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1.
J Cardiovasc Med (Hagerstown) ; 10(4): 298-302, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19430339

ABSTRACT

OBJECTIVE: Plasma levels of brain natriuretic peptide (BNP) and its inactive fragment N-terminal pro-BNP are recognized as reliable markers of ventricular dysfunction in adults. We aimed to verify BNP applications in children. METHODS: A review of the literature on this subject was carried out. RESULTS: When dealing with paediatric patients, age and sex-related normal values must be considered. Higher BNP plasma levels are reported in children with chronic heart failure; they are related with the type of dysfunction and with prognosis. Moreover, increased BNP levels have been reported in asymptomatic children and adolescents pretreated with anthracyclines, who are at risk for ventricular dysfunction. CONCLUSION: BNP and pro-BNP also seem to be effective markers of ventricular dysfunction in paediatric patients. Clinical use may be extended not only for the characterization of heart dysfunction, but also for monitoring asymptomatic patients at specific risk. To this purpose, wider application in clinical trials appears warranted.


Subject(s)
Heart Defects, Congenital/diagnosis , Heart Failure/diagnosis , Natriuretic Peptide, Brain/blood , Peptide Fragments/blood , Ventricular Dysfunction/diagnosis , Adolescent , Age Factors , Anthracyclines/adverse effects , Antibiotics, Antineoplastic/adverse effects , Biomarkers/blood , Child , Chronic Disease , Female , Heart Defects, Congenital/blood , Heart Failure/blood , Humans , Male , Predictive Value of Tests , Prognosis , Reference Values , Risk Factors , Sex Factors , Ventricular Dysfunction/blood , Ventricular Dysfunction/etiology
2.
J Cardiovasc Med (Hagerstown) ; 9(11): 1127-9, 2008 Nov.
Article in English | MEDLINE | ID: mdl-18852585

ABSTRACT

Echocardiographic diagnosis of absent pulmonary valve syndrome and muscular ventricular septal defect was made in a fetus of gestational age 25 weeks referred for marked dilation of the right ventricle at obstetric ultrasound examination. Delivery was planned in a tertiary-level center. The neonate became severely symptomatic for respiratory distress and heart failure during the second day of life. His clinical condition dramatically improved after surgical closure of a large ductus arteriosus. The child is still asymptomatic 30 months later. In the minority of cases with absent pulmonary valve not associated with tetralogy of Fallot, irrespective of the presence of muscular ventricular septal defect, early closure of the ductus may be crucial to improve hemodynamic conditions and postpone surgical correction.


Subject(s)
Abnormalities, Multiple/diagnostic imaging , Ductus Arteriosus, Patent/diagnostic imaging , Heart Septal Defects, Ventricular/diagnostic imaging , Pulmonary Atresia/diagnostic imaging , Ultrasonography, Prenatal , Abnormalities, Multiple/physiopathology , Abnormalities, Multiple/surgery , Cardiac Surgical Procedures , Cesarean Section , Ductus Arteriosus, Patent/physiopathology , Ductus Arteriosus, Patent/surgery , Echocardiography, Doppler , Gestational Age , Heart Septal Defects, Ventricular/physiopathology , Heart Septal Defects, Ventricular/surgery , Hemodynamics , Humans , Infant, Newborn , Male , Pulmonary Atresia/physiopathology , Pulmonary Atresia/surgery , Syndrome , Tetralogy of Fallot/diagnostic imaging
3.
J Cardiovasc Med (Hagerstown) ; 8(7): 527-30, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17568287

ABSTRACT

Congenital coronary artery anomalies are a rare cause of major cardiovascular events in adolescents who practise sports activities. Therefore, symptoms suggestive of cardiac ischaemia should always be carefully considered and subjects should undergo a complete cardiovascular assessment. We describe the case of a young non-competitive athlete, referring episodes of exertional chest pain and syncope, in whom multiple imaging techniques allowed the diagnosis of intramural course of the left anterior descending coronary artery.


Subject(s)
Coronary Vessel Anomalies/diagnosis , Diagnostic Imaging , Adolescent , Chest Pain/etiology , Humans , Sports , Syncope/etiology
4.
J Cardiovasc Med (Hagerstown) ; 8(4): 281-3, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17413306

ABSTRACT

An unusual case of severe supravalvular stenosing ring of the left atrium associated with tricuspid valve dysplasia in an adult symptomatic patient affected by congenitally corrected transposition and unrestrictive ventricular septal defect is reported. The stenosis of the systemic atrioventricular valve possibly prevented the development of obstructive pulmonary vascular disease; removal of the membrane, attached to the tricuspid annulus, together with pulmonary banding was carried out. Clinical conditions improved after surgery. The unusual stenotic lesion of the systemic right ventricular inflow allowed conservative surgical palliation in this adult patient.


