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1.
Congenit Heart Dis ; 10(6): 537-41, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25912000

RESUMO

OBJECTIVE: The purpose of this study was to compare neurological development of children with cyanotic or hemodynamically impaired congenital heart disease (CHD) and healthy controls by using "Bayley Scales of Infant and Toddler Development Screening Test, Third Edition" (Bayley-III). PATIENTS: Children with CHD (n = 37) and healthy controls (n = 24) aged between 1 and 41 months who were admitted to the Department of Pediatric Cardiology at our university hospital were included. The participants were assessed using Bayley-III test. All patients had cyanotic or hemodynamically impaired CHD. Weight, height, body mass index (BMI), mid-arm circumference (MAC), triceps skinfold thickness (TSF), and head circumference (HC) were measured and standard deviation scores (SDSs) were determined. RESULTS: SDS values of weight, height, BMI, MAC, and TSF of the patients as well as HC values were significantly lower than the control group (P < .001). Compared with controls, the patients had significantly lower mean scores in all Bayley-III subscales (P < .001). We observed similar results in Bayley-III scores including the mean values of cognitive, language, and global motor scores for the CHD patients with and without cardiac surgery (P > .05). CONCLUSION: This study demonstrated that children with cyanotic or hemodynamically impaired CHD have delayed neurodevelopmental outcomes compared with healthy children as assessed using Bayley-III.


Assuntos
Cognição/fisiologia , Deficiências do Desenvolvimento/diagnóstico , Cardiopatias Congênitas/complicações , Hemodinâmica/fisiologia , Pré-Escolar , Deficiências do Desenvolvimento/etiologia , Feminino , Seguimentos , Cardiopatias Congênitas/fisiopatologia , Humanos , Lactente , Recém-Nascido , Masculino , Testes Neuropsicológicos , Prognóstico
2.
Life Sci ; 90(21-22): 838-45, 2012 Jun 06.
Artigo em Inglês | MEDLINE | ID: mdl-22525380

RESUMO

AIMS: Perinatal hypoxic-ischemic insult has acute and long term deleterious effects on many organs including heart. Although tumor necrosis factor alpha (TNF-α) has been reported to increase soon after hypoxia, the inhibition of this mediator has not been documented. The aim of this study was to investigate the effects of a TNF-α inhibitor (etanercept) on contractility and ultrastructure of rat heart muscles exposed to hypoxia-ischemia during neonatal period. MAIN METHODS: Forty-five seven-day old rats divided into three groups were included in this study. The right carotid arteries of Saline and Etanercept groups of rats were ligated and kept in a hypoxia chamber containing 8% oxygen for 2h. Immediately after hypoxia, while Etanercept group was administered 10mg/kg etanercept, Saline group had only saline intraperitoneally. The carotid arteries of rats in Sham group were located without ligation and hypoxia. Mechanical activity of heart was recorded and tissue samples were examined by electron microscopy in the sixteenth week following the hypoxia-ischemia. KEY FINDINGS: While atrial contractile force in Etanercept group was similar to Sham group, there was significant decrease in Saline group (p<0.001). However, there was only non-significant decrease in ventricular contractility of Saline group comparing to Sham group (p>0.05). After hypoxia-ischemia, ultrastructural degenerative changes and mitochondrial damage in atriums of Etanercept group were significantly less severe than Saline group. SIGNIFICANCE: This study demonstrated that neonatal hypoxia-ischemia caused long term cardiac dysfunction and ultrastructural degenerative changes in the heart of rats. TNF-α inhibitor administration soon after hypoxia-ischemia may have heart protective effect.


Assuntos
Hipóxia/fisiopatologia , Imunoglobulina G/farmacologia , Isquemia Miocárdica/fisiopatologia , Fator de Necrose Tumoral alfa/antagonistas & inibidores , Animais , Animais Recém-Nascidos , Etanercepte , Fatores Imunológicos/farmacologia , Masculino , Contração Miocárdica/efeitos dos fármacos , Miocárdio/patologia , Miocárdio/ultraestrutura , Ratos , Ratos Wistar , Receptores do Fator de Necrose Tumoral , Índice de Gravidade de Doença , Fatores de Tempo
3.
Pediatr Int ; 53(3): 345-9, 2011 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20723103

RESUMO

BACKGROUND: Children with congenital heart disease are under risk of delayed growth and development. We evaluated physical growth parameters and neurodevelopment in these patients in comparison with normal children and examined the effect of hemodynamic status. METHODS: Patients with congenital heart disease (n= 76) and healthy children (n= 51) aged 1-72 months applied to Mersin University Hospital, Mersin, Turkey were included. Patients with heart failure and those requiring intervention or surgery were classified as hemodynamically impaired (HI group, n= 30), and the others, hemodynamically normal (HN group, n= 46). Growth parameters including weight, height, body mass index (BMI), mid-arm circumference (MAC), and triceps skin fold thickness (TSF) were measured and standard deviations (SD) were determined. Functional development was assessed by Denver Developmental Screening Test-II (DDST II). RESULTS: MAC and BMI values of the group with impaired hemodynamic status were significantly lower than the hemodynamically normal and control groups (MAC P < 0.05 and BMI P < 0.01). In the DDST II, the group with hemodynamic abnormality had more failures in gross motor and fine motor skills than HN group and controls (gross motor P= 0.011, P < 0.001 and fine motor P= 0.028, P= 0.001, respectively) and more failures in language development than the control group (P= 0.001). CONCLUSION: The results showed the importance of hemodynamic status in growth and neurodevelopment of children with congenital heart disease. Besides routine growth parameters, more detailed examinations such as BMI, MAC, TSF, and developmental screening tests appear useful in identifying children with cardiac disease who are under risk for delayed growth and development.


