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Surgical strategies for the management of end‐stage heart failure in infants and children: A 15‐year experience with a patient‐tailored approach

End‐stage heart failure (ESHF) in pediatric age is an ongoing challenge. Heart transplantation is the final option, but its long‐term outcomes are still suboptimal in children. An alternative patient‐tailored surgical protocol to manage ESHF in children is described. Retrospective, single‐center ana...

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Published in:Artificial organs 2021-12, Vol.45 (12), p.1543-1553
Main Authors: Ponzoni, Matteo, Frigo, Anna C., Castaldi, Biagio, Cerutti, Alessia, Di Salvo, Giovanni, Vida, Vladimiro L., Padalino, Massimo A.
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container_title Artificial organs
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creator Ponzoni, Matteo
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description End‐stage heart failure (ESHF) in pediatric age is an ongoing challenge. Heart transplantation is the final option, but its long‐term outcomes are still suboptimal in children. An alternative patient‐tailored surgical protocol to manage ESHF in children is described. Retrospective, single‐center analysis of pediatric patients admitted to our institution between April 2004 and February 2021 for ESHF. Our current protocol is as follows: (a) Patients
doi_str_mv 10.1111/aor.14057
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Heart transplantation is the final option, but its long‐term outcomes are still suboptimal in children. An alternative patient‐tailored surgical protocol to manage ESHF in children is described. Retrospective, single‐center analysis of pediatric patients admitted to our institution between April 2004 and February 2021 for ESHF. Our current protocol is as follows: (a) Patients &lt;1 year with isolated left ventricular dysfunction due to dilated cardiomyopathy underwent pulmonary artery banding (PAB). (b) Patients &lt;10 years and &lt;20 kg, who did not meet previous criteria were managed with Berlin Heart EXCOR. (c) Patients &gt;10 years or &gt;20 kg, underwent placement of intracorporeal Heartware. Primary outcomes were survival, transplant incidence, and postoperative adverse events. A total of 24 patients (mean age 5.3 ± 5.9 years) underwent 26 procedures: PAB in 6 patients, Berlin Heart in 11, and Heartware in 7. Two patients shifted from PAB to Berlin Heart. Overall survival at 1‐year follow‐up and 5‐year follow‐up was 78.7% (95%CI = 62%‐95.4%) and 74.1% (95%CI = 56.1%‐92.1%), respectively. Berlin Heart was adopted in higher‐risk settings showing inferior outcomes, whereas a PAB enabled 67% of patients to avoid transplantation, with no mortality. An integrated, patient‐tailored surgical strategy, comprehensive of PAB and different types of ventricular assist devices, can provide satisfactory medium‐term results for bridging to transplant or recovery. The early postoperative period is critical and requires strict clinical vigilance. Selected infants can benefit from PAB that has demonstrated to be a safe bridge to recovery. 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Heart transplantation is the final option, but its long‐term outcomes are still suboptimal in children. An alternative patient‐tailored surgical protocol to manage ESHF in children is described. Retrospective, single‐center analysis of pediatric patients admitted to our institution between April 2004 and February 2021 for ESHF. Our current protocol is as follows: (a) Patients &lt;1 year with isolated left ventricular dysfunction due to dilated cardiomyopathy underwent pulmonary artery banding (PAB). (b) Patients &lt;10 years and &lt;20 kg, who did not meet previous criteria were managed with Berlin Heart EXCOR. (c) Patients &gt;10 years or &gt;20 kg, underwent placement of intracorporeal Heartware. Primary outcomes were survival, transplant incidence, and postoperative adverse events. A total of 24 patients (mean age 5.3 ± 5.9 years) underwent 26 procedures: PAB in 6 patients, Berlin Heart in 11, and Heartware in 7. Two patients shifted from PAB to Berlin Heart. 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Heart transplantation is the final option, but its long‐term outcomes are still suboptimal in children. An alternative patient‐tailored surgical protocol to manage ESHF in children is described. Retrospective, single‐center analysis of pediatric patients admitted to our institution between April 2004 and February 2021 for ESHF. Our current protocol is as follows: (a) Patients &lt;1 year with isolated left ventricular dysfunction due to dilated cardiomyopathy underwent pulmonary artery banding (PAB). (b) Patients &lt;10 years and &lt;20 kg, who did not meet previous criteria were managed with Berlin Heart EXCOR. (c) Patients &gt;10 years or &gt;20 kg, underwent placement of intracorporeal Heartware. Primary outcomes were survival, transplant incidence, and postoperative adverse events. A total of 24 patients (mean age 5.3 ± 5.9 years) underwent 26 procedures: PAB in 6 patients, Berlin Heart in 11, and Heartware in 7. Two patients shifted from PAB to Berlin Heart. Overall survival at 1‐year follow‐up and 5‐year follow‐up was 78.7% (95%CI = 62%‐95.4%) and 74.1% (95%CI = 56.1%‐92.1%), respectively. Berlin Heart was adopted in higher‐risk settings showing inferior outcomes, whereas a PAB enabled 67% of patients to avoid transplantation, with no mortality. An integrated, patient‐tailored surgical strategy, comprehensive of PAB and different types of ventricular assist devices, can provide satisfactory medium‐term results for bridging to transplant or recovery. The early postoperative period is critical and requires strict clinical vigilance. Selected infants can benefit from PAB that has demonstrated to be a safe bridge to recovery. An integrated and patient‐tailored surgical protocol for end‐stage heart failure in children, comprehensive of pulmonary artery banding for left ventricular rehabilitation and long‐term mechanical circulatory support devices, can provide very good early and medium‐term survival.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>34461675</pmid><doi>10.1111/aor.14057</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-4472-6287</orcidid><orcidid>https://orcid.org/0000-0002-0343-8118</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adverse events
Cardiomyopathy
Cardiomyopathy, Dilated - surgery
Child
Child, Preschool
Children
Congestive heart failure
Dilated cardiomyopathy
Female
Heart Defects, Congenital - surgery
Heart failure
Heart Failure - surgery
Heart transplantation
Heart Transplantation - statistics & numerical data
Heart-Assist Devices
Humans
Infant
Infants
Main Text
Male
mechanical circulatory support
Patients
pediatric heart failure
Pediatrics
Postoperative Complications
Pulmonary arteries
Pulmonary artery
Pulmonary Artery - surgery
pulmonary artery banding
Recovery
Retrospective Studies
Survival
Survival Analysis
Transplantation
Transplants & implants
Treatment Outcome
Ventricle
Ventricular assist devices
Ventricular Dysfunction, Left - surgery
ventricular rehabilitation
Vigilance
title Surgical strategies for the management of end‐stage heart failure in infants and children: A 15‐year experience with a patient‐tailored approach
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