Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Objectives: Recommendations for surgical repair of a congenital heart defect in children with trisomy 13 or trisomy 18 remain controversial, are subject to biases, and are largely unsupported with limited empirical data. This has created significant distrust and uncertainty among parents and could potentially lead to suboptimal care for patients. A working group, representing several clinical specialties involved with the care of these children, developed recommendations to assist in the decision-making process for congenital heart defect care in this population. The goal of these recommendations is to provide families and their health care teams with a framework for clinical decision making based on the literature and expert opinions.

Methods: This project was performed under the auspices of the AATS Congenital Heart Surgery Evidence-Based Medicine Taskforce. A Patient/Population, Intervention, Comparison/Control, Outcome process was used to generate preliminary statements and recommendations to address various aspects related to cardiac surgery in children with trisomy 13 or trisomy 18. Delphi methodology was then used iteratively to generate consensus among the group using a structured communication process.

Results: Nine recommendations were developed from a set of initial statements that arose from the Patient/Population, Intervention, Comparison/Control, Outcome process methodology following the groups' review of more than 500 articles. These recommendations were adjudicated by this group of experts using a modified Delphi process in a reproducible fashion and make up the current publication. The Class (strength) of recommendations was usually Class IIa (moderate benefit), and the overall level (quality) of evidence was level C-limited data.

Conclusions: This is the first set of recommendations collated by an expert multidisciplinary group to address specific issues around indications for surgical intervention in children with trisomy 13 or trisomy 18 with congenital heart defect. Based on our analysis of recent data, we recommend that decisions should not be based solely on the presence of trisomy but, instead, should be made on a case-by-case basis, considering both the severity of the baby's heart disease as well as the presence of other anomalies. These recommendations offer a framework to assist parents and clinicians in surgical decision making for children who have trisomy 13 or trisomy 18 with congenital heart defect.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jtcvs.2023.11.054DOI Listing

Publication Analysis

Top Keywords

congenital heart
24
children trisomy
20
trisomy trisomy
20
heart defect
20
trisomy congenital
12
trisomy
11
recommendations
9
care children
8
decision making
8
patient/population intervention
8

Similar Publications

Outcomes of Left Atrial Appendage Patency After Device Closure Detected by Cardiac CT: A Meta-Analysis.

JACC Cardiovasc Imaging

September 2025

Department of Cardiothoracic Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania, USA; UPMC Heart and Vascular Institute, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA. Electronic address:

Background: Residual leaks are common after left atrial appendage occlusion (LAAO).

Objectives: The authors aimed to systematically evaluate the prognostic implications of residual left atrial appendage (LAA) patency and peridevice leaks (PDLs) detected by cardiac computed tomography (CT) following LAAO.

Methods: The authors used traditional meta-analytical methods and a Bayesian framework to assess the probability of increased risks associated with these residual leaks.

View Article and Find Full Text PDF

Large Cerebral Abscess in a Patient of Tetralogy of Fallot.

Ann Afr Med

September 2025

Department of Medicine, KGMU, Lucknow, Uttar Pradesh, India.

Brain abscess is a rare but dangerous suppurative infection. Incidence of congenital heart disease varies from 5% to 18.7%.

View Article and Find Full Text PDF

Maternal causes of offspring congenital heart disease.

Eur Heart J

September 2025

Department of Cardiology, Cardiovascular Institute, Thorax Center, Erasmus MC, Room Rg-435, Dr. Molewaterplein 40, Rotterdam 3000, The Netherlands.

View Article and Find Full Text PDF

Objectives: We sought to review the outcomes of patients with Ebstein anomaly (EA) after the Fontan operation.

Methods: Patients with EA were identified from a large binational registry about the Fontan operation. Data were collected from hospital records, registry data, and clinical correspondence.

View Article and Find Full Text PDF