Quantification of systemic delivery of substrates for intermediate metabolism during citrate anticoagulation of continuous renal replacement therapy
Language English Country Switzerland Media print-electronic
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
22212643
DOI
10.1159/000334641
PII: 000334641
Knihovny.cz E-resources
- MeSH
- Acute Kidney Injury therapy MeSH
- Anticoagulants metabolism therapeutic use MeSH
- Equipment Design MeSH
- Glucose analogs & derivatives metabolism therapeutic use MeSH
- Heparin therapeutic use MeSH
- Citric Acid metabolism therapeutic use MeSH
- Lactic Acid metabolism MeSH
- Humans MeSH
- Renal Replacement Therapy instrumentation methods MeSH
- Prospective Studies MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- acid citrate dextrose MeSH Browser
- Anticoagulants MeSH
- Glucose MeSH
- Heparin MeSH
- Citric Acid MeSH
- Lactic Acid MeSH
BACKGROUND: There are limited data on systemic delivery of metabolic substrates during citrate anticoagulation. The direct citrate measurements are usually not available. METHODS: Patients on 2.2% acid-citrate-dextrose (ACD, n = 41) were compared to a control group on unfractionated heparin (n = 17). All were treated on 1.9-m(2) polysulfone filters. Samples were taken from the central venous catheter, ports pre- and post-filter and from effluent. RESULTS: The gain of citrate in CVVH (n = 18) was not different from CVVHDF (n = 23, p = 0.8). Mean gain of citrate was 25.4 ± 6.4 mmol/h. The systemic loads of lactate (p = 0.12) and glucose (p = 0.23) in CVVH were similar to CVVHDF. Mean inputs of lactate and glucose were 62.9 ± 21.1 and 26.6 ± 10.4 mmol/h, respectively. The mean difference between post- and prefilter unmeasured anions (d-UA) correlated with mean difference of citrate concentrations (p < 0.0001, r(2) = 0.66). The estimated caloric load of the citrate modalities was 5,536 ± 1,385 kJ/ 24 h. CONCLUSIONS: ACD might represent a significant load of metabolic substrates, particularly if used with lactate buffer. Systemic delivery of citrate can be predicted using d-UA in the extracorporeal circuit.
References provided by Crossref.org
Nutrition in Critically Ill Children with AKI on Continuous RRT: Consensus Recommendations