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Remote Ischemic Preconditioning After Cardiac Surgery

Not Applicable
Conditions
Cardiac Surgery, Aortocoronary Bypass
Interventions
Procedure: Remote ischemic preconditioning (RIPC)
Registration Number
NCT02997748
Lead Sponsor
University Hospital Muenster
Brief Summary

Acute kidney injury (AKI) is a well-recognized complication after cardiac surgery with cardiopulmonary bypass (CPB). The aim of this study is to reduce the incidence of AKI by implementing remote ischemic preconditioning and to evaluate the dose-response relationship using the biomarkers urinary \[TIMP-2\] \*\[IGFBP7\] in high risk patients undergoing cardiac surgery.

Detailed Description

Acute kidney injury (AKI) complicates 7-19% of cardiac surgical procedures. The investigators recently found that remote ischemic preconditioning (RIPC) using transient external compression of the upper arm prior to cardiac surgery was effective for reducing the occurrence of AKI (37.5% compared to 52.5% with sham; absolute risk reduction (ARR),15%; 95% CI, 2.56% to 27.44%; P=0.02). Fewer patients treated with RIPC received renal replacement therapy (RRT) (5.8% versus 15.8%; ARR, 10%; 95% CI, 2.25% to 17.75%; P=0.01). Moreover, the investigators found that the effectiveness of this intervention was strongly associated with the release of cell-cycle arrest biomarkers into the urine. Patients with urinary tissue inhibitor of metalloproteinases-2 and insulin-like growth factor-binding protein 7 (\[TIMP-2\]•\[IGFBP7\]) ≥ 0.5 (ng/ml)(ng/ml)/1000 before surgery had a significantly reduced rate of AKI compared to patients with lower urinary \[TIMP-2\]•\[IGFBP7\] concentration (relative risk (RR), 67%; 95% CI, 53% to 83%, P\<0.001) whereas the biomarker concentrations after surgery predicted AKI as previously shown. This effect makes sense because cell-cycle arrest is thought to be part of the protective mechanisms endothelial cells use when exposed to stress. Stimulating these responses with RIPC should reduce AKI. Importantly, only 56% of patients treated with RIPC achieved an increase in urine \[TIMP-2\]•\[IGFBP7\] to ≥ 0.5, and only in this group was the intervention effective-patients that did not achieve this level showed no benefit.

Our goal is to eventually design and conduct a Bayesian 2-stage adaptive design sequence trial to evaluate the effectiveness of RIPC to prevent AKI in patients undergoing cardiac surgery. The dimensions of dose include duration, intensity and number of cycles. However, before this trial can be designed we need to answer 4 questions: i. Do baseline urinary \[TIMP-2\]•\[IGFBP7\] levels predict AKI (enrichment)? ii. Do \[TIMP-2\]•\[IGFBP7\] changes elicited by RIPC predict protection (RIPC efficacy measure)? iii. Is there a dose-response relationship between RIPC "dose" and \[TIMP-2\]•\[IGFBP7\]? iv. Is a dose-escalation RIPC protocol where doses are increased for non-responders, feasible and safe within the anesthesia workflow for cardiac surgery cases (practical)?

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
180
Inclusion Criteria
  • Patients who are scheduled to undergo cardiac surgery with cardiopulmonary bypass
  • Cleveland Clinic Score >=6
Exclusion Criteria
  • Acute myocardial infarction up to 7 days before surgery
  • Age < 18 years
  • Off-pump cardiac surgery
  • Preexisting AKI
  • Chronic kidney disease (GFR < 30 ml/min)
  • Kidney transplantation within the last 12 months
  • Peripheral arterial occlusive disease
  • Pregnancy
  • Hepatorenal syndrome
  • Sulfonamide or thiazide medication within the last 7 days
  • Participation in another interventional trial

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Sham RIPCRemote ischemic preconditioning (RIPC)Three cycles of 5- min upper limb sham ischemia
RIPC-Group 4Remote ischemic preconditioning (RIPC)Three Cycles of 5-min upper limb ischemia. If there is no response this will be followed by 2 cycles of 10-min upper-limb ischemia
RIPC-Group 3Remote ischemic preconditioning (RIPC)Three cycles of 10-min upper limb ischemia
RIPC-Group 1Remote ischemic preconditioning (RIPC)Three cycles of 5- min upper limb ischemia
RIPC-Group 2Remote ischemic preconditioning (RIPC)Three cycles of 7-min upper limb ischemia
Primary Outcome Measures
NameTimeMethod
Change in urinary [TIMP-2]*[IGFBP7]within 12 hours after CPB

Biomarkers will be measured at different time points after to evaluate the effect of RIPC on \[TIMP-2\]\*\[IGFBP7\]

Secondary Outcome Measures
NameTimeMethod
MAKE 9090 days

major adverse kidney events

Dialysis within 7 days of surgery7 days
All-cause-mortality at 90 days90 d
AKI within 72 hours72 h
Dialysis at day 9090 days
Renal recovery at day 9090 days

Trial Locations

Locations (1)

University Hospital Muenster

🇩🇪

Muenster, Germany

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