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Very low birth weight infants with congenital heart disease: A multicenter cohort study in Japan
Yasumi Nakashima1, Yoshiki Mori1, Hiroshi Sugiura2
1Division of Pediatric Cardiology, Seirei Hamamatsu General Hospital, Hamamatsu, Japan.
Insights
Mortality for very low birth weight infants with congenital heart disease is high, especially with chromosomal anomalies. Sepsis is a significant risk factor for death in these vulnerable infants.
Area of Science:
- Neonatalogy
- Pediatric Cardiology
- Medical Genetics
Background:
- Limited data exists on the frequency, mortality, and morbidity of very low birth weight (VLBW) infants with congenital heart disease (CHD) in Asian populations.
- Risk factors for mortality in VLBW infants with CHD remain largely unknown.
Purpose of the Study:
- To investigate the frequency of CHD in VLBW infants in Asian countries.
- To identify risk factors associated with mortality in VLBW infants diagnosed with CHD.
Main Methods:
- A retrospective, multicenter cohort study included VLBW infants with CHD born between 2006 and 2010.
- Infants were followed up to 5 years of age.
- Multiple logistic regression analysis was used to determine risk factors for death.
Main Results:
- Of 3247 VLBW infants, 126 (3.9%) had CHD. Common CHDs included ventricular septal defect and tetralogy of Fallot.
- Trisomy 18 and 13 were present in 25.4% of VLBW infants with CHD. Overall mortality was 35.7% by 5 years.
- Serious CHD, sepsis, chromosomal anomalies, and non-invasive treatments were associated with increased mortality. Sepsis remained a significant independent risk factor after excluding chromosomal anomalies.
Conclusions:
- Chromosomal anomalies like Trisomy 18 and 13 are frequently observed in VLBW infants with CHD.
- Mortality rates for VLBW infants with CHD remain high, even without chromosomal anomalies.
- Sepsis significantly contributes to the mortality of VLBW infants diagnosed with congenital heart disease.
Background:
The frequency, mortality, and morbidity of very low birth weight (VLBW) infants with congenital heart disease (CHD) in Asian countries are limited. In addition, little is known about the risk factors of death in these infants.
Methods:
A retrospective, multicenter cohort study was conducted. VLBW infants with CHD born between 2006 and 2010, and followed to 5 years of age, were included in the analysis. Multiple logistic regression analysis was performed to identify the risk factors of death.
Results:
Among 3247 VLBW infants, 126 various CHDs (3.9 %) were identified. The most common lesions were ventricular septal defect, tetralogy of Fallot (TOF), and coarctation of the aorta/interrupted aortic arch, in that order. The proportions of left-sided and right-sided outflow obstruction (TOF, pulmonary stenosis) were 15.1 % and 15.9 %, respectively. Trisomy 18 and trisomy 13 were present in 32 (25.4 %) of 126 VLBW infants with CHD. Nine patients were lost to follow-up. Overall, 45 patients (35.7 %) died up to 5 years of age. Serious CHD [odds ratio (OR), 19.2; 95 % confidential interval (CI), 3.94-93.11; p < 0.0001], sepsis (OR, 42.3; 95 % CI, 5.39-332.22; p < 0.0001), chromosomal /named anomalies (OR, 7.50; 95%CI, 2.09-26.94; p = 0.001), and no-invasive treatments (OR, 9.89; 95%CI, 2.28-42.91; p = 0.001) were associated with death. On excluding chromosomal anomalies, twelve of 71 patients (16.9 %) died, and only sepsis (OR, 35.5, 95%CI, 2.63-477.1; p = 0.0008) was an independent risk factor.
Conclusions:
Trisomy 18 and trisomy 13 of chromosomal anomalies are frequently associated with VLBW infants with CHD. The mortality of VLBW infants with CHD is high, even when chromosomal anomalies are excluded. Sepsis has a significant impact on death in VLBW infants with CHD.
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