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Reducing Acute Kidney Injury Occurence by Administering Angiotensin II

Phase 3
Completed
Conditions
Cardiac Surgery
Vasoplegia
Hyperreninemia
Interventions
Registration Number
NCT05199493
Lead Sponsor
Universität Münster
Brief Summary

The aim of this study is to evaluate whether adding angiotensin II to the standard of care is superior compared to the standard of care alone with respect to kidney damage (personalized approach) after cardiac surgery.

Detailed Description

Vasoplegic syndrome is a form of distributive shock that is characterized by low arterial pressure with reduced systemic vascular resistance and normal or elevated cardiac output that occurs in 5 to 25% of patients undergoing cardiac surgery. Patients with vasoplegic shock after cardiac surgery are at higher risk of organ failure, including acute kidney injury (AKI). Postsurgical AKI is associated with several adverse outcomes. Attempts to prevent AKI have largely been futile so far. Prior studies often started with the interventions after an AKI event, when a decline of kidney function (i.e. glomerular filtration rate) was already established. Application of norepinephrine is currently considered as the first-line therapy for vasoplegic shock, but all catecholamines have adverse effects, including myocardial ischemia and arrhythmias. In a recent observational trial, we demonstrated that there is a dysregulation in the renin-angiotensin-aldosterone system (RAAS) likely caused by a reduced angiotensin-converting enzyme (ACE) activity after cardiac surgery. Elevated renin levels identified patients at risk for AKI and were associated with cardiovascular instability and increased AKI rate after cardiac surgery. Furthermore, elevated renin levels could be used to identify high-risk patients for cardiovascular instability and AKI who would benefit from timely intervention with angiotensin II that could improve their outcomes. Therefore, the application of angiotensin II to treat a postoperative hypotension would mean a hormone substitution.Shock after cardiac surgery is associated with increased mortality. Cardiopulmonary bypass (CPB) represents a common clinical setting of sympathetic nervous system activation and cardiovascular instability. Vasoplegia is a form of distributive shock that is characterized by low arterial pressure with reduced systemic vascular resistance and normal or elevated cardiac output. It occurs in 5 to 25% of patients undergoing cardiac surgery. Patients with vasoplegia after cardiac surgery are at higher risk of organ failure, including AKI, and have an increased mortality rate and longer hospital length of stay.

Clinical trials focusing on septic patients suggest that AT-II is a potent vasopressor. However, no human data exist whether the application of AT-II in cardiac surgery patients with y hyperreninemia high-risk patients identified by renin levels (individualized approach) reduces kidney damage and improves kidney function after cardiac surgery.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
64
Inclusion Criteria
  • Adult patients undergoing cardiac surgery with CPB
  • Cardiac index 2.1l/min per square meter
  • Written informed consent
  • D-renin (difference between post- and preoperative) ≥ 3.7 micro Unit/ml 4 h after CPB
  • Postoperative hypotension requiring vasopressors
Exclusion Criteria
  • Preexisting AKI (stage 1 and higher)
  • Patients with cardiac assist devices
  • Pregnant women, nursing women and women of childbearing potential
  • Known (Glomerulo-) Nephritis, interstitial nephritis or vasculitis
  • chronic kidney disease with estimated glomerular filtration rate (eGFR) < 30 ml/min
  • Dialysis dependent chronic kidney disease
  • Prior kidney transplant within the last to 12 months
  • Emergency surgery in the context of an acute coronary syndrome
  • Hypersensitivity to the active substance, or to any of the excipients of the study medication
  • Bronchospasm
  • Liver failure
  • Mesenteric ischemia
  • Participation in another intervention trial in the past 3 months
  • Persons with any kind of dependency on the investigator or employed by the institution responsible or investigator
  • Persons held in an institution by legal or official order

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
ControlControlIntravenous infusion placebo (matched infusion volume) over 12 h after start of infusion
Angiotensin IIAngiotensin IIIntravenous infusion of max. 80 ng/kg/min Angiotensin II (titrated for each individual patient by effect) over 12 h after start of infusion
Primary Outcome Measures
NameTimeMethod
• kidney damage after cardiac surgery identified by the difference between [TIMP-2]*[IGFBP7] levels 12h after randomization and [TIMP-2]*[IGFBP7] levels at randomization12 hours after start of intervention

The presence of tissue inhibitor of metalloproteinases (TIMP-2) and insulin-like growth-factor binding protein 7 (IGFBP7) in the urine will be measured.

Secondary Outcome Measures
NameTimeMethod
Mortality90 days after cardiac surgery
Severity of Acute Kidney Injury72 hours after cardiac surgery

Number of patients with KDIGO stage 1, KDIGO stage 2 or KDIGO stage 3)

Amount of volume application12 hours after start of intervention
Fluid status12 hours after start of intervention
Dose of vasopressor use during interventionDuring intervention, an average of 12 hours
Occurence of Acute Kidney Injury (AKI) according to the Kidney Disease: Improving Global Outcomes (KDIGO) criteria72 hours after cardiac surgery
Creatinine clearance on day one after cardiac surgeryOne day after cardiac surgery
Free-days through day 28 of vasoactive medications and mechanical ventilation28 days after cardiac surgery
Renal Recovery90 days after cardiac surgery

Renal recovery is defined as serum creatinine levels \< 0.5 mg/dL higher than baseline serum creatinine

Length of ICU (Intensive Care Unit) stayup to 90 days after cardiac surgery (until discharge)
Length of hospital stayup to 90 days after cardiac surgery (until discharge)
Use and duration of renal replacement therapyup to 90 days after cardiac surgery

Number of patients with renal replacement therapy

Major adverse kidney events (MAKE)90 days after cardiac surgery

Major adverse kidney events consisting of mortality, dialysis dependency, persistent renal dysfunction (defined as serum creatinine ≥ 2x compared to baseline value)

Effect of Angiotensin converting enzyme inhibitor (ACEi)/angiotensin II receptor blocker (ARBs) use on the effect of angiotensin II12 hours after intervention
Correlation between the severity of hyperreninemia and the effect of angiotensin II12 hours after intervention

Trial Locations

Locations (1)

University Hospital Muenster

🇩🇪

Münster, Germany

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