Metabolic and coagulation effects of citrate: down to the last detail!

The recently published Liver Citrate Anticoagulation Threshold (L-CAT) trial convincingly showed that continuous renal replacement therapy with regional citrate anticoagulation (CRRT-RCA) was safe and effective in patients with severely impaired liver function. Striking findings were a relatively low incidence of acid–base disorders and a markedly long 72-h filter survival [1]. Nonetheless, we would like to comment on two important metabolic issues. First, the low (2 %) incidence of severe metabolic alkalosis, defined as a pH >7.55, is probably highly underestimated. Indeed, we recently evaluated the occurrence of metabolic alkalosis defined either as a pH >7.50 or as an apparent strong ion difference (SIDa) >45 mmol/L according to the Stewart-Figge methodology [2] in patients undergoing CRRT-RCA with an isonatremic low-chloride containing diluted citrate solution. Calculating SIDa revealed a ninefold increase in the percentage of metabolic alkalosis [3]! Accordingly, applying the SIDa approach likely will uncover a substantially higher incidence of severe metabolic alkalosis in the L-CAT patients. Second, the L-CAT investigators attributed the long filter lifespan to a more automated fine-tuning of citrate and calcium dosing. However, we recently demonstrated that keeping post-filter ionized calcium (iCa) within tight limits (i.e., 0.2–0.3 mmol/L) during CRRT-RCA resulted in a 72-h filter survival comparable with that observed in the L-CAT trial [4]. Post-filter iCa levels in all L-CAT trial groups were within the same range and thus may have accounted for a better preserved filter patency.

The recently published Liver Citrate Anticoagulation Threshold (L-CAT) trial convincingly showed that continuous renal replacement therapy with regional citrate anticoagulation (CRRT-RCA) was safe and effective in patients with severely impaired liver function. Striking findings were a relatively low incidence of acid-base disorders and a markedly long 72-h filter survival [1]. Nonetheless, we would like to comment on two important metabolic issues. First, the low (2 %) incidence of severe metabolic alkalosis, defined as a pH >7.55, is probably highly underestimated. Indeed, we recently evaluated the occurrence of metabolic alkalosis defined either as a pH >7.50 or as an apparent strong ion difference (SIDa) >45 mmol/L according to the Stewart-Figge methodology [2] in patients undergoing CRRT-RCA with an isonatremic low-chloride containing diluted citrate solution. Calculating SIDa revealed a ninefold increase in the percentage of metabolic alkalosis [3]! Accordingly, applying the SIDa approach likely will uncover a substantially higher incidence of severe metabolic alkalosis in the L-CAT patients. Second, the L-CAT investigators attributed the long filter lifespan to a more automated fine-tuning of citrate and calcium dosing. However, we recently demonstrated that keeping post-filter ionized calcium (iCa) within tight limits (i.e., 0.2-0.3 mmol/L) during CRRT-RCA resulted in a 72-h filter survival comparable with that observed in the L-CAT trial [4]. Post-filter iCa levels in all L-CAT trial groups were within the same range and thus may have accounted for a better preserved filter patency.

Torsten Slowinski and Detlef Kindgen-Milles
We agree with Honoré et al. that the use of the Stewart-Figge approach probably would have discovered a higher incidence of alkalosis in the study population of the L-CAT study [1]. However, in clinical practice as well as in other studies investigating RCA the Henderson and Hasselbalch approach is used. For practical reasons in this multicenter trial and to allow better comparisons with other studies, we decided to use the latter approach in the L-CAT study.
The major outcome parameter for safety in the L-CAT study was the incidence of severe acidosis (pH ≤7.2) or alkalosis (pH ≥7.5) in patients with different degrees of liver failure. Most important, we found no significant difference between these groups and this was true not only for pH, but also for bicarbonate concentration. Thus, even if the overall incidence of alkalosis might have been slightly different using the Stewart-Figge approach, most probably no differences between the study groups would have been detected this way.
Regarding the problem of metabolic alkalosis during RCA, it is of note that other colleagues, i.e., Oudemannsvan Straaten et al. [5], reported a significantly higher incidence of metabolic alkalosis (bicarbonate >30 mmol/L) in patients treated with conventional bicarbonate containing solutions in systemic anticoagulated continuous venovenous hemofiltration (CVVH; 26 %) compared with those who were treated with RCA-CVVH (9 %). This observation clearly shows an urgent need to analyze different protocols in CRRT with regard to their efficiency to control acid-base state.
Of note, we agree that keeping ionized calcium concentrations within the extracorporeal circuit in tight limits is the most important task in terms of avoiding filter clotting in RCA-CRRT. In vitro data showed that iCa