scholarly journals A study to determine the prevalence of pulmonary arterial hypertension in children with Down syndrome and congenital heart disease

2013 ◽  
Vol 69 (3) ◽  
pp. 241-245 ◽  
Author(s):  
Mukti Sharma ◽  
Sanjeev Khera ◽  
Vishal Sondhi ◽  
Amit Devgan
2020 ◽  
Vol 4 (S1) ◽  
Author(s):  
Zoya Rashid ◽  
Robert Tulloh

Abstract Background Management of patients with pulmonary arterial hypertension associated with congenital heart disease and trisomy 21 is complex due to uncertainty over the best first-line agent to use for treatment, and the outcome measures for assessing response to therapy. There are also ethical issues around therapeutic decisions which may require ‘best interests’ meetings of carers and health care professionals. Case presentation We present a case of a 35-year-old man with Down syndrome, with un-operated atrioventricular septal defect, right ventricular hypertrophy and moderate left atrioventricular valve regurgitation. In the clinic he was visibly cyanosed with peripheral oxygen saturations of 78% at rest. He had very limited walk distance and was in WHO class III. Conclusions We discuss the decisions made around the best therapy for his Eisenmenger syndrome taking into account patient and family views on therapy and considering the psychosocial burden of treatment.


2018 ◽  
Vol 82 (6) ◽  
pp. 1513-1514 ◽  
Author(s):  
Susumu Hosokawa ◽  
Rebecca R. Vanderpool ◽  
Taku Ishii ◽  
Mitsunori Nishiyama ◽  
Shozaburo Doi

2007 ◽  
Vol 6 (3) ◽  
pp. 121-125 ◽  
Author(s):  
Ingram Schulze-Neick ◽  
John E. Deanfield

Adults with congenital heart disease (CHD) have become a rapidly expanding group of complex patients requiring multidisciplinary care in specialty centers by those trained in CHD. They represent one of the most challenging subgroups of patients with pulmonary arterial hypertension (PAH) due to the presence of structural heart disease with or without coexisting cyanosis and its complications. The primary focus of attention for these patients is the lungs, whose vascular system is affected by shunt flow, or is also congenitally malformed, or has been altered by surgical procedures. When PAH develops, it affects physical exercise tolerance, travel to high altitudes, pregnancy, operability, and anesthesia (myocardial failure due to pulmonary hypertensive crisis), and thus general morbidity and mortality in this special patient group.


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