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Your search keyword '"Wysińska, Julia"' showing total 8 results
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8 results on '"Wysińska, Julia"'

1. Immunosuppressive Therapy of Biopsy-Proven, Virus-Negative, Autoimmune/Immune-Mediated Myocarditis—Focus on Azathioprine: A Review of Existing Evidence and Future Perspectives

Author

Grzechocińska, Justyna, primary, Tymińska, Agata, additional, Giordani, Andrea Silvio, additional, Wysińska, Julia, additional, Ostrowska, Ewa, additional, Baritussio, Anna, additional, Caforio, Alida Linda Patrizia, additional, Grabowski, Marcin, additional, Marcolongo, Renzo, additional, and Ozierański, Krzysztof, additional

Published
2023
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2. Protamine sulfate during transcatheter aortic valve implantation (PS TAVI) — a single-center, single-blind, randomized placebo-controlled trial

Author

Zbroński, Karol, primary, Grodecki, Kajetan, additional, Gozdowska, Roksana, additional, Ostrowska, Ewa, additional, Wysińska, Julia, additional, Rymuza, Bartosz, additional, Scisło, Piotr, additional, Wilimski, Radosław, additional, Kochman, Janusz, additional, Filipiak, Krzysztof J, additional, Opolski, Grzegorz, additional, and Huczek, Zenon, additional

Published
2021
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7. Use of protamine sulfate during transfemoral transcatheter aortic valve implantation – a preliminary assessment of administration rate and impact on complications

Author

Zbroński, Karol, primary, Grodecki, Kajetan, additional, Gozdowska, Roksana, additional, Jędrzejczyk, Szymon, additional, Ostrowska, Ewa, additional, Wysińska, Julia, additional, Rymuza, Bartosz, additional, Scisło, Piotr, additional, Wilimski, Radosław, additional, Kochman, Janusz, additional, Filipiak, Krzysztof J., additional, Opolski, Grzegorz, additional, and Huczek, Zenon, additional

Published
2020
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8. Cardiac Arrhythmias in Muscular Dystrophies Associated with Emerinopathy and Laminopathy: A Cohort Study

Author

Agnieszka Madej-Pilarczyk, Vincenzo Russo, Agata Tymińska, Roman Steckiewicz, Ewa Ostrowska, Julia Wysińska, Marcin Grabowski, Michał Marchel, Grzegorz Opolski, Marchel, Michał, Madej-Pilarczyk, Agnieszka, Tymińska, Agata, Steckiewicz, Roman, Ostrowska, Ewa, Wysińska, Julia, Russo, Vincenzo, Grabowski, Marcin, and Opolski, Grzegorz

Subjects
LMNA, medicine.medical_specialty, Emerin, lcsh:Medicine, Laminopathy, 030204 cardiovascular system & hematology, Ventricular tachycardia, Article, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Emery–Dreifuss muscular dystrophy, medicine, EMD, cardiovascular diseases, Muscular dystrophy, lamin A/C, Atrial standstill, emerin, business.industry, lcsh:R, Atrial fibrillation, General Medicine, medicine.disease, Cardiology, cardiovascular system, business, 030217 neurology & neurosurgery
Abstract

Introduction: Cardiac involvement in patients with muscular dystrophy associated with Lamin A/C mutations (LMNA) is characterized by atrioventricular conduction abnormalities and life-threatening cardiac arrhythmias. Little is known about cardiac involvement in patients with emerin mutation (EMD). The aim of our study was to describe and compare the prevalence and time distribution of cardiac arrhythmias at extended follow-up. Patients and methods: 45 consecutive patients affected by muscular dystrophy associated to laminopathy or emerinopathy were examined. All patients underwent clinical evaluation, 12-lead surface electrocardiogram (ECG), 24 h electrocardiographic monitoring, and cardiac implanted device interrogation. Results: At the end of 11 (5.0–16.6) years of follow-up, 89% of the patients showed cardiac arrhythmias. The most prevalent was atrial standstill (AS) (31%), followed by atrial fibrillation/flutter (AF/Afl) (29%) and ventricular tachycardia (22%). EMD patients presented more frequently AF/AFl compared to LMNA (50% vs. 20%, p = 0.06). Half of the EMD patients presented with AS, whilst there was no occurrence of such in the LMNA (p = 0.001). Ventricular arrhythmias were found in 60% of patients with laminopathy compared to 3% in patients with emerinopathy (p &lt, 0.001). The age of AVB occurrence was higher in the LMNA group (32.8 +/− 10.6 vs. 25.1 +/− 9.1, p = 0.03). Conclusions: Atrial arrhythmias are common findings in patients with muscular dystrophy associated with EMD/LMNA mutations, however, they occurred earlier in EMD patients. Ventricular arrhythmias were very common (60%) in LMNA and occurred definitely earlier compared to the EMD group.

Published
2021

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