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Published on: July 7, 2016
[Haemodynamic and coronary effects of Risordan injection in patients with coronary disease (author's transl)]
Insights
Nitro-compounds like Risordan prevent myocardial ischemia by improving coronary blood flow and reducing heart workload. This study shows Risordan effectively reversed ischemia induced by rapid atrial stimulation in patients.
Area of Science:
- Cardiology
- Pharmacology
- Physiology
Context:
- Myocardial ischemia is a critical condition often exacerbated by increased cardiac workload.
- Nitro-compounds are known for their vasodilatory effects, potentially improving coronary perfusion.
- Assessing the efficacy of intravenous Risordan in acute myocardial ischemia models is crucial.
Purpose:
- To investigate the hemodynamic, coronary, and metabolic effects of intravenous Risordan infusions in patients with acute myocardial ischemia.
- To evaluate Risordan's ability to counteract ischemia induced by rapid atrial stimulation (RAS).
- To assess changes in myocardial oxygen consumption and lactate extraction.
Summary:
- Rapid atrial stimulation (RAS) in 15 male patients induced myocardial ischemia, evidenced by increased cardiac workload and anaerobic metabolism (negative lactate extraction).
- Intravenous Risordan (5 mg/h) administration led to a decrease in aortic pressure and cardiac index, with a slight increase in heart rate.
- Risordan effectively corrected RAS-induced myocardial ischemia, normalizing lactate extraction and reducing cardiac workload indicators.
Impact:
- Intravenous Risordan demonstrates efficacy in mitigating acute myocardial ischemia.
- The findings support the use of Risordan in managing ischemic heart conditions.
- Understanding Risordan's effects on myocardial metabolism and hemodynamics can guide clinical treatment strategies.
Abstract:
Nitro-compounds exert a preventive action on myocardial ischaemia through their peripheral effects (reduction of left ventricular preload) and their effects on the coronary system (increase of collateral flow and imprevement in the endocardium: epicardium perfusion ratio). The haemodynamic, coronary and metabolic effects of Risordan i.v. infusions (5 mg/h) in acute myocardial ischaemia induced by rapid atrial stimulation (RAS) were investigated in 15 male patients with angiographic or ECG signs of non-perfusion of the coronary network. Coronary sinus blood flow was measured by the thermodilution method. The values measured or calculated were: heart rate (HR), cardiac index (CI), aortic pressure (PAo), pulmonary capillary pressure (PCP), right atrial pressure (RAP), systemic arterial resistance (SAR), double product (DP), coronary blood flow (QCcor), total coronary resistance (TCR), O2 arterio venous difference (DAVO2), myocardial O2 consumption (MVO2) and myocardial lactate extraction (K %). RAS produced a significant increase of PAo, CI, DP, MVO2 and QCcor, with inversion of K % (-3.3%) indicatif anaerobic metabolism by myocardial ischaemia. Risordan produced significant diminution of PAo and CI with subsequent increase of HR; there was little increase of DP, MVO2 and QCcor and little change n myocardial metabolism (K % = 14 %). Risordan corrected the myocardial ischaemia induced by RAS, with decrease of PAo, PCP, RAP, CI, DP and QCcor, K % became positive (+ 11.5 % vs -3.3 % during RAS) suggesting a decrease in myocardial ischaemia.
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