Pediatric convective hemofiltration: Normocarb replacement fluid and citrate anticoagulation

被引:42
作者
Bunchman, TE
Maxvold, NJ
Brophy, PD
机构
[1] DeVos Childrens Hosp, Grand Rapids, MI 49503 USA
[2] Univ Michigan, Ann Arbor, MI 48109 USA
关键词
continuous venovenous hemofiltration (CVVH); normocarb; citrate anticoagulation; anticoagulant citrate dextrose solution formula A (ACD-A);
D O I
10.1053/j.ajkd.2003.08.026
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Continuous venovenous hemofiltration (CVVH) may be preferable over continuous venovenous hemodialysis (CVVHD) in sepsis; however, CVVH use is limited by the lack of commercially produced bicarbonate replacement solutions in the United States. Anticoagulation used for hemofiltration traditionally has been either heparin or citrate based, but to date, citrate protocols have been used predominately in CVVHD. When CVVH has been used with citrate anticoagulation, replacement solutions have had to be custom made in the pharmacy. Methods: We describe a protocol used in a series of 9 children with sepsis who underwent CVVH with the use of a commercially available bicarbonate solution (Normocarb; Dialysis Solutions Inc, Richmond Hill, Ontario, Canada) and a commercially available citrate solution (Anticoagulant Citrate Dextrose Solution Formula A [ACD-A]; Baxter Health Care, Deerfield, IL). This simplified approach to citrate anticoagulation with CVVH used Normocarb as a prefilter replacement solution under provisions of the 1997 Food and Drug Administration Modernization Act. Results: All patients had acceptable levels of solute and ultrafiltration clearance with this approach. CVVH circuit life averaged 71 hours (range, 37 to 131 hours), influenced in part by the industry recommendation to change the circuit at 72 hours, whereas no complications from this protocol were identified. Conclusion: Similar to CVVHD, this protocol is. effective and simple in its components, using industry-produced solutions, avoiding the need for pharmacy-made solutions, and limiting cost and potential risk for compounding errors. Although not the purpose of this report, the patient survival rate was 55%. (C) 2003 by the National Kidney Foundation, Inc.
引用
收藏
页码:1248 / 1252
页数:5
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