Literature DB >> 31302722

Early palliative balloon pulmonary valvuloplasty in neonates and young infants with tetralogy of Fallot.

Jun Muneuchi1, Mamie Watanabe2, Yuichiro Sugitani2, Naoki Kawaguchi2, Ryohei Matsuoka2, Yusuke Ando3, Yoshie Ochiai3.   

Abstract

We aim to clarify the efficacy of early palliative balloon pulmonary valvuloplasty (BPV) in neonates and young infants (< 60 days) with tetralogy of Fallot (TOF). We performed palliative BPV in 31 subjects, regardless of the presence of cyanosis, with Z score of the pulmonary valve diameter (PVD) less than - 2.00. Primary and secondary endpoints were to avoid early surgical interventions for subjects within 6 months of age and to undergo the pulmonary valve-sparing procedure at corrective surgery, respectively. We studied factors associated with these outcomes among them. BPV was performed at 19 days (14-33) of age and with a weight of 3.34 kg (3.02-3.65). Systemic oxygen saturation, Z score of the PVD, and pulmonary arterial index (PAI) were 87% (81-91), - 3.56 (- 4.15 to - 2.62), and 128 mm2/m2 (102-157), respectively. There were 16 and 13 subjects who avoided early surgical interventions and transannular repair, respectively. At the primary endpoint, there was no significant difference in age, weight, systemic oxygen saturation, and Z score of the PVD and PAI between the groups. However, there was a significant difference in the infundibular morphology (severe: mild-to-moderate, 8:8 vs 13:2, P = 0.029) between the groups. We performed prophylactic BPV within 30 days after birth in 7 acyanotic TOF patients with severe infundibular obstruction, among whom 5 avoided early surgical intervention. At the secondary endpoint, there were no significant difference in weight, systemic oxygen saturation, but in sex, age at BPV, and Z score of the PVD. Early palliative BPV prevented early surgical intervention in half of the neonates and young infants with TOF, which depended upon the degree of infundibular obstruction. However, early palliative BPV did not contribute to avoid transanular patch right-ventricular outflow repair among them.

Entities:  

Keywords:  Catheter intervention; Congenital heart disease; Pulmonary valve; Right-ventricular outflow tract

Year:  2019        PMID: 31302722     DOI: 10.1007/s00380-019-01468-0

Source DB:  PubMed          Journal:  Heart Vessels        ISSN: 0910-8327            Impact factor:   2.037


  3 in total

1.  Conal Septal Hypoplasia in Tetralogy of Fallot-Impact on Clinical Course, Treatment Strategies, and Outcomes After Surgical Intervention.

Authors:  Kirsten E Borsheim; Ronald K Woods; Evelyn M Kuhn; Peter C Frommelt
Journal:  Pediatr Cardiol       Date:  2022-07-19       Impact factor: 1.838

2.  Palliation Strategy to Achieve Complete Repair in Symptomatic Neonates with Tetralogy of Fallot.

Authors:  Mark A Law; Andrew C Glatz; Jennifer C Romano; Paul J Chai; Christopher E Mascio; Christopher J Petit; Courtney E McCracken; Michael S Kelleman; George T Nicholson; Jeffery J Meadows; Jeffrey D Zampi; Shabana Shahanavaz; Sarosh P Batlivala; Joelle Pettus; Amy L Pajk; Kristal M Hock; Bryan H Goldstein; Athar M Qureshi
Journal:  Pediatr Cardiol       Date:  2022-04-05       Impact factor: 1.838

3.  Biventricular strain and strain rate impairment shortly after surgical repair of tetralogy of Fallot in children: A case-control study.

Authors:  Bahar Dehghan; Alireza Ahmadi; Shima Sarfarazi Moghadam; Mohammad Reza Sabri; Mehdi Ghaderian; Chehreh Mahdavi; Mohsen Sedighi; Hamid Bigdelian
Journal:  Health Sci Rep       Date:  2022-05-03
  3 in total

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