Concealed pre-excitation causing paroxysmal reciprocating atrioventricular tachycardia in infancy.
Identifieur interne : 001555 ( Main/Corpus ); précédent : 001554; suivant : 001556Concealed pre-excitation causing paroxysmal reciprocating atrioventricular tachycardia in infancy.
Auteurs : K A Hallidie-Smith ; D. Krikler ; A. MithchellSource :
- Archives of Disease in Childhood [ 0003-9888 ] ; 1978-08.
Abstract
We report 3 infants with Wolff-Parkinson-White (WPW) syndrome who presented with life-threatening paroxysmal reciprocating atrioventricular tachycardia in their first month of life. The diagnosis was confirmed by electrophysiological studies at ages 2--4 years, but the characteristic ECG of pre-excitation has not been shown in one patient and was first recorded at 2 and 3 years in the other two. In 2 patients the tachycardia proved refractory to treatment with digoxin alone but responded to the addition of propranalol or verapamil. One of these infants was converted to sinus rhythm by DC countershock, giving time to reconsider his treatment with drugs. Digoxin is a well-tried treatment acting by slowing AV conduction and interrupting the re-entry circuit. However, it may act more slowly than other agents that act on the AV node--such as intravenous verapamil. Our patients illustrate the value of long follow-up as the diagnosis of WPW syndrome could not be made in infancy. Many infants who present with paroxysmal supraventricular tachycardia in infancy may have an inapparent bypass and be examples of the WPW syndrome.
Url:
DOI: 10.1136/adc.53.8.668
Links to Exploration step
ISTEX:A605AFAA1952D11B69B3E8A9A65D7E9C32F29DB2Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Concealed pre-excitation causing paroxysmal reciprocating atrioventricular tachycardia in infancy.</title><author><name sortKey="Hallidie Smith, K A" sort="Hallidie Smith, K A" uniqKey="Hallidie Smith K" first="K A" last="Hallidie-Smith">K A Hallidie-Smith</name></author><author><name sortKey="Krikler, D" sort="Krikler, D" uniqKey="Krikler D" first="D" last="Krikler">D. Krikler</name></author><author><name sortKey="Mithchell, A" sort="Mithchell, A" uniqKey="Mithchell A" first="A" last="Mithchell">A. Mithchell</name></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:A605AFAA1952D11B69B3E8A9A65D7E9C32F29DB2</idno><date when="1978-08-01" year="1978">1978-08-01</date><idno type="doi">10.1136/adc.53.8.668</idno><idno type="url">https://api.istex.fr/document/A605AFAA1952D11B69B3E8A9A65D7E9C32F29DB2/fulltext/pdf</idno><idno type="wicri:Area/Main/Corpus">001555</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Concealed pre-excitation causing paroxysmal reciprocating atrioventricular tachycardia in infancy.</title><author><name sortKey="Hallidie Smith, K A" sort="Hallidie Smith, K A" uniqKey="Hallidie Smith K" first="K A" last="Hallidie-Smith">K A Hallidie-Smith</name></author><author><name sortKey="Krikler, D" sort="Krikler, D" uniqKey="Krikler D" first="D" last="Krikler">D. Krikler</name></author><author><name sortKey="Mithchell, A" sort="Mithchell, A" uniqKey="Mithchell A" first="A" last="Mithchell">A. Mithchell</name></author></analytic><monogr></monogr><series><title level="j">Archives of Disease in Childhood</title><title level="j" type="abbrev">Arch Dis Child</title><idno type="ISSN">0003-9888</idno><idno type="eISSN">1468-2044</idno><imprint><publisher>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</publisher><date type="published" when="1978-08">1978-08</date><biblScope unit="volume">53</biblScope><biblScope unit="issue">8</biblScope><biblScope unit="page" from="668">668</biblScope></imprint><idno type="ISSN">0003-9888</idno></series><idno type="istex">A605AFAA1952D11B69B3E8A9A65D7E9C32F29DB2</idno><idno type="DOI">10.1136/adc.53.8.668</idno><idno type="href">archdischild-53-668.pdf</idno><idno type="PMID">708105</idno><idno type="local">archdischild;53/8/668</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0003-9888</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">We report 3 infants with Wolff-Parkinson-White (WPW) syndrome who presented with life-threatening paroxysmal reciprocating atrioventricular tachycardia in their first month of life. The diagnosis was confirmed by electrophysiological studies at ages 2--4 years, but the characteristic ECG of pre-excitation has not been shown in one patient and was first recorded at 2 and 3 years in the other two. In 2 patients the tachycardia proved refractory to treatment with digoxin alone but responded to the addition of propranalol or verapamil. One of these infants was converted to sinus rhythm by DC countershock, giving time to reconsider his treatment with drugs. Digoxin is a well-tried treatment acting by slowing AV conduction and interrupting the re-entry circuit. However, it may act more slowly than other agents that act on the AV node--such as intravenous verapamil. Our patients illustrate the value of long follow-up as the diagnosis of WPW syndrome could not be made in infancy. Many infants who present with paroxysmal supraventricular tachycardia in infancy may have an inapparent bypass and be examples of the WPW syndrome.