Campara M, Shord S S, Haaf C M
Department of Pharmacy Practice, University of Illinois, Chicago, IL, USA.
J Clin Pharm Ther. 2009 Apr;34(2):207-13. doi: 10.1111/j.1365-2710.2008.00994.x.
The optimal rasburicase dose for adult patients has not been determined.
To retrospectively examine use of rasburicase in our centre and to evaluate the effect of a single dose of rasburicase on urate and serum creatinine levels in our adult patients.
A retrospective chart review was conducted of all adult patients who received rasburicase for treatment of tumour lysis syndrome-associated hyperuricaemia at our academic, urban medical centre from July 2002 to October 2006.
Twenty-one patients received rasburicase with an average first dose of 0.15 +/- 0.03 mg/kg. The drug dosing was calculated based on the patients' ideal body weight (IBW) or adjusted body weight (aBW) for those who were more than 30% above their IBW. Patients experienced a mean serum urate reduction of 89.7 +/- 9.0% from the baseline through the first 24 h after a single rasburicase dose (11.4 +/- 4.5 mg/dL vs. 1.4 +/- 1.4 mg/dL, respectively, P < 0.001). The urate levels remained within normal limits (<8 mg/dL) in all the patients for 48 h after a single dose of rasburicase. The major limitation of our study is that in 18 of 21 patients we lacked adequate documentation to ascertain that the blood samples sent for urate analysis after drug administration were handled according to the manufacturer's recommendations. However, in this small group of patients, we observed that the effect of rasburicase on serum urate was similar to the total study population. The effect was sustained for 48 h after a single dose. Serum creatinine levels at 24-72 h after the single rasburicase dose were not significantly different from baseline (1.8 mg/dL vs. 2.3 mg/dL, respectively, P = 0.14).
Rasburicase is an effective treatment for patients with hyperuricaemia and may aid in the prevention of hyperuricaemia-associated nephrotoxicity. From our experience, a single dose of 0.15 mg/kg (IBW or aBW) of rasburicase appears to effectively decrease and maintain urate levels within normal limits for 48 h.
成人患者的最佳拉布立酶剂量尚未确定。
回顾性研究我院中心拉布立酶的使用情况,并评估单剂量拉布立酶对成年患者尿酸和血清肌酐水平的影响。
对2002年7月至2006年10月在我院学术性城市医疗中心接受拉布立酶治疗肿瘤溶解综合征相关高尿酸血症的所有成年患者进行回顾性病历审查。
21例患者接受了拉布立酶治疗,平均首剂剂量为0.15±0.03mg/kg。药物剂量根据患者的理想体重(IBW)计算,对于体重超过IBW 30%以上的患者,则根据调整体重(aBW)计算。患者在单次服用拉布立酶后的前24小时内,血清尿酸平均从基线水平降低了89.7±9.0%(分别为11.4±4.5mg/dL和1.4±1.4mg/dL,P<0.001)。单次服用拉布立酶后,所有患者的尿酸水平在48小时内均保持在正常范围内(<8mg/dL)。本研究的主要局限性在于,21例患者中有18例缺乏充分的记录,无法确定给药后送检进行尿酸分析的血样是否按照制造商的建议处理。然而,在这一小部分患者中,我们观察到拉布立酶对血清尿酸的影响与整个研究人群相似。单次给药后,这种效果持续了48小时。单次服用拉布立酶后24 - 72小时的血清肌酐水平与基线水平无显著差异(分别为1.8mg/dL和2.3mg/dL,P = 0.14)。
拉布立酶是治疗高尿酸血症患者的有效药物,可能有助于预防高尿酸血症相关的肾毒性。根据我们的经验,单次剂量0.15mg/kg(IBW或aBW)的拉布立酶似乎能有效降低尿酸水平并使其在48小时内维持在正常范围内。