaminergic polymorphic ventricular tachycardia 2</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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||
</div>
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<div class="portlet mgSection" id="ID_112">
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||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_320273"><div><strong>Sick sinus syndrome 2, autosomal dominant</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>320273</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C1834144</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Sick sinus syndrome (also known as sinus node dysfunction) is a group of related heart conditions that can affect how the heart beats. "Sick sinus" refers to the sino-atrial (SA) node, which is an area of specialized cells in the heart that functions as a natural pacemaker. The SA node generates electrical impulses that start each heartbeat. These signals travel from the SA node to the rest of the heart, signaling the heart (cardiac) muscle to contract and pump blood. In people with sick sinus syndrome, the SA node does not function normally. In some cases, it does not produce the right signals to trigger a regular heartbeat. In others, abnormalities disrupt the electrical impulses and prevent them from reaching the rest of the heart.\n\nSick sinus syndrome occurs most commonly in older adults, although it can be diagnosed in people of any age. The condition increases the risk of several life-threatening problems involving the heart and blood vessels. These include a heart rhythm abnormality called atrial fibrillation, heart failure, cardiac arrest, and stroke.\n\nSick sinus syndrome tends to cause the heartbeat to be too slow (bradycardia), although occasionally the heartbeat is too fast (tachycardia). In some cases, the heartbeat rapidly switches from being too fast to being too slow, a condition known as tachycardia-bradycardia syndrome. Symptoms related to abnormal heartbeats can include dizziness, light-headedness, fainting (syncope), a sensation of fluttering or pounding in the chest (palpitations), and confusion or memory problems. During exercise, many affected individuals experience chest pain, difficulty breathing, or excessive tiredness (fatigue). Once symptoms of sick sinus syndrome appear, they usually worsen with time. However, some people with the condition never experience any related health problems.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/320273">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_393837"><div><strong>Catecholaminergic polymorphic ventricular tachycardia 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>393837</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C2677794</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Catecholaminergic polymorphic ventricular tachycardia (CPVT) is characterized by episodic syncope occurring during exercise or acute emotion. The underlying cause of these episodes is the onset of fast ventricular tachycardia (bidirectional or polymorphic). Spontaneous recovery may occur when these arrhythmias self-terminate. In other instances, ventricular tachycardia may degenerate into ventricular fibrillation and cause sudden death if cardiopulmonary resuscitation is not readily available. The mean onset of symptoms (usually a syncopal episode) is between age seven and 12 years; onset as late as the fourth decade of life has been reported. If untreated, CPVT is highly lethal, as approximately 30% of affected individuals experience at least one cardiac arrest and up to 80% have one or more syncopal spells. Sudden death may be the first manifestation of the disease.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/393837">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_462813"><div><strong>Catecholaminergic polymorphic ventricular tachycardia 3</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>462813</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C3151463</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Catecholaminergic polymorphic ventricular tachycardia (CPVT) is characterized by episodic syncope occurring during exercise or acute emotion. The underlying cause of these episodes is the onset of fast ventricular tachycardia (bidirectional or polymorphic). Spontaneous recovery may occur when these arrhythmias self-terminate. In other instances, ventricular tachycardia may degenerate into ventricular fibrillation and cause sudden death if cardiopulmonary resuscitation is not readily available. The mean onset of symptoms (usually a syncopal episode) is between age seven and 12 years; onset as late as the fourth decade of life has been reported. If untreated, CPVT is highly lethal, as approximately 30% of affected individuals experience at least one cardiac arrest and up to 80% have one or more syncopal spells. Sudden death may be the first manifestation of the disease.