Key result
In a pig model of acute ischemic heart failure, dobutamine and ivabradine increased stroke volume (26 to 33 mL), whereas omecamtiv mecarbil prolonged early relaxation time (42 to 62 msec).
Why the study?
Does omecamtiv mecarbil compared to dobutamine and ivabradine improve diastolic function and stroke volume in a pig model of acute ischemic heart failure?
Does omecamtiv mecarbil compared to dobutamine and ivabradine improve diastolic function and stroke volume in a pig model of acute ischemic heart failure?
In a pig model of acute ischemic heart failure, dobutamine and ivabradine improved early relaxation and stroke volume, whereas omecamtiv mecarbil worsened lusitropy.
Answers are grounded in this paper and cite their sources.
Omecamtiv mecarbil may impair lusitropy in acute ischemic HF models; leaves open its net effects versus inotropes in patients.
Acute ischemic cardiogenic shock is associated with poor prognosis, and the impact of inotropic support on diastolic function in this context is unclear. We assessed two suggested new inotropic strategies in a clinically relevant pig model of ischemic acute heart failure (AHF): treatment with the myosin activator omecamtiv mecarbil (OM) or dobutamine and ivabradine (D+I). Left ventricular (LV) ischemia was induced in anesthetized pigs by coronary microembolization (n = 12). The animals then received OM (bolus 0.75 mg/kg, followed by 0.5 mg/kg per h) (n = 6) or D+I (5 μg/kg per min + 0.29 ± 0.16 mg/kg) (n = 6), respectively. Ischemia reduced the stroke volume (SV), despite the increased left atrial pressure associated with impaired LV early relaxation, systolic dilatation, and LV late diastolic stiffness. Both treatments improved systolic ejection, but only D+I increased the SV from 26 ± 5 to 33 ± 5 mL. D+I enhanced LV early relaxation (Tau; from 45 ± 11 to 29 ± 4 msec) and prolonged the diastolic time (DT) from 338 ± 60 to 352 ± 40 msec. In contrast, OM prolonged Tau (42 ± 5 to 62 ± 10 msec) and shortened the DT (from 326 ± 68 to 248 ± 84 msec). Our data suggest that enhanced early relaxation by D+I improves LV pump function in postischemic acute heart failure. In contrast, OM worsened lusitropy in this model.
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Rønning et al. (2018) studied Acute ischemic heart failure (n=12). Omecamtiv mecarbil vs. Dobutamine and ivabradine (5 μg/kg per min + 0.29 ± 0.16 mg/kg) was evaluated on Stroke volume, LV early relaxation (Tau), and diastolic time. In a pig model of acute ischemic heart failure, dobutamine and ivabradine increased stroke volume (26 to 33 mL), whereas omecamtiv mecarbil prolonged early relaxation time (42 to 62 msec).
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