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Dive into the research topics where Gerald R. Marx is active.

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Featured researches published by Gerald R. Marx.


Journal of The American Society of Echocardiography | 2009

Recommendations for Evaluation of Prosthetic Valves With Echocardiography and Doppler Ultrasound. A Report From the American Society of Echocardiography's Guidelines and Standards Committee and the Task Force on Prosthetic Valves, Developed in Conjunction With the American College of Cardiology Cardiovascular Imaging Committee, Cardiac Imaging Committee of the American Heart Association

William A. Zoghbi; John Chambers; Jean G. Dumesnil; Elyse Foster; John S. Gottdiener; Paul A. Grayburn; Bijoy K. Khandheria; Robert A. Levine; Gerald R. Marx; Fletcher A. Miller; Satoshi Nakatani; Miguel A. Quinones; Harry Rakowski; L. Leonardo Rodriguez; Madhav Swaminathan; Alan D. Waggoner; Neil J. Weissman; Miguel Zabalgoitia

A Report From the American Society of Echocardiography’s Guidelines and Standards Committee and the Task Force on Prosthetic Valves, Developed in Conjunction With the American College of Cardiology Cardiovascular Imaging Committee, Cardiac Imaging Committee of the American Heart Association, the European Association of Echocardiography, a registered branch of the European Society of Cardiology, the Japanese Society of Echocardiography and the Canadian Society of Echocardiography, Endorsed by the American College of Cardiology Foundation, American Heart Association, European Association of Echocardiography, a registered branch of the European Society of Cardiology, the Japanese Society of Echocardiography, and Canadian Society of Echocardiography


Circulation | 2004

Balloon Dilation of Severe Aortic Stenosis in the Fetus Potential for Prevention of Hypoplastic Left Heart Syndrome: Candidate Selection, Technique, and Results of Successful Intervention

Wayne Tworetzky; Louise Wilkins-Haug; Russell W. Jennings; Mary E. van der Velde; Audrey C. Marshall; Gerald R. Marx; Steven D. Colan; Carol B. Benson; James E. Lock; Stanton B. Perry

Background—Preventing the progression of fetal aortic stenosis (AS) to hypoplastic left heart syndrome (HLHS) requires identification of fetuses with salvageable left hearts who would progress to HLHS if left untreated, a successful in utero valvotomy, and demonstration that a successful valvotomy promotes left heart growth in utero. Fetuses meeting the first criterion are undefined, and previous reports of fetal AS dilation have not evaluated the impact of intervention on in utero growth of left heart structures. Methods and Results—We offered fetal AS dilation to 24 mothers whose fetuses had AS. At least 3 echocardiographers assigned a high probability that all 24 fetuses would progress to HLHS if left untreated. Twenty (21 to 29 weeks’ gestation) underwent attempted AS dilation, with technical success in 14. Ideal fetal positioning for cannula puncture site and course of the needle (with or without laparotomy) proved to be necessary for procedural success. Serial fetal echocardiograms after intervention demonstrated growth arrest of the left heart structures in unsuccessful cases and in those who declined the procedure, while ongoing left heart growth was seen in successful cases. Resumed left heart growth led to a 2-ventricle circulation at birth in 3 babies. Conclusions—Fetal echocardiography can identify midgestation fetuses with AS who are at high risk for developing HLHS. Timely and successful aortic valve dilation requires ideal fetal and cannula positioning, prevents left heart growth arrest, and may result in normal ventricular anatomy and function at birth.


Circulation | 2009

Predictors of Technical Success and Postnatal Biventricular Outcome After In Utero Aortic Valvuloplasty for Aortic Stenosis With Evolving Hypoplastic Left Heart Syndrome

Doff B. McElhinney; Audrey C. Marshall; Louise Wilkins-Haug; David W. Brown; Carol B. Benson; Virginia Silva; Gerald R. Marx; Arielle Mizrahi-Arnaud; James E. Lock; Wayne Tworetzky

