113 results match your criteria: "Herma Heart Center[Affiliation]"

Human Genetics of Hypoplastic Left Heart Syndrome.

Adv Exp Med Biol

June 2024

Department of Pediatrics, Herma Heart Center, Children's Hospital of Wisconsin, Medical College of Wisconsin, Milwaukee, WI, USA.

Article Synopsis
  • Hypoplastic left heart syndrome (HLHS) is a serious heart defect involving underdevelopment of the left ventricle and associated structures, leading to significant health risks despite advances in treatment.
  • Genetic factors play a key role in HLHS, with links to cytogenetic abnormalities, familial patterns, and identified genomic regions, suggesting a hereditary basis.
  • Identifying specific genetic causes is challenging; HLHS appears to result from complex inheritance rather than a single variant, prompting researchers to adopt more sophisticated models in their studies.
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Bivalirudin offers several important advantages of relevance to the management of extracorporeal membrane oxygenation (ECMO) patients. This multicenter retrospective analysis evaluated the bivalirudin dosing in pediatric ECMO and correlated these doses with the severity of renal dysfunction. A total of 75 patients were included in this analyses: estimated glomerular filtration rate (eGFR) > 60 ml/min/1.

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Background: Elevated total cell-free DNA (TCF) concentration has been associated with critical illness in adults and elevated donor fraction (DF), the ratio of donor specific cell-free DNA to total cell-free DNA present in the recipient's plasma, is associated with rejection following cardiac transplantation. This study investigates relationships between TCF and clinical outcomes after heart transplantation.

Methods: A prospective, blinded, observational study of 87 heart transplantation recipients was performed.

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Objective: To characterise the parenting priorities of mothers and fathers of infants hospitalised with CHD and generate recommendations to support parenting during infant hospitalisation.

Study Design: Through online crowdsourcing, an innovative research methodology to create an online community to serve as a research sample, 79 parents of young children with CHD responded to questions about parenting during hospitalisation via private social networking site. Responses were analysed using qualitative research methods.

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Methadone's Effect on Cardiac Repolarization: Safety in the PICU.

Pediatr Crit Care Med

September 2020

Division of Critical Care, Department of Pediatrics, Children's Hospital of Wisconsin, The Medical College of Wisconsin, Milwaukee, WI.

Objectives: Opioids are routinely used in the PICU. Methadone is an effective method of preventing and treating iatrogenic opioid withdrawal; however, it carries an Food and Drug Administration Boxed Warning due to the potential to prolong the corrected QT interval and potentially lead to life-threatening arrhythmias. Guidelines on the safe use of methadone have limited applicability to children since their cardiac intervals differ from those of adults.

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Predictability in Fetal Supraventricular Tachycardia Management.

J Am Coll Cardiol

August 2019

Department of Pediatrics, Medical College of Wisconsin, Herma Heart Center, Milwaukee, Wisconsin. Electronic address:

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Aortic stenosis of the neonate: A single-center experience.

J Thorac Cardiovasc Surg

January 2019

Herma Heart Center, Division of Congenital Heart Surgery, Children's Hospital of Wisconsin, Milwaukee, Wis.

Objectives: Because data for neonates are limited, optimal management of critical aortic stenosis remains controversial (balloon valvotomy [BV] or open valvoplasty [OV]). In a center with balanced experience in both methods, we hypothesized that OV can provide a better individualized approach than blunt BV and better serve long-term outcomes.

Methods: A retrospective review of data and follow-up (survival, freedom from operation/replacement) of all neonates, suitable for biventricular repair, undergoing aortic valve procedure (1989-2015), was performed.

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Background:  Neonates undergoing cardiopulmonary bypass (CPB) surgery to correct congenital heart defects often experience excessive bleeding. Exposure of blood to artificial materials during CPB may activate coagulation, complement and inflammatory pathways. In addition, the surgical stress placed on the haemostatic system may result in cross-activation of other plasma proteolytic cascades, which could further complicate physiological responses to the surgical procedure and post-operative recovery.

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Validation of a definition of excessive postoperative bleeding in infants undergoing cardiac surgery with cardiopulmonary bypass.

J Thorac Cardiovasc Surg

May 2018

Herma Heart Center, Children's Hospital of Wisconsin, Milwaukee, Wis; Division of Pediatric Cardiothoracic Surgery, Department of Surgery, Medical College of Wisconsin, Milwaukee, Wis.

Objective: To derive and validate an objective definition of postoperative bleeding in neonates and infants undergoing cardiac surgery with cardiopulmonary bypass.

Methods: Using a retrospective cohort of 124 infants and neonates, we included published bleeding definitions and cumulative chest tube output over different postoperative periods (eg, 2, 12, or 24 hours after intensive care unit admission) in a classification and regression tree model to determine chest tube output volumes that were associated with red blood cell transfusions and surgical re-exploration for bleeding in the first 24 hours after intensive care unit admission. After the definition of excessive bleeding was determined, it was validated via a prospective cohort of 77 infants and neonates.

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We sought to describe the acute results and short- to medium-term durability of transcatheter tricuspid valve-in-valve (TVIV) implantation within surgical bioprostheses among patients with Ebstein anomaly (EA). Cases were identified from a voluntary, multicenter, international registry of 29 institutions that perform TVIV. Demographic, clinical, procedural, and follow-up data were analyzed.

