Clinical and Pathologic Comparison of Simple Left-to-Right Shunt Congenital Heart Disease and Transposition of the Great Arteries with Ventricular Septal Defect

Authors

  • Jing-bin Huang
  • Jian Liang
  • Ming Du

DOI:

https://doi.org/10.1532/HSF98.20111127

Abstract

Background: This study aimed to compare clinical and pathologic data for selected patients with congenital heart disease (CHD) and severe pulmonary hypertension (PH) treated with a diagnostic-treatment-and-repair strategy and to compare results for patients with pulmonary vascular disease (PVD) with simple left-to-right shunt CHD with patients with transposition of the great arteries (TGA) and ventricular septal defect (VSD).

Methods: Group I comprised 38 patients with simple left-to-right shunt CHD and severe PH; group II included 11 older patients with TGA with VSD and severe PH; and group III comprised 6 autopsy cases of individuals with a normal circulation. The nature of the pulmonary arteries was determined by the Heath-Edwards classification system. All specimens were quantitatively analyzed.

Results: Group I showed 31 patients with a change to grade I, 3 patients were grade II, 3 patients were grade III, and only 1 patient was grade IV. Group II showed 7 patients with a change to grade I, 2 patients were grade II, 1 patient was grade III, and only 1 patient was grade IV. The media wall thickness percentage (%MT), the media wall area percentage (%MS), and arteriole density were significantly higher in groups I and II than in group III. %MS was significantly higher in group II than in group I; no significant differences in %MT and arteriole density could be found between groups I and II.

Conclusions: The PVD in these selected patients with CHD and severe PH who were cared for with a diagnostic-treatment-and-repair strategy is generally reversible, and the changes in PVD in the patients with TGA and VSD were similar to those in the patients with simple left-to-right shunt CHD.

References

Allcock RJ, O'Sullivan JJ, Corris PA. 2003. Atrial septostomy for pulmonary arterial hypertension. Heart 89:1344-7.nAnderson RA, Levy AM, Naeye RL, Tabakin BS. 1967. Rapidly progressing pulmonary vascular obstructive disease. Association with ventricular septal defects. Am J Cardiol 19:854-8.nDimopoulos K, Peset A, Gatzoulis MA. 2008. Evaluating operability in adults with congenital heart disease and the role of pretreatment with targeted pulmonary arterial hypertension therapy. Int J Cardiol 129:163-71.nEdgar AN, Milton HP, Alexander JM, Farouk SI. 1974. Pulmonary vascular disease in complete transposition of the great arteries: a study of 200 patients. Am J Cardiol 34:75-82.nEpting CL, Wolfe RR, Abman SH, Deutsch GH, Ivy D. 2002. Reversal of pulmonary hypertension associated with plexiform lesions in congenital heart disease: a case report. Pediatr Cardiol 23:182-5.nHuang JB, Liu YL, Sun PW, Lv XD, Bo K, Fan XM. 2010. Novel strategy for treatment of pulmonary arterial hypertension: enhancement of apoptosis. Lung 2010;188:179-89.nHuang JB, Liu YL, Yu CT, et al. 2011. Lung biopsy findings in previously inoperable patients with severe pulmonary hypertension associated with congenital heart disease. Int J Card 151:76-83.nHumbert M, Sitbon O, Simonneau G. Treatment of pulmonary arterial hypertension. N Engl J Med 2004;351:1425-36.nKlepetko W, Mayer E, Sandoval J, et al. 2004. Interventional and surgical modalities of treatment for pulmonary arterial hypertension. J Am Coll Cardiol 43:73S-80S.nKurzyna M, Dabrowski M, Bielecki D, et al. 2007. Atrial septostomy in treatment of end-stage right heart failure in patients with pulmonary hypertension. Chest 131:977-83.nLiebman J, Cullum L, Belloc NB. 1969. Natural history of transposition of the great arteries. Anatomy and birth and death characteristics. Circulation 40:237-62.nLiu YL, Hu SS, Shen XD, et al. 2010. Safety and efficacy of arterial switch operation in previously inoperable patients. J Card Surg 25:400-5.nLiu YL, Hu SS, Shen XD, et al. 2010. Midterm results of arterial switch operation in older patients with severe pulmonary hypertension. Ann Thorac Surg 90:848-55.nMicheletti A, Hislop AA, Lammers A, et al. 2006. Role of atrial septostomy in the treatment of children with pulmonary arterial hypertension. Heart 92:969-72.nMooi WJ, Grünberg K. 2006. Histopathology of pulmonary hypertensive diseases. Curr Diagn Pathol 2006;12:429-40.nNakajima Y, Momma K, Seguchi M, Nakazawa M, Imai Y. 1996. Pulmonary hypertension in patients with complete transposition of the great arteries: midterm results after surgery. Pediatr Cardiol 17:104-7.nWagenvoort CA, Wagenvoort N, Draulans-Noe Y. 1984. Reversibility of plexogenic pulmonary arteriopathy following banding of the pulmonary artery. J Thorac Cardiovasc Surg 87:876-86.nWagenvoort CA, Wagenvoort N. 1974. Pathology of the Eisenmenger syndrome and primary pulmonary hypertension. Adv Cardiol 11:123-30.nYamaki S, Wagenvoort CA. 1981. Plexogenic pulmonary arteriopathy: significance of medial thickness with respect to advanced pulmonary vascular lesions. Am J Pathol 105:70-5.n

Published

2012-04-26

How to Cite

Huang, J.- bin, Liang, J., & Du, M. (2012). Clinical and Pathologic Comparison of Simple Left-to-Right Shunt Congenital Heart Disease and Transposition of the Great Arteries with Ventricular Septal Defect. The Heart Surgery Forum, 15(2), E97-E102. https://doi.org/10.1532/HSF98.20111127

Issue

Section

Article