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Presence and utility of electrocardiographic abnormalities in long-term childhood cancer survivors.
de Baat, Esmée C; Merkx, Remy; Leerink, Jan M; Boerhout, Coen; van der Pal, Heleen J H; van Dalen, Elvira C; Loonen, Jacqueline; Bresters, Dorine; van Dulmen-den Broeder, Eline; van der Heiden-van der Loo, Margriet; van den Heuvel, Marry M; Kok, Judith L; Louwerens, Marloes; Neggers, Sebastian J C M M; Ronckers, Cecline M; Teepen, Jop C; Tissing, Wim J E; de Vries, Andrica C; Kapusta, Livia; Kremer, Leontien C M; Mavinkurve-Groothuis, Annelies M C; Kok, Wouter E M; Feijen, Elizabeth A M.
Afiliação
  • de Baat EC; Princess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands e.c.debaat-2@prinsesmaximacentrum.nl.
  • Merkx R; Medical Imaging, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Leerink JM; Department of Cardiology, Amsterdam UMC, Amsterdam, The Netherlands.
  • Boerhout C; Department of Cardiology, Amsterdam UMC, Amsterdam, The Netherlands.
  • van der Pal HJH; Princess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • van Dalen EC; Princess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Loonen J; Pediatric Hematology and Oncology, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Bresters D; Princess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • van Dulmen-den Broeder E; Leiden University Medical Center, Willem Alexander Children's Hospital, Leiden, The Netherlands.
  • van der Heiden-van der Loo M; Amsterdam University Medical Centres, Amsterdam, The Netherlands.
  • van den Heuvel MM; Princess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Kok JL; Princess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Louwerens M; Department of Pediatric Oncology, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Neggers SJCMM; Princess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Ronckers CM; Medical Oncologist, Department of Internal Medicine, Leiden University Medical Center, Leiden, The Netherlands.
  • Teepen JC; Princess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Tissing WJE; Erasmus Medical Center, Rotterdam, The Netherlands.
  • de Vries AC; University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
  • Kapusta L; Princess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Kremer LCM; Princess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Mavinkurve-Groothuis AMC; University Medical Centre Groningen, Beatrix Children's Hospital, Groningen, The Netherlands.
  • Kok WEM; Princess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Feijen EAM; Erasmus Medical Center, Rotterdam, The Netherlands.
Heart ; 110(10): 726-734, 2024 Apr 25.
Article em En | MEDLINE | ID: mdl-38503487
ABSTRACT

BACKGROUND:

We assessed the prevalence and diagnostic value of ECG abnormalities for cardiomyopathy surveillance in childhood cancer survivors.

METHODS:

In this cross-sectional study, 1381 survivors (≥5 years) from the Dutch Childhood Cancer Survivor Study part 2 and 272 siblings underwent a long-term follow-up ECG and echocardiography. We compared ECG abnormality prevalences using the Minnesota Code between survivors and siblings, and within biplane left ventricular ejection fraction (LVEF) categories. Among 880 survivors who received anthracycline, mitoxantrone or heart radiotherapy, logistic regression models using least absolute shrinkage and selection operator identified ECG abnormalities associated with three abnormal LVEF categories (<52% in male/<54% in female, <50% and <45%). We assessed the overall contribution of these ECG abnormalities to clinical regression models predicting abnormal LVEF, assuming an absence of systolic dysfunction with a <1% threshold probability.

RESULTS:

16% of survivors (52% female, mean age 34.7 years) and 14% of siblings had major ECG abnormalities. ECG abnormalities increased with decreasing LVEF. Integrating selected ECG data into the baseline model significantly improved prediction of sex-specific abnormal LVEF (c-statistic 0.66 vs 0.71), LVEF <50% (0.66 vs 0.76) and LVEF <45% (0.80 vs 0.86). While no survivor met the preset probability threshold in the first two models, the third model used five ECG variables to predict LVEF <45% and was applicable for ruling out (sensitivity 93%, specificity 56%, negative predictive value 99.6%). Calibration and internal validation tests performed well.

CONCLUSION:

A clinical prediction model with ECG data (left bundle branch block, left atrial enlargement, left heart axis, Cornell's criteria for left ventricular hypertrophy and heart rate) may aid in ruling out LVEF <45%.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Volume Sistólico / Eletrocardiografia / Sobreviventes de Câncer Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male País como assunto: Europa Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Volume Sistólico / Eletrocardiografia / Sobreviventes de Câncer Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male País como assunto: Europa Idioma: En Ano de publicação: 2024 Tipo de documento: Article