Introduction
Acute kidney injury (AKI) is a frequent complication of critical illness. It commonly occurs in the context of sepsis, multi-organ failure, major surgery or trauma, and is considered a pro-inflammatory condition. Our aim is to highlight the lack of high-quality data related to nutrition in AKI.
Malnutrition, defined by the World Health Organisation as “deficiency, excess or imbalance in a person’s intake of energy and/or nutrients”, is common in AKI. The main causes are critical illness (systemic inflammation, immobility, muscle breakdown) and pre-existing malnourishment. Increased protein breakdown, impairment of lipolysis, insulin resistance and altered hormonal regulation have also been reported [1]. The effects of retained uremic waste products and middle molecules, altered amino acid pattern and fluid accumulation, are likely to play a role in the development of malnutrition in AKI, too [2] (Supplementary Fig. 1).
In patients receiving renal replacement therapy (RRT), nutritional status may also be affected by the removal of amino acids, trace elements, glucose and water-soluble vitamins [3–5]. The extent varies depending on the modality, dose and duration of RRT and the concentrations of nutrients in serum. During continuous renal replacement therapy (CRRT), amino acid losses up to 10–15 g/day have been reported [4]. However, most studies are small, relatively old and not always reflective of current clinical practice. Nevertheless, a recent study showed that 80% of patients on CRRT had below-normal levels of at least one important micronutrient measured i.e. thiamine, pyridoxine, ascorbic acid, folate, zinc or copper [6]. However, it should be acknowledged that the presence of low plasma nutrient concentrations during CRRT does not necessarily mean that elimination across the filter is the only cause. For instance, Story et al. measured serum concentrations of vitamin C, vitamin E, selenium, zinc, chromium and copper in critically ill patients with and without CRRT and in healthy controls [5]. They showed that CRRT patients had significantly lower serum concentrations compared to healthy controls but there was no difference between both critically ill cohorts. This suggests that acute illness has a greater impact than CRRT per se.
Nutritional assessment
All critically ill patients should undergo a general clinical assessment of nutritional status [7]. However, there is no validated screening tool to assess nutritional requirements specifically in AKI patients [8]. Indirect calorimetry is not widely available, and equations estimating resting energy requirement are unreliable and have not been validated in AKI. Until a specific tool has been validated, it is recommended that a general nutritional assessment should include the exploration of weight loss before ICU admission, a physical examination and an assessment of body composition, muscle mass and muscle strength [7].
Nutritional support
During critical illness, amino acids are released from muscle to support gluconeogenesis and the production of inflammatory mediators. Nutrition can only improve protein and energy balance and possibly protein synthesis but cannot suppress critical illness-induced catabolism.
There is consensus that nutritional support should be individualised and tailored to the severity of hypercatabolism and the underlying disease, comorbidities, the need for RRT, and pre-existing nutritional status [1, 7, 9–11]. Evidence-based data are limited and randomized controlled trials (RCT) specifically in AKI patients have not been performed. However, recent studies in the general ICU population (including AKI patients) showed important results related to type and timing of nutrition that are likely to be applicable to critically ill patients with AKI [7, 12, 13]. These findings were incorporated in latest guidelines, including the recommendations by the European Society for Clinical Nutrition and Metabolism (ESPEN) [7].
Energy expenditure (EE) tends to be higher during critical illness compared with reference values in healthy individuals [14], but both under- and overfeeding are associated with delayed recovery and increased mortality [13, 15, 16]. The ESPEN guideline recommends hypocaloric nutrition in the early phase of illness, progressing slowly to full targeted nutrition after day 3 with the aim to achieve more than 70% of EE but not more than 100% [7]. Full nutritional support provided early may cause overfeeding as it fails to suppress endogenous energy production which cannot be measured. It also cannot reverse muscle catabolism and may induce refeeding [17]. There is no evidence that caloric targets should be different in AKI patients with and without RRT. However, in patients on CRRT, citrate contributes to caloric delivery and should be accounted for.
If possible, oral diet should be the initial route of nutrition [1, 7, 10, 11]. In patients with insufficient oral intake, enteral feeding within 24–48 h is recommended [7]. Limited data suggest that bolus and continuous enteral feeding can achieve similar targets [7]. When enteral nutrition is contraindicated, parenteral nutrition is recommended within 3–7 days.
With regards to protein targets, the evidence is low. Observational data in the general ICU population suggest that high protein intake is associated with lower mortality; however, a slow progression to target on days 3–5 may be beneficial [15, 16, 18]. Official guidelines vary in their recommendations (Table 1). Whilst some guidelines recommend a higher protein intake [11] based on older reports, certain well-conducted RCTs showed harm with the provision of early supplemental parenteral nutrition during the first week or supplemental high dose glutamine in patients with multiple organ failure, especially AKI (increased ureagenesis with a potentially increased requirement for RRT, suppression of autophagy, failure to suppress catabolism, increased mortality) [12, 13]. Trials comparing low and high amounts of calories and/or protein are ongoing (ClinicalTrials.gov NCT03292237 and NCT03573739). The most recent ESPEN guidelines recommend to deliver 1.3 g/kg protein equivalents per day gradually [7]. For patients receiving CRRT, experts suggest to administer water-soluble vitamins and trace elements routinely but controversy exists about the type, dose and duration [1] (Table 1).
Unmet needs and future research
Nutrition in AKI is an under-researched area. There are no RCTs on nutrition in patients with AKI. The exact role of routine micronutrient supplementation in patients receiving CRRT remains unknown. More well-designed RCTs are urgently required, in particular to investigate whether different protein targets in combination with hypocaloric nutrition and the supplementation of micronutrients improves outcomes in AKI.
