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Chronic Kidney Disease without Renal Replacement Therapy (KDIGO Stage 3-5) 

Definition

Chronic Kidney Disease (CKD) is defined as the presence of kidney damage (typically indicated by albuminuria of ≥30 mg/day or equivalent markers such as Cystatin C or Beta-2-microglobulin) or decreased kidney function (estimated glomerular filtration rate [eGFR] 1. CKD is associated with an increased risk of cardiovascular disease, infections, malignancies, and higher mortality rates.
Assessment of the severity (staging) of chronic kidney disease is based on the KDIGO guidelines (Kidney Disease Improving Guidelines) 1.

Assessment of Chronic Kidney Disease Staging

Definition

GFR [mL/min/1.73 m²]

Stage 3a

Mild to moderate decrease in GFR 45 - 59

Stage 3b

Moderate to severe decrease in GFR 30 - 44

Stage 4

Severe decrease in GFR 15 - 29

Stage 5

End-stage kidney disease <15

GFR = Glomerular Filtration Rate

Impact on Nutritional Status

Patients with CKD are at a high risk of malnutrition due to reduced appetite, decreased food intake, and gastrointestinal uremic side effects. These are further exacerbated by uremia-associated factors (nausea, vomiting), chronic inflammation, metabolic acidosis, hypermetabolism, hormonal changes, and potential comorbidities. A U.S. study demonstrated that in older adults (≥60 years), a decrease in eGFR to  <30 ml/min/1.73 m² was associated with malnutrition (Odds Ratio [OR] 3.6), independent of the overall health status 2.

Nutrient needs for patients with chronic kidney disease. Adjustments are necessary for malnourished patients, physical activity, and patient age. The weight used is Adjusted Body Weight (ADJ) if BMI is ≥28; otherwise, pre-hospitalization body weight is used.  
BW = Body Weight; d = Day 

Nutrient Daily requirement (per kg bw)
Protein 0.6 0.8

g/d 1 

  Diabetes mellitus 0.8 0.9

g/d 4

  Comorbidity/Weight Loss < 1.3

g/d 1

Energy <60 years 35

kcal/d 1

  ≥60 years 30

kcal/d 1

Fluid free /

as prescribed / per medical order* 1

Please fill out the weight

Vitamins, Minerals, and Trace Elements

  • Phosphate**
    • Target Serum Level: <1.5 mmol/L 4
    • Requirement: 600 – 1000 mg/day (19 – 32 mmol/day) 5
  • Potassium***
    • Target Serum Level: 3.5 – 5.0 mmol/L 4
    • Requirement: 1500 – 2000 mg/day (38 – 51 mmol/day) 5
  • Sodium*
    • Requirement: 1.8 – 2.5 g/day (78 – 108 mmol/day)
    • Equivalent NaCl: 4.6 – 6.4 g/day (78 – 108 mmol/day) 5

* Sodium: Sodium and intravascular volume balance is typically maintained by homeostatic mechanisms until eGFR falls below 10 to 15 mL/min/1.73 m². However, patients with mild to moderate CKD, despite relative volume stability, have a reduced ability to respond to high sodium intake, making them prone to fluid overload. Therefore, sodium intake should be limited to a maximum of 2.5 g/day (6.4 g NaCl), unless contraindications exist, such as salt-losing nephropathy.

** Phosphate: Excess phosphate is excreted via urine to maintain a fasting serum concentration of <1.5 mmol/L (4.6 mg/dL) with normal kidney function 6. If eGFR falls below 40 mL/min/1.73 m², the likelihood of hyperphosphatemia increases, triggering a cascade of adverse effects 4. Common complications include disturbances in mineral and bone metabolism, leading to increased vascular calcification, osteoporosis, or atherosclerosis 7, and an increased risk of CKD progression and mortality 8. Restriction of oral phosphorus intake to 600 – 1000 mg (19 – 32 mmol) per day or reducing absorption with phosphate binders is typically indicated if fasting serum levels are ≥1.5 mmol/L 4.

*** Potassium: About 90% of daily potassium intake is excreted through urine with normal kidney function. The risk of hyperkalemia increases with declining kidney function, posing a higher risk of hypertension, ventricular arrhythmias, and sudden death, particularly when eGFR falls below 15 mL/min/1.73 m²  9. Treatment involves avoiding hyperkalemia-inducing medications and potassium-rich foods.

Goals of Nutritional Therapy

  • Maintain/improve nutritional status and body function.
  • Prevent malnutrition and nutrient deficiencies.
  • Reduce acidosis.
  • Prevent osteopenia, osteoporosis, and atherosclerosis.
  • Delay the progression of kidney function decline. 5

To detect malnutrition early, a Nutritional Risk Screening should be conducted at least twice a year.

Energy and protein needs should, whenever possible, be met through oral nutrition. If less than 75% of the requirements are met using fortified foods, snacks, or oral supplements, enteral nutrition should be introduced as a supplement after 5 days. Complementary parenteral nutrition is indicated if less than 75% of needs are met through oral and/or enteral nutrition.

