Deleterious effects of intravenous verapamil in Wolff-Parkinson-White patients and atrial fibrillation
Identifieur interne : 001F82 ( Main/Corpus ); précédent : 001F81; suivant : 001F83Deleterious effects of intravenous verapamil in Wolff-Parkinson-White patients and atrial fibrillation
Auteurs : Boris Strasberg ; Alex Sagie ; Eldad Rechavia ; Amos Katz ; A. Ovsyscher ; Samuel Sclarovsky ; Jacob AgmonSource :
- Cardiovascular Drugs and Therapy [ 0920-3206 ] ; 1989-01-01.
Abstract
Summary: Three patients presented to the emergency room with atrial fibrillation and fast ventricular response with wide preexcited QRS complexes (Wolff-Parkinson-White syndrome). All three patients received intravenous verapamil (5–10mg). The first patient developed ventricular fibrillation requiring several defibrillations; the second patient developed severe hemodynamic deterioration requiring urgent cardioversion; in the third patient a marked increment in the ventricular response was noted, however, there was no hemodynamic impairment. Verapamil may cause detrimental results when given to patients with the Wolff-Parkinson-White syndrome and atrial fibrillation. Its administration should therefore be considered as an absolute contraindication in these patients.
Url:
DOI: 10.1007/BF00133211
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<front><div type="abstract" xml:lang="en">Summary: Three patients presented to the emergency room with atrial fibrillation and fast ventricular response with wide preexcited QRS complexes (Wolff-Parkinson-White syndrome). All three patients received intravenous verapamil (5–10mg). The first patient developed ventricular fibrillation requiring several defibrillations; the second patient developed severe hemodynamic deterioration requiring urgent cardioversion; in the third patient a marked increment in the ventricular response was noted, however, there was no hemodynamic impairment. Verapamil may cause detrimental results when given to patients with the Wolff-Parkinson-White syndrome and atrial fibrillation. Its administration should therefore be considered as an absolute contraindication in these patients.</div>
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<Abstract ID="Abs1" Language="En"><Heading>Summary</Heading>
<Para>Three patients presented to the emergency room with atrial fibrillation and fast ventricular response with wide preexcited QRS complexes (Wolff-Parkinson-White syndrome). All three patients received intravenous verapamil (5–10mg). The first patient developed ventricular fibrillation requiring several defibrillations; the second patient developed severe hemodynamic deterioration requiring urgent cardioversion; in the third patient a marked increment in the ventricular response was noted, however, there was no hemodynamic impairment.</Para>
<Para>Verapamil may cause detrimental results when given to patients with the Wolff-Parkinson-White syndrome and atrial fibrillation. Its administration should therefore be considered as an absolute contraindication in these patients.</Para>
</Abstract>
<KeywordGroup Language="En"><Heading>Key Words</Heading>
<Keyword>verapamil</Keyword>
<Keyword>Wolff-Parkinson-White</Keyword>
<Keyword>arrhythmias</Keyword>
</KeywordGroup>
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<NoBody></NoBody>
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<mods version="3.6"><titleInfo lang="en"><title>Deleterious effects of intravenous verapamil in Wolff-Parkinson-White patients and atrial fibrillation</title>
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<titleInfo type="alternative" contentType="CDATA" lang="en"><title>Deleterious effects of intravenous verapamil in Wolff-Parkinson-White patients and atrial fibrillation</title>
</titleInfo>
<name type="personal" displayLabel="corresp"><namePart type="given">Boris</namePart>
<namePart type="family">Strasberg</namePart>
<affiliation>Israel and Ione Massada Center for Heart Diseases, Beilinson Medical Center, Petah Tikva, Israel</affiliation>
<affiliation>Tel Aviv University Sackler School of Medicine, Tel Aviv, Israel</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">Alex</namePart>
<namePart type="family">Sagie</namePart>
