Concurrent centrifugation plasmapheresis and continuous venovenous hemodiafiltration |
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Authors: | P. D. Yorgin D. K. Eklund A. Al-Uzri L. Whitesell A. A. Theodorou |
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Affiliation: | (1) Section of Nephrology, Department of Pediatrics, University of Arizona, Steele Memorial Children’s Research Center, Tucson, AZ 85724, USA e-mail: pyorgin@peds.arizona.edu Tel.: +1-520-626-6182, Fax: +1-520-626-5009, US;(2) Department of Pathology, University of Arizona, Steele Memorial Children’s Research Center, Tucson, AZ 85724, USA, US;(3) Section of Hematology and Oncology, Department of Pediatrics, University of Arizona, Steele Memorial Children’s Research Center, Tucson, AZ 85724, USA, US;(4) Section of Critical Care Medicine, Department of Pediatrics, University of Arizona, Steele Memorial Children’s Research Center, Tucson, AZ 85724, USA, US |
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Abstract: | Continuous venovenous hemofiltration/hemodiafiltration (CVVH/D) is commonly used to provide renal replacement therapy for critically ill patients who are hemodynamically unstable. Occasionally, the addition of plasmapheresis therapy is necessary for some conditions, including immune-mediated acute renal failure, sepsis, fulminant hepatic failure, and thrombotic thrombocytopenic purpura/hemolytic uremic syndrome. Most tertiary care facilities provide centrifugation plasmapheresis instead of membrane plasmapheresis, because of the requirement for both therapeutic plasma exchange and pheresis of cellular blood products. We report a new technique where centrifugation plasmapheresis and CVVHD (P-CVVHD) are combined and used concurrently. Blood from the patient was concurrently filtered utilizing a Hospal BSM 22 machine with a Multiflow 60 hemofilter and a Cobe Spectra continuous cell separator in a parallel configuration. P-CVVHD is technically possible and can be used for long periods of time with limited risks. There may be advantages to P-CVVHD compared with discontinuous combined CVVH/D and plasmapheresis therapy. Received: 10 June 1998 / Revised: 4 January 1999 / Accepted: 6 January 1999 |
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Keywords: | Hemofiltration Sepsis Acute renal failure Hemolytic anemia |
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