Phosphate binder

Source: Wikipedia, the free encyclopedia.

Phosphate binders are

chronic kidney failure
(CKF), who are less able to excrete phosphate, resulting in an elevated serum phosphate.

Mechanism of action

These agents work by binding to phosphate in the

insoluble compound. Phosphate binders such as sevelamer may also be polymeric structures which bind to phosphate and are then excreted.[citation needed
]

Medical use

For people with chronic kidney failure, controlling

bone pathology and regulated together with serum calcium by the parathyroid hormone (PTH).[1]

They are also used in hypoparathyroidism which presents with hypocalcemia with hyperphosphatemia.[citation needed]

Adverse effects

With regard to phosphate binders, aluminium-containing compounds (such as

hypercalcemia and tissue-damaging calcinosis. One may avoid these adverse effects by using phosphate binders that do not contain calcium or aluminium as active ingredients, such as lanthanum carbonate or sevelamer
.

Choice of agent

There have been limited trials comparing phosphate binders to placebo in the treatment of hyperphosphatemia in people with chronic kidney disease. When compared with people receiving calcium-based binders, people taking sevelamer have a reduced all-cause mortality.[1]

Types

Summary of Common Oral Phosphate Binders[2]
Phosphate Binder Brands Advantages Disadvantages
Aluminum salts
Alucaps Calcium free Risk of aluminum toxicity
Basaljel High binder efficiency regardless of pH Requires frequent monitoring-extra cost
Cheap
Moderate tablet burden
Calcium carbonate Calcichew Aluminum free Calcium containing-potential risk of hypercalcemia and ectopic calcification
Titralac Moderate binding efficacy Parathyroid hormone oversuppression
Relatively low cost Gastrointestinal side effects
Moderate tablet burden Efficacy pH dependent
Chewable
Calcium acetate Lenal Ace Aluminum free Calcium containing-potential risk of hypercalcemia and ectopic calcification
PhosLo Higher efficacy than calcichew/sevelamer Parathyroid hormone oversuppression
Moderately cheap Gastrointestinal side effects
Lower calcium load than calcium carbonate Large tablets & capsules, nonchewable formulation
Sevelamer hydrochloride/Sevelamer carbonate Renagel Aluminium and calcium free Relatively costly
Renvela No gastrointestinal absorption High pill burden
Moderate efficacy Large tablets, nonchewable formulation
Reduces total and low-density lipoprotein cholesterol Gastrointestinal side effects
Binds fat-soluble vitamins
Lanthanum carbonate Fosrenol Aluminum and calcium free Relatively costly
Minimal gastrointestinal absorption Gastrointestinal side effects
High efficacy across full pH range Larger tablet size may cause choking if not chewed well
Chewable formulation
Palatable
Low tablet burden
Ferric Citrate Auryxia Iron based Very costly
Tablets can be toxic to young children
Stool discoloration - may turn them black, obscuring intestinal bleeding

References

  1. PMID 26668024
    .
  2. ^ Burtis, C.A.; Ashwood, E.R. and Bruns, D.E. Tietz Textbook of Clinical Chemistry and Molecular Diagnostics. 5th Edition. Elsevier. pp1552
  1. ^ Lederer E, Ouseph R, Erbeck K. Hyperphosphatemia, eMedicine.com, URL: Hyperphosphatemia: Practice Essentials, Background, Pathophysiology, Accessed on July 14, 2005.
  2. PMID 17971314
    .

External links

Common Phosphate Binders