Nitrite Infusion in High Risk Patients Undergoing Cardiopulmonary Bypass
Mots clés
Abstrait
La description
Acute kidney injury is one of the most untoward consequences of cardiac-surgery with the use of CPB. As such it is associated with a high mortality and morbidity and health care expense. Unfortunately, currently, there is no effective preventive or treatment strategy for cardiac surgery-associated (CSA) AKI other than renal replacement therapy.
It is postulated that a major mechanism of CSA-AKI is created by the ischemia reperfusion injury (IRI) resulting from aortic cross clamping and unclamping. This creates a cascade of events culminating in inflammation, microvascular dysfunction and tubular cell maladaptation and eventually renal tissue damage. Current treatment modalities that target the microcirculation such as blood pressure and cardiac output fails to prevent renal abnormalities and as such may be deleterious to the renal tissue microcirculation. The PI hypothesizes that a therapeutic strategy that limits IRI such as the administration of inhaled nitric oxide (NO) or sodium nitrite (NaNO2) would ameliorate CSA-AKI by limiting inflammatory injury to the kidney.
The anion nitrite (NO2-) releases NO in biological systems and has been demonstrated to inhibit IR injury in the heart, liver and kidneys created by various pathologic states1-3 and improve outcomes in patients with acute myocardial infarction, in patients with pulmonary hypertension and is the putative active mediator of protection in liver-transplantation patients receiving inhaled nitric oxide4.
The objective of this study is to determine whether the NO donor, nitrite will prevent I/R injury in patients at high risk of development of CSA-AKI undergoing open-heart surgery with cardiopulmonary bypass.
Rendez-vous
| Dernière vérification: | 08/31/2018 |
| Première soumission: | 10/19/2017 |
| Inscription estimée soumise: | 10/30/2017 |
| Première publication: | 11/05/2017 |
| Dernière mise à jour soumise: | 09/24/2018 |
| Dernière mise à jour publiée: | 09/26/2018 |
| Date de début réelle de l'étude: | 09/30/2018 |
| Date d'achèvement primaire estimée: | 05/31/2019 |
| Date estimée d'achèvement de l'étude: | 11/30/2020 |
Condition ou maladie
Intervention / traitement
Drug: Saline
Drug: Sodium Nitrite
Phase
Groupes d'armes
| Bras | Intervention / traitement |
|---|---|
| Placebo Comparator: Control group saline infusion will be administered after induction of general anesthesia | |
| Active Comparator: Sodium Nitrite sodium nitrite will start after induction of general anesthesia via a dedicated IV line for 6 hrs. |
Critère d'éligibilité
| Âges éligibles aux études | 19 Years À 19 Years |
| Sexes éligibles à l'étude | All |
| Accepte les bénévoles en santé | Oui |
| Critères | Inclusion Criteria: - Patients CCFS score ≥ 6 (Table 1) - Patients admitted to UAB cardiac intensive care unit (CICU) following elective cardiac surgery with cardiopulmonary bypass under general endotracheal anesthesia - 19 years old - Estimated glomerular filtration rate (eGFR) ≥ 30 ml/min/1.73 m2 Exclusion Criteria: - Prisoners directly admitted from a correctional facility. - Children < 19 years or under 50 kg body weight if age is unknown. - Patients enrolled in a concurrent ongoing interventional, randomized clinical trial. - Patients with end stage renal disease or preexisting GFR <30 mL/min/1.73 m2 or need for dialysis. 34 - Patients with end stage heart disease on the cardiac transplant list. - Patients undergoing procedures without the use of CPB - All transplant patients. - Patients on ventricular assist devices. - Patients undergoing emergency procedures. - Patients with glucose 6-dehydrogenase deficiency - Pregnancy |
Résultat
Mesures des résultats primaires
1. Nitrite Metabolome Levels [baseline to 73 hrs post-operatively]
2. Biomarkers of Hemolysis [baseline to 73 hrs post-operatively]
3. Biomarkers of Kidney Injury [baseline to 73 hrs post-operatively]
4. Cell Cycle Stress [baseline to 73 hrs post-operatively]
Mesures des résultats secondaires
1. Biomarkers of Hepatic injury [baseline to 24 hours post-operatively]
2. Biomarkers of Kidney Injury [baseline to 24 hours post-operatively]
3. Cell Cycle Stress [baseline to 24 hours post-operatively]
4. Biomarkers of Myocardial Injury [baseline to 24 hours post-operatively]
5. Urine Output [baseline to 73 hrs post-operatively]
6. Vasopressors Usage [baseline to 73 hrs post-operatively]
