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Circulatory Management and Acute Kidney Injury in Patients Undergoing Partial Nephrectomy

Not Applicable
Completed
Conditions
Acute Kidney Injury
Interventions
Other: Goal-directed circulatory management
Other: Routine circulatory management
Registration Number
NCT02803372
Lead Sponsor
Peking University First Hospital
Brief Summary

The purpose of this study is to investigate whether circulatory management based on LiDCOrapid hemodynamic monitoring can reduce the incidence of acute kidney injury in patients undergoing partial nephrectomy when compared with routine circulatory management based on blood pressure and urine output monitoring

Detailed Description

Previous studies found that the incidence of acute kidney injury afer partial nephrectomy is higher than 30%. In addition to nephron loss induced by renal parenchyma resection, ischemia/reperfusion injury produced by clamping/unclamping of renal arteries is also an important reason. However, studies investigating the effect of circulatory management on the incidence of acute kidney injury after partial nephrectomy are limited.

It has been shown that perioperative hemodynamic optimization protected renal function in surgical patients. And in patients undergoing renal transplantation, adequate hydration and optimal perfusion enhances early graft function. The investigators hypothesize that hydration and circulatory management to guarantee optimal renal perfusion may decrease the occurrence of acute kidney injury after partial nephrectomy. The purpose of this study is to investigate whether circulatory management based on LiDCOrapid hemodynamic monitoring can reduce the incidence of acute kidney injury in patients undergoing partial nephrectomy when compared with routine circulatory management based on blood pressure and urine output monitoring.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
144
Inclusion Criteria
  1. Age > 18 years;
  2. Planning to undergo partial nephrectomy;
Exclusion Criteria
  1. Patients with renal function damage (chronic kidney disease stage 3-5) before surgery;
  2. Patients with arrhythmia or aortic valve diseases (moderate or higher degree stenosis/regurgitation);
  3. Patients who has participated in other trials.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention groupGoal-directed circulatory managementIn addition to routine monitoring, invasive LiDCOrapid is used to monitor mean arterial pressure (MAP), stroke volume variation (SVV) and cardiac index (CI). Intraoperative goal-directed circulatory management is performed, i.e., to maintain MAP \> 95 mmHg, SVV \< 6%, and CI 3.0-4.0 L/min/m2, started from renal artery clamping and maintained until the end of surgery.
Control groupRoutine circulatory managementRoutine monitoring is performed, which includes invasive blood pressure and urine output. Intraoperative routine circulatory management is performed, i.e., to maintain blood pressure within 20% from baseline level and urine output \> 0.5 ml/kg/h.
Primary Outcome Measures
NameTimeMethod
Incidence of acute kidney injury after surgeryDuring the first 3 days after surgery

Acute kidney injury is diagnosed according to KDIGO (Kidney Disease: Improving Global Outcomes) criteria

Secondary Outcome Measures
NameTimeMethod
Serum creatinine concentrationAt 3 and 6 months after surgery

Serum creatinine concentration

Length of stay in hospital after surgeryFrom end of surgery to 30 days after surgery

Length of stay in hospital after surgery

Incidence of postoperative complicationsFrom end of surgery to 30 days after surgery

Incidence of complications within 30 days after surgery

Trial Locations

Locations (1)

Department of Anesthesiology and Critical Care Medicine, Peking University First Hospital

🇨🇳

Beijing, Beijing, China

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