Key result
Inhaled iloprost significantly decreased the transpulmonary gradient (8.2 vs 11.2 mmHg, P<0.05) in heart transplant recipients with post-bypass acute right ventricular dysfunction.
Why the study?
Does inhaled iloprost improve hemodynamics and right ventricular function in heart transplant recipients with post-bypass acute right ventricular dysfunction?
Case Report (n=8)
Does inhaled iloprost improve hemodynamics and right ventricular function in heart transplant recipients with post-bypass acute right ventricular dysfunction?
Absolute Event Rate: 8.2% vs 11.2%
p-value: p=< 0.05
Inhaled iloprost safely and effectively improves hemodynamics and right ventricular function in heart transplant recipients experiencing post-bypass acute right ventricular dysfunction.
May support inhaled iloprost in select post-transplant RV dysfunction; hypothesis-generating and requires prospective trials before practice change.
BACKGROUND: During heart transplantation, weaning from cardiopulmonary bypass may be particularly laborious as a result of superimposed acute right ventricular dysfunction in the setting of pre-existing pulmonary hypertension. Research in recent years has focused on inhaled vasodilatory treatment modalities which selectively target the pulmonary circulation. METHODS: We present a series of eight patients in whom inhaled iloprost, a synthetic prostacyclin analog, was used to treat pulmonary hypertension and right ventricular dysfunction detected by transesophageal echocardiography during a heart transplant procedure. In addition to conventional inotropic support, 20 mug of inhaled iloprost was administered via nebulized aerosol for a 20-min period. Complete sets of hemodynamic measurements were obtained before inhalation and during and after cessation of the inhalation period. RESULTS: Inhaled iloprost decreased the transpulmonary gradient at the end of the inhalation period relative to baseline (8.2 +/- 1.6 mmHg vs. 11.2 +/- 0.9 mmHg, P < 0.05). The mean pulmonary artery pressure to systemic artery pressure ratio decreased over this period (0.24 +/- 0.07 vs. 0.44 +/- 0.09, P < 0.05). A statistically significant decrease in the pulmonary vascular resistance to systemic vascular resistance ratio was also observed (0.10 +/- 0.02 vs. 0.19 +/- 0.02, P < 0.05). Improved indices of right ventricular function were observed in echocardiographic monitoring. CONCLUSION: During heart transplantation procedures, episodes of pulmonary hypertension can be successfully treated with inhaled iloprost administration, without untoward side-effects or significant systemic impact.
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Theodoraki et al. (2006) conducted a case report in post-bypass acute right ventricular dysfunction (n=8). Inhaled iloprost vs. baseline was evaluated on transpulmonary gradient (p=< 0.05). Inhaled iloprost significantly decreased the transpulmonary gradient (8.2 vs 11.2 mmHg, P<0.05) in heart transplant recipients with post-bypass acute right ventricular dysfunction.
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