ASN's Mission

To create a world without kidney diseases, the ASN Alliance for Kidney Health elevates care by educating and informing, driving breakthroughs and innovation, and advocating for policies that create transformative changes in kidney medicine throughout the world.

learn more

Contact ASN

1401 H St, NW, Ste 900, Washington, DC 20005

email@asn-online.org

202-640-4660

The Latest on X

Kidney Week

Please note that you are viewing an archived section from 2023 and some content may be unavailable. To unlock all content for 2023, please visit the archives.

Abstract: TH-PO508

Regional Citrate Anticoagulation in Continuous Renal Replacement Therapy in Children: Opportunities for Optimization

Session Information

  • Pediatric Nephrology - I
    November 02, 2023 | Location: Exhibit Hall, Pennsylvania Convention Center
    Abstract Time: 10:00 AM - 12:00 PM

Category: Pediatric Nephrology

  • 1900 Pediatric Nephrology

Authors

  • Santana, Danilo, Universidade de Sao Paulo Hospital das Clinicas, Sao Paulo, São Paulo, Brazil
  • Ortega, Caroline Sartori, Universidade de Sao Paulo Hospital das Clinicas, Sao Paulo, São Paulo, Brazil
  • Nóbrega, Lilian Caroline da Silva, Universidade de Sao Paulo Hospital das Clinicas, Sao Paulo, São Paulo, Brazil
  • Luglio, Michele, Universidade de Sao Paulo Hospital das Clinicas, Sao Paulo, São Paulo, Brazil
  • Watanabe, Andreia, Universidade de Sao Paulo Hospital das Clinicas, Sao Paulo, São Paulo, Brazil
  • Carvalho, Werther Brunow de, Universidade de Sao Paulo Hospital das Clinicas, Sao Paulo, São Paulo, Brazil
Background

Regional citrate anticoagulation (RCA) is based on blood citrate concentration of 3-4 mmol/L to reach post filter ionized calcium (Cai) of 0,25-0,40 mmol/L in continuous hemodiafiltration (CVVHDF). However, it can lead to metabolic complications of citrate accumulation.

Methods

From May 2019 to Dec 2022, 5,5% (109/1970) of patients admitted in a PICU were submitted to CVVHDF using RCA with 2,2% citrate. 25 patients were excluded for CVVHDF <24h, and 3 others for prior CVVHDF. Data related to minimum magnesemia was analyzed to sensitize the results.

Results

From the 81 patients included, 56,8% were girls, the age was 4.2 years (1.1-12.8) and the weight 13 kg (8,1-36,3). Organic dysfunctions were cardiovascular in 64,2%, pulmonary in 70,4% and hepatic in 65,4%, and the mortality rate was 51.9%. Hypomagnesemia (Mg<1,7mg/dL) was observed in 64% of patients, and the minimum magnesemia was 1,6mg/dL (1,4-1,8), where blood flow rate was 6ml/kg/min (3,4-7,5), the replacement+dialisate fluid rate of 65 ml/kg/h (47-92), blood citrate concentration of 1,7 mmol/L (1,4-2,6), citrate dosage of 0,6mmol/kg/h (0,35-0,85), reaching CaT/Cai (citrate GAP) of 2,01 (1,89-2,03). Only 4 patients presented citrate acummulation (citrate GAP >2,5). Patients <1 years of age reached larger blood flow rate [7,7 (6,7-11,7) vs 4,8 (3-6,5), p<0,001], smaller blood citrate concentration [1,5 (1,4-1,9) vs 1,9 (1,4-2,80), p=0,048], larger citrate dosage [0,75 (0,64-1,09) vs 0,53 (0,32-0,77), p=0,008], and larger citrate GAP [2,14 (1,96-2,33) vs 1,96 (1,79-2,09), p=0,035]. Blood citrate concentration tended to be smaller in the circuits with <36 horas of duration (48,7%), [1,7mmol/L (1,3-2,0) vs 1,9 (1,4-2,8) vs p=0,062], and no difference was observed in the citrate dose (p=0,117) or post filter Cai (p=0,385).

Conclusion

The low circuit patency obtained is probably associated with the low blood citrate concentration used. Children <1 year of age presented good tolerance to high doses of citrate, with a low rate of citrate accumulation. It is possible that children tolerate citrate dosages of 0,6-0,85 mmol/kg/h, reaching blood citrate concentration of 3mmol/L by adjusting the blood flow rate to 2-5 ml/kg/min, improving circuits patency without major metabolic consequences.