Subject(s)
Atrial Fibrillation/complications , Atrial Flutter/complications , Heart Failure/etiology , Heart Septal Defects, Ventricular/complications , Transposition of Great Vessels/complications , Tricuspid Valve Insufficiency/complications , Tricuspid Valve Stenosis/complications , Anti-Arrhythmia Agents/therapeutic use , Atrial Fibrillation/drug therapy , Atrial Flutter/drug therapy , Cardiac Surgical Procedures , Echocardiography, Doppler , Heart Failure/surgery , Humans , Male , Middle Aged , Treatment Outcome , Tricuspid Valve Insufficiency/etiology , Tricuspid Valve Insufficiency/surgery , Tricuspid Valve Stenosis/etiology , Tricuspid Valve Stenosis/surgery
5.
Pediatr Nephrol ; 21(7): 1027-30, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16773417

ABSTRACT

In this report we present the case of a 15-month-old girl with hyponatraemic-hypertensive syndrome (HHS) caused by stenosis of the left renal artery. On sonographic examination the contralateral non-stenotic kidney appeared enlarged and with cortical hyperechogenicity mimicking a parenchymal lesion. After successful percutaneous transluminal angioplasty, when the girl became normotensive, her serum electrolyte and acid-base balance became normal within a few days. The contralateral non-stenotic kidney hyperechogenicity also disappeared, but only after a period of 6 months, suggesting parenchymal damage due to tubulointerstitial injury, even though reversible. Our case confirms that renovascular hypertension may rarely also be present with HHS in children and that metabolic and morphological alterations are reversible after the resolution of arterial stenosis.


Subject(s)
Hypertension, Renovascular/etiology , Hyponatremia/etiology , Renal Artery Obstruction/complications , Child , Female , Humans , Hypertension, Renovascular/therapy , Hyponatremia/therapy , Syndrome
6.
Ital Heart J Suppl ; 5(6): 492-6, 2004 Jun.
Article in Italian | MEDLINE | ID: mdl-15471155

ABSTRACT

Renal artery stenosis, mainly due to fibromuscular dysplasia, is the second more common cause of arterial hypertension in children, after aortic coarctation. Two children sent to our Center of Pediatric Cardiology, one for arterial hypertension and the other for renal failure (associated with severe hypertension not previously recognized) are reported. In both of them the diagnosis of renal artery stenosis was established at Doppler ultrasonography, performed at the time of Doppler echocardiography. Both children were submitted to successful percutaneous transluminal angioplasty; short- and medium-term results are evaluated by Doppler ultrasonography. Renovascular disease is a potentially curable cause of renal artery stenosis in children. Renal artery evaluation by Doppler ultrasound is recommended in all hypertensive children who undergo Doppler echocardiography.


Subject(s)
Renal Artery Obstruction/diagnostic imaging , Renal Artery Obstruction/therapy , Angiography , Angioplasty, Balloon , Child, Preschool , Echocardiography, Doppler , Electrocardiography , Female , Follow-Up Studies , Humans , Hypertension, Renovascular/etiology , Hypertrophy, Left Ventricular/complications , Hypertrophy, Left Ventricular/diagnosis , Infant , Renal Artery/diagnostic imaging , Renal Artery Obstruction/complications , Renal Insufficiency/etiology , Time Factors , Treatment Outcome , Ultrasonography, Doppler, Color
8.
Eur J Pediatr ; 161(3): 149-50, 2002 Mar.
Article in English | MEDLINE | ID: mdl-11998912

ABSTRACT

UNLABELLED: Chylothorax may be spontaneous or a complication of thoracic surgery. Treatment of this potentially harmful condition is not well established and may comprise dietary interventions and surgery. Somatostatin seems effective in the management of chylothorax, although its mechanism of action is unclear. CONCLUSION: octreotide, a somatostatin analogue, may be effective in the treatment of post-operative chylothorax.


Subject(s)
Cardiac Surgical Procedures , Chylothorax/drug therapy , Octreotide/therapeutic use , Postoperative Complications , Child , Chylothorax/etiology , Drainage , Humans
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