Targeted Blood-pressure Management and Acute Kidney Injury After Coronary Artery Bypass Surgery

Overview

Acute renal injury (AKI) is a common complication after cardiac surgery and is associated with worse outcomes. It is now realized that intraoperative hypotension is an important risk factor for the development of AKI. In a recent randomized controlled trial of patients undergoing major noncardiac surgery, intraoperative individualized blood-pressure management reduced the incidence of postoperative organ dysfunction. The investigators hypothesize that, for patients undergoing off-pump CABG, targeted blood-pressure management during surgery may also reduce the incidence of postoperative AKI.

Full Title of Study: “Impact of Targeted Blood-pressure Management on Incidence of Acute Kidney Injury After Off-pump Coronary Artery Bypass Surgery: A Randomized Controlled Trial”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Prevention
    • Masking: Double (Participant, Outcomes Assessor)
  • Study Primary Completion Date: December 2025

Detailed Description

Acute renal injury (AKI) is a common complication after cardiac surgery. In patients undergoing noncardiac surgery, intraoperative hypotension may lead to hypoperfusion of important organs and result in organ injuries such as AKI, myocardial injury, and stroke. The development of organ injuries is associated with wose outcomes including higher 30-day or even 1-year mortality. In a recent randomized controlled trial, patients undergoing major noncardiac surgery received either individualized (systolic blood pressure [SBP] maintained within 10% of the reference level) or standard (SBP maintained above 80 mmHg or within 40% of the reference level) blood-pressure management strategy during surgery. The results showed that individualized blood-pressure management reduced the incidence of postoperative organ dysfunction. Intraoperative hypotension is very common during off-pump coronary artery bypass grafting (CABG) surgery. The investigators hypothesize that, for patients undergoing off-pump CABG, good blood-pressure management with norepinephrine may also reduce the incidence of postoperative AKI. The purpose of this study is to investigate the effect of targeted blood-pressure management during off-pump CABG surgery on the incidence of postoperative AKI.

Interventions

  • Drug: Targeted blood-pressure management
    • Prophylactic norepinephrine infusion is started before anesthetic induction and maintained throughout surgery. The target is to maintain systolic blood pressure at 110 mmHg or higher.
  • Drug: Routine blood-pressure management
    • Phenylephrine (25-50 ug) is injected or vasopressors is infused only when necessary. The target is to maintain systolic blood pressure at 90 mmHg or higher during surgery.

Arms, Groups and Cohorts

  • Experimental: Targeted blood-pressure management
    • Prophylactic norepinephrine infusion is started at the beginning of anesthetic induction and maintained throughout surgery. The target is to maintain systolic blood pressure at 110 mmHg or higher during surgery.
  • Active Comparator: Routine blood-pressure management
    • Phenylephrine (25-50 ug) is injected or vasopressors is infused only when necessary. The target is to maintain systolic blood pressure at 90 mmHg or higher during surgery.

Clinical Trial Outcome Measures

Primary Measures

  • Incidence of acute kidney injury (AKI) within 7 days after surgery
    • Time Frame: Up to 7 days after surgery
    • Development of AKI within 7 days after surgery is diagnosed according to the Kidney Disease Improving Global Outcomes (KDIGO) criteria

Secondary Measures

  • Classification of AKI within 7 days after surgery
    • Time Frame: Up to 7 days after surgery
    • Development of AKI within 7 days after surgery is diagnosed according to the KDIGO criteria
  • Incidence of delirium within 7 days after surgery
    • Time Frame: Up to 7 days after surgery
    • Development of delirium within 7 days after surgery is assessed with the Confusion Assessment Method (3D-CAM for patients without mechanical ventilation and CAM-ICU for patients with mechanical ventilation).
  • Duration of mechanical ventilation after surgery
    • Time Frame: Up to 30 days after surgery
    • Duration of mechanical ventilation after surgery
  • Length of stay in intensive care unit (ICU) after surgery
    • Time Frame: Up to 30 days after surgery
    • Length of stay in intensive care unit (ICU) after surgery
  • Length of stay in hospital after surgery
    • Time Frame: Up to 30 days after surgery
    • Length of stay in hospital after surgery
  • Incidence of major adverse cardiovascular events (MACEs) within 30 days after surgery
    • Time Frame: Up to 30 days after surgery
    • MACEs within 30 days after surgery include cardiovascular death, non-fatal cardiac arrest, acute myocardial infarction, revascularization, and stroke.
  • Incidence of non-MACE complications within 30 days after surgery
    • Time Frame: Up to 30 days after surgery
    • Non-MACE complications within 30 days after surgery indicate new-onset medical conditions other than MACEs that produce harmful effects on patients’ recovery and required therapeutic intervention.
  • All-cause 30-day mortality
    • Time Frame: At 30 days after surgery
    • All-cause 30-day mortality
  • 2-year overall survival after surgery
    • Time Frame: Up to 2 years after surgery
    • 2-year overall survival after surgery
  • 2-year major adverse cardiovascular event (MACE)-free survival after surgery
    • Time Frame: Up to 2 years after surgery
    • MACEs within 2 years after surgery include cardiovascular death, non-fatal cardiac arrest, acute myocardial infarction, revascularization, and stroke.
  • Cognitive function in 1- and 2-year survivors
    • Time Frame: At the end of the 1st and 2nd years after surgery
    • Cognitive function in 1- and 2-year survivors is assessed with the modified Telephone Interview for Cognitive Status (TICS-m, score ranges from 0 to 40, with higher score indicating better function).
  • Quality of life in 1- and 2- year survivors: SF-36
    • Time Frame: At the end of the 1st and 2nd years after surgery
    • Quality of life in 1- and 2-year survivors is assessed with the 36-Item Short Form Health Survey (SF-36). The SF-36 evaluates 8 different domains of quality of life, i.e., physical functioning, role physical, bodily pain, general health, vitality, social functioning, role emotional, and mental health. The score of each domain ranges from 0 to 100, with high score indicating better function.

Participating in This Clinical Trial

Inclusion Criteria

  • Age ≥ 50 years; – Scheduled to undergo off-pump CABG surgery. Exclusion Criteria:

  • Refuse to participate; – Untreated or uncontrolled severe hypertension (systolic blood pressure ≥180 mmHg or diastolic blood pressure ≥110 mmHg); – Chronic kidney disease with a glomerular filtration rate < 30 ml/min/1.73 m2 or end-stage renal disease requiring renal-replacement therapy; – Inability to communicate during the preoperative period because of coma, profound dementia, language barrier, or end-stage disease; – Requirement of vasopressors/inotropics to maintain blood pressure before surgery; – Second or emergency surgery; – Expected survival of less than 24 hours.

Gender Eligibility: All

Minimum Age: 50 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Peking University First Hospital
  • Provider of Information About this Clinical Study
    • Principal Investigator: Dong-Xin Wang, Professor and Chairman, Department of Anaesthesiology and Critical Care Medicine – Peking University First Hospital
  • Overall Official(s)
    • Dong-Xin Wang, MD, PhD, Principal Investigator, Peking University First Hospital
  • Overall Contact(s)
    • Dong-Xin Wang, MD, PhD, 8610-83572784, wangdongxin@hotmail.com

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