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Article Dans Une Revue BMC Nephrology Année : 2017

No increase in small-solute transport in peritoneal dialysis patients treated without hypertonic glucose for fifty-four months

Résumé

BACKGROUND: Glucose is widely used as an osmotic agent in peritoneal dialysis (PD), but exerts untoward effects on the peritoneum. The potential protective effect of a reduced exposure to hypertonic glucose has never been investigated. METHODS: The cohort of PD patients attending our center which tackled the challenge of a restricted use of hypertonic glucose solutions has been prospectively followed since 1992. Small-solute transport was assessed using an equivalent of the glucose peritoneal equilibration test after 6 months, and then every year. Study was stopped on July 1st, 2008, before use of biocompatible solutions. Repeated measures in patients treated with PD for 54 months were analyzed by using (1) the slopes of the linear regression for D4/D0 ratios over time computed for each individual, and (2) a linear mixed model. RESULTS: In the study period, 44 patients were treated for a total of 2376 months, 2058 without hypertonic glucose. There was one episode of peritoneal infection every 18 patient-months. The mean of slopes of the linear regression for D4/D0 ratios was found to be significantly positive (Student's test, p < .001) and the results of the mixed model reflected a similar significant increase for D4/D0 ratios over time. These results reflected a significant decrease of small-solute transport. CONCLUSION: In this large series, minimizing the use of hypertonic glucose solutions was associated in patients on long term PD with an overall decrease of small-solute transport within 54 months, despite a high rate of peritoneal infection.
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inserm-02080157 , version 1 (26-03-2019)

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Dominique Pagniez, Alain Duhamel, Eric Boulanger, Celia Lessore de Sainte Foy, Jean-Baptiste Beuscart. No increase in small-solute transport in peritoneal dialysis patients treated without hypertonic glucose for fifty-four months. BMC Nephrology, 2017, 18 (1), pp.278. ⟨10.1186/s12882-017-0690-7⟩. ⟨inserm-02080157⟩
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