Midgestation Fetal Pulmonary Annulus Size Is Predictive of Outcome in Tetralogy of Fallot. (3rd July 2013)

• Record Type: Journal Article
• Authors: Friedman, Kevin; Balasubramanian, Sowmya; Tworetzky, Wayne
• Is Part Of: Congenital heart disease. Volume 9:Number 3(2014)
• Page Start: 187
• Page End: 193
• Publication Date: 2013-07-03
• Subjects: Congenital heart disease -- Periodicals; 616.1204305
• DOI: 10.1111/chd.12120
• Languages: English
• ISSNs: 1747-079X

Abstract

<abstract abstract-type="main"> <title>Abstract</title> <sec id="chd12120-sec-0001" sec-type="section"> <title>Background</title> <p>Surgical management of tetralogy of Fallot (TOF) is increasingly moving toward valve‐sparing approaches rather than transannular patch (TAP). We evaluate whether fetal pulmonary valve (PV) size is predictive of postnatal course and surgical approach in TOF.</p> </sec> <sec id="chd12120-sec-0002" sec-type="section"> <title>Methods</title> <p>In this retrospective study, fetal and postnatal demographic, clinical, and echocardiographic data on 66 patients diagnosed prenatally with TOF were collected. We compared those with midgestation PV <italic>z</italic>‐score > −3.5 to those with <italic>z</italic>‐score ≤−3.5. We analyzed fetal and postnatal PV size and growth and outcomes between groups</p> </sec> <sec id="chd12120-sec-0003" sec-type="section"> <title>Results</title> <p>Gestational age at first fetal echo was 23 weeks (range 18–28). PV diameter and <italic>z</italic>‐score on midgestation echo were 3.5 mm (1.3–6.0) and −2.8 (−0.5 to −6.0) respectively. Patients with PV <italic>z</italic>‐score ≤ −3.5 on first fetal echo had smaller PV diameter (4.5 vs. 5.0 mm, <italic>P</italic> = .047) and PV <italic>z</italic>‐score (−3.8 vs. −2.8, <italic>P</italic> < .001) in late gestation and at time of surgery (6.0 mm vs. 7.0 mm, <italic>P</italic> = .01; <italic>z</italic>‐score = −2.9 vs. −1.7, <italic>P</italic> = .007). Similarly, those with smaller fetal PV <italic>z</italic>‐score had smaller main and branch pulmonary arteries at time of surgery. PV growth rate over gestation was similar between groups, while after‐birth PV growth rate was lower in those with smaller PV (0 mm/month vs. 0.6 mm/month, <italic>P</italic> = .002).</p> <p>Those with smaller pulmonary valve were more likely to be cyanotic (<italic>P</italic> = .05), to undergo surgery at <1 month (<italic>P</italic> < .01), and to have a TAP repair (<italic>P</italic> = .01). Among patients undergoing valve‐sparing repair, those with smaller PV underwent more reinterventions for residual valvar PS (<italic>P</italic> < .01).</p> </sec> <sec id="chd12120-sec-0004" sec-type="section"> <title>Conclusion</title> <p>Midgestation fetal PV size is predictive of postnatal PV and PA size in TOF. Midgestation PV size has implications for timing and type of surgical management as well as for need for reintervention in valve‐sparing repair patients and is therefore important to consider in prenatal counseling for TOF fetuses.</p> </sec> </abstract>