Abstract

BackgroundRegional citrate anticoagulation may cause a negative calcium balance, systemic hypocalcemia and parathormone (PTH) activation but randomzed studies are not available. Aim was to determine the effect of citrate dose on calcium (Ca) and magnesium (Mg) balance, PTH and Vitamin D.MethodsSingle center prospective randomized study. Patients, requiring continuous venovenous hemofiltration (CVVH) with citrate, randomized to low dose citrate (2.5 mmol/L) vs. high dose (4.5 mmol/L) for 24 h, targeting post-filter ionized calcium (pfiCa) of 0.325–0.4 mmol/L vs. 0.2–0.275 mmol/L, using the Prismaflex® algorithm with 100% postfilter calcium replacement. Extra physician-ordered Ca and Mg supplementation was performed aiming at systemic iCa > 1.0 mmol/L. Arterial blood, effluent and post-filter aliquots were taken for balance calculations (area under the curve), intact (i), oxidized (ox) and non-oxidized (nox) PTH, 25-hydroxy-Vitamin D (25D) and 1,25-dihydroxy-Vitamin D (1,25D).Results35 patients were analyzed, 17 to high, 18 to low citrate. Mean 24-h Ca balance was - 9.72 mmol/d (standard error 1.70) in the high vs − 1.18 mmol/d (se 1.70)) (p = 0.002) in the low citrate group and 24-h Mg-balance was − 25.99 (se 2.10) mmol/d vs. -17.63 (se 2.10) mmol/d (p = 0.008) respectively. Physician-ordered Ca supplementation, higher in the high citrate group, resulted in a positive Ca-balance in both groups. iPTH, oxPTH or noxPTH were not different between groups. Over 24 h, median PTH decreased from 222 (25th–75th percentile 140–384) to 162 (111–265) pg/ml (p = 0.002); oxPTH from 192 (124–353) to 154 pg/ml (87–231), p = 0.002. NoxPTH did not change significantly. Mean 25 D (standard deviation), decreased from 36.5 (11.8) to 33.3 (11.2) nmol/l (p = 0.003), 1,25D rose from 40.9 pg/ml (30.7) to 43.2 (30.7) pg/ml (p = 0.046), without differences between groups.ConclusionsA higher citrate dose caused a more negative CVVH Ca balance than a lower dose, due to a higher effluent Calcium loss. Physician-ordered Ca supplementation, targeting a systemic iCa > 1.0 mmol/L, higher in the high citrate group, resulted in a positive Ca-balance in both groups. iPTH and oxPTH declined, suggesting decreased oxidative stress, while noxPTH did not change. 25D decreased while 1,25-D rose. Mg balance was negative in both groups, more so in the high citrate group.Trial registrationClinicalTrials.gov: NCT02194569. Registered 18 July 2014.

Highlights

  • Regional citrate anticoagulation may cause a negative calcium balance, systemic hypocalcemia and parathormone (PTH) activation but randomzed studies are not available

  • Post-filter ionized calcium (iCa) was measured using the ABL800 Flex blood gas analyzer (Radiometer, Copenhagen, Denmark). This habit is common, though the reliability of measuring iCa in this low range has been challenged [28]. This randomized controlled trial in critically ill patients on citrate continuous venovenous hemofiltration (CVVH) is the first to demonstrate that calcium loss depends on citrate dose

  • Physician-ordered Ca supplementation, targeting a systemic iCa > 1.0 mmol/L higher in the high citrate group, prevented a negative Ca balance. iPTH was increased, both at baseline and at 24-h but declined during the first 24 h of citrate CVVH. This decline in iPTH seems to be related to the systemic iCa target used

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Summary

Introduction

Regional citrate anticoagulation may cause a negative calcium balance, systemic hypocalcemia and parathormone (PTH) activation but randomzed studies are not available. Regional anticoagulation with citrate is recommended as first-line anticoagulation for patients on continuous renal replacement therapy (CRRT) [1]. This method is based on pre-filter administration of citrate, which lowers ionized calcium (iCa) by chelation, thereby inhibiting the clotting cascade within the filter, and on the concomitant replacement of calcium (Ca) via the post-filter circuit or a separate line. Insufficient replacement of the increased loss of Ca as Ca citrate complexes in the effluent may lead to a negative Ca balance, systemic hypocalcemia [2,3,4,5] and further activation of parathormone (PTH), which may already be activated due to renal dysfunction. Monitoring of the total to ionized calcium ratio (T/ iCa) is generally utilized as a marker to detect citrate accumulation

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