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/462813">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_815866"><div><strong>Catecholaminergic polymorphic ventricular tachycardia 5</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>815866</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C3809536</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Catecholaminergic polymorphic ventricular tachycardia (CPVT) is characterized by episodic syncope occurring during exercise or acute emotion. The underlying cause of these episodes is the onset of fast ventricular tachycardia (bidirectional or polymorphic). Spontaneous recovery may occur when these arrhythmias self-terminate. In other instances, ventricular tachycardia may degenerate into ventricular fibrillation and cause sudden death if cardiopulmonary resuscitation is not readily available. The mean onset of symptoms (usually a syncopal episode) is between age seven and 12 years; onset as late as the fourth decade of life has been reported. If untreated, CPVT is highly lethal, as approximately 30% of affected individuals experience at least one cardiac arrest and up to 80% have one or more syncopal spells. Sudden death may be the first manifestation of the disease.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/815866">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_864108"><div><strong>Long QT syndrome 14</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>864108</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C4015671</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">LQT14 is a cardiac arrhythmia disorder characterized by ventricular arrhythmias, often life-threatening, occurring very early in life, frequent episodes of T-wave alternans, markedly prolonged QTc intervals, and intermittent 2:1 atrioventricular block (Crotti et al., 2013). Patients with LQT14, LQT15 (616249), or LQT16 (618782), resulting from mutation in calmodulin genes CALM1, CALM2 (114182), or CALM3 (114183), respectively, typically have a more severe phenotype, with earlier onset, profound QT prolongation, and a high predilection for cardiac arrest and sudden death, than patients with mutations in other genes (Boczek et al., 2016).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/864108">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_864132"><div><strong>Long QT syndrome 15</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>864132</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C4015695</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">LQT15 is a cardiac arrhythmia disorder characterized by ventricular arrhythmias, often life-threatening, occurring very early in life, frequent episodes of T-wave alternans, markedly prolonged QTc intervals, and intermittent 2:1 atrioventricular block (Crotti et al., 2013). Patients with LQT14 (616247), LQT15, or LQT16 (618782), resulting from mutation in calmodulin genes CALM1 (114180), CALM2, or CALM3 (114183), respectively, typically have a more severe phenotype, with earlier onset, profound QT prolongation, and a high predilection for cardiac arrest and sudden death, than patients with mutations in other genes (Boczek et al., 2016).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/864132">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_393837" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Catecholaminergic polymorphic ventricular tachycardia 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_462813" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Catecholaminergic polymorphic ventricular tachycardia 3</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_815866" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Catecholaminergic polymorphic ventricular tachycardia 5</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_864108" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Long QT syndrome 14</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_864132" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Long QT syndrome 15</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_320273" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Sick sinus syndrome 2, autosomal dominant</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/34363988">2021 PACES Expert Consensus Statement on the Indications and Management of Cardiovascular Implantable Electronic Devices in Pediatric Patients.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Writing Committee Members,
