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DOI 10.1016/j.clinph.2026.2111849

Медицинская библиотека · Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2026

Hemodialysis fistula-related ischemic neuropathy in end stage renal failure: an electrophysiological study.

Posa Andreas, Langer Thomas Martin, Kresse Susanne, Kornhuber Malte Erich

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Аннотация

OBJECTIVE

Hemodialysis access (HA) may induce distal ischemia and impair peripheral nerve function in the ipsilateral limb. Peripheral neuropathy is common in end-stage renal disease (ESRD) and may remain subclinical without electrophysiological testing. This study evaluated the effect of arteriovenous fistula (AVF) on electrophysiological parameters of the median (MN) and ulnar (UN) nerves and examined the impact of HA localization and flow.

METHODS

Ninety ESRD patients with functioning AVF underwent bilateral nerve conduction studies (DML, CMAP, CSAP, MCV, SCV) one hour before dialysis. HA flow was measured by Doppler sonography. Sensory symptoms and clinical tests (Phalen, Tinel) were recorded.

RESULTS

Compared to the contralateral arm, the HA arm showed longer DML and reduced CMAP, CSAP, MCV, and SCV in both MN and UN. CSAP and MCV reductions were significant in both nerves, CMAP in UN. Electrophysiological impairment was greater with forearm HA and high flow (>979 ml/min). Patients with sensory complaints exhibited significantly worse parameters than asymptomatic patients.

CONCLUSIONS

AVF is associated with mixed axonal sensory-motor neuropathy, likely due to chronic distal ischemia. Sensory fibers are particularly vulnerable. Forearm location and high flow exacerbate deficits.

SIGNIFICANCE: Early electrophysiological screening may enable timely detection and intervention.

Для цитирования: Posa Andreas, Langer Thomas Martin, Kresse Susanne, Kornhuber Malte Erich. Hemodialysis fistula-related ischemic neuropathy in end stage renal failure: an electrophysiological study.. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 2026. DOI: 10.1016/j.clinph.2026.2111849.

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