About this trial
Cardiac surgery is a procedure that is commonly performed worldwide. Despite these technological advances, cardiac surgery remains a high-risk surgery. Among post-operative complications, acute kidney injury, respiratory failure, myocardial infarction, and stroke as well as cognitive dysfunction are significant causes of mortality in patients undergoing and following cardiac surgery. Inhaled nitric oxide (NO) therapy as a selective pulmonary vasodilator in cardiac surgery has been one of the most significant pharmacological advances in managing pulmonary hemodynamics and life threatening right ventricular dysfunction and failure. In addition, newer applications show greater promise of inhaled NO as a therapy in the area of cardiac surgery associated acute kidney injury and ischemia reperfusion. However, this remarkable expectation to inhaled NO has experienced a roller-coaster ride with high hopes and nearly universal demonstration of physiological benefits but disappointing translation of these benefits to harder clinical outcomes, like mortality. Most of our understanding on the iNO field in cardiac surgery stems from small observational or single center randomized trials, which failed to ascertain strong evidence base. As a consequence, there are only week clinical practice guidelines on the field and only European expert opinion for the use of iNO in routine and more specialized cardiac surgery. There is need for a large multicenter randomized controlled study to confirm the administration of iNO as an effective weapon for the battle against life threatening complication in high risk cardiac surgical patients.
In a previous meta analysis with 27 studies included, we demonstrated that inhaled nitric oxide (NO) could reduce the duration of mechanical ventilation and reducing biomarkers of organ injury and clinical signs of organ dysfunction in cardiac surgery under cardiopulmonary bypass (CPB) , but had no significance in the ICU stay, hospital stay, and mortality. This may be attributed to the small sample size of the most included studies (of the 27 studies included, 20 studies with sample size less than 100) and heterogeneity in timing, dosage and duration of iNO administration. Well-designed, large-scale, multicenter clinical trials are needed to further explore the effect of iNO in improving postoperative prognosis in cardiovascular surgical patients.
We are planning a large multicenter controlled randomized trial to demonstrate that inhaled nitric oxide can reduce composite outcome of death and Major Adverse Events (MAEs), including need for intensive supports due to heart failure, low cardiac output sydrome, or renal failure, respiratory failure, etc., and myocardial infarction, stroke, and sepsis at 30 days after surgery from 20% to 16% in patient undergoing cardiac surgery with cardiopulmonary bypass.
If the hypothesis had been proved and validated, the results of this study can provide strong evidence for guidelines to facilitate the routine use of iNO in all cardiopulmonary bypass assisted cardiac procedures with 31,800 postoperative outcomes improved per year in US and in China.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age ≥18 years.
Elective cardiac or aortic surgery requiring CPB
Without history of previous open heart surgery.
Disqualifiers
Immediate emergency cardiac surgery;
Cardiac surgery that requires deep hypothermic circulatory arrest;
Planned cardiac surgery for congenital heart disease repair;
Planned for heart transplatation
Trial design
Parallel
Treatments tested in this trial
Nitric Oxide Gas
DrugPatients will receive 80 parts per million (ppm) NO during CPB through the oxygenator. After weaning of CPB, test gases will be delivered via inspiration limb of ventilator at a dose range of 40-80 ppm until 6 hours after ICU admission or until extubation after surgery, whichever comes first.
Standard Care Arm
DrugPatients in this group will receive standard care and 80 ppm nitrogen (N2, control group) are added to the gas mixture as control. In the circumstances when the N2 is not applicable, such as when the plasma-chemical NO synthesis device is employed for NO generatiaon and delivery, the device will be connected to the CPB and ventilator circuits, but the synthesis will remain inactive in the control group. Consequently, the circuit will be supplied with air devoid of NO.
Treatment groups
Trial outcomes
Primary outcomes
Composite outcome of death and major adverse events requiring intensive life supports
It is composite outcome including: * all cause mortality; * ischemic events(myocardial infarction, ischemic stroke, and pulmonary embolism) , * Cardiac arrest that had been successfully resuscitated or new onset of acute cardiac failure (low output syndrome) requiring IABP, ECMO, left ventricular assist device, cardiac dysfunction need for large dose of inotrope support, ---Stage 3 AKI or Renal failure that required renal replacement therapy, * prolonged mechanical ventilation (\> 24h ), * re-sternotomy for any indication, * major arrhythmia ((Ventricular fibrilliation or ventricular tachycardia after weaning-off cardiopulmonary bypass, new onset atrial fibrillation requiring anticoagulant therapy or other intervention upon discharge from the hospital); * sepsis
Secondary outcomes
Total number of major adverse events (MAEs)
Total number of major adverse events( MAEs) listed as the components of the primary outcomes.
Incidence of the MAEs
Incidence of the MAEs listed as the components of the primary outcomes.
All AKI incidence
AKI incidence which will be diagnosed by KDIGO criteria
Length of mechanical ventilation
Length of mechanical ventilation in hours
Other outcomes
Blood transfusion
Amount of each type of blood product transfused (red blood cells, fresh frozen plasma, platelets)
Blood loss
Total amount of blood loss (chest tube drainage) in ml
Incidence of prolonged cardiovascular support
cardiovascular support by using inotropes for more than 48 hours
Maximum vasoactive-inotropic score (VIS)
The VIS will be calculated using the formula: Dopamine dose (mcg/Kg/min) + Dobutamine dose (mcg/Kg/min) + 100 x Epinephrine dose (mcg/Kg/min) + 100 x Norepinephrine dose (mcg/Kg/min) + 50 x Levosimendan dose (mcg/Kg/min) + Enoximone dose (mcg/Kg/min) + 10.000 x Vasopressin dose (UI/kg/min). The maximum VIS will be recorded each day.
Sponsors and contacts
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Xijing Hospital
Lead sponsor
Nikolay O. Kamenshchikov., M.D., Tomsk National Research Medical Center of the Russian Academy of Sciences
Collaborator
Lorenzo Berra., M.D., Massachusetts General Hospital
Collaborator
Jiange Han, Tianjin Chest Hospital, Tianjin, China
Collaborator
Qingping Wu, Wuhan Union Hospital, Wuhan, China
Collaborator
Evgeniy Grigoriev, Research Institute for Complex Issues of Cardiovascular Diseases, Kemerovo, Russian Federation
Collaborator
Vladimir Boboshko, E. Meshalkin National Medical Research Center, Novosibirsk, Russian Federation
Collaborator
Andrei Bautin, The Almazov National Medical Research Centre, St. Petersburg, Russian Federation
Collaborator
Vladimir Pichugin, Specialized Cardiac Surgery Clinical Hospital named after Academician B.A. Korolev, Nizhny Novgorod, Russian Federation
Collaborator
Evgeniy Rosseykin, Federal Center of Cardiovascular Surgery, Khabarovsk, Russian Federation
Collaborator
Jing Shi, The Afffliated Hospital of Guizhou Medical University, Guiyang, China.
Collaborator
Grigoryev Evgeny, Scientific Research Insitute for Complex Issues of Cardiovascular Diseases, Kemerovo, Russia.
Collaborator
Mikhail Vasilev, Meshalkin National Medical Research Center, Мeshalkin of the ministry of health of the Russian Federation,Novosibirsk,Russia.
Collaborator
Jia Min, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Collaborator
Jiawan Wang, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China
Collaborator
Zongbin Song, Xiangya Hospital, Central South University, Changsha, China.
Collaborator