- IRMS - Nicolae Testemitanu SUMPh
- 1. COLECȚIA INSTITUȚIONALĂ
- Congresul consacrat aniversării a 75-a de la fondarea Universității de Stat de Medicină și Farmacie „Nicolae Testemițanu” din Republica Moldova
- Culegere de postere
Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12710/12971
Title: | Study of the cardioprotective metabolic effects of mildronate |
Authors: | Chetruș, Olga |
Keywords: | cardioprotective;metabolic effect;angina pectoris |
Issue Date: | Oct-2020 |
Publisher: | Universitatea de Stat de Medicină şi Farmacie "Nicolae Testemiţanu" |
Abstract: | Introduction.
Diseases of the cardiovascular system are the leading cause of death in most
countries of the world. The epidemiological situation in Moldova is characterized by
the term “over-mortality” due to cardiovascular diseases, compared to
economically developed countries. Purpose
Study of possible pharmacodynamic effects, mechanisms of action and
toxicity of metabolic drugs - mildronate based on the molecular structure of
the pharmaceutical substance.Material and methods
An open randomized clinical trial was performed that included 160 patients with
CPI (117 men and 43 women) with a mean age of 59.26 ± 0.74 years. 142 patients
had stable angina pectoris from different functional classes, and 21 - unstable
angina pectoris. The control group included 30 practically healthy people. The
observation period was 6 weeks.
Results
There was an improvement in the repolarization phase in the form of a reduction in
the depth of the "T" wave from 1.5 mm to 0.2 mm (p<0.05). At the end of the
observation period, patients treated with mildronate increased exercise tolerance
from 310.66±24.74 meters to 476.50±43.5 meters (p <0.05). Mildronate provided a
hemodynamic effect in the form of a decrease in blood pressure - systolic from
161.76±4.39 mmHg to 143.4±5.13 mm Hg (p<0.05) and diastolic from 95.09±2.88
mmHg to 87.54±2.52 mmHg (p=0.06). The summary efficacy coefficient of the basic
therapy was 15.55±4.21%, and of the complex pharmacotherapy with mildronate
59.16±3.31% (p<0.001), which is actually 4 times higher.
ConclusionsIn patients with stable exertional angina pectoris, a 4-fold increase in
the efficacy of pharmacotherapy was added to the addition of mildronate due to the
more pronounced antianginal effect, improved physical performance, potentiation of
positive and hypotensive inotropic effects. |
URI: | https://stiinta.usmf.md/ro/manifestari-stiintifice/zilele-universitatii http://repository.usmf.md/handle/20.500.12710/12971 |
Appears in Collections: | Culegere de postere
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