Effect of Dialysate and Plasma Sodium on Mortality in a Global Historical Hemodialysis Cohort
- PMID: 37967469
- PMCID: PMC10843362
- DOI: 10.1681/ASN.0000000000000262
Effect of Dialysate and Plasma Sodium on Mortality in a Global Historical Hemodialysis Cohort
Abstract
Significance statement: This large observational cohort study aimed to investigate the relationship between dialysate and plasma sodium concentrations and mortality among maintenance hemodialysis patients. Using a large multinational cohort of 68,196 patients, we found that lower dialysate sodium concentrations (≤138 mmol/L) were independently associated with higher mortality compared with higher dialysate sodium concentrations (>138 mmol/L). The risk of death was lower among patients exposed to higher dialysate sodium concentrations, regardless of plasma sodium levels. These results challenge the prevailing assumption that lower dialysate sodium concentrations improve outcomes in hemodialysis patients. The study confirms that until robust evidence from randomized trials that are underway is available, nephrologists should remain cautious in reconsideration of dialysate sodium prescribing practices to optimize cardiovascular outcomes and reduce mortality in this population.
Background: Excess mortality in hemodialysis (HD) patients is largely due to cardiovascular disease and is associated with abnormal fluid status and plasma sodium concentrations. Ultrafiltration facilitates the removal of fluid and sodium, whereas diffusive exchange of sodium plays a pivotal role in sodium removal and tonicity adjustment. Lower dialysate sodium may increase sodium removal at the expense of hypotonicity, reduced blood volume refilling, and intradialytic hypotension risk. Higher dialysate sodium preserves blood volume and hemodynamic stability but reduces sodium removal. In this retrospective cohort, we aimed to assess whether prescribing a dialysate sodium ≤138 mmol/L has an effect on survival outcomes compared with dialysate sodium >138 mmol/L after adjusting for plasma sodium concentration.
Methods: The study population included incident HD patients from 875 Fresenius Medical Care Nephrocare clinics in 25 countries between 2010 and 2019. Baseline dialysate sodium (≤138 or >138 mmol/L) and plasma sodium (<135, 135-142, >142 mmol/L) concentrations defined exposure status. We used multivariable Cox regression model stratified by country to model the association between time-varying dialysate and plasma sodium exposure and all-cause mortality, adjusted for demographic and treatment variables, including bioimpedance measures of fluid status.
Results: In 2,123,957 patient-months from 68,196 incident HD patients with on average three HD sessions per week dialysate sodium of 138 mmol/L was prescribed in 63.2%, 139 mmol/L in 15.8%, 140 mmol/L in 20.7%, and other concentrations in 0.4% of patients. Most clinical centers (78.6%) used a standardized concentration. During a median follow-up of 40 months, one third of patients ( n =21,644) died. Dialysate sodium ≤138 mmol/L was associated with higher mortality (multivariate hazard ratio for the total population (1.57, 95% confidence interval, 1.25 to 1.98), adjusted for plasma sodium concentrations and other confounding variables. Subgroup analysis did not show any evidence of effect modification by plasma sodium concentrations or other patient-specific variables.
Conclusions: These observational findings stress the need for randomized evidence to reliably define optimal standard dialysate sodium prescribing practices.
Copyright © 2023 by the American Society of Nephrology.
