Pediatric Cardiology

, Volume 38, Issue 7, pp 1317–1323 | Cite as

Postnatal Outcomes of Fetal Supraventricular Tachycardia: a Multicenter Study

  • Kevin A. Hinkle
  • Shabnam Peyvandi
  • Corey Stiver
  • Stacy A. S. Killen
  • Hsin Yi Weng
  • Susan P. Etheridge
  • Michael D. Puchalski
Original Article
  • 556 Downloads

Abstract

Supraventricular tachycardia (SVT), the most common fetal tachycardia, can be difficult to manage in utero. We sought to better understand predictors of the postnatal clinical course in neonates who experienced fetal SVT. We hypothesized that fetuses with hydrops or those with refractory SVT (failure of first-line SVT therapy) are more likely to experience postnatal SVT. This was a retrospective multicenter cohort study of subjects diagnosed with fetal SVT between 2006 and 2014. Fetuses with structural heart disease were excluded. Descriptive comparative statistics and univariate analysis with logistic regression were utilized to determine factors that most strongly predicted postnatal SVT and preterm delivery. The cohort consisted of 103 subjects. Refractory SVT was found in 37% (N = 38) of the cohort with this group more likely to be delivered prematurely (median = 36 vs. 37.5 weeks, p = 0.04). Refractory SVT did not increase the risk of postnatal SVT (p = 0.09). Postnatal SVT was seen in 61% (N = 63). Of those, 68% (N = 43) had postnatal SVT at ≤2 days of age. Postnatal SVT was associated with a later fetal SVT diagnosis (median = 30 vs. 27.5 weeks, p = 0.006). We found a strong correlation between postnatal SVT and later gestational age at fetal SVT diagnosis. Subjects with refractory SVT or hydrops did not have a higher risk of postnatal SVT. We propose strong consideration for term delivery in the absence of significant clinical compromise. Further studies to assess whether outcomes vary for preterm delivery versus expectant management in those with refractory SVT should be performed.

Keywords

Supraventricular tachycardia Clinical studies Fetal echocardiography 

Notes

Funding

This investigation was supported by the University of Utah Study Design and Biostatistics Center, with funding in part from the National Center for Research Resources and the National Center for Advancing Translational Sciences, the National Institutes of Health, through Grant 8UL1TR000105 (formerly UL1RR025764).

Compliance with Ethical Standards

Conflicts of Interest

Kevin Hinkle, Shabnam Peyvandi, Corey Stiver, Stacy A. S. Killen, Hsin Yi Weng, Susan P. Etheridge, Michael Puchalski declares no conflict of interest.

Ethical approval

This article does not contain any studies with human participants or animals performed by any of the authors.

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Copyright information

© Springer Science+Business Media, LLC 2017

Authors and Affiliations

  • Kevin A. Hinkle
    • 1
  • Shabnam Peyvandi
    • 2
  • Corey Stiver
    • 3
  • Stacy A. S. Killen
    • 4
  • Hsin Yi Weng
    • 1
  • Susan P. Etheridge
    • 1
  • Michael D. Puchalski
    • 1
  1. 1.University of UtahSalt Lake CityUSA
  2. 2.University of California San FranciscoSan FranciscoUSA
  3. 3.Nationwide Children’s HospitalColumbusUSA
  4. 4.Vanderbilt University Medical CenterNashvilleUSA

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