|
||
Shah MJ,
|
||
Silka MJ,
|
||
Silva JNA,
|
||
Balaji S,
|
||
Beach CM,
|
||
Benjamin MN,
|
||
Berul CI,
|
||
Cannon B,
|
||
Cecchin F,
|
||
Cohen MI,
|
||
Dalal AS,
|
||
Dechert BE,
|
||
Foster A,
|
||
Gebauer R,
|
||
Gonzalez Corcia MC,
|
||
Kannankeril PJ,
|
||
Karpawich PP,
|
||
Kim JJ,
|
||
Krishna MR,
|
||
Kubuš P,
|
||
LaPage MJ,
|
||
Mah DY,
|
||
Malloy-Walton L,
|
||
Miyazaki A,
|
||
Motonaga KS,
|
||
Niu MC,
|
||
Olen M,
|
||
Paul T,
|
||
Rosenthal E,
|
||
Saarel EV,
|
||
Silvetti MS,
|
||
Stephenson EA,
|
||
Tan RB,
|
||
Triedman J,
|
||
Bergen NHV,
|
||
Wackel PL</span><br />
|
||
<span class="medgenPMjournal">Heart Rhythm</span>
|
||
2021 Nov;18(11):1888-1924.
|
||
Epub 2021 Jul 29
|
||
doi: 10.1016/j.hrthm.2021.07.038.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34363988" target="_blank">34363988</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30446242">An Update on the Diagnosis and Management of Catecholaminergic Polymorphic Ventricular Tachycardia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pflaumer A,
|
||
Davis AM</span><br />
|
||
<span class="medgenPMjournal">Heart Lung Circ</span>
|
||
2019 Mar;28(3):366-369.
|
||
Epub 2018 Nov 7
|
||
doi: 10.1016/j.hlc.2018.10.016.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30446242" target="_blank">30446242</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21698509">Anesthetic management of patients with Brugada syndrome: a case series and literature review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kloesel B,
|
||
Ackerman MJ,
|
||
Sprung J,
|
||
Narr BJ,
|
||
Weingarten TN</span><br />
|
||
<span class="medgenPMjournal">Can J Anaesth</span>
|
||
2011 Sep;58(9):824-36.
|
||
Epub 2011 Jun 23
|
||
doi: 10.1007/s12630-011-9546-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/21698509" target="_blank">21698509</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22polymorphic%20ventricular%20tachycardia%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (116)</a></div></div>
|
||
</div>
|
||
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
|
||
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
|
||
<div class="portlet mgSection" id="ID_103">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37622576">Risk stratification of sudden cardiac death: a review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tfelt-Hansen J,
|
||
Garcia R,
|
||
Albert C,
|
||
Merino J,
|
||
Krahn A,
|
||
Marijon E,
|
||
Basso C,
|
||
Wilde AAM,
|
||
Haugaa KH</span><br />
|
||
<span class="medgenPMjournal">Europace</span>
|
||
2023 Aug 25;25(8)
|
||
doi: 10.1093/europace/euad203.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37622576" target="_blank">37622576</a><a href="/pmc/articles/PMC10450787" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35353122">Outcomes of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia Treated With β-Blockers.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mazzanti A,
|
||
Kukavica D,
|
||
Trancuccio A,
|
||
Memmi M,
|
||
Bloise R,
|
||
Gambelli P,
|
||
Marino M,
|
||
Ortíz-Genga M,
|
||
Morini M,
|
||
Monteforte N,
|
||
Giordano U,
|
||
Keegan R,
|
||
Tomasi L,
|
||
Anastasakis A,
|
||
Davis AM,
|
||
Shimizu W,
|
||
Blom NA,
|
||
Santiago DJ,
|
||
Napolitano C,
|
||
Monserrat L,
|
||
Priori SG</span><br />
|
||
<span class="medgenPMjournal">JAMA Cardiol</span>
|
||
2022 May 1;7(5):504-512.
|
||
doi: 10.1001/jamacardio.2022.0219.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35353122" target="_blank">35353122</a><a href="/pmc/articles/PMC8968697" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33730522">Brugada syndrome clinical update.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rojas R,
|
||
Kaul R,
|
||
Frenkel D,
|
||
Hoch EG,
|
||
Iwai S,
|
||
Jacobson JT,
|
||
Aronow WS</span><br />
|
||
<span class="medgenPMjournal">Hosp Pract (1995)</span>
|
||
2021 Oct;49(4):255-261.
|
||
Epub 2021 Mar 30
|
||
doi: 10.1080/21548331.2021.1906012.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33730522" target="_blank">33730522</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29473523">Drug-induced QT Interval Prolongation in the Intensive Care Unit.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Etchegoyen CV,
|
||
Keller GA,
|
||
Mrad S,
|
||
Cheng S,
|
||
Di Girolamo G</span><br />
|
||
<span class="medgenPMjournal">Curr Clin Pharmacol</span>
|
||
2017;12(4):210-222.
