Comparing Continuous Venovenous Hemodiafiltration and Peritoneal Dialysis in Critically Ill Patients with Acute Kidney Injury: A Pilot Study

2011 ◽  
Vol 31 (4) ◽  
pp. 422-429 ◽  
Author(s):  
Jacob George ◽  
Sandeep Varma ◽  
Sajeev Kumar ◽  
Jose Thomas ◽  
Sreepa Gopi ◽  
...  

BackgroundThere are few reports on the role of peritoneal dialysis in critically ill patients requiring continuous renal replacement therapies.MethodsPatients with acute kidney injury and multi-organ involvement were randomly allotted to continuous venovenous hemodiafiltration(CVVHDF, group A) or to continuous peritoneal dialysis (CPD, group B). Cause and severity of renal failure were assessed at the time of initiating dialysis. Primary outcome was the composite correction of uremia, acidosis, fluid overload, and hyperkalemia. Secondary outcomes were improvement of sensorium and hemodynamic instability, survival, and cost.ResultsGroups A and B comprised 25 patients each with mean ages of 45.32 ± 17.53 and 48.44 ± 17.64 respectively. They received 21.68 ± 13.46 hours and 66.02 ± 69.77 hours of dialysis respectively ( p = 0.01). Composite correction was achieved in 12 patients of group A (48%) and in 14 patients of group B (56%). Urea and creatinine clearances were significantly higher in group A (21.72 ± 10.41 mL/min and 9.36 ± 4.93 mL/min respectively vs. 22.13 ± 9.61 mL/min and 10.5 ± 6.07 mL/min, p < 0.001). Acidosis was present in 21 patients of group A (84%) and in 16 of group B (64%); correction was better in group B ( p < 0.001). Correction of fluid overload was faster and the amount of ultrafiltrate was significantly higher in group A (20.31 ± 21.86 L vs. 5.31 ± 5.75 L, p < 0.001). No significant differences were seen in correction of hyperkalemia, altered sensorium, or hemodynamic disturbance. Mortality was 84% in group A and 72% in group B. Factors that influenced outcome were the APACHE (Acute Physiology and Chronic Health Evaluation) II score ( p = 0.02) and need for ventilatory support ( p < 0.01). Cost of disposables was higher in group A than in group B [INR7184 ± 1436 vs. INR3009 ± 1643, p < 0.001 (US$1 = INR47)].ConclusionsBased on this pilot study, CPD may be a cost-conscious alternative to CVVHDF; differences in metabolic and clinical outcomes are minimal.

Critical Care ◽  
2008 ◽  
Vol 12 (4) ◽  
pp. 169 ◽  
Author(s):  
Sean M Bagshaw ◽  
Patrick D Brophy ◽  
Dinna Cruz ◽  
Claudio Ronco

2011 ◽  
Vol 2011 ◽  
pp. 1-8 ◽  
Author(s):  
Masanori Abe ◽  
Noriaki Maruyama ◽  
Shiro Matsumoto ◽  
Kazuyoshi Okada ◽  
Takayuki Fujita ◽  
...  

We conducted a prospective, randomized study to compare conventional continuous venovenous hemodiafiltration (CVVHDF) with sustained hemodiafiltration (SHDF) using an acetate-free dialysate. Fifty critically ill patients with acute kidney injury (AKI) who required renal replacement therapy were treated with either CVVHDF or SHDF. CVVDHF was performed using a conventional dialysate with an effluent rate of 25 mL⋅kg−1⋅h−1, and SHDF was performed using an acetate-free dialysate with a flow rate of 300−500 mL/min. The primary study outcome, 30 d survival rate was 76.0% in the CVVHDF arm and 88.0% in the SHDF arm (NS). Both the number of patients who showed renal recovery (40.0% and 68.0%, CVVHDF and SHDF, resp.;P<.05), and the hospital stay length (42.3 days and 33.7 days, CVVHDF and SHDF, resp.;P<.05), significantly differed between the two treatments. Although the total convective volumes did not significantly differ, the dialysate flow rate was higher and mean duration of daily treatment was shorter in the SHDF treatment arm. Our results suggest that compared with conventional CVVHDF, more intensive renal support in the form of post-dilution SHDF with acetate-free dialysate may accelerate renal recovery in critically ill patients with AKI.


2010 ◽  
Vol 29 (4) ◽  
pp. 331-338 ◽  
Author(s):  
Jorge Cerda ◽  
Geoffrey Sheinfeld ◽  
Claudio Ronco

2020 ◽  
Vol 52 (2) ◽  
pp. 351-361 ◽  
Author(s):  
Eman Salah Albeltagy ◽  
Abeer Mohammed Abdul-Mohymen ◽  
Doaa Refaat Amin Taha

2016 ◽  
Vol 60 (6) ◽  
pp. 3587-3590 ◽  
Author(s):  
Joost B. Koedijk ◽  
Corinne G. H. Valk-Swinkels ◽  
Tom A. Rijpstra ◽  
Daan J. Touw ◽  
Paul G. H. Mulder ◽  
...  

The objective of this study was to describe the pharmacokinetics of cefotaxime (CTX) in critically ill patients with acute kidney injury (AKI) when treated with continuous renal replacement therapy (CRRT) in the intensive care unit (ICU). This single-center prospective observational pilot study was performed among ICU-patients with AKI receiving ≥48 h concomitant CRRT and CTX. CTX was administered intravenously 1,000 mg (bolus) every 6 h for 4 days. CRRT was performed as continuous venovenous hemofiltration (CVVH). Plasma concentrations of CTX and its active metabolite desacetylcefotaxime (DAC) were measured during CVVH treatment. CTX plasma levels and patient data were used to construct concentration-time curves. By using this data, the duration of plasma levels above 4 mg/liter (four times the MIC) was calculated and analyzed. Twenty-seven patients were included. The median CTX peak level was 55 mg/liter (range, 19 to 98 mg/liter), the median CTX trough level was 12 mg/liter (range, 0.8 to 37 mg/liter), and the median DAC plasma level was 15 mg/liter (range, 1.5 to 48 mg/liter). Five patients (19%) had CTX plasma levels below 4 mg/liter at certain time points during treatment. In at least 83% of the time any patient was treated with CTX, the CTX plasma level stayed above 4 mg/liter. A dosing regimen of 1,000 mg of CTX given four times daily is likely to achieve adequate plasma levels in patients with AKI treated with CVVH. Dose reduction might be a risk for suboptimal treatment.


2017 ◽  
Vol 18 (1) ◽  
Author(s):  
Nawal Salahuddin ◽  
Mustafa Sammani ◽  
Ammar Hamdan ◽  
Mini Joseph ◽  
Yasir Al-Nemary ◽  
...  

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