Hostname: page-component-74656f9884-j7cmm Total loading time: 0 Render date: 2026-11-07T21:56:15.881Z Has data issue: false hasContentIssue false

Surgical versus transcatheter palliation for insufficient pulmonary blood supply in infants with cyanotic CHD

Published online by Cambridge University Press:  24 May 2021

Andrew B. Ho
Affiliation:
Congenital Cardiology, Leeds General Infirmary, Great George Street, Leeds, United Kingdom University Hospitals Southampton NHS Trust, Tremona Road, Southampton, United Kingdom
Thomas Perry
Affiliation:
Department of Biomedical Sciences, University of Plymouth, Plymouth, United Kingdom
Ines Hribernik
Affiliation:
Congenital Cardiology, Leeds General Infirmary, Great George Street, Leeds, United Kingdom
John D. Thomson
Affiliation:
Congenital Cardiology, Leeds General Infirmary, Great George Street, Leeds, United Kingdom
James R. Bentham*
Affiliation:
Congenital Cardiology, Leeds General Infirmary, Great George Street, Leeds, United Kingdom
*
Author for correspondence: Dr James Bentham, Congenital Cardiology, Leeds General Infirmary, Great George Street, Leeds, LS1 3EX, United Kingdom. Tel: +441132432799. E-mail: James.Bentham@nhs.net
Rights & Permissions [Opens in a new window]

Abstract

Infants with complex cyanotic CHD can become symptomatic from insufficient pulmonary blood supply following either ductal closure or due to outflow tract obstruction. Blalock–Taussig shunt mortality remains significant and recent studies have highlighted the advantages of using transcatheter alternatives. We present here our experience in changing our primary choice of palliation from the Blalock–Taussig shunt to transcatheter palliation with either a ductal stent or, if antegrade flow is present, a right ventricular outflow tract stent.

This is a retrospective, single-unit cohort study. Eighty-seven infants underwent palliation for insufficient pulmonary blood flow at under 3 months of age between 2012 and 2019. On an intention-to-treat basis, 29 underwent insertion of a Blalock–Taussig shunt, 36 duct stents, and 22 right ventricular outflow tract stents at median ages of 15, 9, and 32 days, respectively, and median weights of 3.3, 3.1, and 3.1 kg, respectively. No primary Blalock–Taussig shunts have been performed in our institution since 2017.

At 30-days there had been one death in each group (univariable p = 0.93) and deaths prior to repair totalled three in the shunt group, four in the ductal stent group, and two in the right ventricular outflow tract stent group (univariable p = 0.93). Reintervention on the pulmonary circuit prior to next stage of surgery was more frequent in those undergoing transcatheter intervention, reaching statistical significance by logrank (p = 0.012).

In conclusion, within this work we provide further evidence of the safety and efficacy of transition from a primary surgical to primary transcatheter palliation pathway in infants with insufficient pulmonary blood supply.

Information

Type
Original Article
Copyright
© The Author(s), 2021. Published by Cambridge University Press
Figure 0

Table 1. Baseline demographics

Figure 1

Table 2. Anatomical diagnoses of palliated patients

Figure 2

Figure 1. Bar chart showing number of each procedure per annum. Note data collection ended July 2019 so the 2019 data comprises an incomplete year.

Figure 3

Figure 2. Scatter charts of procedural and fluoroscopy times by procedure over time with linear regression lines and 95% confidence intervals overlaid.

Figure 4

Table 3. Primary outcomes

Figure 5

Figure 3. Flowchart of patient outcomes.

Figure 6

Table 4. Secondary outcomes for patients reaching next stage surgery. Reported Nakata index is prior to complete repair/Glenn shunt

Figure 7

Table 5. Branch PA sizes

Figure 8

Figure 4. Kaplan–Meier curves for mortality, with the plot on the left for mortality prior to repair and the plot on the right for mortality at any time following palliation (median follow-up = 3.9 years). Reported p values are by logrank.

Figure 9

Table 6. Serious adverse events and reintervention prior to complete repair or Glenn shunt

Figure 10

Figure 5. Kaplan–Meier curve of reintervention prior to either complete repair or Glenn shunt. Patients are censored at death prior to complete repair or complete repair. Reported p value is by logrank.