Abstract
Introduction
Newborns with congenital diaphragmatic hernia (CDH) have varying degrees of pulmonary hypoplasia and pulmonary hypertension (PH), and there is limited evidence that cardiac dysfunction is present. We sought to study early neonatal biventricular function and performance in these patients by reviewing early post-natal echocardiography (ECHO) measurements and comparing them to normal term newborns.
Methods
Retrospective case–control study reviewing clinical and ECHO data on term newborns with CDH and normal controls born between 2009 and 2016. Patients were excluded if major anomalies, genetic syndromes, or no ECHO available. PH was assessed by ductal shunting and tricuspid regurgitant jet velocity. Speckle-tracking echocardiography was used to assess myocardial deformation using velocity vector imaging.
Results
Forty-four patients with CDH and 18 age-matched controls were analyzed. Pulmonary pressures were significantly higher in the CDH cohort (systolic pulmonary arterial pressure to systolic blood pressure of 103 ± 13 vs. 78 ± 29%, p = 0.0001). CDH patients had decreased RV fractional area change (FAC − 28.6 ± 11.1 vs. 36.2 ± 9.6%, p = 0.02), tricuspid annular plane of systolic excursion (TAPSE—5.6 ± 1.6 vs. 8.6 ± 1.6 mm, p = 0.0001), and RV outflow tract stroke distance (8.6 ± 2.7 vs. 14.0 ± 4.5 cm, p = 0.0001) compared with controls. The left ventricular (LV) ejection fraction was similar in both groups, but CDH patients had a decreased LV end-diastolic volume by Simpson’s rule (2.7 ± 1.0 vs. 5.0 ± 1.8 mL, p = 0.0001) and LVOT stroke distance (9.7 ± 3.4 vs. 12.6 ± 3.6 cm, p = 0.004). Biventricular global longitudinal strain (GLS) was markedly decreased in the CDH population compared to controls (RV-GLS: − 9.0 ± 5.3 vs. − 19.5 ± 1.4%, p = 0.0001; LV GLS: − 13.2 ± 5.8 vs. − 20.8 ± 3.5%, p = 0.0001).
Conclusion
CDH newborns have evidence of biventricular dysfunction and decreased cardiac output. Abnormal function may be a factor in the non-response to pulmonary arterial vasodilators in CDH patients. A two-pronged management strategy aimed at improving cardiac function, as well as reducing pulmonary artery pressure in CDH newborns, may be warranted.
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Abbreviations
- BP:
-
Blood pressure
- CDH:
-
Congenital diaphragmatic hernia
- DICOM:
-
Digital imaging and communications in medicine format
- EDSR:
-
Early diastolic strain rate
- EF:
-
Ejection fraction
- EDV:
-
End-diastolic volume
- ECMO:
-
Extracorporeal membrane oxygenation
- FAC:
-
Fractional area change
- GLS:
-
Global longitudinal strain
- GLSR:
-
Global longitudinal strain rate
- LV:
-
Left ventricle
- EI:
-
Eccentricity index
- LVOT:
-
Left ventricular outflow tract
- MPA:
-
Main pulmonary artery
- PDA:
-
Patent ductus arteriosus
- PAP:
-
Pulmonary artery pressure
- RV:
-
Right ventricle
- RVOT:
-
Right ventricular outflow tract
- STE:
-
Speckle-tracking echocardiography
- SD:
-
Standard deviation
- TAPSE:
-
Tricuspid annular plane systolic excursion
- TR:
-
Tricuspid regurgitant jet velocity
- VTI:
-
Velocity time integral
- VVI:
-
Velocity vector imaging
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We have no conflicts of interest related to the content of this study. Gabriel Altit is the author that wrote the first draft. There was no payment, grant, or honorarium given to anyone to produce the manuscript.
Ethical Approval
This study was approved by the institutional review board of Stanford University (protocol—IRB-39501).
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Altit, G., Bhombal, S., Van Meurs, K. et al. Diminished Cardiac Performance and Left Ventricular Dimensions in Neonates with Congenital Diaphragmatic Hernia. Pediatr Cardiol 39, 993–1000 (2018). https://doi.org/10.1007/s00246-018-1850-7
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DOI: https://doi.org/10.1007/s00246-018-1850-7