Results 11 to 20 of about 5,715 (232)

Comparison of morrow procedure and transapical beating-heart septal myectomy in patients with hypertrophic obstructive cardiomyopathy: a systematic review and meta-analysis [PDF]

open access: yesFrontiers in Surgery
IntroductionTransaortic surgical myectomy is the established gold-standard treatment for hypertrophic obstructive cardiomyopathy (HOCM). In contrast, the less invasive transapical beating-heart septal myectomy (TABSM) has recently gained attention as a ...
Maxat Zhakayev   +3 more
doaj   +2 more sources

PlasmaBlade-assisted surgical septal myectomy: technique and our experience [PDF]

open access: yesFrontiers in Cardiovascular Medicine
BackgroundThe pulsed-electron avalanche knife (PEAK) PlasmaBlade provides an atraumatic, scalpel-like cutting precision and electrocautery-like hemostasis. PlasmaBlade operates near body temperature, and its long, thin, and malleable tip can overcome the
Pankaj Garg   +5 more
doaj   +2 more sources

Bimanual examination for septal myectomy for hypertrophic cardiomyopathy [PDF]

open access: bronzeInteractive CardioVascular and Thoracic Surgery, 2014
Left ventricular septal myectomy is the therapeutic 'gold standard' for patients with obstructive hypertrophic cardiomyopathy whose symptoms are refractory to medical therapy. We describe our initial clinical experience with a new surgical technique for septal myectomy utilizing the 'bimanual examination' in order to more reliably complete extended ...
Shinichi Fukuhara   +3 more
openalex   +3 more sources

Left ventricle myocardial remodeling following septal myectomy in patients with hypertrophic obstructive cardiomyopathy [PDF]

open access: yesJournal of Cardiovascular Magnetic Resonance
Background: Left ventricular (LV) reverse myocardial remodeling occurs following septal myectomy in hypertrophic obstructive cardiomyopathy (HOCM), but it remains unclear whether diffuse fibrosis is reversible during this period.
Guanyu Lu   +12 more
doaj   +2 more sources

Comparing long‐term outcomes of septal myectomy and mitral valve replacement in hypertrophic cardiomyopathy patients: A retrospective cohort study in Iran [PDF]

open access: yesHealth Science Reports
Background Hypertrophic cardiomyopathy (HCM) affects millions of individuals worldwide. In severe cases, it can cause life‐threatening conditions such as left ventricular outflow tract (LVOT) obstruction, mitral regurgitation (MR), and sudden cardiac ...
Aryan Ayati   +4 more
doaj   +2 more sources

Transapical Approach to Septal Myectomy for Hypertrophic Cardiomyopathy. [PDF]

open access: yesLife (Basel)
A 63-year-old symptomatic female with apical hypertrophic cardiomyopathy and diastolic disfunction was admitted to the hospital. What is the best way to manage this patient? This study is a literature review that was performed to answer this question. The following PubMed search strategy was used: ‘Hypertrophic obstructive cardiomyopathy’ [All Fields ...
Afanasyev A   +9 more
europepmc   +4 more sources

Successful Percutaneous Septal Alcohol Ablation After Surgical Myectomy

open access: yesBiomolecules & Biomedicine, 2010
Hypertrophic obstructive cardiomyopathy (HOCM) is a primary, usually familial and genetically fixed myocardial hypertrophy, with dynamic left ventricular outflow tract obstruction.
Mehmed Kulić   +6 more
doaj   +4 more sources

Clinical Effect of the Modified Morrow Septal Myectomy Procedure for Biventricular Hypertrophic Cardiomyopathy [PDF]

open access: yesReviews in Cardiovascular Medicine
Background: Right ventricular involvement in hypertrophic cardiomyopathy is uncommon. This study aimed to evaluate clinical outcomes of the modified septal myectomy in patients diagnosed with biventricular hypertrophic cardiomyopathy (BHCM), a subject ...
Tong Tan   +10 more
doaj   +2 more sources

Role of Septal Myectomy in Pediatric Hypertrophic Cardiomyopathy [PDF]

open access: bronzeKardiyovasküler Tıp E Dergisi/E Journal of Cardiovascular Medicine
Hypertrophic cardiomyopathy is a prevalent cause of sudden cardiac death among young people. This distinctive genetic condition can manifest at any age from infancy to adulthood.
Sameh M. Said
doaj   +2 more sources

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