Oral Nutrition

A moderate protein restriction of 0.6-0.8 g/kg body weight per day is recommended for stable patients without malnutrition. For diabetic patients, a slightly higher intake of 0.8-0.9 g protein per kg body weight is suggested to achieve better glycemic control 4. The extent of phosphorus and potassium restriction should be tailored based on serum levels and in consultation with the treating medical specialist or managed with medication (e.g., phosphate and potassium binders). Overall acid intake should be reduced, for example, by including fiber-rich foods (such as fruits, vegetables, and whole grains), which can reduce the formation of uremic toxins and positively impact inflammation 10.

CKD-specific oral supplements often contain reduced amounts of protein, potassium, and phosphorus 5. A reduction in protein intake to below 0.6 g/kg body weight is not common practice in Switzerland and requires close monitoring of nutritional status and amino acid supplementation 4.

Practical Tips for Restrictions (if indicated):

  • Protein: Include a protein source in each main meal, combining animal and plant-based proteins. Adjust protein intake to individual needs (consider portion sizes, replace protein-rich foods with lower-protein alternatives, and focus on a good protein/phosphorus ratio). Limit to a maximum of 3 portions of dairy products and 1 portion of meat, fish, eggs, legumes, or tofu per day.
  • Phosphate: Avoid foods with artificial phosphate additives and high phosphate content, especially processed foods with the following additives: [E 338, E 339, E 340, E 341, E 343, E 442, E 450, E 451, E 452, E 541, E 1410, E 1413, E 1414, E 1442]. Note: Organic meat products do not contain phosphate additives 11.
  • Potassium: Reduce potassium-rich foods and opt for lower-potassium alternatives: Limit potatoes to 120 g, a maximum of three times per week. Replace whole grain products (such as whole grain pasta, bread, rice) with white flour products and white rice. Avoid dried products (such as dried fruits, beans, mushrooms). Pay attention to preparation methods, portion size, and consumption frequency.
  • Salt: Use salt moderately during preparation and avoid additional salting at the table. Increase the use of herbs, garlic, and onions for seasoning. Note: Spice mixes, bouillon, liquid seasonings, soy sauce, and ready-made sauces often have a high salt content. Favor cooking methods like steaming or braising instead of boiling in salted water. Consume salty foods like processed foods, canned goods, salty snacks, and charcuterie in moderation. Caution: Some diet and herbal salts contain potassium chloride instead of sodium chloride. These are suitable for patients with high blood pressure but not for those with kidney disease.
  • Acid Reduction: Moderate consumption of animal products. Prefer plant-based protein sources. Include fiber-rich foods like fruits, vegetables, and whole grains (note potassium content).

Enteral and Parenteral Nutrition

Enteral and/or parenteral nutrition is generally required only for patients with an additional acute illness that increases nutrient needs, which cannot be adequately met through oral or enteral intake 12.

Monitoring

  • Monitoring serum concentrations of proteins, glucose, phosphate, potassium, sodium, parathyroid hormone (PTH), bicarbonate, and Vitamin D3:
    • Prevent malnutrition due to protein restriction.
    • Manage hyperglycemia caused by peripheral insulin resistance and hepatic gluconeogenesis through appropriate dietary intake 13.
    • Estimate salt intake via 24-hour urine collection: Sodium in mmol / 17.1 mmol = salt intake in grams (e.g., 50 mmol Na+ ≈ 3 g NaCl, 100 mmol ≈ 6 g NaCl, 150 mmol ≈ 9 g NaCl). Assumption: Patient in steady state, all sodium in urine originates from dietary salt.
    • Prevent hydrogen ion (H⁺) retention and subsequent metabolic acidosis. Substitute bicarbonate (HCO3⁻) if serum levels are
    • Substitute calcitriol (1,25-OH-Vitamin D) for patients with CKD Stages 4 and 5 (KDIGO) as kidney-derived calcitriol synthesis decreases with eGFR
  • If anemia is present:
    • Exclude and treat iron deficiency. If unresolved, administer erythropoiesis-stimulating agents (ESA). Anemia in CKD is typically normocytic and normochromic, caused by reduced erythropoietin production and shortened red blood cell lifespan, particularly with eGFR 14.
  • Evaluate nutritional therapy measures three times in the first year after initiation, then annually.

