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Haemodialysate: long neglected, difficult to optimize, may modify hard outcomes
Maria Vanessa Perez-Gomez1, Emilio Gonzalez-Parra1, Alberto Ortiz2
1IIS-Fundacion Jimenez Diaz, School of Medicine , Universidad Autonoma de Madrid, Fundacion Renal Iñigo Alvarez de Toledo-IRSIN and REDINREN , Madrid , Spain.
Insights
Optimizing hemodialysate composition is crucial for patient outcomes. Personalized medicine approaches and further clinical trials are needed to guide hemodialysis fluid customization and improve patient care.
Area of Science:
- Nephrology
- Clinical Medicine
- Dialysis Therapy
Background:
- Hemodialysate composition is increasingly linked to adverse patient outcomes.
- Limited clinical trial data restricts guideline recommendations for hemodialysis fluid management.
- Expert opinion is vital due to the scarcity of evidence-based practices.
Purpose of the Study:
- To highlight the importance of hemodialysate composition in patient care.
- To discuss the challenges in balancing rapid correction of imbalances with gradual adjustment.
- To explore personalized medicine approaches for optimizing hemodialysate.
Main Methods:
- Review of recent expert opinions and observational studies on hemodialysate composition.
- Analysis of the complexities in hemodialysis fluid design considering patient variability.
- Discussion on the need for novel clinical trial designs.
Main Results:
- Observational studies suggest a link between hemodialysate composition and adverse events.
- Current guidelines offer limited positive recommendations, focusing more on restrictions.
- Individual patient factors significantly complicate optimal hemodialysate formulation.
Conclusions:
- A personalized medicine approach to hemodialysate composition holds promise for improved patient outcomes.
- Further research, including robust clinical trial designs, is essential to validate individualized hemodialysis strategies.
- Balancing acute correction needs with gradual physiological adaptation is key in hemodialysate prescription.
Abstract:
In two recent CKJ reviews, experts (Basile and Lomonte and Locatelli et al.) have reviewed haemodialysate composition. A long-neglected issue, observational studies have associated the composition of haemodialysate to adverse outcomes. However, the scarcity of clinical trial-derived information results in limited guideline recommendations on the issue. Indeed, guidelines have more frequently indicated what not to do rather than what to do. In this setting, expert opinion becomes invaluable. In designing haemodialysate composition, a balance should be struck between the need to correct within a time frame of around 4 hours the electrolyte and water imbalances that take 48 to 72 h to build, with the need for gradual correction of these imbalances. The issue is complicated further by the impact of individual variability in dietary habits, medications and comorbidities. In this regard, a personalized medicine approach to individualization of haemodialysate composition offers the best chance of improving patient outcomes. But how can haemodialysate individualization be achieved, and what clinical trial design will best test the impact of such approaches on patient outcomes?
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