15,387 results match your criteria: "Pulmonic Valvular Stenosis"

Article Synopsis
  • Dextro-transposition of the great arteries (D-TGA) is a serious congenital heart defect where the heart’s two main arteries are switched, leading to separation of pulmonary and systemic blood flow.
  • The condition can occur on its own or alongside other heart issues and is influenced by a mix of genetic and environmental factors.
  • Surgical intervention during infancy, including necessary procedures like balloon atrial septostomy and various corrective surgeries, is crucial for improving outcomes, as early diagnosis and treatment significantly enhance the chances of survival into adulthood.
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Rupture of the ascending aorta 6 months after TAVI procedure caused by TAVI prosthesis.

J Cardiothorac Surg

August 2024

Department of Cardiac, Vascular and Endovascular Surgery and Transplantology, Silesian Center for Heart Diseases, Medical University of Silesia in Katowice, Marii Skłodowskiej-Curie 9, Zabrze, 41-800, Poland.

Background: Transcatheter aortic valve implantation (TAVI) is indicated for elderly patients who often have severe comorbidities and high operative risk. Despite many advantages, it carries the potential for both early and late complications. The literature reports mainly periprocedural problems.

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APOE-NOTCH axis governs elastogenesis during human cardiac valve remodeling.

Nat Cardiovasc Res

August 2024

Perinatal Institute, Division of Pulmonary Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

Valve remodeling is a process involving extracellular matrix organization and elongation of valve leaflets. Here, through single-cell RNA sequencing of human fetal valves, we identified an elastin-producing valve interstitial cell (VIC) subtype (apolipoprotein E (APOE), elastin-VICs) spatially located underneath valve endothelial cells (VECs) sensing unidirectional flow. APOE knockdown in fetal VICs resulted in profound elastogenesis defects.

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Isolated Pulmonic Valve Endocarditis: A Rare Clinical Entity.

Clin Med Insights Case Rep

August 2024

Department of Internal Medicine, School of Medicine, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.

Article Synopsis
  • Isolated pulmonic valve endocarditis is a rare heart valve infection, making up only 1-2% of all infective endocarditis cases, and was diagnosed using modified Duke's criteria in this case.
  • A 52-year-old male presented with symptoms like body swelling, prolonged fever, cough, and discolored urine, alongside signs of heart failure and other health issues detected during examination and lab tests.
  • Diagnosis was confirmed by echocardiography showing vegetations on the pulmonic valve, supported by the presence of one major and three minor criteria from the modified Duke's criteria, leading to significant improvement after two weeks of intravenous treatment.
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Background: We present a case series of right ventricle (RV) rehabilitation after the Starnes procedure in patients with Ebstein anomaly (EA), applying the Cone repair of the tricuspid valve (TV) to achieve 2-ventricle or 1.5-ventricle physiology.

Methods: This is a retrospective database analysis from 2 institutions in North America.

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Article Synopsis
  • A study in South Korea aimed to investigate the prevalence of congenital heart disease (CHD) in children, filling a gap in national epidemiological data.
  • Researchers analyzed data from the National Health Insurance Service from 2014-2018, focusing on critical CHDs that require immediate intervention after birth.
  • Results showed that prevalence rates for certain defects varied significantly between East Asian and Western populations, indicating unique patterns in CHD types in Korean children.
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Background: Balloon Pulmonary Valvuloplasty (BPV) is a procedure for Pulmonary Stenosis (PS) treatment. In this study, right ventricle (RV) performance was determined through 2D-Speckle Tracking Echocardiography (2D-STE).

Methods: The study involved 25 diagnosed children with PS undergoing BPV and 25 normal children.

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Bronchoscopy using a flexible bronchoscope is considered a safe procedure and has been used for diagnosing and treating airway and parenchymal lung diseases. Bronchoscopic interventions in selected patients with emphysema, airway stenosis, and air leaks provide new treatment options. The application of multidetector computed tomography (MDCT) planning prior to bronchoscopy is comprehensively addressed.

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Article Synopsis
  • The study investigated patients with significant tricuspid regurgitation (TR) in the context of severe mitral or aortic valvular disease, analyzing their characteristics and long-term outcomes.
  • A total of 975 patients with moderate to severe TR were sorted into four groups based on their specific valvular conditions, with the primary goal to examine all-cause death rates and heart failure-related outcomes.
  • Results showed that patients with severe aortic stenosis and TR had poorer outcomes; however, after adjusting for various factors, differences in death rates between groups became insignificant, highlighting the serious impact of TR across different valvular diseases.
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Surgical aortic valve replacement (SAVR) prolongs life and improves its quality in patients with severe aortic stenosis (AS). Unplanned SAVR is a failure of AS screening and follow-up programmes. We identified all elective, first, isolated SAVRs performed between 1 January and 31 December 2019 in a Welsh tertiary cardiac centre, and documented the clinical and echocardiographic variables, and reasons for unplanned SAVR.

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Tricuspid regurgitation (TR) is common after a heart transplant and is associated with worse clinical outcomes. The incidence ranges from 34% immediately after transplant to 20% by 10 years. Most patients can be managed medically; however, severe TR and symptomatic right heart failure warrant tricuspid valve replacement.