Assuntos
Desenvolvimento Infantil , Cardiopatias Congênitas/fisiopatologia , Hemodinâmica/fisiologia , Desempenho Psicomotor/fisiologia , Índice de Massa Corporal , Pré-Escolar , Feminino , Seguimentos , Cardiopatias Congênitas/psicologia , Humanos , Lactente , Recém-Nascido , Masculino , Prognóstico , Estudos Retrospectivos
4.
Ann Noninvasive Electrocardiol ; 9(4): 339-44, 2004 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-15485511

RESUMO

BACKGROUND: The aim of the present study was to determine the potential role of P wave duration and P wave dispersion for risk assessment of atrial tachyarrhythmias in patients with corrected tetralogy of Fallot (ToF). METHODS: The maximum P wave duration, minimum P wave duration, and the P wave dispersion from the 12-lead surface electrocardiogram of the patients and controls were measured. Electrophysiological study was performed only in the patient group. RESULTS: The study group consisted of 25 patients with corrected ToF with a mean age of 16.4 +/- 4.25 years and 25 age-matched healthy control subjects. Patients underwent repair at a mean age of 4.6 +/- 3.41 years (range: 1-19), and the mean duration of follow-up of 11.8 +/- 1.7 years (range: 9-15) after surgery. On electrophysiological study sinus node dysfunction was detected in 3 patients (12%), atrial tachyarrythmias-atrial flutter or fibrillation-in 5 patients (20%), both sinus node dysfunction and atrial flutter in 1 patient (4%), and AV conduction delay in 1 patient (4%). P wave dispersion is significantly higher in patients with atrial tachyarrhythmia inducible by electrophysiological study than in other patients (P < 0.05). A P wave dispersion value of >35 ms has a high predictive accuracy (sensitivity = 83% and specificity = 89%) for inducible atrial tachyarrhythmia in patients with corrected tetralogy of Fallot. CONCLUSION: P wave dispersion is an easily measured electrocardiographic marker with a good sensitivity and specificity for predicting atrial arrhythmias in patients after correction of ToF.


Assuntos
Fibrilação Atrial/fisiopatologia , Flutter Atrial/fisiopatologia , Eletrocardiografia , Tetralogia de Fallot/fisiopatologia , Adolescente , Adulto , Fibrilação Atrial/etiologia , Flutter Atrial/etiologia , Estudos de Casos e Controles , Criança , Ecocardiografia , Eletrocardiografia Ambulatorial , Feminino , Humanos , Masculino , Estatísticas não Paramétricas , Tetralogia de Fallot/complicações , Tetralogia de Fallot/cirurgia
5.
Int J Cardiol ; 92(1): 93-7, 2003 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-14602223

RESUMO

BACKGROUND: Leptin has been shown to be an integral component of energy homeostasis and regulation of body weight. Leptin regulates adipose tissue mass and correlates with the fat mass, however the circulating levels are altered by energy intake. Research on the physiological function of leptin has primarily focused on its role in the pathogenesis of obesity. However, its role in the negative energy imbalance is unclear. Increased energy expenditure is a primary factor in the reduced growth in infants with cyanotic congenital heart disease. The objective of this study was to examine the possible role of leptin on growth and nutrition in children with cyanotic and acyanotic congenital heart disease. METHODS AND RESULTS: In this study, plasma leptin levels, nutritional and growth status were evaluated in 28 cyanotic and 20 acyanotic patients with congenital heart disease. Although standard deviation (S.D.) of height (P<0.01), mid arm circumference (MAC) (P<0.001) and body mass index (BMI) (P<0.05) were significantly low in cyanotic group, plasma leptin levels were similar. Energy intake was high in cyanotic group. In both cyanotic and acyanotic group, plasma leptin levels were correlated with BMI (R: 0.388, P<0.05 and R: 0.789, P<0.001, respectively). In addition, leptin levels were significantly correlated with the height (R: 0.415, P<0.05), MAC (R: 0.482, P<0.05) and BMI (R: 0.377, P<0.05) S.D. in cyanotic subjects. CONCLUSIONS: Our results suggest that the leptin regulating axis is intact in cyanotic patients and leptin does not contribute to the cachexia of cyanotic heart disease.


Assuntos
Cianose/sangue , Cardiopatias Congênitas/sangue , Leptina/sangue , Adolescente , Estatura , Índice de Massa Corporal , Peso Corporal , Caquexia/sangue , Criança , Pré-Escolar , Metabolismo Energético , Cardiopatias Congênitas/fisiopatologia , Humanos , Estado Nutricional
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