Respiratory exacerbation in a young adult with cystic fibrosis and tricuspid atresia

Jamie Wood, Abbey Sawyer, Siobhain Mulrennan, Andrew Bullock

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Abstract

Tricuspid atresia (TAt) is a complex congenital heart defect (CHD) characterized by the absence of the tricuspid valve and right ventricular hypoplasia requiring surgery in childhood, the Fontan procedure. We present a case of a 21-year-old male with TAt and cystic fibrosis (CF), who underwent a Fontan procedure in childhood, presenting to an adult CF clinic with severe deterioration in his respiratory status and multi-organ dysfunction associated with CF. This report describes problems associated with the management of a CF respiratory exacerbation and extrapulmonary manifestations of CF in the unique situation of a Fontan circulation, a circulation with absence of a subpulmonary ventricle and pulsatile pulmonary arterial blood flow where maintenance of systemic cardiac output is totally dependent on good respiratory function and low pulmonary artery pressures.

Original languageEnglish
Article numbere00318
JournalRespirology Case Reports
Volume6
Issue number5
Publication statusPublished - 1 Jul 2018

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