Why the study?
Incremental peritoneal dialysis improves outcomes in patients with residual kidney function, but the most appropriate recipients based on peritoneal solute transfer rate have not been identified.
Does incremental peritoneal dialysis improve mortality and anuria compared to full-dose peritoneal dialysis in patients with residual kidney function initiating CAPD?
Does incremental peritoneal dialysis improve mortality and anuria compared to full-dose peritoneal dialysis in patients with residual kidney function initiating CAPD?
Incremental peritoneal dialysis is associated with lower mortality and cardiovascular mortality compared to full-dose PD in patients with non-fast peritoneal solute transfer rates.
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Introduction Previous studies have shown that incremental peritoneal dialysis (iPD) improves the prognosis of patients with PD and tolerable residual kidney function (RKF). The peritoneal solute transfer rate (PSTR) characterizes peritoneal ultrafiltration and solute transfer. However, the most appropriate recipients of iPD have not been identified. Therefore, we hypothesized that patients with different PSTRs would experience different clinical benefits of iPD therapy. Methods We studied patients with RKF who initiated CAPD at our center. The enrolled patients were allocated to fast and non-fast PSTR groups, and then to iPD or full-dose PD. To mitigate the influence of confounding factors, propensity score matching was employed. The clinical outcomes associated with iPD and full-dose PD in the fast and non-fast PSTR groups were compared. Results A total of 974 CAPD patients were enrolled. The median duration of maintenance using iPD for the non-fast PSTR group was longer than that for the fast PSTR group (21.0 vs. 15.6 months, P =0.011). Patients in non-fast PSTR group who underwent iPD had lower risks of mortality [hazard ratio (HR) 0.25, P =0.002], anuria (HR 0.53, P =0.003), and cardiovascular mortality (HR 0.36, P =0.047) than those who underwent full-dose PD after matching. However, these clinical benefits of iPD therapy were not present in the fast PSTR group. Conclusions Patients who show non-fast PSTR maintain iPD longer and experience superior clinical benefits than those who undergo fast PSTR. Therefore, patients who experience non-fast PSTR may be more suitable for iPD therapy than those who experience fast PSTR.
iPD benefits may differ by PSTR in PD patients; leaves open optimal selection for incremental regimens.
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Guo et al. (2025) studied this question.
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