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Implantation of Total Artificial Heart in Congenital Heart Disease
Published on: July 18, 2014
Growth status of Iranian children with hemodynamically important congenital heart disease
Mohammad Dalili1, Seyed Mahmood Meraji, Paridokht Davari
1Department of Pediatric Cardiology, Shaheed Rajaei Cardiovascular Medical and Research Center, Tehran University of Medical Sciences, Iran. drdalili@yahoo.com
Insights
Congenital heart disease (CHD) in Iranian children is linked to significant growth failure. Female children and those with cyanosis showed lower body weights, requiring targeted nutritional and psychosocial support.
Area of Science:
- Pediatrics
- Cardiology
- Growth and Development
Background:
- Congenital heart disease (CHD) is known to correlate with growth retardation.
- Understanding growth patterns in pediatric CHD populations is crucial for early intervention.
Purpose of the Study:
- To investigate the growth condition of Iranian children with significant congenital heart disease (CHD).
- To compare the growth findings with international research on pediatric CHD.
Main Methods:
- Studied 469 Iranian children (1 month to 18 years) with important CHD.
- Excluded infants with prematurity, genetic, or neurological disorders affecting growth.
- Assessed cardiac conditions via clinical exams, ECG, echocardiography, catheterization, and angiography; measured weight and height against standard charts.
Main Results:
- All patients exhibited significantly lower body weight and height compared to the normal population.
- Growth failure was more pronounced in female children's weight.
- Risk factors for growth failure included large left-to-right shunts, pulmonary hypertension, and cyanosis.
Conclusions:
- Iranian children with CHD experience growth failure, with specific differences noted compared to global data.
- Cyanotic patients and female children with CHD require enhanced nutritional and psychosocial support due to lower body weights.
Abstract:
The relationship between congenital heart disease (CHD) and growth retardation is well documented. We investigated the growth condition of Iranian children with several types of congenital heart disease (CHD) and compared it with worldwide researches. Growth condition was investigated in 469 patients with important CHD aged from 1 month to 18 years. The patients were divided into two groups; infants (aged 12 months or less), and children (1-18 yrs of age). Children with hemodynamically unimportant small VSDs or small ASDs were not studied. Other exclusion criteria were prematurity, known genetic disorders and neurologic disease affecting growth. All patients' cardiac diagnoses were made on the basis of clinical and laboratory examinations; including electrocardiography, echocardiography, cardiac catheterization, and angiography. Body weight and height of all patients were measured using conventional methods and compared with standard growth charts. In all patients body weights and heights were significantly lower than normal population. This difference was greater in the weight of female children. Other risk factors for growth failure were large left-to-right intracardiac shunts, pulmonary hypertension and cyanosis. Iranian children with CHD have growth failure somewhat different from other countries. Lower body weights of cyanotic patients and female children indicated that these patients need more nutritional and psychosocial attention.
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