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Taussig-Bing complex--a pathologic study of eight cases.

U B Khanolkar1, S G Kinare

  • 1Department of Cardiology, Seth G.S. Medical College, Bombay.

Indian Heart Journal
|May 1, 1990
PubMed
Summary
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Taussig-Bing Complex, a rare heart defect, occurred in 7.2% of double outlet right ventricle cases. This complex congenital heart disease impacts survival, with a mean age at death of 23.5 months.

Area of Science:

  • Pediatric Cardiology
  • Congenital Heart Disease
  • Cardiac Surgery

Background:

  • Taussig-Bing Complex is an uncommon congenital heart anomaly.
  • Double outlet right ventricle (DORV) is a complex cardiac malformation.

Purpose of the Study:

  • To investigate the incidence and associated features of Taussig-Bing Complex in DORV.
  • To analyze the clinical presentation and outcomes of patients with Taussig-Bing Complex.

Main Methods:

  • Retrospective analysis of 110 hearts with DORV.
  • Detailed examination of cardiac morphology, great vessel relationships, and associated anomalies.

Main Results:

  • Taussig-Bing Complex was identified in 8 (7.2%) of DORV cases.

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  • Mean age at death was 23.5 months, with survival up to 10 years.
  • Associated anomalies included VSD, subpulmonary stenosis, and mitral valve abnormalities.

    • Conclusions:

    • Taussig-Bing Complex is a significant, though uncommon, component of DORV.
    • Early diagnosis and management are crucial for improving outcomes in these complex congenital heart defects.