monitor with HMG CoA reductase inhibitors (statins)
Jump to navigation
Jump to search
Monitor
- liver function tests (baseline, 12 weeks, then yearly)
- slight difference in recommendations for each statin[2]
- discontinue if ALT or AST > 3x upper limit of normal
- increased liver function tests (< 10-fold normal) NOT associated with increased risk of hepatotoxicity[3]
- creatine kinase
- baseline levels on ALL patients
- recheck patients who develop myalgias or brown urine
- discontinue if 10x upper limit of normal
- monitor elevated levels < 10x normal weekly
- routine monitoring NOT recommended
- lipid panel 6-8 weeks after initiation or increasing dose
- serum TSH & if myalgia or muscle weakness
More general terms
References
- ↑ Prescriber's Letter 17(7): 2010 Recommended Lab Monitoring for Common Medications Detail-Document#: http://prescribersletter.com/(5bhgn1a4ni4cyp2tvybwfh55)/pl/ArticleDD.aspx?li=1&st=1&cs=&s=PRL&pt=3&fpt=25&dd=260704&pb=PRL (subscription needed) http://www.prescribersletter.com
- ↑ 2.0 2.1 Prescriber's Letter 17(6): 2010 Characteristics of the Various Statins Detail-Document#: http://prescribersletter.com/(5bhgn1a4ni4cyp2tvybwfh55)/pl/ArticleDD.aspx?li=1&st=1&cs=&s=PRL&pt=3&fpt=25&dd=260611&pb=PRL (subscription needed) http://www.prescribersletter.com
- ↑ 3.0 3.1 Chalasani N, Aljadhey H, Kesterson J, Murray MD, Hall SD. Patients with elevated liver enzymes are not at higher risk for statin hepatotoxicity. Gastroenterology. 2004 May;126(5):1287-92. PMID: https://www.ncbi.nlm.nih.gov/pubmed/15131789