Key result
Oral milrinone reduces pulmonary wedge pressure ~30% and increases cardiac index in severe HF.
Why the study?
The effects of oral milrinone on systemic hemodynamics, regional blood flow, and neurohormonal parameters in severe chronic congestive heart failure were not fully characterized.
Does oral milrinone improve systemic hemodynamics, regional blood flow, and neurohormonal parameters in patients with severe chronic congestive heart failure?
Does oral milrinone improve systemic hemodynamics, regional blood flow, and neurohormonal parameters in patients with severe chronic congestive heart failure?
Absolute Event Rate: 19% vs 27%
p-value: p=<0.02
One month of oral milrinone therapy in severe heart failure improves systemic and forearm hemodynamics, but has heterogeneous effects on renal blood flow depending on cardiac index increases.
May support short-term hemodynamic gains with oral milrinone in severe HF; leaves open effects on renal flow and outcomes.
We measured systemic hemodynamics, regional blood flow, and neurohormonal parameters in 13 patients with severe chronic congestive heart failure before and after 1 month of therapy with oral milrinone, a bipyridine cardiotonic agent. After milrinone there were significant reductions in pulmonary wedge pressure (27 +/- 2 to 19 +/- 3 mm Hg; P less than 0.02) and systemic vascular resistance (1866 +/- 152 to 1393 +/- 93 dyne X sec/cm5; P less than 0.05) that were associated with increases in cardiac index (1.85 +/- 0.15 to 2.47 +/- 0.20 L/min/m2; P less than 0.02). There was a marked improvement in forearm blood flow (1.98 +/- 0.14 to 3.02 +/- 0.16 ml/min/dl; P less than 0.01) and a reduction in forearm vascular resistance (45 +/- 3 to 30 +/- 3 U; P less than 0.01). Overall there was no significant change in renal blow flow, renal vascular resistance, or glomerular filtration rate. However, there was a heterogeneous response of renal blood flow and glomerular filtration rate, such that both were directly correlated with the magnitude of increase of cardiac index (r = 0.587 [P less than 0.05] and r = 0.721 [P less than 0.01], respectively). After milrinone there were no significant overall or subgroup changes in urinary sodium excretion, blood volume, plasma renin activity, urinary aldosterone levels, plasma or platelet vasopressin levels, or plasma norepinephrine levels. Thus 1 month of therapy with milrinone improves systemic and forearm hemodynamics, but its effects on renal blood flow and function were heterogeneous. These heterogeneous effects on regional blood flow may depend on the relative vasodilator and inotropic effects of milrinone.
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Cody et al. (1986) studied severe chronic congestive heart failure (n=13). oral milrinone vs. baseline was evaluated on pulmonary wedge pressure (p=<0.02). One month of oral milrinone therapy in severe congestive heart failure significantly reduced pulmonary wedge pressure from 27 to 19 mm Hg (P<0.02) and increased cardiac index.
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