Growing Heart Valve Implants for Children

Haley Konsek1, Curry Sherard1, Cora Bisbee1

  • 1Department of Surgery, College of Medicine, Medical University of South Carolina, Charleston, SC 29425, USA.

Insights

Pediatric heart valve replacements fail to grow with children. This review explores tissue-engineered valves and partial heart transplants as potential solutions for growing pediatric heart valves, addressing long-term clinical needs.

Area of Science:

  • Biomedical Engineering
  • Regenerative Medicine
  • Pediatric Cardiology

Background:

  • Current heart valve implants for pediatric patients with congenital valvular disease do not accommodate somatic growth.
  • This limitation prevents long-term clinical success in children requiring valve replacement.
  • There is a critical need for pediatric heart valve solutions that can grow with the patient.

Purpose of the Study:

  • To review recent advancements in tissue-engineered heart valves (TEHVs) and partial heart transplantation.
  • To evaluate these approaches as potential growing heart valve implants for pediatric patients.
  • To discuss the barriers hindering clinical translation of these innovative therapies.

Main Methods:

  • Review of in vitro and in situ designs for tissue-engineered heart valves.
  • Analysis of large animal studies and clinical translational research.
  • Identification of challenges in the clinical application of growing heart valve technologies.

Main Results:

  • Tissue engineering and partial transplantation show promise as growing heart valve alternatives.
  • Significant progress has been made in designing and testing TEHVs.
  • Translational research in large animals provides a basis for clinical application.

Conclusions:

  • Tissue-engineered heart valves and partial heart transplantation represent promising avenues for pediatric growing heart valve solutions.
  • Overcoming barriers in design, manufacturing, and clinical integration is crucial for successful translation.
  • These regenerative approaches offer hope for improved long-term outcomes in children with congenital valvular disease.

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