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• W3087281788 abstract "Abstract Background Cystic fibrosis may lead to left ventricular (LV) dysfunction. This dysfunction can be documented by methods such as tissue Doppler echocardiographic (TDI) imaging and two‐dimensional speckle tracking echocardiography (STE) in early stage. Study design This was prospective cohort study. Methods A total of 34 patients diagnosed with cystic fibrosis (mean age and SD 9.9 ± 4.9 years) and 37 healthy control subjects with a comparable gender and age distribution (mean age 9.8 ± 4.3) were studied. The results for the two groups were compared along with the results of published reports. Results No significant relationship was found between the groups in terms of systolic and diastolic measurements of the interventricular septum and posterior left ventricular wall, and ejection fraction ( P > .05). Myocardial performance indexes of left ventricular free wall and interventricular septum increased in the patient group compared with the controls ( P < .05). As measured by STE, seven segments in the LV myocardial longitudinal strain and three segments in the LV myocardial circumferential strain showed significant reductions in patients with cystic fibrosis compared with controls ( P < .05). The longitudinal global, circumferential global, and total global strain values had no significant difference between the groups ( P > .05). Longitudinal strain rates and circumferential strain rates were both lower in five segments in the patient group ( P < .05). Conclusions Tissue Doppler echocardiographic imaging and STE may help identifying subclinical LV dysfunction in cystic fibrosis patients with unremarkable conventional echocardiography. They may be considered for the routine follow‐up of cystic fibrosis patients." @default.
• W3087281788 created "2020-09-25" @default.
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• W3087281788 date "2020-09-19" @default.
• W3087281788 modified "2023-09-27" @default.
• W3087281788 title "Tissue Doppler and speckle tracking echocardiography assessment of left ventricular function in children with cystic fibrosis" @default.
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• W3087281788 doi "https://doi.org/10.1111/echo.14860" @default.
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