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Background: The development of heart failure is a turning point in the natural course of aortic stenosis (AS). Pulmonary oedema and elevated left ventricular pressure (LVP) are cardinal features of heart failure. Evaluating pulmonary oedema by lung ultrasound involves taking the upper hand with a bedside noninvasive tool that may reflect LVP.

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Acute urticaria and cardiovascular diseases.

Am J Med Sci

August 2024

Leumit Health Services, Tel Aviv-Yafo 6473817, Israel; Department of Family Medicine, Sackler Faculty of Medicine, Tel-Aviv University, Tel Aviv-Yafo 6997801.

Article Synopsis
  • The study explores the link between acute urticaria (AU) and cardiovascular conditions, aiming to identify common comorbidities among AU patients compared to a control group.
  • Results showed higher levels of various health indicators (like blood pressure and BMI) in AU patients and significant associations with several cardiovascular issues, including heart diseases and arrhythmias.
  • The findings highlight the need for medical professionals to be aware of cardiovascular risks in AU patients, suggesting that these conditions might share underlying mechanisms, warranting further investigation.
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Severe aortic valve stenosis (AS) and pulmonary hypertension (PH) are life-threatening cardiovascular conditions, necessitating early detection and intervention. Recent studies have explored the role of Insulin-like Growth Factor-Binding Protein 2 (IGF-BP2) in cardiovascular pathophysiology. Understanding its involvement may offer novel insights into disease mechanisms and therapeutic targets for these conditions.

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Trans-pulmonary stent placement for pulmonary stenosis in a dog with a type R2A coronary artery anomaly.

J Vet Cardiol

October 2024

Department of Veterinary Clinical Sciences, College of Veterinary Medicine, University of Minnesota, 1365 Gortner Ave, St Paul, MN 55108, USA.

Article Synopsis
  • A one-year-old male American bulldog was evaluated for severe pulmonary stenosis, with a significant pressure gradient of 240 mmHg identified through echocardiography.
  • Angiography revealed a type R2A coronary anomaly, characterized by an unusual left coronary artery ending up in the right coronary ostium.
  • A trans-pulmonary stent was successfully implanted, reducing the pressure gradient to 68 mmHg post-surgery without causing coronary compression, marking a unique application of coronary compression testing in this context.
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Air pollution may be a potential cause of congenital heart defects (CHDs), but racial disparities in this association are unexplored. We conducted a statewide population-based cohort study using North Carolina birth data from 2003-2015 (N=1,225,285) to investigate the relationship between air pollution and CHDs (specifically pulmonary valve atresia/stenosis, Tetralogy of Fallot (TOF), and atrioventricular septal defect (AVSD)). Maternal exposure to particulate matter ≤2.

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Background: While communicable diseases have long been the primary focus of healthcare in Africa, the rising impact of paediatric and congenital heart disease (CHD) cannot be overlooked. This research aimed to estimate the frequency and pattern of heart diseases in children who underwent their first echocardiography at a national cardiac referral hospital in Tanzania.

Methods: A retrospective observational study was conducted on children aged 0 to 18 years referred for first-time cardiological evaluation from January 2017 to December 2022.

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Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a group of systemic diseases caused by a combination of many factors, including genetics, environment, and immunity. AAV is characterized by predominantly small-vessel involvement and has a variety of clinical manifestations. Small-vessel lesions of the kidneys and lungs are common, and lesions of medium-sized arteries may also present, but the involvement of large arteries and their primary branches is very rare.

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Objective: Shone's complex comprises of a combination of congenital cardiac anomalies causing obstructions in the left ventricle's inflow and outflow tracts. This systematic review aims to evaluate the clinical features and surgical outcomes of Shone's complex.

Methods: An electronic literature search of PubMed and Scopus was performed to identify relevant studies related to the presentation, management, and outcomes of Shone's complex.

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The Ross Procedure in Children and Infants: A Systematic Review With Pooled Analyses.

CJC Pediatr Congenit Heart Dis

June 2024

Department of Medicine, Montreal Heart Institute, Université de Montréal, Montreal, Québec, Canada.

Background: The Ross procedure is a surgical option for congenital aortic stenosis that involves replacing the diseased aortic valve with a pulmonary autograft. Little is known about outcomes in children, particularly those younger than 1 year.

Methods: A systematic review with pooled analyses was conducted according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) criteria.

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Article Synopsis
  • Absent Pulmonary Valve Syndrome (APVS) is a rare heart defect characterized by the missing or underdeveloped pulmonary valve, often occurring with Tetralogy of Fallot (TOF).
  • A case study of a 33-year-old woman showed her infant had severe pulmonary stenosis and a large ventricular septal defect, which were surgically treated, leading to an asymptomatic outcome after two years.
  • Advances in surgical techniques have improved long-term survival rates for APVS, highlighting the importance of early detection and tailored surgical approaches for better patient outcomes.
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Article Synopsis
  • * The case study discusses an infant with recurrent infections, diagnosed with TOF, highlighting additional cardiac issues like ventricular septal defects and pulmonary stenosis found during echocardiography.
  • * The condition is associated with DiGeorge syndrome and poses unique surgical management challenges due to its complex embryological origins and multiple cardiac anomalies.
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