Background— Aortic stenosis in the midgestation fetus with a normal-sized or dilated left ventricle predictably progresses to hypoplastic left heart syndrome when associated with certain physiological findings. Prenatal balloon aortic valvuloplasty may improve left heart growth and function, possibly preventing evolution to hypoplastic left heart syndrome. Methods and Results— Between March 2000 and October 2008, 70 fetuses underwent attempted aortic valvuloplasty for critical aortic stenosis with evolving hypoplastic left heart syndrome. We analyzed this experience to determine factors associated with procedural and postnatal outcome. The median gestational age at intervention was 23 weeks. The procedure was technically successful in 52 fetuses (74%). Relative to 21 untreated comparison fetuses, subsequent prenatal growth of the aortic and mitral valves, but not the left ventricle, was improved after intervention. Nine pregnancies (13%) did not reach a viable term or preterm birth. Seventeen patients had a biventricular circulation postnatally, 15 from birth. Larger left heart structures and higher left ventricular pressure at the time of intervention were associated with biventricular outcome. A multivariable threshold scoring system was able to discriminate fetuses with a biventricular outcome with 100% sensitivity and modest positive predictive value. Conclusions— Technically successful aortic valvuloplasty alters left heart valvar growth in fetuses with aortic stenosis and evolving hypoplastic left heart syndrome and, in a subset of cases, appeared to contribute to a biventricular outcome after birth. Fetal aortic valvuloplasty carries a risk of fetal demise. Fetuses undergoing in utero aortic valvuloplasty with an unfavorable multivariable threshold score at the time of intervention are very unlikely to achieve a biventricular circulation postnatally.


Bone Marrow Transplantation | 2006

Isolation of mesenchymal stem cells from G-CSF-mobilized human peripheral blood using fibrin microbeads.

Ibrahim Kassis; Lior Zangi; Rachel Rivkin; Lilia Levdansky; S Samuel; Gerald R. Marx; Raphael Gorodetsky

Adult mesenchymal stem cells (MSC) that are able to differentiate into various mesenchymal cell types are typically isolated from bone marrow, but their significant presence in human peripheral blood (PB) is controversial. Fibrin microbeads (FMB) that bind matrix-dependent cells were used to isolate MSC from the mononuclear fraction of mobilized PB of adult healthy human donors treated with a granulocyte colony-stimulating factor. Isolation by plastic adherence resulted in a negligible number of MSC in all samples tested, whereas FMB-based isolation yielded spindle-shaped cell samples that could further expand on plastic or on FMB in eight out of the 11 samples. The yield of these cells at days 17–18 after the harvest was ∼0.5% of the initial cell number. The isolated cells were grown on plastic and characterized by FACS analysis and immunohistochemistry for specific markers. Following culturing and first passage, the FMB-isolated cells stained positive for mesenchymal stromal cell markers CD90 and CD105, expressed vimentin and fibronectin and were negative for hematopoietic markers CD45 and CD34. These cells could differentiate into osteoblasts, adipocytes and chondrocytes. This study indicates that FMB may have special advantage in isolating MSC from sources such as mobilized PB, where the number of such cells is scarce.


European Journal of Anaesthesiology | 2004

Assessing fluid responsiveness by stroke volume variation in mechanically ventilated patients with severe sepsis

Gerald R. Marx; T. Cope; L. McCrossan; S. Swaraj; C. Cowan; S. M. Mostafa; R. Wenstone; Martin Leuwer

Background and objective: Our hypothesis was that stroke volume variation during mechanical ventilation of the lungs would allow accurate prediction and monitoring of changes in cardiac index in response to fluid loading in patients with severe sepsis. Methods: This was a prospective clinical study in a university hospital. Ten mechanically ventilated patients with severe sepsis or septic shock were given fluid loading with 500 mL 10% hydroxyethylstarch 200/0.5 over 30 min. Before and after fluid loading pulmonary arterial occlusion pressure and central venous pressure were measured. Intrathoracic blood volume index, stroke volume variation and cardiac index were measured by the transpulmonary thermodilution technique. After verifying normal distribution of the data (skewness <1.0) the paired t-test was used for statistical analysis. Results: After fluid loading stroke volume variation decreased significantly, whereas central venous pressure, pulmonary arterial occlusion pressure, intrathoracic blood volume index and cardiac index increased significantly. Changes of cardiac index in response to fluid loading were correlated to baseline values of stroke volume variation (r = 0.64, P = 0.02) and intrathoracic blood volume index (r = −0.73, P = 0.009). Changes in cardiac index were significantly correlated to percentage changes in stroke volume variation (r = −0.65, P < 0.001) and changes in intrathoracic blood volume index (r = 0.52, P = 0.002), whereas changes in cardiac index revealed no significant correlation to changes in central venous pressure (r = 0.28, P = 0.07) and changes in pulmonary arterial occlusion pressure (r = 0.29, P = 0.06). Conclusions: Measuring stroke volume variation may be a useful way of guiding fluid therapy in ventilated patients with severe sepsis because it allows estimation of preload and prediction of cardiac index changes in response to fluid loading.


