# Uremic Pruritus in Hemodialysis: Mechanisms, Burden, and Emerging Therapies

**Authors:** Marina Kljajić, Ena Parać, Armin Atić, Nikolina Bašić-Jukić

PMC · DOI: 10.3390/jcm15020494 · Journal of Clinical Medicine · 2026-01-08

## TL;DR

Uremic pruritus is a common and burdensome skin condition in hemodialysis patients, with multiple contributing factors and a range of treatment options including topical and systemic therapies.

## Contribution

This review provides an updated summary of emerging therapies and evolving mechanisms of uremic pruritus in hemodialysis patients.

## Key findings

- Topical therapies like emollients and humectants consistently improve symptoms of uremic pruritus.
- Gabapentinoids show the most robust efficacy among systemic therapies for treating uremic pruritus.
- Emerging therapies like AST-120, omega-3 fatty acids, and dupilumab show promising but preliminary results.

## Abstract

Background/Objectives: Uremic pruritus is a common complication in patients with end-stage kidney disease undergoing maintenance hemodialysis. Despite its high prevalence and substantial impact on sleep, psychological well-being, and overall quality of life, its pathophysiology remains multifactorial and incompletely understood. This narrative review summarizes contemporary evidence (2015–2025) on therapeutic strategies for uremic pruritus, with an emphasis on emerging treatments and evolving mechanistic insights. Methods: A PubMed search was conducted for original clinical studies published between 1 January 2015, and 31 October 2025, evaluating treatments for uremic pruritus in adult hemodialysis patients. Eligible study designs included randomized controlled trials and observational interventional studies. Non-English articles, pediatric studies, peritoneal dialysis studies, reviews, case reports, and studies of mixed-etiology pruritus were excluded. Earlier literature was reviewed to contextualize epidemiology and pathophysiology. Results: The review identifies multiple interacting mechanisms—including uremic toxins, immune dysregulation, mineral abnormalities, xerosis, neuropathic changes, and dysregulated opioid signaling—contributing to itch generation. Topical therapies, especially emollients and humectants, consistently improved symptoms with excellent safety profiles. Optimization of dialysis adequacy and membrane selection showed benefit in selected patients. Among systemic therapies, gabapentinoids demonstrated the most robust efficacy but required cautious dosing. Sertraline, nalbuphine, and difelikefalin showed significant antipruritic effects in controlled trials. Emerging therapies, including AST-120, omega-3 fatty acids, and the biologic dupilumab, demonstrated promising but preliminary results. Conclusions: Management of uremic pruritus requires a multifaceted, individualized approach integrating skin-directed therapies, dialysis optimization, and targeted systemic treatments. Ongoing research is needed to identify reliable biomarkers and to develop safer, more effective, mechanism-based therapies.

## Linked entities

- **Diseases:** end-stage kidney disease (MONDO:0004375)

## Full-text entities

- **Diseases:** mineral abnormalities (MESH:D012080), end-stage kidney disease (MESH:D007676), Uremic Pruritus (MESH:D011537), immune dysregulation (OMIM:614878), uremic toxins (MESH:D006463), neuropathic changes (MESH:D009437)
- **Chemicals:** difelikefalin (MESH:C000657129), nalbuphine (MESH:D009266), AST-120 (MESH:C040896), dupilumab (MESH:C582203), gabapentinoids (-), Sertraline (MESH:D020280), omega-3 fatty acids (MESH:D015525)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

132 references — full list in the complete paper: https://tomesphere.com/paper/PMC12842320/full.md

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Source: https://tomesphere.com/paper/PMC12842320