<affiliation>Israel and Ione Massada Center for Heart Diseases, Beilinson Medical Center, Petah Tikva, Israel</affiliation>
<affiliation>Tel Aviv University Sackler School of Medicine, Tel Aviv, Israel</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">Eldad</namePart>
<namePart type="family">Rechavia</namePart>
<affiliation>Israel and Ione Massada Center for Heart Diseases, Beilinson Medical Center, Petah Tikva, Israel</affiliation>
<affiliation>Tel Aviv University Sackler School of Medicine, Tel Aviv, Israel</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">Amos</namePart>
<namePart type="family">Katz</namePart>
<affiliation>Cardiology Division, Soroka Medical Center, Beersheva, Israel</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">Ilya</namePart>
<namePart type="given">A.</namePart>
<namePart type="family">Ovsyscher</namePart>
<affiliation>Cardiology Division, Soroka Medical Center, Beersheva, Israel</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">Samuel</namePart>
<namePart type="family">Sclarovsky</namePart>
<affiliation>Israel and Ione Massada Center for Heart Diseases, Beilinson Medical Center, Petah Tikva, Israel</affiliation>
<affiliation>Tel Aviv University Sackler School of Medicine, Tel Aviv, Israel</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">Jacob</namePart>
<namePart type="family">Agmon</namePart>
<affiliation>Israel and Ione Massada Center for Heart Diseases, Beilinson Medical Center, Petah Tikva, Israel</affiliation>
<affiliation>Tel Aviv University Sackler School of Medicine, Tel Aviv, Israel</affiliation>
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<originInfo><publisher>Kluwer Academic Publishers</publisher>
<place><placeTerm type="text">Dordrecht</placeTerm>
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<dateIssued encoding="w3cdtf">1989-01-01</dateIssued>
<copyrightDate encoding="w3cdtf">1989</copyrightDate>
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<language><languageTerm type="code" authority="rfc3066">en</languageTerm>
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<abstract lang="en">Summary: Three patients presented to the emergency room with atrial fibrillation and fast ventricular response with wide preexcited QRS complexes (Wolff-Parkinson-White syndrome). All three patients received intravenous verapamil (5–10mg). The first patient developed ventricular fibrillation requiring several defibrillations; the second patient developed severe hemodynamic deterioration requiring urgent cardioversion; in the third patient a marked increment in the ventricular response was noted, however, there was no hemodynamic impairment. Verapamil may cause detrimental results when given to patients with the Wolff-Parkinson-White syndrome and atrial fibrillation. Its administration should therefore be considered as an absolute contraindication in these patients.</abstract>
<note>Calcium Antagonists</note>
<relatedItem type="host"><titleInfo><title>Cardiovascular Drugs and Therapy</title>
</titleInfo>
<titleInfo type="abbreviated"><title>Cardiovasc Drug Ther</title>
</titleInfo>
<genre type="Journal" displayLabel="Archive Journal"></genre>
<originInfo><dateIssued encoding="w3cdtf">1989-01-01</dateIssued>
<copyrightDate encoding="w3cdtf">1989</copyrightDate>
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<subject><genre>Medicine & Public Health</genre>
<topic>Cardiology</topic>
</subject>
<identifier type="ISSN">0920-3206</identifier>
<identifier type="eISSN">1573-7241</identifier>
<identifier type="JournalID">10557</identifier>
<identifier type="IssueArticleCount">19</identifier>
<identifier type="VolumeIssueCount">6</identifier>
<part><date>1989</date>
<detail type="volume"><number>2</number>
<caption>vol.</caption>
</detail>
<detail type="issue"><number>6</number>
<caption>no.</caption>
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<extent unit="pages"><start>801</start>
<end>806</end>
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<recordInfo><recordOrigin>Kluwer Academic Publishers, 1989</recordOrigin>
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<identifier type="DOI">10.1007/BF00133211</identifier>
<identifier type="ArticleID">Art14</identifier>
<identifier type="ArticleID">BF00133211</identifier>
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