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Continuous renal replacement therapy and its impact on hyperammonaemia in acute liver failure
Stephen Warrillow, Caleb Fisher, Heath Tibballs, Michael Bailey, Colin McArthur, Pia Lawson-Smith, Bheemasenachar Prasad, Matthew Anstey, Bala Venkatesh, Gemma Dashwood, James Walsham, Andrew Holt, Ubbo Wiersema, David Gattas, Matthew Zoeller, Mercedes García Álvarez, Rinaldo Bellomo, On behalf of the Australasian Management of Acute Liver Failure Investigators (AMALFI)
Crit Care Resusc 2020; 22 (2): 158-165
- Stephen Warrillow 1, 2
- Caleb Fisher 1
- Heath Tibballs 1
- Michael Bailey 2, 3
- Colin McArthur 4, 5
- Pia Lawson-Smith 5
- Bheemasenachar Prasad 6
- Matthew Anstey 7
- Bala Venkatesh 8
- Gemma Dashwood 8
- James Walsham 8
- Andrew Holt 9
- Ubbo Wiersema 9
- David Gattas 10
- Matthew Zoeller 10
- Mercedes García Álvarez 11
- Rinaldo Bellomo 1, 2, 12, 13
- On behalf of the Australasian Management of Acute Liver Failure Investigators (AMALFI) 14
OBJECTIVE: Hyperammonaemia contributes to complications in acute liver failure (ALF) and may be treated with continuous renal replacement therapy (CRRT), but current practice is poorly understood.
DESIGN: We retrospectively analysed data for baseline characteristics, ammonia concentration, CRRT use, and outcomes in a cohort of Australian and New Zealand patients with ALF.
SETTING: All liver transplant ICUs across Australia and New Zealand.
PARTICIPANTS: Sixty-two patients with ALF.
MAIN OUTCOME MEASURES: Impact of CRRT on hyperammonaemia and patient outcomes.
RESULTS: We studied 62 patients with ALF. The median initial (first 24 h) peak ammonia was 132 μmol/L (interquartile range [IQR], 91–172), median creatinine was 165 μmol/L (IQR, 92–263) and median urea was 6.9 mmol/L (IQR, 3.1–12.0). Most patients (43/62, 69%) received CRRT within a median of 6 hours (IQR, 2–12) of ICU admission. At CRRT commencement, three-quarters of such patients did not have Stage 3 acute kidney injury (AKI): ten patients (23%) had no KDIGO creatinine criteria for AKI, 12 (28%) only had Stage 1, and ten patients (23%) had Stage 2 AKI. Compared with non-CRRT patients, those treated with CRRT had higher ammonia concentrations (median, 141 μmol/L [IQR, 102–198] v 91 μmol/L [IQR, 54–115]; P = 0.02), but a nadir Day 1 pH of only 7.25 (standard deviation, 0.16). Prevention of extreme hyperammonaemia (> 140 μmol/L) after Day 1 was achieved in 36 of CRRT-treated patients (84%) and was associated with transplant-free survival (55% v 13%; P = 0.05).
CONCLUSION: In Australian and New Zealand patients with ALF, CRRT is typically started early, before Stage 3 AKI or severe acidaemia, and in the presence hyperammonaemia. In these more severely ill patients, CRRT use was associated with prevention of extreme hyperammonaemia, which in turn, was associated with increased transplant-free survival.
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Interest is growing in measuring and rapidly treating hyperammonaemia in patients with ALF, despite the lack of evidence to guide the best means to achieve its correction. 14, 15, 16
Given the above considerations, in patients with ALF treated in all Australian and New Zealand liver transplant ICUs, we conducted an exploratory evaluation of CRRT utilisation and associated biochemical monitoring in response to hyperammonaemia. Our primary hypothesis was that, in most ALF patients, CRRT initiation would occur early, before overt evidence of renal failure and in the presence of severe hyperammonaemia. We further hypothesised that such CRRT treatment would be associated with the correction or avoidance of extreme hyperammonaemia in most patients.
