Optimal Mode of clearance in critically ill patients with Acute Kidney Injury (OMAKI) - a pilot randomized controlled trial of hemofiltration versus hemodialysis: a Canadian Critical Care Trials Group project

Critical Care - Tập 16 - Trang 1-9 - 2012
Ron Wald1,2, Jan O Friedrich2,3,4, Sean M Bagshaw5, Karen EA Burns2,3,4, Amit X Garg6, Michelle A Hladunewich7,8, Andrew A House6, Stephen Lapinsky4,9, David Klein2,3,4,10, Neesh I Pannu11, Karen Pope10, Robert M Richardson12, Kevin Thorpe10, Neill KJ Adhikari4,7
1Division of Nephrology, St.Michael's Hospital, Toronto, Canada
2Keenan Research Centre in the Li Ka Shing Knowledge Institute of St Michael's Hospital, Toronto, Canada
3Critical Care and Medicine Departments, St, Michael's Hospital, Toronto, Canada
4Interdepartmental Division of Critical Care, University of Toronto, Toronto, Canada
5Division of Critical Care Medicine, University of Alberta, Edmonton, Canada
6Division of Nephrology, London Health Sciences Centre, London, Canada
7Division of Nephrology, Sunnybrook Health Sciences Centre, Toronto, Canada
8Department of Critical Care Medicine and Sunnybrook Research Institute, Sunnybrook Health Sciences Centre, Toronto, Canada
9Division of Critical Care,, Mt.Sinai Hospital, Toronto, Canada
10Applied Health Research Centre, Li Ka Shing Knowledge Institute, St. Michael’s Hospital, Toronto, Canada
11Division of Nephrology, University of Alberta Hospital, Edmonton, Canada
12Division of Nephrology, University Health Network, Toronto, Canada

Tóm tắt

Among critically ill patients with acute kidney injury (AKI) needing continuous renal replacement therapy (CRRT), the effect of convective (via continuous venovenous hemofiltration [CVVH]) versus diffusive (via continuous venovenous hemodialysis [CVVHD]) solute clearance on clinical outcomes is unclear. Our objective was to evaluate the feasibility of comparing these two modes in a randomized trial. This was a multicenter open-label parallel-group pilot randomized trial of CVVH versus CVVHD. Using concealed allocation, we randomized critically ill adults with AKI and hemodynamic instability to CVVH or CVVHD, with a prescribed small solute clearance of 35 mL/kg/hour in both arms. The primary outcome was trial feasibility, defined by randomization of >25% of eligible patients, delivery of >75% of the prescribed CRRT dose, and follow-up of >95% of patients to 60 days. A secondary analysis using a mixed-effects model examined the impact of therapy on illness severity, defined by sequential organ failure assessment (SOFA) score, over the first week. We randomized 78 patients (mean age 61.5 years; 39% women; 23% with chronic kidney disease; 82% with sepsis). Baseline SOFA scores (mean 15.9, SD 3.2) were similar between groups. We recruited 55% of eligible patients, delivered >80% of the prescribed dose in each arm, and achieved 100% follow-up. SOFA tended to decline more over the first week in CVVH recipients (-0.8, 95% CI -2.1, +0.5) driven by a reduction in vasopressor requirements. Mortality (54% CVVH; 55% CVVHD) and dialysis dependence in survivors (24% CVVH; 19% CVVHD) at 60 days were similar. Our results suggest that a large trial comparing CVVH to CVVHD would be feasible. There is a trend toward improved vasopressor requirements among CVVH-treated patients over the first week of treatment. ClinicalTrials.gov: NCT00675818

Tài liệu tham khảo

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