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Featured researches published by Arman Bilgiç.


International Journal of Cardiology | 1995

Double-chambered right ventricle: experience with 52 cases

Ergun Cil; Muhsin Saraçlar; Süheyla Özkutlu; Şencan Özme; Arman Bilgiç; Sema Özer; Alpay Çeliker; Kürşad Tokel; Metin Demircin

The presence of anomalous muscle bundles may produce a pressure gradient between the inflow and outflow portions of the right ventricle, thus resulting in double-chambered right ventricle bearing troublesome clinically in its diagnosis. The aim of the present study was to review the diagnostic criteria. Fifty-two patients with a double-chambered right ventricle were seen during an 8-year period. They ranged in age at the catheterization from 4 months to 17 years (mean 7.5 +/- 4.4 years). Diagnosis was confirmed in 51 patients at cardiac catheterization and in other one on operation. The majority of the patients had associated cardiac anomalies: there were 33 ventricular septal defect (63%), 21 pulmonary valve stenosis (40%), nine atrial septal defect (17%), and four double-outlet right ventricle. The electrocardiograms revealed upright T waves alone in right precordial leads suggesting right ventricular hypertrophy in 33% of the patients. At cardiac catheterization, there was a pressure gradient of 20-160 mmHg between the right ventricular inflow and outflow portions. Forty patients have had surgery and four have undergone balloon pulmonary valvuloplasty. Surgical treatment was planned for two patients and other six had no indication for treatment.


Pediatric Cardiology | 1996

Parameters of iron deficiency in children with cyanotic congenital heart disease

L. Olcay; Sema Özer; A. Gürgey; Muhsin Saraçlar; Sencan Özme; Arman Bilgiç; Süheyla Özkutlu; Alpay Çeliker

A group of 67 children with cyanotic congenital heart disease (CCHD) were studied, and 35 were given iron treatment according to a regimen that gives iron to patients with a hematocrit (Hct) below 60%. The patients were categorized as iron-deficient and iron-sufficient according to their transferrin saturation and ferritin values. The pretreatment hemoglobin (Hb) and Hct values of the groups were similar. The mean Hct was nearly three times as much as the mean Hb in the iron-sufficient group and more than three times as much as the Hb in the iron-deficient group. Excessive erythrocytosis in the iron-deficient group was impressive. Mean corpuscular volume (MCV) values were below 72.7 fl in all of the iron-deficient patients. After treatment the Hb, Hct, transferrin saturation, and ferritin increased significantly in both groups, with the increments greater in the iron-deficient group. Increments in the erythrocyte (RBC) count were significant in the iron-sufficient group but insignificant in the iron-deficient one. Increments of MCV in the iron-deficient group were significant but insignificant in the iron-sufficient group. Our study demonstrated that prediction of Hb, RBC count, and MCV, measurements of which are easy and inexpensive and require little blood, can suffice for the diagnosis of iron deficiency in patients with CCHD without altering systemic perfusion.


Pediatrics International | 1996

Transcatheter closure of patent ductus arteriosus using controlled-release coils

Alpay Çeliker; Arman Bilgiç; Dursun Alehan; Naci Ceviz; Mustafa Koray Lenk

Controlled‐release coils have become available recently for the closure of patent ductus arteriosus (PDA). Transcatheter closure of patent arterial ducts was attempted in 13 patients, ranging in age from 5 months to 15 years, mean 4.1 years. Implantation of controlled‐release PDA coils was attempted via the femoral artery through 5 Fr catheters in all cases except one, in whom both the femoral arterial and venous routes were used. The procedure was successful in 10 of the 13 patients. In these, the pulmonary artery systolic pressure ranged between 25 and 42 mmHg and the duct diameter varied from 1.5 to 6 mm at its narrowest point. Six of the patients received a single coil. Two coils were inserted in three patients and three coils in one patient. In three patients the ducts were too large for safe release of the coils, despite attempted implantation of up to three coils simultaneously. These coils were easily withdrawn into the catheter Immediately at the end of the procedure, the duct was completely occluded in nine of the 10 patients, and in one patient there was a small residual flow. The procedure time varied between 35 min and 2.5 h, mean 81 min and the fluoroscopy time varied from 5 to 78 min, mean 25 min. None of the patients experienced hemorrhage, diminished lower extremity pulse, hemolysis or infection. In one patient, a 5 mm coil embolized into the right pulmonary artery soon after release. It was retrieved with a snare, then 8 mm and a 5 mm coil were implanted satisfactorily in the arterial duct. At follow‐up by color Doppler echocardiography, the duct was completely occluded in all patients.


