Heart Transplantation in a 14-Year-Old Boy in the Presence of Severe Out-of-Proportion Pulmonary Hypertension due to Restrictive Left Heart Disease: A Case Report

A 14-year-old boy after balloon valvuloplasty of severe aortic valve stenosis in the neonatal period was referred for heart-lung transplantation because of high grade pulmonary hypertension and left heart dysfunction due to endocardial fibroelastosis with severe mitral insufficiency. After heart cat...

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Main Authors: Martin Schwienbacher, Ulrich Schweigmann, Nikolaus Neu, Elisabeth Schermer, Corinna Velik-Salchner, Ina Michel-Behnke, Erentraud Irnberger, Christina Maria Steger, Jörg Ingolf Stein, Ralf Geiger
Format: Article
Language:English
Published: Hindawi Limited 2013-01-01
Series:Case Reports in Cardiology
Online Access:http://dx.doi.org/10.1155/2013/418565
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spelling doaj-2b562d9091554cb2aac52349ce7bd2a32020-11-24T22:43:10ZengHindawi LimitedCase Reports in Cardiology2090-64042090-64122013-01-01201310.1155/2013/418565418565Heart Transplantation in a 14-Year-Old Boy in the Presence of Severe Out-of-Proportion Pulmonary Hypertension due to Restrictive Left Heart Disease: A Case ReportMartin Schwienbacher0Ulrich Schweigmann1Nikolaus Neu2Elisabeth Schermer3Corinna Velik-Salchner4Ina Michel-Behnke5Erentraud Irnberger6Christina Maria Steger7Jörg Ingolf Stein8Ralf Geiger9Department of Pediatrics, Division of Cardiology, Pulmology, Allergology and Cystic Fibrosis, Innsbruck Medical University, 6020 Innsbruck, AustriaDepartment of Pediatrics, Division of Cardiology, Pulmology, Allergology and Cystic Fibrosis, Innsbruck Medical University, 6020 Innsbruck, AustriaDepartment of Pediatrics, Pediatric Intensive Care Unit, Innsbruck Medical University, 6020 Innsbruck, AustriaDepartment of Pediatrics, Division of Cardiology, Pulmology, Allergology and Cystic Fibrosis, Innsbruck Medical University, 6020 Innsbruck, AustriaDepartment of Anaesthesiology and Critical Care Medicine, Innsbruck Medical University, 6020 Innsbruck, AustriaDepartment of Pediatric Cardiology, Medical University of Vienna, 1090 Vienna, AustriaDepartment of Pediatrics, Salzburg State Hospital, 5020 Salzburg, AustriaDepartment of Pathology, Innsbruck Medical University, 6020 Innsbruck, AustriaDepartment of Pediatrics, Division of Cardiology, Pulmology, Allergology and Cystic Fibrosis, Innsbruck Medical University, 6020 Innsbruck, AustriaDepartment of Pediatrics, Division of Cardiology, Pulmology, Allergology and Cystic Fibrosis, Innsbruck Medical University, 6020 Innsbruck, AustriaA 14-year-old boy after balloon valvuloplasty of severe aortic valve stenosis in the neonatal period was referred for heart-lung transplantation because of high grade pulmonary hypertension and left heart dysfunction due to endocardial fibroelastosis with severe mitral insufficiency. After heart catheterization, hemodynamic parameters were invasively monitored: a course of levosimendan and initiation of diuretics led to a decrease of pulmonary capillary wedge pressure (from maximum 35 to 24 mmHg). Instead of an expected decrease, mean pulmonary artery pressures (mPAP) increased up to 80 mmHg with increasing transpulmonary pressure gradient (TPG) up to 55 mmHg. Oral bosentan and intravenous epoprostenol then led to a ~50% decrease of mPAP (TPG between 16 and 22 mmHg). The boy was listed solely for heart transplantation which was successfully accomplished 1 month later.http://dx.doi.org/10.1155/2013/418565
collection DOAJ
language English
format Article
sources DOAJ
author Martin Schwienbacher
Ulrich Schweigmann
Nikolaus Neu
Elisabeth Schermer
Corinna Velik-Salchner
Ina Michel-Behnke
Erentraud Irnberger
Christina Maria Steger
Jörg Ingolf Stein
Ralf Geiger
spellingShingle Martin Schwienbacher
Ulrich Schweigmann
Nikolaus Neu
Elisabeth Schermer
Corinna Velik-Salchner
Ina Michel-Behnke
Erentraud Irnberger
Christina Maria Steger
Jörg Ingolf Stein
Ralf Geiger
Heart Transplantation in a 14-Year-Old Boy in the Presence of Severe Out-of-Proportion Pulmonary Hypertension due to Restrictive Left Heart Disease: A Case Report
Case Reports in Cardiology
author_facet Martin Schwienbacher
Ulrich Schweigmann
Nikolaus Neu
Elisabeth Schermer
Corinna Velik-Salchner
Ina Michel-Behnke
Erentraud Irnberger
Christina Maria Steger
Jörg Ingolf Stein
Ralf Geiger
author_sort Martin Schwienbacher
title Heart Transplantation in a 14-Year-Old Boy in the Presence of Severe Out-of-Proportion Pulmonary Hypertension due to Restrictive Left Heart Disease: A Case Report
title_short Heart Transplantation in a 14-Year-Old Boy in the Presence of Severe Out-of-Proportion Pulmonary Hypertension due to Restrictive Left Heart Disease: A Case Report
title_full Heart Transplantation in a 14-Year-Old Boy in the Presence of Severe Out-of-Proportion Pulmonary Hypertension due to Restrictive Left Heart Disease: A Case Report
title_fullStr Heart Transplantation in a 14-Year-Old Boy in the Presence of Severe Out-of-Proportion Pulmonary Hypertension due to Restrictive Left Heart Disease: A Case Report
title_full_unstemmed Heart Transplantation in a 14-Year-Old Boy in the Presence of Severe Out-of-Proportion Pulmonary Hypertension due to Restrictive Left Heart Disease: A Case Report
title_sort heart transplantation in a 14-year-old boy in the presence of severe out-of-proportion pulmonary hypertension due to restrictive left heart disease: a case report
publisher Hindawi Limited
series Case Reports in Cardiology
issn 2090-6404
2090-6412
publishDate 2013-01-01
description A 14-year-old boy after balloon valvuloplasty of severe aortic valve stenosis in the neonatal period was referred for heart-lung transplantation because of high grade pulmonary hypertension and left heart dysfunction due to endocardial fibroelastosis with severe mitral insufficiency. After heart catheterization, hemodynamic parameters were invasively monitored: a course of levosimendan and initiation of diuretics led to a decrease of pulmonary capillary wedge pressure (from maximum 35 to 24 mmHg). Instead of an expected decrease, mean pulmonary artery pressures (mPAP) increased up to 80 mmHg with increasing transpulmonary pressure gradient (TPG) up to 55 mmHg. Oral bosentan and intravenous epoprostenol then led to a ~50% decrease of mPAP (TPG between 16 and 22 mmHg). The boy was listed solely for heart transplantation which was successfully accomplished 1 month later.
url http://dx.doi.org/10.1155/2013/418565
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