The effects of oral sodium bicarbonate

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The effects of oral sodium bicarbonate on extracellular water in patients with chronic kidney
disease (CKD)
Louise Wells, Lead Specialist and Team Leader for Renal Dietetics, York Hospital
Introduction: Progressive renal failure is characterised by a worsening metabolic acidosis. Metabolic
acidosis may lead to adverse effects on bone and protein metabolism and exacerbate hyperkalaemia.
In addition recent studies have suggested that oral sodium bicarbonate may delay progression of
kidney disease in CKD patients. However deteriorating renal function is also characterised by sodium
and fluid retention. As well as causing peripheral or pulmonary oedema, this may exacerbate
hypertension which is a frequent complication of renal failure. There are therefore concerns about
administering oral sodium bicarbonate to these patients, although there is very little evidence on the
effect of sodium bicarbonate on extracellular fluid in renal failure. We have therefore undertaken a
study of the effects of sodium bicarbonate on extracellular water in CKD patients.
Methods: This was a double blind randomised comparison of oral sodium bicarbonate versus placebo.
The null hypotheses were that sodium bicarbonate increases neither blood pressure nor extracellular
fluid in patients with CKD.
Patients with stage 3-5 CKD were randomised to either oral sodium bicarbonate 1.5 g (3 x 500 mg
tablets) three times a day (54 mmol sodium/day) or oral placebo (3 tablets 3 times per day) for 4
weeks. Patients were assessed at baseline and at 4 weeks by means of height, weight, blood pressure,
medication history, and clinical assessment for peripheral oedema. Blood was analysed for serum
creatinine, electrolytes and venous bicarbonate and 24 hour urine for sodium excretion. Extracellular
fluid volume and total body water were determined by sodium bromide and deuterium oxide (2H2O)
dilution respectively. The significance of differences between the active (bicarbonate) and placebo
groups at week 4 was analysed by ANCOVA with week 0 (baseline) data as the covariate. A value of
<0.05 was taken as statistically significance.
Results: The study has now been completed and the results will be presented to the BRS research
forum.
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