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Exercise testing in children with Wolff-Parkinson-white syndrome

Identifieur interne : 000875 ( Main/Corpus ); précédent : 000874; suivant : 000876

Exercise testing in children with Wolff-Parkinson-white syndrome

Auteurs : J. Timothy Bricker ; Co-Burn J. Porter ; Arthur Garson Jr. ; Paul C. Gillette ; Pat Mcvey ; Malinda Traweek ; Dan G. Mcnamara

Source :

RBID : ISTEX:98FA83D3432857B4980AF1987B8FB20E3F87FB25

Abstract

Exercise testing using a modified Bruce treadmill protocol was performed by 17 children with Wolff-Parkinson-White (WPW) syndrome. All had intracardiac electrophysiology studies as well. Endurance time, heart rate and blood pressure were normal during exercise. Ventricular premature complexes were seen with exercise in 2 patients and supraventricular tachycardia with exercise testing was seen in 2. Disappearance of the delta wave with exercise correlated with a long anterograde effective refractory period of the Kent bundle (360 to 390 ms). Children with partial normalization of the QRS during exercise had a longer anterograde effective refractory period of the Kent bundle than those in whom preexcitation persisted. In 1 patient, disappearance of the delta wave with exercise confirmed the diagnosis of WPW syndrome. Preexcitation was seen only after exercise in 1 patient. Exercise testing is of value in the evaluation of children with WPW syndrome; children with WPW syndrome who have total normalization of the QRS interval during exercise and few or no symptoms of tachycardia do not require electrophysiologic study. Address for reprints: J. Timothy Bricker, MD, Pediatric Cardiology, Texas Children's Hospital, 6621 Fannin, Houston, Texas 77030.

Url:
DOI: 10.1016/0002-9149(85)90734-9

Links to Exploration step

ISTEX:98FA83D3432857B4980AF1987B8FB20E3F87FB25

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<ce:sup loc="post">a</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="AFF2">
<ce:sup loc="post">b</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:author>
<ce:given-name>Dan G.</ce:given-name>
<ce:surname>McNamara</ce:surname>
<ce:degrees>MD</ce:degrees>
<ce:cross-ref refid="AFF1">
<ce:sup loc="post">a</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="AFF2">
<ce:sup loc="post">b</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:affiliation id="AFF1">
<ce:label>a</ce:label>
<ce:textfn>From the Lillie Frank Abercrombie Section of Cardiology, Department of Pediatrics, Baylor College of Medicine USA</ce:textfn>
</ce:affiliation>
<ce:affiliation id="AFF2">
<ce:label>b</ce:label>
<ce:textfn>From the Texas Children's Hospital, Houston, Texas, USA</ce:textfn>
</ce:affiliation>
<ce:correspondence id="COR1">
<ce:label></ce:label>
<ce:text>Address for reprints: J. Timothy Bricker, MD, Pediatric Cardiology, Texas Children's Hospital, 6621 Fannin, Houston, Texas 77030.</ce:text>
</ce:correspondence>
</ce:author-group>
<ce:date-received day="8" month="11" year="1984"></ce:date-received>
<ce:date-revised day="26" month="12" year="1984"></ce:date-revised>
<ce:date-accepted day="31" month="12" year="1984"></ce:date-accepted>
<ce:abstract class="author">
<ce:section-title>Abstract</ce:section-title>
<ce:abstract-sec>
<ce:simple-para view="all" id="simple-para.0010">Exercise testing using a modified Bruce treadmill protocol was performed by 17 children with Wolff-Parkinson-White (WPW) syndrome. All had intracardiac electrophysiology studies as well. Endurance time, heart rate and blood pressure were normal during exercise. Ventricular premature complexes were seen with exercise in 2 patients and supraventricular tachycardia with exercise testing was seen in 2. Disappearance of the delta wave with exercise correlated with a long anterograde effective refractory period of the Kent bundle (360 to 390 ms). Children with partial normalization of the QRS during exercise had a longer anterograde effective refractory period of the Kent bundle than those in whom preexcitation persisted. In 1 patient, disappearance of the delta wave with exercise confirmed the diagnosis of WPW syndrome. Preexcitation was seen only after exercise in 1 patient. Exercise testing is of value in the evaluation of children with WPW syndrome; children with WPW syndrome who have total normalization of the QRS interval during exercise and few or no symptoms of tachycardia do not require electrophysiologic study. Address for reprints: J. Timothy Bricker, MD, Pediatric Cardiology, Texas Children's Hospital, 6621 Fannin, Houston, Texas 77030.</ce:simple-para>
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<namePart type="given">Arthur</namePart>
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<affiliation>From the Lillie Frank Abercrombie Section of Cardiology, Department of Pediatrics, Baylor College of Medicine USA</affiliation>
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</name>
<name type="personal">
<namePart type="given">Malinda</namePart>
<namePart type="family">Traweek</namePart>
<namePart type="termsOfAddress">MS</namePart>
<affiliation>From the Lillie Frank Abercrombie Section of Cardiology, Department of Pediatrics, Baylor College of Medicine USA</affiliation>
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<roleTerm type="text">author</roleTerm>
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<abstract lang="en">Exercise testing using a modified Bruce treadmill protocol was performed by 17 children with Wolff-Parkinson-White (WPW) syndrome. All had intracardiac electrophysiology studies as well. Endurance time, heart rate and blood pressure were normal during exercise. Ventricular premature complexes were seen with exercise in 2 patients and supraventricular tachycardia with exercise testing was seen in 2. Disappearance of the delta wave with exercise correlated with a long anterograde effective refractory period of the Kent bundle (360 to 390 ms). Children with partial normalization of the QRS during exercise had a longer anterograde effective refractory period of the Kent bundle than those in whom preexcitation persisted. In 1 patient, disappearance of the delta wave with exercise confirmed the diagnosis of WPW syndrome. Preexcitation was seen only after exercise in 1 patient. Exercise testing is of value in the evaluation of children with WPW syndrome; children with WPW syndrome who have total normalization of the QRS interval during exercise and few or no symptoms of tachycardia do not require electrophysiologic study. Address for reprints: J. Timothy Bricker, MD, Pediatric Cardiology, Texas Children's Hospital, 6621 Fannin, Houston, Texas 77030.</abstract>
<note>This study was supported in part by General Clinic Research Branch Grant RR-00188, United States Public Health Service Grant HL-07190, Research Career Development Award HL-00571, and Young Investigator's Award HL-24916 from the National Institutes of Health, Bethesda, Maryland, and the Women's Auxiliary of Texas Children's Hospital, Houston, Texas.</note>
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