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Regional citrate anticoagulation for continuous renal replacement therapy
- Source :
- Current opinion in critical care. 24(6)
- Publication Year :
- 2018
-
Abstract
- The delivery of an effective dialysis dose in continuous renal replacement therapy (CRRT) depends on adequate anticoagulation of the extracorporeal circuit. In most patients, either systemic heparin anticoagulation (SHA) or regional citrate anticoagulation (RCA) is used. This review will outline the basics and rationale of RCA and summarize data on safety and efficacy of both techniques.The basic principle of RCA is to reduce the level of ionized calcium in the extracorporeal circuit via infusion of citrate. This way, effective anticoagulation restricted to the extracorporeal circuit is achieved. SHA and RCA were compared in a variety of studies. RCA significantly prolonged filter lifetime, reduced bleeding complications and provided excellent control of uremia and acid-base status. RCA was also safe in the majority of patients with impaired liver function, whereas caution must be exerted in those with severe multiorgan failure and persistent hyperlactatemia.RCA per se is safe and effective for anticoagulation of CRRT. Compared to SHA, efficacy of anticoagulation is improved and adverse effects are reduced. RCA can be recommended as the anticoagulation mode of choice for CRRT in most ICU patients.
- Subjects :
- Dose-Response Relationship, Drug
business.industry
medicine.medical_treatment
Critical Illness
030232 urology & nephrology
Anticoagulants
030208 emergency & critical care medicine
Guidelines as Topic
Heparin
Acute Kidney Injury
Critical Care and Intensive Care Medicine
Extracorporeal
Citric Acid
Renal Replacement Therapy
03 medical and health sciences
0302 clinical medicine
Anesthesia
Citrate anticoagulation
Medicine
Humans
Renal replacement therapy
business
Dialysis
medicine.drug
Subjects
Details
- ISSN :
- 15317072
- Volume :
- 24
- Issue :
- 6
- Database :
- OpenAIRE
- Journal :
- Current opinion in critical care
- Accession number :
- edsair.doi.dedup.....8b8490ee9fa06bb7256d79b08cc663e3