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Pannus, thrombus, calcium-Bioprosthetic mitral replacement in young children has it all.

J Thorac Cardiovasc Surg

February 2018

Division of Pediatric Cardiothoracic Surgery, Department of Surgery, Medical College of Wisconsin, Milwaukee, Wis; Herma Heart Center, Children's Hospital of Wisconsin, Milwaukee, Wis.

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Stress and quality of life among parents of children with congenital heart disease referred for psychological services.

Congenit Heart Dis

January 2018

Department of Pediatrics, Medical College of Wisconsin, Herma Heart Center, Children's Hospital of Wisconsin, Milwaukee, Wisconsin, USA.

Objective: The study examined parent stress and health-related quality of life (HRQOL) among families of children with congenital heart disease (CHD) referred for psychological services.

Methods: Parents of 54 children (85% boys) aged 3 to 13 (M  = 7.48, SD = 2.

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Excellence, Like Beauty, May Be in the Eyes of the Beholder.

Semin Thorac Cardiovasc Surg

June 2018

Division of Cardiothoracic Surgery, Department of Surgery, Medical College of Wisconsin, and Herma Heart Center, Children's Hospital of Wisconsin, Milwaukee, Wisconsin. Electronic address:

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Treating a 20 mm Hg gradient alleviates myocardial hypertrophy in experimental aortic coarctation.

J Surg Res

October 2017

Department of Biomedical Engineering, Marquette University and Medical College of Wisconsin, Milwaukee, Wisconsin; Division of Cardiovascular Medicine, Department of Medicine and Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin. Electronic address:

Background: Children with coarctation of the aorta (CoA) can have a hyperdynamic and remodeled left ventricle (LV) from increased afterload. Literature from an experimental model suggests the putative 20 mm Hg blood pressure gradient (BPG) treatment guideline frequently implemented in CoA studies may permit irreversible vascular changes. LV remodeling from pressure overload has been studied, but data are limited following correction and using a clinically representative BPG.

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Background: We sought to compare clinical outcomes and resource utilization for two surgical approaches for single-stage repair of coarctation of the aorta and ventricular septal defect (VSD).

Methods: This was a retrospective chart review of 21 consecutive neonates and infants undergoing single-stage repair of coarctation of the aorta and VSD. Group 1 included 13 patients with both arch repair and VSD repair completed via sternotomy.

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Contemporary results of aortic valve repair for congenital disease: lessons for management and staged strategy.

Eur J Cardiothorac Surg

September 2017

Division of Congenital Heart Surgery, Children's Hospital of Wisconsin, Herma Heart Center, Milwaukee, WI, USA.

Objectives: Any aortic valve (AoV) operation in children (repair, Ross or mechanical replacement) is a palliation and reinterventions are frequent. AoV repair is a temporary solution primarily aimed at allowing the patient to grow to an age when more definitive solutions are available. We retrospectively analysed AoV repair effectiveness across the whole age spectrum of children, excluding neonates and AoV disease secondary to congenital heart disease.

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Objective: Children with hypoplastic left heart syndrome are at a risk for neurodevelopmental delays. Current guidelines recommend systematic evaluation and management of neurodevelopmental outcomes with referral for early intervention services. The Single Ventricle Reconstruction Trial represents the largest cohort of children with hypoplastic left heart syndrome ever assembled.

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The young infant diaphragm: What goes up should come down.

J Thorac Cardiovasc Surg

November 2017

Division of Pediatric Cardiothoracic Surgery, Department of Surgery, Medical College of Wisconsin, Milwaukee, Wis; Herma Heart Center, Children's Hospital of Wisconsin, Milwaukee, Wis. Electronic address:

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Genetic testing is routinely performed on infants with critical congenital heart disease (CHD). This project reviewed the effect of implementing a genetic testing protocol in this population. Charts of infants with critical CHD were reviewed for genetic testing and results across two time periods: the time before implementation of a genetic testing protocol (pre-protocol) and the time after implementation (post-protocol).

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Background: We sought to report the frequency, types, and outcomes of left-sided reoperations (LSRs) after an arterial switch operation (ASO) for patients with D-transposition of the great arteries (D-TGA) and double-outlet right ventricle (DORV) TGA-type.

Methods: Seventeen centers belonging to the European Congenital Heart Surgeons Association (ECHSA) contributed to data collection. We included 111 patients who underwent LSRs after 7,951 ASOs (1.

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Blood Harvested? Cord Cut? Aortic Purse-string Please.

Semin Thorac Cardiovasc Surg

August 2017

Division of Pediatric Cardiothoracic Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin; Herma Heart Center, Children's Hospital of Wisconsin, Milwaukee, Wisconsin. Electronic address:

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Background: Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare condition that can be difficult to diagnose by echocardiography alone. The purpose of this study was to describe the clinical and echocardiographic presentation of ALCAPA, create a set of critical echocardiographic diagnostic criteria, and report outcomes.

Methods: A retrospective review was conducted of all patients diagnosed with isolated ALCAPA at two major cardiac centers between 1990 and 2015.

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