Commentary: the Heart of Symptomatic Neonatal Ebstein Anomaly: Negative Interventricular Interaction and Ventricular Myopathy.

Central MessageSymptomatic newborn infants with Ebstein anomaly have physiologic and anatomic pathology that benefit from Starnes palliation when operative intervention is necessary.See Article page 128. Symptomatic newborn infants with Ebstein anomaly have physiologic and anatomic pathology that benefit from Starnes palliation when operative intervention is necessary. See Article page 128. Patients with Ebstein anomaly demonstrate a wide array of clinical presentations primarily rooted in their heterogenous anatomy. Severe defects recognized on prenatal ultrasound screening and/or triggering symptoms in the neonatal period are particularly hazardous. Despite modern advances in surgical and critical care, neonatal Ebstein anomaly exhibits a perinatal mortality of 45%.1Freud L.R. Escobar-Diaz M.C. Kalish B.T. Komarlu R. Puchalski M.D. Jaeggi E.T. et al.Outcomes and predictors of perinatal mortality in fetuses with Ebstein anomaly or tricuspid valve dysplasia in the current era: a multicenter study.Circulation. 2015; 132: 481-489Crossref PubMed Scopus (79) Google Scholar Knott-Craig and Boston2Knott-Craig C.J. Boston U.S. Current surgical techniques in the management of the symptomatic neonate with severe Ebstein's anomaly: too much, too little, or just enough?.J Thorac Cardiovasc Surg Tech. 2021; 9: 128-134Scopus (1) Google Scholar have devoted their careers to the care of these children and contributed enormously to our understanding of the best management strategies. Their article concludes that most symptomatic neonates can undergo biventricular repair but the ideal timing for that operation is at age of 3 to 5 months. This marks an important transition away from their prior reports.3Knott-Craig C.J. Overholt E.D. Ward K.E. Razook J.D. Neonatal repair of Ebstein's anomaly: indications, surgical technique, and medium-term follow-up.Ann Thorac Surg. 2000; 69: 1505-1510Abstract Full Text Full Text PDF PubMed Scopus (59) Google Scholar, 4Boston U.S. Goldberg S.P. Ward K.E. Overholt E.D. Spentzas T. Chin T.K. et al.Complete repair of Ebstein anomaly in neonates and young infants: a 16-year follow-up.J Thorac Cardiovasc Surg. 2011; 141: 1163-1169Abstract Full Text Full Text PDF PubMed Scopus (43) Google Scholar, 5Goldberg S.P. Jones R.C. Boston U.S. Haddad L.M. Wetzel G.T. Chin T.K. et al.Current trends in the management of neonates with Ebstein's anomaly.World J Pediatr Congenit Heart Surg. 2011; 2: 554-557Crossref PubMed Scopus (9) Google Scholar, 6Knott-Craig C.J. Goldberg S.P. Ballweg J.A. Boston U.S. Surgical decision making in neonatal Ebstein's anomaly: an algorithmic approach based on 48 consecutive neonates.World J Pediatr Congenit Heart Surg. 2012; 3: 16-20Crossref PubMed Scopus (26) Google Scholar, 7Knott-Craig C.J. Kumar T.K. Arevalo A.R. Joshi V.M. Surgical management of symptomatic neonates with Ebstein's anomaly: choice of operation.Cardiol Young. 2015; 25: 1119-1123Crossref PubMed Scopus (14) Google Scholar Symptomatic newborn infants fall into 2 major categories: those who need time to transition from fetal life and those who are unable to survive without intervention. The number of newborn infants in each category is relatively equal.8Freud L.R. McElhinney D.B. Kalish B.T. Escobar-Diaz M.C. Komarlu R. Puchalski M.D. et al.Risk factors for mortality and circulatory outcome among neonates prenatally diagnosed with Ebstein anomaly or tricuspid valve dysplasia: a multicenter study.J Am Heart Assoc. 2020; 9: e016684Crossref PubMed Scopus (5) Google Scholar It has been our experience that children who are able to transition and go home have a reasonable-sized true right ventricle (RV) and/or little to no tricuspid regurgitation. They do not usually develop symptoms or require surgical intervention within their first year of life. Conversely, neonates who need intervention often have tenuous pulmonary blood flow and significant right heart distension that compromises left ventricular (LV) filling and outflow via interventricular septal shift. The most appropriate intervention must secure blood flow and eliminate the cause of septal shift. Admittedly, our group is biased. It has always been our opinion that features inherent to Ebstein anomaly favor initial Starnes palliation. The most relevant are right ventricular myopathy and failed tricuspid valve delamination.9Stephens E.H. Dearani J.A. Qureshi M.Y. Ammash N. Maleszewski J.J. The congenital tricuspid valve spectrum: from Ebstein to dysplasia.World J Pediatr Congenit Heart Surg. 2020; 11: 783-791Crossref PubMed Google Scholar A myopathic RV is unable to effectively overcome the elevated pulmonary vascular resistance and oft-underdeveloped branch pulmonary arteries of symptomatic neonates. Secondarily, thin and attenuated valvular tissue in newborn infants makes any attempt at effective valve repair impractical. Finally, if the valvular tissue cannot be relocated to the true annulus along with a restoration of valvular competency, an atrialized RV remains at risk for distension with subsequent displacement of the interventricular septum toward the LV. We congratulate the evolution of the management algorithm presented within this article,2Knott-Craig C.J. Boston U.S. Current surgical techniques in the management of the symptomatic neonate with severe Ebstein's anomaly: too much, too little, or just enough?.J Thorac Cardiovasc Surg Tech. 2021; 9: 128-134Scopus (1) Google Scholar but have several critiques based on the limitations outlined above. Primarily, the presence of LV compression must be accounted for. Isolated Blalock-Taussig shunt does not address this problem. There are several areas where it is recommended, but we caution providers to consider the presence of LV compression before committing to an isolated shunt. In addition, the timing recommended for biventricular repair following neonatal palliation is 3 to 5 months. RV myopathy is of important concern in these newborn infants. Although rehabilitation of this ventricle is feasible for future 1.5- or 2-ventricle repairs, it appears to be a process that takes longer than 3 to 5 months.10Da Silva J.P. Viegas M. Castro-Medina M. Da Fonseca Da Silva L. The Da Silva cone operation after the Starnes procedure for Ebstein's anomaly: new surgical strategy and initial results.J Thorac Cardiovasc Surg Tech. 2020; 3: 281-283Google Scholar Waiting longer may also allow for a lesser need for bidirectional Glenn. Overall, our field has come a long way since 1991,11Starnes V.A. Pitlick P.T. Bernstein D. Griffin M.L. Choy M. Shumway N.E. Ebstein's anomaly appearing in the neonate. A new surgical approach.J Thorac Cardiovasc Surg. 1991; 101: 1082-1087Abstract Full Text PDF PubMed Google Scholar and the future for these children has never been more optimistic. Current surgical techniques in the management of the symptomatic neonate with severe Ebstein anomaly: Too much, too little, or just enough?JTCVS TechniquesVol. 9PreviewThe management of severely symptomatic neonates with Ebstein anomaly is challenging during the early neonatal period. Initial management goals should focus on mitigating a central shunt; providing respiratory mechanical support; providing an adequate but not excessive source of pulmonary blood flow; and minimizing pulmonary vascular resistance. For most patients thus stabilized, definitive repair should be prudently deferred until it is safe for a bailout bidirectional Glenn anastomosis to be added, usually at age 3 to 4 months. Full-Text PDF Open Access