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Erschienen in: Canadian Journal of Anesthesia/Journal canadien d'anesthésie 8/2019

12.02.2019 | Reports of Original Investigations

Effect of iloprost inhalation on postoperative outcome in high-risk cardiac surgical patients: a prospective randomized-controlled multicentre trial (ILOCARD)

verfasst von: Michael Winterhalter, MD, Steffen Rex, MD, Christian Stoppe, MD, Peter Kienbaum, MD, Hans-Helge Müller, PhD, Ines Kaufmann, MD, Hermann Kuppe, MD, Aristidis Dongas, MD, Bernhard Zwissler, MD, ILOCARD Investigators

Erschienen in: Canadian Journal of Anesthesia/Journal canadien d'anesthésie | Ausgabe 8/2019

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Abstract

Purpose

Perioperative right ventricular (RV) failure due to pressure overload from pulmonary hypertension (PH) worsens postoperative outcomes after cardiac surgery. Inhaled iloprost is a potent pulmonary vasodilator improving RV performance, ameliorating myocardial and pulmonary ischemia-reperfusion injury and attenuating inflammation. We hypothesized that the prophylactic inhalation of iloprost would reduce postoperative ventilation times after cardiac surgery.

Methods

In this phase III, multicentre, randomized, double-blind, placebo-controlled trial, we randomly assigned 253 cardiac surgical patients at high risk of perioperative RV failure to the prophylactic inhalation of 20 µg iloprost or placebo before and during weaning from extracorporeal circulation. The primary endpoint was the duration of postoperative ventilation. Secondary endpoints included perioperative hemodynamics, intensive care unit and hospital length of stay, and 90-day mortality. Safety was assessed by the incidence of adverse events.

Results

Iloprost had no significant effect on the median [interquartile range] duration of postoperative ventilation compared with placebo (720 [470–1170] min vs 778 [541–1219] min, respectively; median decrease, 65 min; 95% confidence interval [CI], − 77 to 210; P = 0.37). While the nebulization of iloprost decreased RV afterload and improved cardiac index, major secondary endpoints were not significantly affected. Ninety-day mortality occurred in 14% of the iloprost patients compared with 14% of the placebo patients (hazard ratio, 0.97; 95% CI, 0.50 to 1.89; P = 0.93). The incidence of adverse events was comparable in both groups.

Conclusions

The prophylactic inhalation of iloprost did not meaningfully improve the outcome in high-risk cardiac surgical patients.

Trial registration

www.​clinicaltrials.​gov (NCT00927654); registered 25 June, 2009.
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Metadaten
Titel
Effect of iloprost inhalation on postoperative outcome in high-risk cardiac surgical patients: a prospective randomized-controlled multicentre trial (ILOCARD)
verfasst von
Michael Winterhalter, MD
Steffen Rex, MD
Christian Stoppe, MD
Peter Kienbaum, MD
Hans-Helge Müller, PhD
Ines Kaufmann, MD
Hermann Kuppe, MD
Aristidis Dongas, MD
Bernhard Zwissler, MD
ILOCARD Investigators
Publikationsdatum
12.02.2019
Verlag
Springer International Publishing
Erschienen in
Canadian Journal of Anesthesia/Journal canadien d'anesthésie / Ausgabe 8/2019
Print ISSN: 0832-610X
Elektronische ISSN: 1496-8975
DOI
https://doi.org/10.1007/s12630-019-01309-8

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