</div></front></TEI><istex><corpusName>bmj</corpusName><author><json:item><name>K A Hallidie-Smith</name></json:item><json:item><name>D Krikler</name></json:item><json:item><name>A Mithchell</name></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>Research Article</value></json:item></subject><language><json:string>eng</json:string></language><abstract>We report 3 infants with Wolff-Parkinson-White (WPW) syndrome who presented with life-threatening paroxysmal reciprocating atrioventricular tachycardia in their first month of life. The diagnosis was confirmed by electrophysiological studies at ages 2--4 years, but the characteristic ECG of pre-excitation has not been shown in one patient and was first recorded at 2 and 3 years in the other two. In 2 patients the tachycardia proved refractory to treatment with digoxin alone but responded to the addition of propranalol or verapamil. One of these infants was converted to sinus rhythm by DC countershock, giving time to reconsider his treatment with drugs. Digoxin is a well-tried treatment acting by slowing AV conduction and interrupting the re-entry circuit. However, it may act more slowly than other agents that act on the AV node--such as intravenous verapamil. Our patients illustrate the value of long follow-up as the diagnosis of WPW syndrome could not be made in infancy. Many infants who present with paroxysmal supraventricular tachycardia in infancy may have an inapparent bypass and be examples of the WPW syndrome.</abstract><qualityIndicators><score>5.356</score><pdfVersion>1.3</pdfVersion><pdfPageSize>516.48 x 705.6 pts</pdfPageSize><refBibsNative>false</refBibsNative><keywordCount>1</keywordCount><abstractCharCount>1134</abstractCharCount><pdfWordCount>3256</pdfWordCount><pdfCharCount>19939</pdfCharCount><pdfPageCount>6</pdfPageCount><abstractWordCount>175</abstractWordCount></qualityIndicators><title>Concealed pre-excitation causing paroxysmal reciprocating atrioventricular tachycardia in infancy.</title><pmid><json:string>708105</json:string></pmid><genre><json:string>research-article</json:string></genre><host><volume>53</volume><pages><first>668</first></pages><issn><json:string>0003-9888</json:string></issn><issue>8</issue><genre></genre><language><json:string>unknown</json:string></language><eissn><json:string>1468-2044</json:string></eissn><title>Archives of Disease in Childhood</title></host><publicationDate>1978</publicationDate><doi><json:string>10.1136/adc.53.8.668</json:string></doi><id>A605AFAA1952D11B69B3E8A9A65D7E9C32F29DB2</id><fulltext><json:item><original>true</original><mimetype>application/pdf</mimetype><extension>pdf</extension><uri>https://api.istex.fr/document/A605AFAA1952D11B69B3E8A9A65D7E9C32F29DB2/fulltext/pdf</uri></json:item><json:item><original>false</original><mimetype>application/zip</mimetype><extension>zip</extension><uri>https://api.istex.fr/document/A605AFAA1952D11B69B3E8A9A65D7E9C32F29DB2/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/A605AFAA1952D11B69B3E8A9A65D7E9C32F29DB2/fulltext/tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">Concealed pre-excitation causing paroxysmal reciprocating atrioventricular tachycardia in infancy.</title><respStmt xml:id="ISTEX-API" resp="Références bibliographiques récupérées via GROBID" name="ISTEX-API (INIST-CNRS)"></respStmt></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</publisher><availability><p>BMJ</p></availability><date>1978-08-01</date></publicationStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Concealed pre-excitation causing paroxysmal reciprocating atrioventricular tachycardia in infancy.