The CardioMEMS HF System (Abbott, Abbott Park, IL) is the first FDA- and CE-Mark-approved device for monitoring patients with heart failure, significantly reducing hospitalizations and improving the quality of life for NYHA class III non-congenital adult patients. This device, implanted percutaneously, allows the direct monitoring of pulmonary arterial pressure with the wireless transfer of pressure data to the clinician, who can adjust the therapy remotely. Limited experience exists regarding its use in patients with congenital heart disease (CHD). CardioMEMS device implantation is feasible and safe in selected adults and children with CHD. The potential of the device to reduce heart failure hospitalizations in this population is enormous, but further multi-center studies are needed to demonstrate its efficacy.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11277830 | PMC |
http://dx.doi.org/10.3390/jcm13144234 | DOI Listing |
Diagnostics (Basel)
November 2024
Cardiology Department, GB Grassi Hospital, ASL Roma 3, 00122 Rome, Italy.
: Heart failure (HF) is a chronic disease with a steadily increasing prevalence, high mortality, and social and economic costs. Furthermore, every hospitalization for acute HF is associated with worsening prognosis and reduced life expectancy. In order to prevent hospitalizations, it would be useful to have instruments that can predict them well in advance.
View Article and Find Full Text PDFEur J Obstet Gynecol Reprod Biol
December 2024
Division of Cardiology, Zucker School of Medicine at Hofstra/Northwell, Manhasset, NY, United States.
Arch Cardiovasc Dis
November 2024
PhyMedExp, Inserm, CNRS, Cardiology Department, INI-CRT, université de Montpellier, 34295 Montpellier, France.
J Soc Cardiovasc Angiogr Interv
June 2024
Department of Pediatric Cardiology, Hospital Universitario La Paz, Madrid, Spain.
Background: The CardioMEMS is an implantable device for hemodynamic monitoring approved by the US Food and Drug Administration for adult patients with heart failure. It has been used in the adult population without structural heart disease and with congenital heart diseases, but we do not have data in the pediatric population.
Methods: We report the initial single-center experience of the CardioMEMS implantation in children.
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