Effect of iloprost inhalation on postoperative outcome in high-risk cardiac surgical patients: a prospective randomized-controlled multicentre trial (ILOCARD)
Autor: | Aristidis Dongas, Bernhard Zwissler, Ines Kaufmann, Ilocard Investigators, Hermann Kuppe, Steffen Rex, Michael Winterhalter, Hans-Helge Müller, Peter Kienbaum, Christian Stoppe |
---|---|
Rok vydání: | 2019 |
Předmět: |
medicine.medical_specialty
Inhalation business.industry Extracorporeal circulation Cardiac index General Medicine Perioperative 030204 cardiovascular system & hematology medicine.disease Pulmonary hypertension Intensive care unit law.invention Cardiac surgery 03 medical and health sciences 0302 clinical medicine Anesthesiology and Pain Medicine 030228 respiratory system law Anesthesia cardiovascular system medicine business Iloprost medicine.drug |
Zdroj: | Canadian Journal of Anesthesia/Journal canadien d'anesthésie. 66:907-920 |
ISSN: | 1496-8975 0832-610X |
DOI: | 10.1007/s12630-019-01309-8 |
Popis: | 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. 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. 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. The prophylactic inhalation of iloprost did not meaningfully improve the outcome in high-risk cardiac surgical patients. www.clinicaltrials.gov (NCT00927654); registered 25 June, 2009. |
Databáze: | OpenAIRE |
Externí odkaz: |