</title><author><persName><forename type="first">K A</forename><surname>Hallidie-Smith</surname></persName></author><author><persName><forename type="first">D</forename><surname>Krikler</surname></persName></author><author><persName><forename type="first">A</forename><surname>Mithchell</surname></persName></author></analytic><monogr><title level="j">Archives of Disease in Childhood</title><title level="j" type="abbrev">Arch Dis Child</title><idno type="pISSN">0003-9888</idno><idno type="eISSN">1468-2044</idno><imprint><publisher>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</publisher><date type="published" when="1978-08"></date><biblScope unit="volume">53</biblScope><biblScope unit="issue">8</biblScope><biblScope unit="page" from="668">668</biblScope></imprint></monogr><idno type="istex">A605AFAA1952D11B69B3E8A9A65D7E9C32F29DB2</idno><idno type="DOI">10.1136/adc.53.8.668</idno><idno type="href">archdischild-53-668.pdf</idno><idno type="PMID">708105</idno><idno type="local">archdischild;53/8/668</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1978-08-01</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>We report 3 infants with Wolff-Parkinson-White (WPW) syndrome who presented with life-threatening paroxysmal reciprocating atrioventricular tachycardia in their first month of life. The diagnosis was confirmed by electrophysiological studies at ages 2--4 years, but the characteristic ECG of pre-excitation has not been shown in one patient and was first recorded at 2 and 3 years in the other two. In 2 patients the tachycardia proved refractory to treatment with digoxin alone but responded to the addition of propranalol or verapamil. One of these infants was converted to sinus rhythm by DC countershock, giving time to reconsider his treatment with drugs. Digoxin is a well-tried treatment acting by slowing AV conduction and interrupting the re-entry circuit. However, it may act more slowly than other agents that act on the AV node--such as intravenous verapamil. Our patients illustrate the value of long follow-up as the diagnosis of WPW syndrome could not be made in infancy. Many infants who present with paroxysmal supraventricular tachycardia in infancy may have an inapparent bypass and be examples of the WPW syndrome.</p></abstract></profileDesc><revisionDesc><change when="1978-08-01">Created</change><change when="1978-08">Published</change><change xml:id="refBibs-istex" who="#ISTEX-API" when="2016-3-14">References added</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><original>false</original><mimetype>text/plain</mimetype><extension>txt</extension><uri>https://api.istex.fr/document/A605AFAA1952D11B69B3E8A9A65D7E9C32F29DB2/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="corpus bmj" wicri:toSee="no header"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="no"</istex:xmlDeclaration><istex:docType PUBLIC="-//NLM//DTD Journal Archiving and Interchange DTD v2.3 20070202//EN" URI="archivearticle.dtd" name="istex:docType"></istex:docType><istex:document><article article-type="research-article" xml:lang="EN"><front><journal-meta><journal-id journal-id-type="hwp">archdischild</journal-id><journal-id journal-id-type="nlm-ta">Arch Dis Child</journal-id><journal-title>Archives of Disease in Childhood</journal-title><abbrev-journal-title abbrev-type="publisher">Arch Dis Child</abbrev-journal-title><issn pub-type="ppub">0003-9888</issn><issn pub-type="epub">1468-2044</issn><publisher><publisher-name>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">708105</article-id><article-id pub-id-type="other">archdischild;53/8/668</article-id><article-id pub-id-type="doi">10.1136/adc.53.8.668</article-id><article-id pub-id-type="other">668</article-id><article-id pub-id-type="other">adc.53.8.668</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title>Concealed pre-excitation causing paroxysmal reciprocating atrioventricular tachycardia in infancy.</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Hallidie-Smith</surname><given-names>K A</given-names></name></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Krikler</surname><given-names>D</given-names></name></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mithchell</surname><given-names>A</given-names></name></contrib></contrib-group><pub-date pub-type="ppub"><month>8</month><year>1978</year></pub-date><pub-date pub-type="epub"><day>1</day><month>8</month><year>1978</year></pub-date><volume>53</volume><volume-id pub-id-type="other">53</volume-id><volume-id pub-id-type="other">53</volume-id><issue>8</issue><issue-id pub-id-type="other">archdischild;53/8</issue-id><issue-id pub-id-type="other">8</issue-id><issue-id pub-id-type="other">53/8</issue-id><fpage>668</fpage><self-uri content-type="pdf" xlink:role="full-text" xlink:href="archdischild-53-668.pdf"></self-uri><abstract><p>We report 3 infants with Wolff-Parkinson-White (WPW) syndrome who presented with life-threatening paroxysmal reciprocating atrioventricular tachycardia in their first month of life. The diagnosis was confirmed by electrophysiological studies at ages 2--4 years, but the characteristic ECG of pre-excitation has not been shown in one patient and was first recorded at 2 and 3 years in the other