Symptomatic presentation influences outcomes in pediatric restrictive cardiomyopathy

IntroductionChildren with restrictive cardiomyopathy (RCM) traditionally have a poor prognosis, with most patients either dying or requiring heart transplantation within 2 years of diagnosis. The development of symptoms in RCM suggests advanced disease. However, as screening practices evolve and lea...

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Main Authors: Melissa Lorenzo (Author), Aine Lynch (Author), Jenna Ashkanase (Author), Linda Fazari (Author), Kristen George (Author), Katelyn Arathoon (Author), Sunghoon Minn (Author), Dawn Nicolson (Author), Aamir Jeewa (Author), Emilie Jean- (Author)
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Published: Frontiers Media S.A., 2023-10-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Melissa Lorenzo  |e author 
700 1 0 |a Aine Lynch  |e author 
700 1 0 |a Jenna Ashkanase  |e author 
700 1 0 |a Linda Fazari  |e author 
700 1 0 |a Kristen George  |e author 
700 1 0 |a Katelyn Arathoon  |e author 
700 1 0 |a Sunghoon Minn  |e author 
700 1 0 |a Dawn Nicolson  |e author 
700 1 0 |a Aamir Jeewa  |e author 
700 1 0 |a Emilie Jean-  |e author 
245 0 0 |a Symptomatic presentation influences outcomes in pediatric restrictive cardiomyopathy 
260 |b Frontiers Media S.A.,   |c 2023-10-01T00:00:00Z. 
500 |a 2296-2360 
500 |a 10.3389/fped.2023.1264751 
520 |a IntroductionChildren with restrictive cardiomyopathy (RCM) traditionally have a poor prognosis, with most patients either dying or requiring heart transplantation within 2 years of diagnosis. The development of symptoms in RCM suggests advanced disease. However, as screening practices evolve and lead to diagnosis of early disease, identifying appropriate timing of transplant listing becomes increasingly important. In this context we compared outcomes of children with RCM presenting with clinical symptoms to those asymptomatic at initial presentation.MethodsThis retrospective cohort study included 25 patients with RCM presenting to a quaternary care center between 2001 and 2018. Times to transplantation, death, and a composite outcome of adverse cardiac events (CPR, cardioversion, inotropic support, mechanical ventilation, mechanical support, or heart transplant) were compared between those symptomatic and asymptomatic at presentation.ResultsAt 2 years following diagnosis, patients asymptomatic at presentation had a significantly better transplant-free survival at 57% compared to 17% for symptomatic patients (p = 0.03). Those asymptomatic at diagnosis also had significantly improved cardiac event-free survival at 71% compared to symptomatic patients at 25% (p = 0.01). In multivariable analysis, cardiac symptoms at presentation remained an independent risk factor for heart-transplant or death [hazard ratio 5.17 (1.28-20.85), p = 0.02].ConclusionPatients with RCM who are symptomatic at time of diagnosis have significantly worse transplant-free survival and cardiac event-free survival. Given current practice variability in timing of transplant listing, the presence of any cardiac symptoms is an important negative prognostic marker and should prompt urgent transplant listing. 
546 |a EN 
690 |a restrictive cardiomyopathy 
690 |a symptoms 
690 |a outcomes 
690 |a heart transplant 
690 |a transplant-free survival 
690 |a Pediatrics 
690 |a RJ1-570 
655 7 |a article  |2 local 
786 0 |n Frontiers in Pediatrics, Vol 11 (2023) 
787 0 |n https://www.frontiersin.org/articles/10.3389/fped.2023.1264751/full 
787 0 |n https://doaj.org/toc/2296-2360 
856 4 1 |u https://doaj.org/article/e721ab8d827641889a0ce6b3fb0ecedb  |z Connect to this object online.