Sevelamer
๐ About Sevelamer
โ ๏ธ Always
check the BNF here
for up-to-date UK prescribing details (formulation, dose ranges, cautions, interactions).
- ๐ง Sevelamer is a non-calcium, non-metal phosphate binder used to treat hyperphosphataemia in chronic kidney disease (CKD), especially in patients on dialysis (HD or PD).
- ๐ง Key aim: reduce phosphate load โ protect bone and blood vessels (CKD-MBD).
๐งฌ Why Phosphate Matters in CKD (Pathophysiology)
- ๐ฉบ In CKD, phosphate excretion falls โ phosphate retention develops.
- ๐ง High phosphate stimulates FGF-23 and reduces calcitriol โ lowers calcium absorption โ drives secondary hyperparathyroidism.
- ๐ฆด This contributes to renal osteodystrophy (bone pain, fractures).
- ๐ซ Chronic hyperphosphataemia accelerates vascular/valvular calcification โ increased cardiovascular mortality.
โ๏ธ Mode of Action
- ๐ฝ๏ธ Sevelamer binds dietary phosphate in the gut lumen.
- ๐ซ The bound phosphate is not absorbed โ passed in stool โ lowers serum phosphate.
- โ
Because it contains no calcium, it helps avoid calcium loading and may reduce calcification risk compared with calcium-based binders in some patients.
๐ฏ Indications
- ๐ฉธ Hyperphosphataemia in patients on haemodialysis or peritoneal dialysis.
- ๐งช Hyperphosphataemia in non-dialysis CKD where dietary measures are insufficient (e.g. serum phosphate > 1.78 mmol/L).
๐ซ Contraindications & Cautions
- โ Bowel obstruction.
- โ ๏ธ Use caution in severe GI motility disorders, dysphagia, prior major GI surgery, or recurrent constipation.
- ๐ง PD patients: maintain vigilance for infective complications and abdominal symptoms.
๐ Interactions (Practical Prescribing Tips)
- ๐ Can reduce ciprofloxacin absorption โ avoid co-administration (separate dosing or choose alternative antibiotic where possible).
- โฑ๏ธ General rule: separate sevelamer from susceptible drugs by at least 1โ3 hours (check BNF for each drug).
- ๐ง If INR control becomes unstable in a warfarin patient who starts a binder, re-check adherence/timing and consider closer monitoring (interaction is usually timing/absorption-related rather than direct).
โ ๏ธ Side Effects
- ๐คข GI: nausea, bloating, abdominal pain, constipation, diarrhoea, dyspepsia.
- ๐งฑ Rare but important: faecal impaction, ileus, bowel obstruction/perforation (red flags = severe pain, vomiting, no bowel movements).
- ๐ก๏ธ Other: headache, rash.
- ๐งซ Peritoneal dialysis: possible association with increased risk of peritonitis in some cohorts (monitor symptoms; treat promptly).
๐ก Dose & Administration (High-Yield)
- ๐ฝ๏ธ Take with meals (it must meet phosphate in the gut to work).
- Initial: 2.4โ4.8 g daily in 3 divided doses with meals.
- Maintenance: often ~6 g daily in 3 divided doses, titrated to response.
- ๐ Adjust every 2โ4 weeks to reach local phosphate targets (guided by renal team).
โ
Clinical pearl: If phosphate remains high despite โbeing on bindersโ, the commonest causes are timing (not with meals), missed doses, and dietary phosphate load.
Ask specifically: โDo you take it with the first few mouthfuls?โ ๐ฝ๏ธ
๐งช Monitoring
- ๐ฉธ Serum phosphate (trend is more useful than single readings).
- ๐ฆด Calcium, PTH, alkaline phosphatase (CKD-MBD picture).
- ๐ฝ๏ธ Diet review with renal dietitian (phosphate additives are a frequent hidden culprit).
๐ References