Echocardiography-a Journal of Cardiovascular Ultrasound and Allied Techniques | 1994

Dynamic three-dimensional echocardiography : methods and clinical potential

Natesa G. Pandian; Jos Roelandt; Navin C. Nanda; Lissa Sugeng; Qi-Ling Cao; Jose Azevedo; Steven L. Schwartz; Mani A. Vannan; Achi Ludomirski; Gerald R. Marx; Michael Vogel

In this article, we will attempt to review basic requirements for three‐dimensional reconstruction, methods of cavity reconstruction, approaches to gray scale tissue‐depiction displays, and current clinical experience, and also present some directions for future development. (ECHOCARDIOGRAPHY, Volume 11, May 1994)


Circulation | 1994

Guidelines for exercise testing in the pediatric age group. From the Committee on Atherosclerosis and Hypertension in Children, Council on Cardiovascular Disease in the Young, the American Heart Association.

Reginald L. Washington; J T Bricker; B S Alpert; Stephen R. Daniels; Richard J. Deckelbaum; Edward A. Fisher; Samuel S. Gidding; J Isabel-Jones; R E Kavey; Gerald R. Marx

Exercise testing of children differs from adult exercise testing in many ways beyond the technical issues related to test performance that are addressed in this report. Disease processes that produce myocardial ischemia are relatively rare in children compared with adults. Exercise testing may be useful in these cases, but the use of testing to assess functional capacity or cardiac rhythms will be encountered more often. Although the precise role of exercise testing in patient evaluation or long-term management of the cardiac patient will vary somewhat from center to center, exercise testing is often essential to diagnose and to direct treatment in a wide variety of clinical problems. An understanding of the role of exercise testing for children with known or suspected heart abnormalities is an essential part of the training of pediatric cardiologists. The staff of the pediatric exercise laboratory should be available to discuss with the clinician when a test might be of value in a specific case in addition to providing advice about the specifics of the performance of the test and offering age- and size-appropriate normal data from the laboratory with test interpretation.


Circulation | 1997

Two- and Three-Dimensional Transesophageal Echocardiography in Patient Selection and Assessment of Atrial Septal Defect Closure by the New DAS–Angel Wings Device Initial Clinical Experience

Giuseppina Magni; Ziyad M. Hijazi; Natesa G. Pandian; Alain Delabays; Lissa Sugeng; Cleo Laskari; Gerald R. Marx

BACKGROUND Transcatheter closure of atrial septal defects (ASDs) has been feasible and successful. Two-dimensional echocardiography (2DE) was applied to patients before selection and during device deployment. Three-dimensional echocardiography (3DE) can provide unique anatomic perspectives that might aid in improving device closure of ASDs. METHODS AND RESULTS Twenty-two consecutive patients were enrolled in an initial protocol for ASD device closure by the new DAS-Angel Wings occluder device. On the basis of transesophageal (TEE) 2DE and 3DE, 13 patients were considered eligible for device closure (9 secundum ASDs and 4 with patent foramen ovale associated with a cerebral vascular accident). Maximal ASD diameter and surrounding rim tissues were compared by TEE 2DE and 3DE and with balloon sizing measurements at catheterization. ASD size measured by TEE 2DE and 3DE correlated well (y = 1.0x + 0.049, r = .95), with good limits of agreement. However, balloon-stretched diameter measurements were systematically larger than echocardiographic measurements. Rim tissue measurements correlated well; however, TEE 3DE could demonstrate the entire shape and perimeter of the defect. Two-dimensional imaging provided reliable information during device deployment and for closure of small ASDs. However, 3DE was superior for imaging the device, especially when abnormally placed. CONCLUSIONS Three-dimensional imaging provides unique images and projections that were essential for understanding the spatial relationship of the device to the atrial septum. Three-dimensional echocardiography significantly enhanced our understanding of two-dimensional images and provided an imaging conceptualization that should aid in future development of device closures.


