Browsing by Author "Kumar, SM"
Now showing 1 - 6 of 6
Results Per Page
Sort Options
Item An Unusual Mediastinal Mass in a Patient with Myocardial Infarction(ECHOCARDIOGRAPHY-A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES, 2013) Kumar, SM; Thajudeen, AAchalasia cardiae is a rare esophageal motility disorder of unknown cause, which can remain asymptomatic for a long time. Diagnosis can be missed in view of the frequent absence of pathognomonic clinical signs and symptoms. We present the case of an elderly gentleman, who had achalasia incidentally detected by transthoracic echocardiography during evaluation of coronary artery disease. (Echocardiography 2013; 30: E7-E9)Item ASD Device Embolization: Caught in the Act(ECHOCARDIOGRAPHY-A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES, 2013) Kumar, SM; Subramanian, V; Krishnamoorthy, KM; Sivasankaran, SItem Myocardial Infarction in a 4-Year-Old Child: Role of Echocardiography in Diagnosis(ECHOCARDIOGRAPHY-A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES, 2013) Kumar, SM; Subramanian, V; Krishnamoorthy, KMItem Percutaneous Closure of a Moderate to Large Tubular or Elongated Patent Ductus Arteriosus in Children Younger Than 3 Years: Is the ADO II Appropriate?(PEDIATRIC CARDIOLOGY, 2013) Kumar, SM; Subramanian, V; Bijulal, S; Krishnamoorthy, KM; Sivasankaran, S; Tharakan, JAProtrusion of the Amplatzer duct occluder (ADO) II device into the aortic isthmus or the pulmonary artery causing obstruction and residual flow has been reported, but the same has not been widely studied in small children with a patent ductus arteriosus (PDA) anatomy not considered suitable for closure with the ADO I device. This study aimed to report the safety and efficacy of the ADO II device in children younger than 3 years with a tubular or elongated PDA and to analyze the possible reasons for residual flow in children with such a PDA. In this study, 17 children younger than 3 years (mean age, 10.3 +/- 7 months; mean weight, 6 +/- 3.6 kg) underwent attempted closure of a tubular or elongated PDA (mean diameter at the narrowest point, 4.1 +/- 1.1 mm) with the ADO II device between July 2010 and July 2012. Of the 17 patients, 16 (2 boys and 14 girls) completed the follow-up evaluation. A complete echocardiographic evaluation was performed on all the patients before PDA closure and at the follow-up visit, and the results were compared with those of previous published studies. Of the 16 patients, the 15 who completed the follow-up evaluation had successful device closure (1 device embolization). Residual flow was present in six patients immediately after deployment, which was reduced to three patients at the last follow-up visit. Five of nine patients closed with a 6-mm-long device had residual flow compared with only one of seven patients closed with a 4-mm-long device. After device closure, significant elevations of the left and right pulmonary artery velocities occurred in three and two patients, respectively; in 12 patients, descending thoracic aortic (DTA) velocities increased mildly. There was trend toward a fall in the elevated pressures at the last follow-up visit, although one patient had an elevation in right pulmonary artery velocity at last the follow-up echocardiogram compared with the echocardiogram immediately after closure. Hence, in children younger than 3 years with or without pulmonary arterial hypertension, closure of a PDA not amenable to closure with the ADO I device is feasible using the ADO II device, with an increased incidence of clinically nonsignificant complications. Selection of device dimensions according to the manufacturer's recommendation may not be the optimal strategy.Item Real-Time 3-Dimensional Transesophageal Echocardiography-Guided Device Closure of Coronary Arteriovenous Fistula(JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2013) Kumar, SM; Venkateshwaran, S; Bijulal, S; Krishnamoorthy, KM; Sivasankaran, S; Tharakan, JAItem Right Pulmonary Artery-to-Left Atrial Fistula: A Rare Cause of Neonatal Cyanosis(PEDIATRIC CARDIOLOGY, 2013) Kumar, SM; Sivasankaran, S