References
Druml W, Joannidis M, John S, Jörres A, Schmitz M, Kielstein J, Kindgen-Milles D, Oppert M, Schwenger V, Willam C, Zarbock A (2018) Metabolic management and nutrition in critically ill patients with renal dysfunction: recommendations from the renal section of the DGIIN, ÖGIAIN, and DIVI. Med Klin Intensivmed Notfmed 113(5):393–400
Carrero JC, Agullera A, Stenvinkel P, Gil F, Selgas R, Lindholm B (2008) Appetite disorders in uremia. J Ren Nutr 18(1):107–113
Berger MM, Shenkin A, Revelly JP, Roberts E, Cayeux MC, Baines M, Chiolero RL (2004) Copper, selenium, zinc and thiamine balances during continuous venovenous hemodiafiltration in critically ill patients. Am J Clin Nutr 80:410–416
Scheinkestel CD, Adams F, Mahony L, Bailey M, Davies AR, Nyulasi I, Tuxen DV (2003) Impact of increasing parenteral protein loads on amino acid levels and balance in critically ill anuric patients on continuous renal replacement therapy. Nutrition 19:733–740
Story DA, Ronco C, Bellomo R (1999) Trace element and vitamin concentrations and losses in critically ill patients treated with continuous venovenous haemofiltration. Crit Care Med 27(1):220–223
Kamel AY, Dave NJ, Zhao VM, Griffith DP, Connor MJ Jr, Ziegler TR (2018) Micronutrient alterations during continuous renal replacement therapy in critically ill adults: a retrospective study. Nutr Clin Pract 33(3):439–446
Singer P, Blaser AR, Berger MM, Alhazzani W, Calder PC, Casaer MP, Hiesmayr M, Mayer K, Montejo JC, Pichard C, Preiser JC, van Zanten ARH, Oczkowski S, Szczeklik W, Bischoff SC (2019) ESPEN guideline on clinical nutrition in the intensive care unit. Clin Nutr 38(1):48–79
Fiaccadori E, Cremaschi E, Regolisti G (2011) Nutritional assessment and delivery in renal replacement therapy patients. Semin Dial 24:169–175
Brown RO, Compher C, The American Society for Parenteral and Enteral Nutrition (A.S.P.E.N.) Board of Directors. A.S.P.E.N. (2010) Clinical guidelines: nutrition support in adult acute and chronic renal failure. JPEN 34:366–377
Kidney Disease Improving Global Outcomes (KDIGO) Acute Kidney Injury Work Group (2012) KDIGO clinical practice guideline for acute kidney injury. Kidney Int 2:1–138
McClave SA, Taylor BE, Martindale RG, Warren MW, Johnson DR, Braunschweig C, McCarthy MS, Davanos E, Rice TW, Cresci GA, Gervasio JM, Sacks GS, Roberts PR, Compher C, The Society of Critical Care Medicine and the American Society for Parenteral and Enteral Nutrition (2016) Guidelines for the provision and assessment of nutrition support therapy in the adult critically ill patient: Society of Critical Care Medicine (SCCM) and American Society for Parenteral and Enteral Nutrition (A.S.P.E.N). JPEN J Parenter Enteral Nutr 40(2):159–211
Heyland DK, Elke G, Cook D, Berger MM, Wischmeyer PE, Albert M, Muscedere J, Jones G, Day AG, Canadian Critical Care Trials Group (2015) Glutamine and antioxidants in the critically ill patient: a post hoc analysis of a large-scale randomized trial. JPEN J Parenter Enteral Nutr 39(4):401–409
Casaer MP, Mesotten D, Hermans G, Wouters PJ, Schetz M, Meyfroidt G, Van Cromphaut S, Ingels C, Meersseman P, Muller J, Vlasselaers D, Debaveye Y, Desmet L, Dubois J, Van Assche A, Vanderheyden S, Wilmer A, Van den Berghe G (2011) Early versus late parenteral nutrition in critically ill adults. N Engl J Med 365:506–517
Mooij CM, Beurskens CJ, Juffermans NP (2013) Energy expenditure in different patient populations on intensive care: one size does not fit all. Neth J Crit Care 7(3):3–8
Weijs PJ, Looijaard WG, Beishuizen A, Girbes AR, Oudemans-van Straaten HM (2014) Early high protein intake is associated with low mortality and energy overfeeding with high mortality in non-septic mechanically ventilated critically ill patients. Crit Care 18(6):701
Zusman O, Theilla M, Cohen J, Kagan I, Bendavid I, Singer P (2016) Resting energy expenditure, calorie and protein consumption in critically ill patients: a retrospective cohort study. Crit Care 20:367
Doig GS, Simpson F, Heighes PT, Bellomo R, Chesher D, Caterson ID, Reade MC, Harrigan PW, Refeeding Syndrome Trial Investigators Group (2015) Restricted versus continued standard caloric intake during the management of refeeding syndrome in critically ill adults: a randomised, parallel-group, multicentre, single-blind controlled trial. Lancet Respir Med 3(12):943–952
Bendavid I, Zusman O, Kagan I, Theilla M, Cohen J, Singer P (2019) Early administration of protein in critically ill patients: a retrospective cohort study. Nutrients 11(1):106
Author information
Authors and Affiliations
Corresponding author
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Electronic supplementary material
Below is the link to the electronic supplementary material.
Rights and permissions
About this article
Cite this article
Ostermann, M., Macedo, E. & Oudemans-van Straaten, H. How to feed a patient with acute kidney injury. Intensive Care Med 45, 1006–1008 (2019). https://doi.org/10.1007/s00134-019-05615-z
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00134-019-05615-z