Circulation | 1996

Understanding Obesity in Youth A Statement for Healthcare Professionals From the Committee on Atherosclerosis and Hypertension in the Young of the Council on Cardiovascular Disease in the Young and the Nutrition Committee, American Heart Association

Samuel S. Gidding; Rudolph L. Leibel; Stephen R. Daniels; Michael Rosenbaum; Linda Van Horn; Gerald R. Marx

Obesity is strongly linked to cardiovascular disease and non–insulin-dependent diabetes mellitus through the promotion of insulin resistance and other associated physiological abnormalities, including dyslipidemia, elevated blood pressure, and increased left ventricular mass.1 2 3 4 Overweight and insulin resistance have been linked to the early development of atheromata in young adults independent of other cardiovascular risk factors.5 Pulmonary, skeletal, dermatologic, immunologic, and endocrinologic systems display obesity-related morbidities (Table 1⇓).6 Adverse social and psychological effects of obesity have also been demonstrated.6 7 8 View this table: Table 1. Morbidity of Obesity in Youth Obesity is a major public health problem with both genetic and environmental causes.9 10 Longitudinal studies of children followed into young adulthood suggest that overweight children may become overweight adults, particularly if obesity is present in adolescence.11 12 13 There is substantial evidence that obesity in childhood lays the metabolic groundwork for adult cardiovascular disease.14 Studies of families and twins have clearly demonstrated a strong genetic component in the etiology of obesity.15 16 17 Just as persuasively, a recent study of secular trends in anthropometry has shown an increase in the prevalence of overweight in children and young adults over the last 10 to 20 years, indicating a potent interaction between environment and genetics.18 This secular trend is associated with worsening cardiovascular risk.19 This statement reviews the medical consequences of obesity in youth. Epidemiology, morbidity (especially cardiovascular), and etiology are considered and approaches to prevention and treatment presented. Areas for additional research are highlighted. Obesity is defined as the presence of excess adipose tissue. In normal individuals the percentage of body tissue that is adipose tissue varies by gender (greater in postpubertal females than males) and age (about 12% at birth, increasing to 25% at 5 months, then decreasing to 15% …


Journal of Cardiovascular Electrophysiology | 1997

Electrocardiographic markers of late sudden death risk in postoperative tetralogy of Fallot children.

Charles I. Berul; Sharon L. Hill; Robert L. Geggel; Ziyad M. Hijazi; Gerald R. Marx; Jonathan Rhodes; Kerri A. Walsh; David R. Eulton

Late Sudden Death Risk in Postoperative TOF. Following surgery for tetralogy of Fallot (TOP), children may develop late onset ventricular arrhythmias. Many patients have both depolarization and repolarization abnormalities, including right bundle branch block (RBBB) and QT prolongation. The goal of this study was to improve prospective risk‐assessment screening for late onset sudden death. Resting ECG markers including QRS duration, QTc, JTc, and interlead QT and JT dispersion were statistically analyzed to identify those patients at risk for ventricular arrhythmias and sudden cardiac death. To determine predictive markers for future development of arrhythmia, we examined 101 resting ECGs in patients (age 12 ± 6 years) with postoperative TOF and RBBB, 14 of whom developed late ventricular tachycardia (VT) or sudden death. These ECGs were also compared with an additional control group of 1000 age‐ and gender‐matched normal ECGs. The mean QRS (± SD) in the VT group was 0.18 ± 0.02 seconds versus 0.14 ± 0.02 seconds in the non‐VT group (P < 0.01). QTc and JTc in the VT group was 0.53 ± 0.05 seconds and 0.33 ± 0.03 seconds compared with 0.50 ± 0.03 seconds and 0.32 ± 0.03 seconds in the non‐VT group (P = NS). There was no increase in QT dispersion among TOF patients with VT or sudden death compared with control patients or TOF patients without VT, although JT dispersion was more common in the TOF groups. A prolonged QRS duration in postoperative TOF with RBBB is more predictive than QTc, JTc, or dispersion indexes for identifying vulnerability to ventricular arrhythmias in this population, while retaining high specificity. The combination of both QRS prolongation and increased JT dispersion had very good positive and negative predictive values. These results suggest that arrhythmogenesis in children following TOF surgery might involve depolarization in addition to repolarization abnormalities. Prospective identification of high‐risk children may be accomplished using these ECG criteria.

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Pedro J. del Nido

Boston Children's Hospital

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Wayne Tworetzky

Boston Children's Hospital

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Sitaram M. Emani

Boston Children's Hospital

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Jonathan Rhodes

Boston Children's Hospital

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David Fulton

Georgia Regents University

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