|
||
doi: 10.2174/1574884713666180223123947.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29473523" target="_blank">29473523</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28912179">Classification, Epidemiology, and Global Burden of Cardiomyopathies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">McKenna WJ,
|
||
Maron BJ,
|
||
Thiene G</span><br />
|
||
<span class="medgenPMjournal">Circ Res</span>
|
||
2017 Sep 15;121(7):722-730.
|
||
doi: 10.1161/CIRCRESAHA.117.309711.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28912179" target="_blank">28912179</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Polymorphic%20ventricular%20tachycardia%22%20AND%20Etiology%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (628)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37558302">Calcium Release Deficiency Syndrome: A New Inherited Arrhythmia Syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kallas D,
|
||
Roberts JD,
|
||
Sanatani S,
|
||
Roston TM</span><br />
|
||
<span class="medgenPMjournal">Card Electrophysiol Clin</span>
|
||
2023 Sep;15(3):319-329.
|
||
Epub 2023 Jun 20
|
||
doi: 10.1016/j.ccep.2023.05.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37558302" target="_blank">37558302</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34669951">Inherited Arrhythmia Syndromes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kim JA,
|
||
Chelu MG</span><br />
|
||
<span class="medgenPMjournal">Tex Heart Inst J</span>
|
||
2021 Sep 1;48(4)
|
||
doi: 10.14503/THIJ-20-7482.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34669951" target="_blank">34669951</a><a href="/pmc/articles/PMC8717759" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34491774">Polymorphic Ventricular Tachycardia: Terminology, Mechanism, Diagnosis, and Emergency Therapy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Viskin S,
|
||
Chorin E,
|
||
Viskin D,
|
||
Hochstadt A,
|
||
Schwartz AL,
|
||
Rosso R</span><br />
|
||
<span class="medgenPMjournal">Circulation</span>
|
||
2021 Sep 7;144(10):823-839.
|
||
doi: 10.1161/CIRCULATIONAHA.121.055783.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34491774" target="_blank">34491774</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28912179">Classification, Epidemiology, and Global Burden of Cardiomyopathies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">McKenna WJ,
|
||
Maron BJ,
|
||
Thiene G</span><br />
|
||
<span class="medgenPMjournal">Circ Res</span>
|
||
2017 Sep 15;121(7):722-730.
|
||
doi: 10.1161/CIRCRESAHA.117.309711.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28912179" target="_blank">28912179</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/23022705">Catecholaminergic polymorphic ventricular tachycardia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Leenhardt A,
|
||
Denjoy I,
|
||
Guicheney P</span><br />
|
||
<span class="medgenPMjournal">Circ Arrhythm Electrophysiol</span>
|
||
2012 Oct;5(5):1044-52.
|
||
Epub 2012 Sep 27
|
||
doi: 10.1161/CIRCEP.111.962027.
|
||
<span class="bold">PMID: </span><a href="/pubmed/23022705" target="_blank">23022705</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Polymorphic%20ventricular%20tachycardia%22%20AND%20Diagnosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (777)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37558302">Calcium Release Deficiency Syndrome: A New Inherited Arrhythmia Syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kallas D,
|
||
Roberts JD,
|
||
Sanatani S,
|
||
Roston TM</span><br />
|
||
<span class="medgenPMjournal">Card Electrophysiol Clin</span>
|
||
2023 Sep;15(3):319-329.
|
||
Epub 2023 Jun 20
|
||
doi: 10.1016/j.ccep.2023.05.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37558302" target="_blank">37558302</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35353122">Outcomes of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia Treated With β-Blockers.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mazzanti A,
|
||
Kukavica D,
|
||
Trancuccio A,
|
||
Memmi M,
|
||
Bloise R,
|
||
Gambelli P,
|
||
Marino M,
|
||
Ortíz-Genga M,
|
||
Morini M,
|
||
Monteforte N,
|
||
Giordano U,
|
||
Keegan R,
|
||
Tomasi L,
|
||
Anastasakis A,
|
||
Davis AM,
|
||
Shimizu W,
|
||
Blom NA,
|
||
Santiago DJ,
|
||
Napolitano C,
|
||
Monserrat L,
|
||
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<div class="nl"><a target="_blank" href="/pubmed/23252797">Electrical storm in children.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Clausen H,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Polymorphic%20ventricular%20tachycardia%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (14)</a></div></div>
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