KDIGO 2026-richtlijn anemie bij chronische nierziekte: Europees commentaar
De KDIGO 2026-richtlijn voor anemie bij CKD is een ingrijpende update met nieuwe aanbevelingen voor intraveneus ijzer en HIF-prolylhydroxylase-remmers. Dit ERBP-commentaar beoordeelt de richtlijn vanuit Europees perspectief en benadrukt dat ESA's eerstelijnstherapie blijven vanwege cardiovasculaire veiligheidszorgen bij HIF-PHI's.
Abstract (original)
The 2026 Kidney Disease: Improving Global Outcomes (KDIGO) Clinical Practice Guideline for Anemia in Chronic Kidney Disease represents a substantial update, more than a decade since the previous KDIGO guideline on the topic. This time lapse was necessary for accumulating new scientific evidence meaningful for an updated guideline. The new guideline now includes updated recommendations and practice points for anaemia management, incorporating recent evidence on intravenous iron therapies and hypoxia-inducible factor prolyl hydroxylase inhibitors (HIF-PHIs). This European Renal Best Practice commentary critically evaluates and comments on relevant and newer recommendations and practice points, focusing on key aspects from a European perspective. The new guideline emphasises the need for a comprehensive evaluation of the patient at the time of diagnosis, to identify additional causes of anaemia other than erythropoietin insufficiency. Coherently, the timing and the type of treatment should be individualised. Moreover, it introduces more proactive thresholds for intravenous iron supplementation, especially for haemodialysis patients. Erythropoiesis-stimulating agents (ESAs) are recommended as the preferred first-line therapy due to persisting concerns regarding cardiovascular safety and methodological limitations of available HIF-PHI trials. The commentary includes considerations on special aspects not considered by the new KDIGO guideline, such as pregnancy, gender-specific considerations, and interactions with SGLT2 inhibitors or inflammation. The commentary also highlights regional regulatory differences between European and US drug approvals for HIF-PHIs. While supporting most recommendations, European nephrologists should consider local contexts, regulatory approvals, and emerging evidence when implementing these guidelines in clinical practice.
Dit artikel is een samenvatting van een publicatie in Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. Voor het volledige artikel, alle details en referenties verwijzen wij u naar de oorspronkelijke bron.
Lees het volledige artikelDOI: 10.1093/ndt/gfag014