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Early experience with intravenous sotalol in children with and without congenital heart disease.

Publication ,  Journal Article
Valdés, SO; Miyake, CY; Niu, MC; de la Uz, CM; Asaki, SY; Landstrom, AP; Schneider, AE; Rusin, CG; Patel, R; Lam, WW; Kim, JJ
Published in: Heart Rhythm
December 2018

BACKGROUND: Arrhythmias are common in the pediatric population. In patients unable to take oral medications or in need of acute therapy, options of intravenous (IV) antiarrhythmic medications are limited. Recently IV sotalol has become readily available, but experience in children is limited. OBJECTIVE: The purpose of this study was to describe our initial experience with the use of IV sotalol in the pediatric population. METHODS: A retrospective study of all pediatric patients receiving IV sotalol was performed. Patient demographic characteristics, presence of congenital heart disease, arrhythmia type, efficacy of IV sotalol use, and adverse effects were evaluated. RESULTS: A total of 47 patients (26 (55%) male and 24 (51%) with congenital heart disease) received IV sotalol at a median age of 2.05 years (interquartile range 0.07-10.03 years) and a median weight of 12.8 kg (interquartile range 3.8-34.2 kg), and 13 (28%) received IV sotalol in the acute postoperative setting. Supraventricular arrhythmias occurred in 40 patients (85%) and ventricular tachycardia in 7 (15%). Among 24 patients receiving IV sotalol for an active arrhythmia, acute termination was achieved in 21 (88%). Twenty-three patients received IV sotalol as maintenance therapy for recurrent arrhythmias owing to inability to take oral antiarrhythmic medications; 19 (83%) were controlled with sotalol monotherapy. No patient required discontinuation of IV sotalol secondary to adverse effects, proarrhythmia, or QT prolongation. CONCLUSION: IV sotalol is an effective antiarrhythmic option for pediatric patients and may be an excellent agent for acute termination of active arrhythmias. It was well tolerated, with no patient requiring discontinuation secondary to adverse effects.

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Published In

Heart Rhythm

DOI

EISSN

1556-3871

Publication Date

December 2018

Volume

15

Issue

12

Start / End Page

1862 / 1869

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Time Factors
  • Tachycardia, Ventricular
  • Sotalol
  • Retrospective Studies
  • Male
  • Infant
  • Humans
  • Heart Defects, Congenital
  • Follow-Up Studies
 

Citation

APA
Chicago
ICMJE
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Valdés, S. O., Miyake, C. Y., Niu, M. C., de la Uz, C. M., Asaki, S. Y., Landstrom, A. P., … Kim, J. J. (2018). Early experience with intravenous sotalol in children with and without congenital heart disease. Heart Rhythm, 15(12), 1862–1869. https://doi.org/10.1016/j.hrthm.2018.07.010
Valdés, Santiago O., Christina Y. Miyake, Mary C. Niu, Caridad M. de la Uz, S Yukiko Asaki, Andrew P. Landstrom, Andrew E. Schneider, et al. “Early experience with intravenous sotalol in children with and without congenital heart disease.Heart Rhythm 15, no. 12 (December 2018): 1862–69. https://doi.org/10.1016/j.hrthm.2018.07.010.
Valdés SO, Miyake CY, Niu MC, de la Uz CM, Asaki SY, Landstrom AP, et al. Early experience with intravenous sotalol in children with and without congenital heart disease. Heart Rhythm. 2018 Dec;15(12):1862–9.
Valdés, Santiago O., et al. “Early experience with intravenous sotalol in children with and without congenital heart disease.Heart Rhythm, vol. 15, no. 12, Dec. 2018, pp. 1862–69. Pubmed, doi:10.1016/j.hrthm.2018.07.010.
Valdés SO, Miyake CY, Niu MC, de la Uz CM, Asaki SY, Landstrom AP, Schneider AE, Rusin CG, Patel R, Lam WW, Kim JJ. Early experience with intravenous sotalol in children with and without congenital heart disease. Heart Rhythm. 2018 Dec;15(12):1862–1869.
Journal cover image

Published In

Heart Rhythm

DOI

EISSN

1556-3871

Publication Date

December 2018

Volume

15

Issue

12

Start / End Page

1862 / 1869

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Time Factors
  • Tachycardia, Ventricular
  • Sotalol
  • Retrospective Studies
  • Male
  • Infant
  • Humans
  • Heart Defects, Congenital
  • Follow-Up Studies