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Transcatheter Mitral Valve-in-Valve Implantation in Pediatric Patients. | LitMetric

AI Article Synopsis

  • - The study investigates the use of transcatheter implantation of the Edwards Sapien 3 valve in four pediatric patients with dysfunctional bioprosthetic mitral valves, a method previously established in adults but not well explored for children.
  • - Results showed significant improvement in patients' conditions, with a drastic reduction in mean transmitral gradient and enhancement in functional status, as the average hospital stay was about four days post-procedure.
  • - The research concludes that this procedure is a safe and effective alternative for high-risk pediatric patients, although further long-term studies with larger groups are recommended to validate these findings.

Article Abstract

Background: Transcatheter implantation of the Edwards Sapien 3 valve (Edwards Lifesciences, Irvine CA) within the bioprosthetic mitral valve (MV) is an established method of treatment in adults. However, it has not been well studied in the pediatric age group.

Methods: Transcatheter mitral valve-in-valve implantation was attempted in 4 symptomatic pediatric patients with a dysfunctional MV bioprosthesis implanted at an earlier stage due to severe MV stenosis or regurgitation. We reviewed our experience with MV implantation in this cohort.

Results: The mean age and weight of the patients at the time of the procedure were 11.4 years (range: 10-14 years) and 36 kg (range: 31-44 kg), respectively. The transmitral mean gradient dropped from a mean of 19.75 mm Hg (range: 15-22 mm Hg) to a mean of 1 mm Hg (range: 0-3 mm Hg) after the procedure. The mean fluoroscopy time was 55.25 minutes (range: 40-72 minutes), and the mean hospital length of stay was 4 days (range: 3-7 days). The patients' functional class improved from New York Heart Association class IV to class I during the follow-up period.

Conclusions: Transcatheter mitral valve-in-valve implantation can be performed safely for dysfunctional bioprosthetic MVs in the pediatric age group with favorable early and midterm outcomes. This procedure offers a viable alternative in patients who have high surgical risk or are deemed unfit for conventional surgery. However, we still recommend a long-term study of this approach in a large cohort, multicentre study.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8767141PMC
http://dx.doi.org/10.1016/j.cjco.2021.08.007DOI Listing

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