Study designAs previously described, 24
Data collected included patient sex, age, comorbidities, aetiology of ALF, illness severity score, components of the King’s College Criteria (KCC), the Kidney Disease: Improving Global Outcomes (KDIGO) criteria for AKI stage, biochemical and haematological test results, critical care interventions, blood product utilisation, and outcomes, including emergency liver transplantation (ELT) and death. We obtained data for interventions and investigations occurring at the time of ICU admission, 6 hours, 12 hours and 24 hours after admission, and then every day for one week. A sample size of 60 patients was considered sufficient on the basis of convenience and feasibility and as representative of about one year of practice. 1
Statistical analysisStatistical analysis was performed using IBM SPSS statistics for Macintosh, version 25 (IBM Corporation, Armonk, NY, USA). Continuous variables are expressed as medians with interquartile ranges (IQR) and categorical variables as frequencies with percentages. Continuous data were compared using Mann–Whitney test. Categorical data were compared using X2 or Fisher exact test as appropriate. The Kruskal–Wallis test was used to compare more than two ordinal variables between groups. Longitudinal data were assessed for normality and log-transformed where appropriate. Differences between groups over time were analysed using repeat measures analysis of variance fitting main effects for group, time and an interaction between group and time to determine if groups behaved differently over time. Results are presented as mean (standard error) or as geometric mean (95% confidence interval [CI]) in accordance with the underlying distribution of the data. A two-sided P of 0.05 was used to indicate statistical significance.
Patient characteristics, aetiology of acute liver failure and clinical outcomesWe studied 62 patients with ALF of whom 33 (53%) had paracetamol overdose-related ALF, with the remaining cases having ALF due to a variety of causes (Online Appendix, supplementary table 1).
Baseline characteristics at the time of admission to ICU are summarised in Table 1. Patients were mostly young and female, with high illness severity, and 37 (60%) fulfilled the KCC for transplantation.
Use of continuous renal replacement therapyThe use of CRRT over the first week of ICU management is presented in Figure 1. Overall, a total of 43 patients with ALF (69%) received CRRT. Patients treated with CRRT had greater illness severity and more patients fulfilled the KCC. They had a significantly lower pH, higher lactate concentration, worse hypofibrinogenaemia, more severe anaemia and more severe hyperammonaemia.
The median time from ICU admission to commencement of CRRT was 6 hours (IQR, 2–12) and all except one patient started CRRT on the day of ICU admission. At CRRT initiation, ten patients did not meet KDIGO creatinine criteria for AKI, 12 met Stage 1, ten met Stage 2, and only 11 (26%) patients met Stage 3 AKI criteria. The median duration of CRRT therapy was 60 hours (IQR, 33–129) and the most common modality was continuous venovenous haemodiafiltration (CVVHDF), which was used in 80% of patients treated with CRRT. No patients were treated with intermittent haemodialysis.
Consistent with greater illness severity, treatment with CRRT was associated with the provision of other advanced critical care interventions (Online Appendix, supplementary figure 1) and complications. Thus, 88% of CRRT patients versus 47% of non-CRRT patients were mechanically ventilated (P = 0.001), and 81% versus 42% of patients received vasopressor therapy (P = 0.002). In addition, more CRRT patients experienced a bleeding episode and received a blood transfusion or were treated with cryoprecipitate (Online Appendix, supplementary table 2).
Safety of early continuous renal replacement therapyHaemostatic parameters at the time of catheter insertion are summarised in the Online Appendix (supplementary table 3). Patients commencing CRRT had a more prolonged activated partial thromboplastin time and slightly worse anaemia, and fresh frozen plasma was used to a greater extent on the day of vascular access insertion compared with non-CRRT patients (median, 2 units [IQR, 0–4.8] v 0 units [IQR, 0–2.5]; P = 0.04). Only one episode of catheter-related bleeding occurred close to the time of CRRT initiation, which required no intervention other than the administration of clotting factors.
Dynamics of biochemical parameters and continuous renal replacement therapy in acute liver failurePeak creatinine (but not peak urea) concentration was higher in CRRT patients (Table 1), and seven patients (16%) never had a serum creatinine above the upper limit of normal. However, the peak ammonia concentration on the first day was 55% higher than in non-CRRT patients (P = 0.02) (Table 1). Despite such high levels and greater illness severity, ammonia concentrations in CRRT patients rapidly and significantly decreased over time and became similar to untreated patients. In contrast, untreated patients had no significant change over time.