two. In 2 patients the tachycardia proved refractory to treatment with digoxin alone but responded to the addition of propranalol or verapamil. One of these infants was converted to sinus rhythm by DC countershock, giving time to reconsider his treatment with drugs. Digoxin is a well-tried treatment acting by slowing AV conduction and interrupting the re-entry circuit. However, it may act more slowly than other agents that act on the AV node--such as intravenous verapamil. Our patients illustrate the value of long follow-up as the diagnosis of WPW syndrome could not be made in infancy. Many infants who present with paroxysmal supraventricular tachycardia in infancy may have an inapparent bypass and be examples of the WPW syndrome.</p></abstract></article-meta></front></article></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Concealed pre-excitation causing paroxysmal reciprocating atrioventricular tachycardia in infancy.</title></titleInfo><titleInfo type="alternative" lang="en" contentType="CDATA"><title>Concealed pre-excitation causing paroxysmal reciprocating atrioventricular tachycardia in infancy.</title></titleInfo><name type="personal"><namePart type="given">K A</namePart><namePart type="family">Hallidie-Smith</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">D</namePart><namePart type="family">Krikler</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">A</namePart><namePart type="family">Mithchell</namePart><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="research-article"></genre><originInfo><publisher>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</publisher><dateIssued encoding="w3cdtf">1978-08</dateIssued><dateCreated encoding="w3cdtf">1978-08-01</dateCreated></originInfo><language><languageTerm type="code" authority="iso639-2b">eng</languageTerm><languageTerm type="code" authority="rfc3066">en</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType></physicalDescription><abstract lang="en">We report 3 infants with Wolff-Parkinson-White (WPW) syndrome who presented with life-threatening paroxysmal reciprocating atrioventricular tachycardia in their first month of life. The diagnosis was confirmed by electrophysiological studies at ages 2--4 years, but the characteristic ECG of pre-excitation has not been shown in one patient and was first recorded at 2 and 3 years in the other two. In 2 patients the tachycardia proved refractory to treatment with digoxin alone but responded to the addition of propranalol or verapamil. One of these infants was converted to sinus rhythm by DC countershock, giving time to reconsider his treatment with drugs. Digoxin is a well-tried treatment acting by slowing AV conduction and interrupting the re-entry circuit. However, it may act more slowly than other agents that act on the AV node--such as intravenous verapamil. Our patients illustrate the value of long follow-up as the diagnosis of WPW syndrome could not be made in infancy. Many infants who present with paroxysmal supraventricular tachycardia in infancy may have an inapparent bypass and be examples of the WPW syndrome.</abstract><relatedItem type="host"><titleInfo><title>Archives of Disease in Childhood</title></titleInfo><titleInfo type="abbreviated"><title>Arch Dis Child</title></titleInfo><genre type="Journal">journal</genre><identifier type="ISSN">0003-9888</identifier><identifier type="eISSN">1468-2044</identifier><identifier type="PublisherID-hwp">archdischild</identifier><identifier type="PublisherID-nlm-ta">Arch Dis Child</identifier><part><date>1978</date><detail type="volume"><caption>vol.</caption><number>53</number></detail><detail type="issue"><caption>no.</caption><number>8</number></detail><extent unit="pages"><start>668</start></extent></part></relatedItem><identifier type="istex">A605AFAA1952D11B69B3E8A9A65D7E9C32F29DB2</identifier><identifier type="DOI">10.1136/adc.53.8.668</identifier><identifier type="href">archdischild-53-668.pdf</identifier><identifier type="PMID">708105</identifier><identifier type="local">archdischild;53/8/668</identifier><recordInfo><recordContentSource>BMJ</recordContentSource></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/ParkinsonV1/Data/Main/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001555 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Corpus/biblio.hfd -nk 001555 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Sante
|area= ParkinsonV1
|flux= Main
|étape= Corpus
|type= RBID
|clé= ISTEX:A605AFAA1952D11B69B3E8A9A65D7E9C32F29DB2
|texte= Concealed pre-excitation causing paroxysmal reciprocating atrioventricular tachycardia in infancy.
}}
| This area was generated with Dilib version V0.6.23. |  |