Consequence

Symptoms

Monitoring

Uremia Anorexia, malnutrition, increased mortality Oral intake, nutritional screenings, urea/nitrogen levels
Metabolic Acidosis Increased protein catabolism, muscle breakdown Bicarbonate levels, serum pH
Hyperkalemia Increased muscle contraction, weakness to paralysis, arrhythmias, cardiac/respiratory failure Potassium levels, serum pH, insulin deficiency, potassium-impacting medications, dietary intake
Hypervolemia Edema/ascites, hypertension, increased cardiac output Weight trends, fluid balance
Anemia Reduced oxygen transport, dyspnea, fatigue Hemoglobin, hematocrit, iron status
Hyperphosphatemia Decreased 1-α-hydroxylation, secondary hyperparathyroidism Phosphate levels, parathyroid hormone, calcium

Adapted from 15

Medications/Supplements

  • Phosphate Binders: Calcium carbonate, Calcium acetate, Alucol®, Phosphonorm®, Renagel®, Renvela®, Fosrenol®, Velphoro®. Timing and dosage should align with the phosphate content of meals.
  • Potassium Ion Exchangers: Resonium®, Veltassa® (initial prescription by cardiologist or nephrologist only). Regular use as prescribed is crucial and does not require administration with meals.
  • Vitamin D Analogues: ViDe-Drops, Rocaltrol®, Zemplar®.
  • Calcimimetics: Cinacalcet (Mimpara®), Etelcalcetide (Parsabiv®).
  • Other Vitamin Supplements: Dialvit®.
  1. Group, K.D.I.G.O.K.C.W., KDIGO 2012 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Kidney inter., Suppl., 2013. 84(3): p. 1-150. (Link NutriBib
  2. Garg, A.X., et al., Association between renal insufficiency and malnutrition in older adults: results from the NHANES III. Kidney Int, 2001. 60(5): p. 1867-74.
  3. Fiaccadori, E., et al., ESPEN guideline on clinical nutrition in hospitalized patients with acute or chronic kidney disease. Clin Nutr, 2021. 40(4): p. 1644-1668. (Link NutriBib)
  4. Ikizler, T.A., et al., KDOQI Clinical Practice Guideline for Nutrition in CKD: 2020 Update. Am J Kidney Dis, 2020. 76(3 Suppl 1): p. S1-s107. (Link NutriBib)
  5. Sobotka, L., BASICS IN CLINICAL NUTRITION. 2020, [S.l.]: GALEN.
  6. Bazydlo, L.A.L., M. Needham, and N.S. Harris, Calcium, Magnesium, and Phosphate. Laboratory Medicine, 2014. 45(1): p. e44-e50.
  7. Moe, S., et al., Definition, evaluation, and classification of renal osteodystrophy: a position statement from Kidney Disease: Improving Global Outcomes (KDIGO). Kidney Int, 2006. 69(11): p. 1945-53.
  8. Barreto, F.C., et al., Strategies for Phosphate Control in Patients With CKD. Kidney Int Rep, 2019. 4(8): p. 1043-1056.
  9. Cupisti, A., et al., Dietary Approach to Recurrent or Chronic Hyperkalaemia in Patients with Decreased Kidney Function. Nutrients, 2018. 10(3).
  10. Chauveau, P., et al., Vegetarianism: advantages and drawbacks in patients with chronic kidney diseases. J Ren Nutr, 2013. 23(6): p. 399-405.
  11. Das Eidgenössische Departement für Wirtschaft, B.u.F.W., Verordnung des WBF über die biologische Landwirtschaft, SR910.181. 22. September 1997 (Stand am 1. Januar 2021).
  12. Cano, N., et al., ESPEN Guidelines on Enteral Nutrition: Adult renal failure. Clin Nutr, 2006. 25(2): p. 295-310. (Link NutriBib)
  13. Fiaccadori, E., G. Regolisti, and U. Maggiore, Specialized nutritional support interventions in critically ill patients on renal replacement therapy. Curr Opin Clin Nutr Metab Care, 2013. 16(2): p. 217-24.
  14. Ikizler, T.A., et al., Prevention and treatment of protein energy wasting in chronic kidney disease patients: a consensus statement by the International Society of Renal Nutrition and Metabolism. Kidney Int, 2013. 84(6): p. 1096-107.
  15. Steiber, A.L., Chronic kidney disease: considerations for nutrition interventions. JPEN J Parenter Enteral Nutr, 2014. 38(4): p. 418-26.

Authorship:

Valentina Huwiler, PhD, Ernährungswissenschaftlerin, Inselspital Bern
Cecilia Czerlau, MD, Nephrologin, Inselspital Bern
Dominik Uehlinger, MD, Nephrologe, Inselspital Bern

Information NutriGo

Application-oriented practical recommendations for nutrition therapy in different clinical situations based on current guidelines

The treatment of malnutrition is a central component in the intial and continuing therapy of hospital patients in order to maintain/improve body function and quality of life and to reduce the risk of complications up to and including mortality. Therapy should be adapted to the underlying disease. NutriGo summarises treatment strategies for different clinical situations and provides practical advice on implementation.

The recommendations are based on the recognised current guidelines for the respective clinical situation. By entering the patient's body weight, the micro- and macronutrient requirements can be calculated using a simple multiplication, if the requirements are specified in the relevant guidelines. Additional adjustments are required for patients with an increased BMI (>28 kg/m2), ascites, underweight, increased age and increased/reduced physical activity.

List of abbreviations

BMI  Body Mass index