臨牀透析 Vol.35 No.6(7)


特集名 AKI診療のエビデンスと課題
題名 急性血液浄化療法における薬物動態と薬の使い方
発刊年月 2019年 06月
著者 山本 武人 東京大学大学院薬学系研究科・医療薬学教育センター
【 要旨 】 急性血液浄化療法導入時には一般に腎排泄型薬物の体内動態が変化しやすい.持続的腎代替療法(CRRT)による薬物除去能力は濾液流量(QE)により決定され,わが国における実施条件ではクレアチニンクリアランス(Ccr)あるいは糸球体濾過量(GFR)として10~30mL/min に相当する.そのため,CRRT導入時の投与量は,原則として腎機能が中等度に低下した患者(CcrあるいはGFRで10~50 mL/min)と同用量でよい.また,持続低効率血液透析(SLED)導入時の投与量についても基本的にはCRRT導入時と同量でよいと考えられるが,情報は不足しており,今後さらなる検証が必要である.
Theme Evidence and issue for clinical practice of acute kidney injury
Title Alteration of pharmacokinetics and strategies of dosage setting during acute blood purification
Author Takehito Yamamoto The Education Center for Clinical Pharmacy, Graduate School of Pharmaceutical Sciences, The University of Tokyo
[ Summary ] Generally, the pharmacokinetics of renally excreted drugs are altered during acute blood purification. Therefore, special consideration is needed for the dosage settings of drugs during acute blood purification such as continuous renal replacement therapy (CRRT) or sustained low-efficiency dialysis (SLED). The effluent flow rate (QE) of CRRT is the major determinant of its drug eliminating capacity, and the drug clearance by CRRT accounts for creatinine clearance (Ccr) or glomerular filtration rate (GFR) of 10-30 mL/min. Therefore, in most cases, dosage during CRRT is as same as those for patients with moderately impaired renal function (i.e. Ccr or GFR of 10-50 mL/min), while the dosage during SLED should be the same as during CRRT. However, the information regarding alteration of pharmacokinetics during SLED is limited and further studies are needed to enable the optimal dosage setting.
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