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Defining the electrocardiogram in the neonate with hypoplastic left heart syndrome
Michael A Monaco1, Leonardo Liberman, Thomas J Starc
1Division of Cardiology, Department of Pediatrics, Morgan Stanley Children's Hospital, Columbia University College of Physicians and Surgeons, 3959 Broadway, CH-2 North, New York, NY, 10032-3784, USA.
Insights
Hypoplastic left heart syndrome (HLHS) shows distinct ECG patterns, including longer PR intervals and wider QRS complexes. These findings help identify this severe congenital heart defect in neonates.
Area of Science:
- Pediatric Cardiology
- Congenital Heart Disease
- Electrocardiography
Background:
- Hypoplastic left heart syndrome (HLHS) is a critical congenital heart defect.
- A defined electrocardiogram (ECG) pattern for HLHS in a large population is lacking.
Purpose of the Study:
- To identify a classic ECG pattern in neonates with HLHS.
- To compare ECG findings in HLHS patients with a control group.
Main Methods:
- Retrospective review of ECGs from 89 neonates with HLHS (2001-2011) before surgery.
- Comparison of ECG parameters between HLHS patients and age-matched controls.
Main Results:
- HLHS patients exhibited longer PR intervals, wider QRS complexes, and decreased left-sided forces (lower voltage S waves in V1, R waves in V6).
- Absence of Q waves in lateral precordial and inferior leads, abnormal frontal plane QRS axis, and preexcited appearance were more common in HLHS.
- 20% of HLHS patients presented with a normal ECG.
Conclusions:
- Specific ECG findings are associated with HLHS, aiding in diagnosis.
- ECG can reveal decreased left ventricular forces and conduction abnormalities in HLHS.
- Despite characteristic findings, a normal ECG does not exclude HLHS.
Abstract:
Hypoplastic left heart syndrome (HLHS) is a severe form of congenital heart disease characterized by underdevelopment of the left heart. There has been no previously defined "classic" ECG pattern in a large homogenous population of patients with HLHS. We performed a retrospective review of ECGs from neonates with HLHS from 2001 to 2011 with electrocardiograms available prior to surgical intervention. Eighty-nine neonates met the inclusion criteria and were compared to a control population. HLHS patients had a longer PR interval 108 ± 18 versus 98 ± 11 ms (p < 0.05), a wider QRS complex 84 ± 17 versus 54 ± 5 ms (p < 0.05), lower voltage S waves in V1 2.0 ± 3.3 versus 5.8 ± 4.6 mm (p < 0.001) or absent S waves in V1 52 versus 4 % (p < 0.001) and lower voltage R waves in V6 7.8 ± 4.8 versus 9.3 ± 4.2 mm (p < 0.05). Patients with HLHS were more likely to have absent Q waves in the lateral precordial leads 78 versus 0 % (p < 0.001) and inferior leads 20 versus 1 % (p < 0.001) and an abnormal frontal plane QRS axis 26 versus 11 % (p < 0.05). HLHS patients were more likely to have a preexcited appearance 11 versus 0 % (p = 0.001). Despite these findings, 20 % of patients with HLHS had a normal ECG. Compared to age-matched controls, patients with HLHS were more likely to exhibit a longer PR interval, a wider QRS complex, decreased left-sided forces, an absence of septal Q waves in the inferior and lateral leads, an abnormal frontal plane QRS axis and a preexcited appearance.
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