Conflict of interest statement
B. Canaud reports Employer: Scientific consultant for Fresenius Medical Care, Germany up to December 2022—Retired from December 2022; and Consultancy: Senior scientist consultant for Fresenius Medical Care up to December 2022. B. Genser received a consulting fee from FMC for conducting the statistical analysis. M. Jardine reports Research Funding: Baxter, CSL, Dimerix with all payments to my institution; Honoraria: AstraZeneca, Bayer, Boehringer Ingelheim, Janssen, MSD, Occuryx and Vifor, and directs honoraria to clinical research programs; Advisory or Leadership Role: Chinook, CSL, Janssen. All honoraria directed to clinical research programs; and Speakers Bureau: AstraZeneca, Boehringer Ingelheim, Janssen, and directs speaker fees to clinical research programs. M.R. Marshall reports Ownership Interest: Microsoft Corporation. J. Pinter received a grant from Fresenius Medical Care for authorship related expenses regarding journal publication, abstract submission, organization, management and travel costs for conference presentations. P. Rossignol reports Consultancy: AstraZeneca, Bayer, Boehringer Ingelheim, CinCor, Idorsia, KBP, NovoNordisk, Sanofi, Servier, Sequana medical, Vifor; Ownership Interest: Cardiorenal cofounder (stocks); G3P (stock options); Research Funding: Relypsa Inc. and Vifor Fresenius Medical Care Renal Pharma, and a Vifor Pharma Group Company; Honoraria: Dr. Rossignol reports personal fees from AstraZeneca, Bayer, Boehringer Ingelheim, CinCor, Idorsia, KBP, NovoNordisk, Sanofi, Sequana medical, Servier, Vifor; Patents or Royalties: CardioRenal cofounder (a company developing a home potassium self-monitoring device); Advisory or Leadership Role: ESH: “hypertension and the kidney” working group board member since 2016; WG board member HFA, Cardio renal (2016–) and translational 2016–2020; WG board member Eurecam ERA-EDTA 2021–2023; WG on biomarkers board member HFA, 2020–2022; KDIDO executive committee member since 2023; and Speakers Bureau. B. Smyth reports Research Funding: In-kind support provided by iX Biopharma (Singapore) for investigator-initiated research; Honoraria: Research Review Australia; CSL-Vifor (funds to institution); and Advisory or Leadership Role: Unpaid committee positions for not-for-profit organisations/clinical trials (ANZSN Research Advisory Committee, INCH-HD study SC, RESOLVE trial SC); Paid position with CSL-Vifor (funds to institution). S. Stuard is an employee of Fresenius Medical Care; Ownership Interest: Fresenius Medical Care; and Patents or Royalties: Fresenius Medical Care. C. Wanner has received honoraria for advisory or educational activities from Amgen, Astellas, AstraZeneca, Bayer, Boehringer Ingelheim, CSL-Vifor, Fresenius Medical Care, Gilead, GSK, MSD, NovoNordisk and grants from Boehringer Ingelheim and Sanofi to the institution. C. Wanner also reports Consultancy: AstraZeneca, Bayer, Boehringer Ingelheim, CSL-Vifor, GSK, MSD, NovoNordisk; Honoraria: Amicus, Chiesi, Eli-Lilly, FMC, Novartis, Sanofi, Stadapharm, Takeda; and Other Interests or Relationships: European Renal Association (ERA). D.C. Wheeler has an ongoing consultancy contract with AstraZeneca. In the last 2 years he has received honoraria/consultancy fees from Astellas, Bayer, Boehringer Ingelheim, Eledon, Galderma, Gilead, GlaxoSmithKline, Janssen, Prokidney, Tricida, Vifor and Zydus for clinical trial related, Advisory or Educational activities. D.C. Wheeler also reports Consultancy: George Clinical, Merck Sharp and Dohme, Pfizer, ProKidney; Advisory Boards, Trial Committees and Consultancy; Honoraria: Amgen, Astellas, AstraZeneca, Bayer, Boehringer Ingelhiem, GalaxoSmithKline, Janssen, Napp, Merck Sharp and Dohme, Napp, Pharmacosmos, Reata, Vifor Fresenius; Advisory or Leadership Role: AstraZeneca; and Speakers Bureau: Amgen, Astellas, AstraZeneca, Janssen, Merck Sharp and Dohme, Mundipharma, Napp, Vifor Fresenius.
Figures
Comment in
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Are Observational Reports on the Association of Dialysate Sodium with Mortality Enough to Change Practice? Perspective from the RESOLVE Study Team.J Am Soc Nephrol. 2024 Feb 1;35(2):229-231. doi: 10.1681/ASN.0000000000000289. Epub 2023 Dec 14. J Am Soc Nephrol. 2024. PMID: 38096088 Free PMC article. No abstract available.
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