Author/Authors :
Maryam Moradian, Rajaie Cardiovascular, Medical, and Research Center - Iran University of Medical Sciences, Tehran, I.R. Iran , Pouraliakbar, Hamidreza Rajaie Cardiovascular, Medical, and Research Center - Iran University of Medical Sciences, Tehran, I.R. Iran , Mahdavi, Mohammad Rajaie Cardiovascular, Medical, and Research Center - Iran University of Medical Sciences, Tehran, I.R. Iran , Ghadrdoost, Behshid Rajaie Cardiovascular, Medical, and Research Center - Iran University of Medical Sciences, Tehran, I.R. Iran , Faritous, Zahra Rajaie Cardiovascular, Medical, and Research Center - Iran University of Medical Sciences, Tehran, I.R. Iran , Shojaei Fard, Maryam Echocardiography Research Center - Rajaie Cardiovascular, Medical, and Research Center - Iran University of Medical Sciences, Tehran, I.R. Iran
Abstract :
Background: Growth retardation following malnutrition is prevalent among patients with
congenital heart diseases (CHDs). This study was designed to evaluate failure to thrive
(FTT) and delay in bone age in children with CHDs who were referred to our hospital and
subsequently to determine their relation with cyanosis and the pulmonary artery pressure.
Methods: We enrolled 120 consecutive patients who were referred to Rajaie Cardiovascular,
Medical, and Research Center for cardiac catheterization or surgical correction. Growth
parameters, comprising height (cm), weight (kg), and head circumference (cm), were
measured by an experienced nurse. Bone age was evaluated by taking an anteroposterior
wrist X-ray and reported by a radiologist, who was not aware of the exact cardiac diagnosis.
The pulmonary artery pressure was measured during cardiac catheterization or surgical
correction.
Results: Bone growth retardation, FTT, short stature, and microcephaly were seen in 46.6%, 43.7%,
29.4%, and 5.1% of the patients, correspondingly. There was a significant relationship
between the presence of cyanosis and delayed bone age, particularly when O2 saturation was
less than 75% (P < 0.0001). The presence of pulmonary hypertension was significantly
related to a higher rate of bone growth retardation (P < 0.0001). FTT and delayed bone age
were significantly different between the cyanotic patients and the children with pulmonary
hypertension and the acyanotic patients and those without pulmonary hypertension
(P < 0.05).
Conclusions: According to our results, delayed bone age and growth retardation are common
findings in children with CHDs. The presence of cyanosis and/or pulmonary hypertension
may further deteriorate these conditions and should be promptly managed.
Keywords :
Congenital heart disease , Cyanosis , Failure to thrive , Pulmonary hypertension , Bone age