International Journal of Cardiology | 1992

Mycotic aneurysm of the descending aorta diagnosed by echocardiography

Süheyla Özkutlu; Nazan Özbarlas; Arman Bilgiç; Ilhan Pasaoglu

We present a 3-yr-old girl with coarctation of aorta and patent ductus arteriosus in whom mycotic aneurysm and bacterial endarteritis developed postoperatively and was diagnosed by two-dimensional and Doppler echocardiography. Five weeks after the operation of ligation of ductus and resection of coarctated segment, the patient was readmitted with complaints of vomiting, fever and coughing. Bacterial endarteritis, empyema and septic arthritis were diagnosed. Suprasternal echocardiographic examination demonstrated an aneurysmatic appearance 60 x 65 mm in size at the location of coarctation. The patient died, most probably due to aortic rupture, before surgical treatment could be undertaken. Autopsy study confirmed our diagnosis.


Pediatric Cardiology | 1994

Single daily dose of digoxin for maintenance therapy of infants and children with cardiac disease: Is it reliable?

Mustafa Bakir; Arman Bilgiç

SummaryBetween July 1990 and September 1991, 30 infants and children, most of whom had a congenital heart defect and who had been treated at least during the previous 20 days by two daily doses of digoxin and were in a stable clinical condition, were selected at random. A maintenance dose of digoxin was administered at 24-h intervals for 7 days in the study group (n=15) no change was made in the 12-h dosage interval in the control group (n=15). When the serum digoxin concentrations were compared, no significant difference was found between pre-and poststudy values in the study group (1.0±0.6 and 0.8±0.3 ng/ml, respectively) or between the control and study groups (0.9±0.6 and 0.8±0.3 ng/ml, respectively) in terms of trough serum digoxin concentrations. Although the peak serum concentrations in the study group were increased significantly (2.3±0.8 ng/ml) compared with prestudy peak levels (1.6±0.7 ng/ml,p<0.05) and with the level in the control groups (1.5±0.8 ng/ml,p<0.05), a toxic concentration was not reached, and toxicity symptoms were not observed clinically. Blood pressure, heart rate, and liver size did not change significantly in any patient during the study.


Catheterization and Cardiovascular Diagnosis | 1996

Abnormal connection of the inferior vena cava to the left atrium with double outlet right ventricle and heterotaxia: A case report

Nazlıhan Günal; Arman Bilgiç; Mustafa Koray Lenk; Yurdakul Yurdakul; Ali Sarigül; Selim Ispir

A 4-year-old boy with abnormal connection of the inferior vena cava to the left atrium and double outlet right ventricle and right atrial isomerism is presented. The anomalies were detected by echocardiography and angiography, and later verified through surgical intervention.


Japanese Heart Journal | 1990

Cardiomyopathies in children. Clinical, epidemiological and prognostic evaluation.

Arman Bilgiç; Nazan Özbarlas; Süheyla Özkutlu; Sema Özer; Sencan Özme


Turkish Journal of Pediatrics | 1982

The absent pulmonary valve syndrome.

Arman Bilgiç; Saraçlar M; Ozme S; Akçoral A; Aytaç A


Turkish Journal of Pediatrics | 1996

Acquired subvalvular aortic stenosis after repair of several congenital cardiac defects.

Tokel K; Ozme S; Ergun Cil; Süheyla Özkutlu; Alpay Çeliker; Saraçlar M; Arman Bilgiç; Sema Özer


Turkish Journal of Pediatrics | 2002

Complications and outcome in left-sided endocarditis in children.

Dursun Alehan; Süheyla Özkutlu; Canan Ayabakan; Arman Bilgiç; Ozme S; Sema Özer; Alpay Çeliker

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