Over 7 days of ICU management, the mean peak Day 1 ammonia was reduced from 155 μmol/L (95% CI, 103–234) to 71μmol/L (95% CI, 45–112) with CRRT; while in non-treated patients, the change over this period was from 83 μmol/L (95% CI, 40–171) to 72 μmol/L (95% CI, 21–246) (Figure 2). In addition, 14 of the 62 patients with ALF had a peak ammonia concentration greater than 140 μmol/L during the first 24 hours. However, these levels were rapidly reduced over a single day in 12 patients (92%). Moreover, among these severely hyperammonaemic patients, eight (57%) had a pH greater than 7.30. Finally, among patients with hyperammonaemia treated with CRRT, the mean nadir pH was 7.25 (SD, 0.16) (Table 1).
After the first ICU day, avoidance of any ammonia levels greater than 140 μmol/L was achieved in 36 CRRT patients (84%). Eight patients in total had a documented ammonia concentration greater than 140 μmol/L at least once after the first day and only one of them achieved ELT-free survival. This compares with ELT-free survival in 30 of the 54 patients without episodes of extreme hyperammonaemia after Day 1 (P = 0.05). Other key biochemical and fluid balance data are summarised in the Online Appendix (supplementary figures 2–6 and supplementary table 5).
Outcomes on the basis of continuous renal replacement therapyClinical outcomes are summarised in the Online Appendix (supplementary table 4). Patients treated with CRRT had a longer ICU length of stay than non-CRRT patients, but hospital length of stay was not significantly different between the two groups. Use of ELT in CRRT patients was not significantly greater; however, ICU mortality was nearly four times higher and ELT-free survival was nearly half that of patients not requiring CRRT.
Key findingsIn our study of patients with ALF treated in Australian and New Zealand liver transplant ICUs, CRRT was started very early in the setting of hyperammonaemia, in the absence of Stage 3 AKI, and in the overall absence of advanced acidaemia or any acidaemia in half of the patients and with a pH greater than 7.3 in most patients with extreme hyperammonaemia. Such CRRT-based treatment strategy was associated with rapid ammonia reduction to safer levels in most patients and avoidance of extreme hyperammonaemia. In contrast, there were only minor changes over time in untreated patients. Moreover, after several days of CRRT, ammonia concentrations became the same as those seen in less severely ill non-CRRT patients. Finally, avoidance of extreme hyperammonaemia was associated with ELT-free survival.
Relationship to previous studiesCRRT was used in a high proportion of Australian and New Zealand patients with ALF. Compared with previous studies, such Australian and New Zealand patients had higher illness severity at the time of admission to ICU, with a lower pH, higher international normalised ratio, higher lactate concentration, and more severe hyperammonaemia. 16, 26
The optimal timing of RRT in critically ill patients is uncertain. 30, 31, 32, 33
Implications of study findingsOur findings suggest that in patients with ALF, Australian and New Zealand intensivists typically start CRRT early and such early commencement of therapy is safe. Moreover, our findings imply that clinicians target correction of severe hyperammonaemia even in the absence of severe AKI or severe acidaemia, suggesting that their major therapeutic target is hyperammonaemia itself. Finally, our findings imply that this approach contributes to rapid reductions of such severe hyperammonaemia to safer levels, which become similar to those of less severely ill patients with ALF.
Strengths and limitationsOur study has several strengths. All liver transplant ICUs in Australia and New Zealand contributed patients to the study ensuring the first full binational study of this aspect of ALF management. Patients with chronic liver disease were excluded, thus removing a key confounder. Data were obtained from patient records at each centre by experienced researchers thus minimising attribution errors. Finally, a clear methodology was used to ensure consistent and complete collection of available data.
Several limitations in this study warrant consideration. The study may appear relatively small, but it includes patients with ALF from every transplant unit in Australia and New Zealand and is the second largest case series worldwide of such patients in 40 years. We studied a convenience-based sample size; however, each ICU chose ten or more sequential patients based only on the diagnostic code of ALF at the time of admission, thus minimising selection bias. We did not obtain detailed data on the technical aspects of CRRT treatments, limiting our ability to ascertain whether specific techniques resulted in different outcomes. However, fluid balance and small solute (eg, ammonia) clearance is readily achieved with any of the commonly used CRRT techniques. In addition, hourly treatment intensity may not be a strong determinant of reductions in ammonia. 23