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1 irst patient received continuous veno-venous hemofiltration.
2 %FO) in the intensive care unit (ICU) before hemofiltration.
3 ately transitioned to continuous veno-venous hemofiltration.
4 and kidney transplantation and responded to hemofiltration.
5 Two patients required continuous venovenous hemofiltration, 1 of whom died and 1 of whom survived.
7 ors can be removed from the circulation with hemofiltration and that adsorption plays an important ro
10 ation cardiac arrest, continuous veno-venous hemofiltration, and hyperbilirubinemia during extracorpo
11 transport on ECLS, minimal anticoagulation, hemofiltration, and optimal systemic oxygen delivery.
13 cial kidney (BAK) consists of a conventional hemofiltration cartridge in series with a renal tubule a
14 tificial kidney consisting of a conventional hemofiltration cartridge in series with a renal tubule a
15 The use of a modified continuous venovenous hemofiltration circuit for rewarming in a juvenile goat
16 imals were placed in a continuous venovenous hemofiltration circuit with either a sham RAD without ce
17 oxygenator (0.65 m) was inserted within the hemofiltration circuit, either upstream (n = 7) or downs
20 s were connected to a continuous veno-venous hemofiltration (CVVH) (filtration: 80 ml/kg/h) or sham c
21 s is not equivalent on continuous venovenous hemofiltration (CVVH) compared with continuous venovenou
23 F-80 dialyzers during continuous venovenous hemofiltration (CVVH) or continuous venovenous hemodialy
25 nstrates that the combination of a synthetic hemofiltration device and a renal tubule cell therapy de
27 mmediately placed in a continuous venovenous hemofiltration extracorporeal circuit with either a sham
29 amine have shown that it is ineffective, and hemofiltration has become increasingly popular as a choi
30 al substitution therapy with hemodialysis or hemofiltration has been the only successful long-term ex
33 d correcting metabolic acidosis, high-volume hemofiltration (HVHF) might halt the vicious circle lead
34 nstrate that the addition of cell therapy to hemofiltration in an acutely uremic animal model with se
35 poreal CO2 removal and continuous venovenous hemofiltration in patients with acute respiratory distre
37 of patients receiving continuous veno-venous hemofiltration or continuous venovenous hemofiltration w
38 e undergone aggressive continuous venovenous hemofiltration or hemodiafiltration at Brooke Army Medic
39 on (2C); equivalency of continuous veno-veno hemofiltration or intermittent hemodialysis (2B); prophy
40 (1A); equivalency of continuous veno-venous hemofiltration or intermittent hemodialysis (2B); prophy
41 echanical fluid removal via ultrafiltration, hemofiltration, or hemodialysis may be needed for refrac
43 uids should be administered judiciously, and hemofiltration should be instituted early to remove flui
45 cal application of human progenitor cells in hemofiltration units, and additional studies may ultimat
46 taneously placed catheter and hepatic venous hemofiltration using a double balloon catheter positione
47 our throughout CPB, simultaneously replacing hemofiltration volume with a balanced salt solution (HF
49 nous hemofiltration or continuous venovenous hemofiltration with a 0.9-m2 polyacrylonitrile filter at
52 ncluding hemoperfusion, plasma exchange, and hemofiltration with hemoperfusion were associated with l
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