McMaster P, Mirza D F, Ismail T, Vennarecci G, Patapis P, Mayer A D
Liver and Hepatobiliary Unit, Queen Elizabeth Hospital, Edgbaston, Birmingham, UK.
Ther Drug Monit. 1995 Dec;17(6):602-5. doi: 10.1097/00007691-199512000-00010.
Initial clinical trials of FK did not incorporate available FK levels, and difficulties were quickly experienced particularly with neurotoxicity and nephrotoxicity. The introduction of routine assay allowed broad parameters to be identified, which assisted in evaluating effective therapeutic parameters. Levels approximately 20 ng/ml were frequently associated with toxicity and the initial therapeutic range between 10-25 ng/ml was probably excessive. Reliable effective assay > 5 ng/ml using the Abbott IMx is not available, and many patients will have excellent hepatic or renal function with what are currently undetectable levels of FK. However, IncStar have an ELISA assay with a sensitivity of 0.5 mg/ml. Clinical practice does not, at this time, dictate elevation of FK, although careful monitoring continues. Education of oral administration from 0.15 mg/kg to 0.1 mg/kg in combination therapy with steroids and 0.05 mg/kg with azathioprine and steroids has led to revision of therapeutic parameters, e.g., 5-15 ng/ml is now widely used. Therapeutic drug monitoring is important to avoid unnecessary toxicity, but the lower limit has not been fully defined. Clearly, many patients with < 5 ng/ml have excellent hepatic function.
FK的初步临床试验未纳入可用的FK水平,很快就遇到了困难,尤其是神经毒性和肾毒性方面。常规检测方法的引入使得能够确定广泛的参数,这有助于评估有效的治疗参数。大约20 ng/ml的水平经常与毒性相关,最初10 - 25 ng/ml的治疗范围可能过大。使用雅培IMx无法进行可靠的大于5 ng/ml的有效检测,许多患者肝功能或肾功能良好,但目前FK水平检测不到。然而,英思科公司有一种灵敏度为0.5 mg/ml的酶联免疫吸附测定法。目前临床实践并不要求提高FK水平,尽管仍需仔细监测。在与类固醇联合治疗时,口服剂量从0.15 mg/kg降至0.1 mg/kg,与硫唑嘌呤和类固醇联合治疗时降至0.05 mg/kg,这导致了治疗参数的修订,例如,现在广泛使用5 - 15 ng/ml。治疗药物监测对于避免不必要的毒性很重要,但下限尚未完全确定。显然,许多FK水平低于5 ng/ml的患者肝功能良好。