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Wyświetlanie 1-2 z 2
Tytuł:
Pediatric cardiology emergencies – the role of Long QT Syndrome among arrhythmias
Autorzy:
Zipser, Mariusz
Zienciuk-Krajka, Agnieszka
Krenska, Dominika D.
Kwiatkowska, Joanna
Powiązania:
https://bibliotekanauki.pl/articles/895795.pdf
Data publikacji:
2019-02-05
Wydawca:
Gdański Uniwersytet Medyczny
Tematy:
long QT syndrome
torsades de pointes
pediatric arrhythmias
Opis:
Long QT syndrome (LQTS) is a hereditary disease with significant mortality, which might be reduced with appropriate management. This cardiac disorder is regarded as rare, but its prevalence remains unknown. The clinical course of LQTS is variable and syncope is a common first manifestation of LQTS. Therefore in each patient after syncope an ECG should be carried out. However, there is no universal QT value applying to all patients (especially infants and children), because it varies depending on age and sex. Genetic testing can be of great importance for the management of families with LQTS and early identification of patient relatives at risk of developing disease. We aimed to show that a very important part of treatment is not only pharmacotherapy, especially beta-blockers, but change of lifestyle plays a significant role.
Źródło:
European Journal of Translational and Clinical Medicine; 2018, 1, 2; 4-10
2657-3148
2657-3156
Pojawia się w:
European Journal of Translational and Clinical Medicine
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Comparison of clinical and echocardiographic parameters in patients with hypertrophic cardiomyopathy under and over 60 years of age
Autorzy:
Wabich, Elżbieta
Raczak, Grzegorz
Rozwadowska, Katarzyna
Zienciuk-Krajka, Agnieszka
Szymanowicz, Wiktor
Kozłowski, Dariusz
Kaleta, Anna M.
Daniłowicz-Szymanowicz, Ludmiła
Powiązania:
https://bibliotekanauki.pl/articles/895757.pdf
Data publikacji:
2019-06-04
Wydawca:
Gdański Uniwersytet Medyczny
Tematy:
hypertrophic cardiomyopathy
echocardiography
speckle-tracking echocardiography
Opis:
Background: Hypertrophic Cardiomyopathy (HCM) is one of the most common genetic myocardial diseases. Transthoracic echocardiography which includes speckle tracking technique is tool for HCM diagnosis and monitoring the course of the disease. The aim of this study was to compare clinical and echocardiographic parameters in HCM patients older and younger than 60 years old (yo). Material and methods: We prospectively enrolled 53 HCM patients, who were divided into two groups: younger and older than 60 yo. Clinical parameters, standard echocardiographic indices, as well as strain parameters were assessed and compared between the groups. Results: The older subgroup was characterized by a higher prevalence of coronary artery disease. In the younger subgroup the incidence of atrial fibrillation was quite high, which occurs far more often than in the general population. Echocardiographic analysis showed worse diastolic function in older, as well as lower volume of the LV. The global longitudinal strain was worse in <60 patients. The 3D strain parameters differed significantly between the groups: the area and radial strains were worse in younger patients. Conclusions: HCM patients older and younger than 60 yo differ significantly in terms of clinical and echocardiographic parameters.
Źródło:
European Journal of Translational and Clinical Medicine; 2019, 2, 1; 28-35
2657-3148
2657-3156
Pojawia się w:
European Journal of Translational and Clinical Medicine
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-2 z 2

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