dc.contributor.author |
Ivanov, R. O. |
|
dc.contributor.author |
Zverkhanovskyi, O. A. |
|
dc.contributor.author |
Sarafiniuk, L. A. |
|
dc.contributor.author |
Androshchuk, O. V. |
|
dc.contributor.author |
Tatarina, O. V. |
|
dc.date.accessioned |
2025-03-09T20:06:15Z |
|
dc.date.available |
2025-03-09T20:06:15Z |
|
dc.date.issued |
2024 |
|
dc.identifier.citation |
Main methodological aspects of determining the chewing efficiency / Ivanov R.O., Zverkhanovskyi O. A., Sarafiniuk, L. A. [etc.] // Вісник проблем біології і медицини. – 2024. – № 1. – P. 24-29 |
uk_UA |
dc.identifier.uri |
https://dspace.vnmu.edu.ua/123456789/7163 |
|
dc.description.abstract |
Heart failure is one of the most urgent problems of medicine, because the number of patients suffering
from this pathology continues to grow steadily. The arsenal of drugs for the treatment of chronic heart failure has
been replenished with new samples that have demonstrated significant effectiveness in improving the course and
prognosis of patients in this cohort. However, the search for other promising drugs continues.
The aim of our work is to summarize existing scientific data on the effect of sodium-glucose cotransporter-2
inhibitors, vericiguat, omecamtiv mecarbil on the clinical course and prognosis in patients with chronic heart failure,
as well as the analysis of current clinical studies aimed at evaluating hemodynamic effects, tolerability and safety of
experimental drugs in patients with chronic heart failure.
The positive effects of sodium-glucose cotransporter-2 inhibitors have led to their inclusion in European
guidelines for treating patients with chronic heart failure, regardless of left ventricular ejection fraction.
Vericiguat is recommended for patients with NYHA class II-IV chronic heart failure and reduced left ventricular
ejection fraction who have decompensated heart failure within the past 3 months despite receiving optimal chronic
heart failure therapy.
Omecamtiv mecarbil has been considered a promising drug for the treatment of heart failure due to its ability to
reduce the primary composite endpoint compared to placebo for many years. However, in 2023, the US Food and
Drug Administration refused to approve omecamtiv mecarbil for the treatment of adult heart failure patients with
reduced left ventricular ejection fraction, citing insufficient evidence of the drug’s effectiveness.
Development of new drugs for patients with chronic heart failure opens up new opportunities to improve the
quality of life and prognosis of patients. Ongoing clinical trials of experimental drugs give hope for breakthrough
results. |
uk_UA |
dc.language.iso |
en |
uk_UA |
dc.publisher |
Вісник проблем біології і медицини |
uk_UA |
dc.subject |
chronic heart failure, drug therapy, sodium-glucose cotransporter-2 inhibitors, vericiguat, omecamtiv mecarbil. |
uk_UA |
dc.title |
Main methodological aspects of determining the chewing efficiency |
uk_UA |
dc.type |
Article |
uk_UA |