Ross-Konno operation for patients with shone complex

Ryo Aeba, Kazuma Okamoto, Ryohei Yozu

Research output: Contribution to journalArticle

Abstract

We report the cases of 2 pediatric patients who had Shone complex. Each child had severe left ventricular outflow tract obstruction and marginal mitral obstruction, and both underwent the Ross-Konno operation. The mitral valve was left alone. Both patients survived the operations, and serial follow-up echocardiography up to 4 years later showed a decreased or decreasing trend in the peak mitral diastolic velocity. The Ross-Konno procedure can be an acceptable approach for a subgroup of patients who have Shone complex.

Original languageEnglish
Pages (from-to)240-241
Number of pages2
JournalTexas Heart Institute Journal
Volume37
Issue number2
Publication statusPublished - 2010 Aug 13

Keywords

  • Aortic valve stenosis/congenital/surgery
  • Cardiac surgical procedures/methods
  • Child, Preschool
  • Heart defects, congenital/mortality/pathology/surgery
  • Mitral valve/abnormalities/pathology/surgery
  • Reoperation
  • Risk assessment
  • Treatment outcome
  • Ventricular outflow obstruction/complications/congenital/surgery

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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  • Cite this

    Aeba, R., Okamoto, K., & Yozu, R. (2010). Ross-Konno operation for patients with shone complex. Texas Heart Institute Journal, 37(2), 240-241.