Original ArticleNeonatal Isolated Critical Aortic Valve Stenosis: Balloon Valvuloplasty or Surgical Valvotomy☆
Introduction
Neonatal critical aortic stenosis is potentially life threatening with a high morbidity and significant mortality despite early intervention.1, 2, 3, 4, 5, 6, 7 It is uncommon and accounts for 1–3% of neonates with significant congenital heart disease.3 Infants may present in cardiac failure and/or in a low output state, many requiring ventilation, inotropic support and prostaglandin E1 infusion, the latter to maintain patency of the arterial duct to assist systemic circulation.2 Cross-sectional echocardiography is able to define the diagnosis accurately and determine other abnormalities.1 Open surgical valvotomy and transcatheter balloon valvuloplasty of the aortic valve are recognized treatment modalities with favorable results.8, 9 A neonatal Ross procedure has been advocated by some authors.10
Previous comparisons of the outcome of balloon valvuloplasty and surgical valvotomy have been published though the numbers were limited, not randomized or from different time periods.8, 9 Other series of critical aortic valve stenosis have included additional malformations with outcomes focussed on predicting mortality arising from multiple anatomical variables.1, 2
The purpose of this study was to compare the short and medium term outcome of neonates with isolated critical aortic stenosis who required intervention during the same time period at a single tertiary institution, to determine their immediate morbidity, the re-stenosis rate and the need for re-intervention. Their duration of hospitalization and intensive care stay were also determined. The procedure selected depended on the preference of the attending cardiologist after discussion with the attending cardiac surgeon, and taking into account the anatomy of the aortic valve. The two groups were therefore not comparable, the surgical group including somewhat sicker infants.
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Materials and Methods
The study group comprised neonates who presented to a tertiary centre with isolated critical valvar aortic stenosis with atrio-ventricular concordance and no associated left heart malformation. All patients required intervention within 6 weeks of life due to heart failure and/or shock. Their records were reviewed and the cross sectional echocardiogram of each infant was studied in detail. The outcome of each patient was determined and their serial Doppler velocities across the aortic valve
Statistics
The results were expressed as frequencies, median with a range, mean and standard deviation. Student's t-test and a p-value of less than or equal to 0.05 was determined as a significant level for continuous data.
Results
Between 1990 and 2000, 25 neonates with critical aortic stenosis required intervention. There were 12 patients in the balloon group and 13 in the surgical group.
Discussion
This study reviewed the treatment currently undertaken at our center for neonates with isolated critical aortic stenosis namely, open surgical valvotomy or transcatheter balloon valvuloplasty. The excellent outcome of surgical aortic valvotomy from this institution4, 5 for neonates with critical aortic valve stenosis with or without other congenital heart abnormalities, provided little impetus to the introduction of balloon valvuloplasty. There was an 18% hospital mortality with a 5-year
Conclusions
Both balloon valvuloplasty and surgical valvotomy offers effective immediate reduction of gradient in critical aortic stenosis resulting in the relief of heart failure and the need for continued ventilation and inotropic support. Patients in the balloon group had a higher re-intervention rate with the main increase of gradient seen within the first months following intervention. Hospital and intensive care stay in the balloon group was shorter as compared to the surgical group.
Either procedure
Acknowledgements
Dr. J. L. Wilkinson provided considerable help in the preparation of the manuscript.
Appreciation is expressed to the staff cardiologists and surgeons who allowed us to review their patients.
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Cited by (23)
The Ross Procedure in Children: The Gold Standard?
2021, Seminars in Thoracic and Cardiovascular Surgery: Pediatric Cardiac Surgery AnnualCitation Excerpt :Both transcatheter balloon valvuloplasty (TBV) and surgical valvotomy (SV) have long been utilized with favorable results.2-4 Seventy-two percent of patients with congenital aortic valve stenosis have been reported to have bicuspid aortic valves.5 The majority of patients exhibit fusion of the intercoronary commissure along with partial fusion of the anterior and posterior commissures.
Neonatal Aortic Stenosis is a Surgical Disease: An Interventional Cardiologist View
2016, Seminars in Thoracic and Cardiovascular Surgery: Pediatric Cardiac Surgery AnnualCitation Excerpt :While overall mortality rates in the Zeevi study were high,9 it was largely attributed to small or hypoplastic left ventricles; a finding that has been reported in other studies.10–12 Recent studies by McCrindle et al13 and Zain et al14 have demonstrated either no differences or a higher mortality rate after SAV. The data presented here demonstrates equivalence for both techniques in the intermediate and longer-term and contemporary mortality rates better than previous reports.
Percutaneous treatment of congenital heart valve diseases
2011, Archives of Cardiovascular Diseases SupplementsHybrid approach as bridge to biventricular repair in a neonate with critical aortic stenosis and borderline left ventricle
2009, European Journal of Cardio-thoracic SurgeryBalloon aortic valvuloplasty in neonates: short- and long-term effects and predictors of successful outcome
2022, Postepy w Kardiologii InterwencyjnejResults of balloon and surgical valvuloplasty in congenital aortic valve stenosis: A 19-year, single-center, retrospective study
2021, Turkish Journal of Thoracic and Cardiovascular Surgery
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Presented in part at the World Congress of Paediatric Cardiology and Cardiac Surgery, Toronto, May 2001.