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Life-Threatening Event Risk in Children With Wolff-Parkinson-White Syndrome: A Multicenter International Study

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F18%3A10375536" target="_blank" >RIV/00216208:11130/18:10375536 - isvavai.cz</a>

  • Alternative codes found

    RIV/00064203:_____/18:10375536

  • Result on the web

    <a href="https://doi.org/10.1016/j.jacep.2017.10.009" target="_blank" >https://doi.org/10.1016/j.jacep.2017.10.009</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jacep.2017.10.009" target="_blank" >10.1016/j.jacep.2017.10.009</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Life-Threatening Event Risk in Children With Wolff-Parkinson-White Syndrome: A Multicenter International Study

  • Original language description

    Objectives: This study sought to characterize risk in children with Wolff-Parkinson-White (WPW) syndrome by comparing those who had experienced a life-threatening event (LTE) with a control population. Background: Children with WPW syndrome are at risk of sudden death. Methods: This retrospective multicenter pediatric study identified 912 subjects LESS-THAN OR EQUAL TO21 years of age with WPW syndrome, using electrophysiology (EPS) studies. Case subjects had a history of LTE: sudden death, aborted sudden death, or atrial fibrillation (shortest pre-excited RR interval in atrial fibrillation [SPERRI] of LESS-THAN OR EQUAL TO250 ms or with hemodynamic compromise); whereas subjects did not. We compared clinical and EPS data between cases and subjects. Results: Case subjects (n = 96) were older and less likely than subjects (n = 816) to have symptoms or documented tachycardia. Mean age at LTE was 14.1 +- 3.9 years of age. The LTE was the sentinel symptom in 65%, consisting of rapidly conducted pre-excited atrial fibrillation (49%), aborted sudden death (45%), and sudden death (6%). Three risk components were considered at EPS: SPERRI, accessory pathway effective refractory period (APERP), and shortest paced cycle length with pre-excitation during atrial pacing (SPPCL), and all were shorter in cases than in control subjects. In multivariate analysis, risk factors for LTE included male sex, Ebstein malformation, rapid anterograde conduction (APERP, SPERRI, or SPPCL LESS-THAN OR EQUAL TO250 ms), multiple pathways, and inducible atrial fibrillation. Of case subjects, 60 of 86 (69%) had GREATER-THAN OR EQUAL TO2 EPS risk stratification components performed; 22 of 60 (37%) did not have EPS-determined high-risk characteristics, and 15 of 60 (25%) had neither concerning pathway characteristics nor inducible atrioventricular reciprocating tachycardia. Conclusions: Young patients may experience LTE from WPW syndrome without prior symptoms or markers of high-risk on EPS.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>SC</sub> - Article in a specialist periodical, which is included in the SCOPUS database

  • CEP classification

  • OECD FORD branch

    30201 - Cardiac and Cardiovascular systems

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    JACC: Clinical Electrophysiology [online]

  • ISSN

    2405-500X

  • e-ISSN

  • Volume of the periodical

    4

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    12

  • Pages from-to

    433-444

  • UT code for WoS article

  • EID of the result in the Scopus database

    2-s2.0-85034441724