Pleasants R A, Sawyer W T, Williams D M, McKenna W R, Brown J M, Powell J R
Department of Pharmacy, North Carolina Memorial Hospital, Chapel, NC 27514.
Clin Pharm. 1988 May;7(5):367-73.
The accuracy of tobramycin delivery by four methods of intermittent intravenous infusion was studied in 11 healthy male volunteers. Subjects received intravenous tobramycin (as the sulfate salt) 1.5 mg/kg by each of four infusion methods in a nonblinded, randomized, four-way crossover design. The methods used for intravenous infusion were (1) minibag via gravity flow (MG), (2) minibag with the secondary infusion tubing inserted below a volumetric infusion pump (MP), (3) metered chamber via volumetric infusion pump (MC), and (4) syringe pump (SP). Doses were diluted to a volume of 50 mL, except for the two minibag methods, for which the dilution was necessarily greater because of manufacturer overfill. Intravenous flow rates for both primary fluid and drug administration were set at 100 mL/hr, and the duration of drug infusion was documented by observation for each administered dose. The fluid volume of 12 minibags was measured to assess manufacturer overfill. Fluid remaining in the secondary i.v. tubing for the minibag methods was collected after the infusion. Seventeen blood samples were obtained before and at various time intervals after each dose and analyzed in duplicate for tobramycin content by fluorescence polarization immunoassay. A mean of 10% of each dose remained in the secondary i.v. tubing at the completion of the infusion for the minibag methods, whereas less than 1% of each dose remained in the secondary tubing for the SP method.(ABSTRACT TRUNCATED AT 250 WORDS)
在11名健康男性志愿者中研究了四种间歇性静脉输注方法给予妥布霉素的准确性。受试者采用非盲、随机、四交叉设计,通过四种输注方法分别接受静脉注射妥布霉素(硫酸盐)1.5mg/kg。静脉输注所用方法为:(1)重力流微型袋(MG);(2)在容量输液泵下方插入二级输液管的微型袋(MP);(3)通过容量输液泵的定量室(MC);(4)注射泵(SP)。除两种微型袋方法外,剂量均稀释至50mL,由于制造商的过量灌装,这两种微型袋方法的稀释度必然更高。主液和药物输注的静脉流速均设定为100mL/hr,每次给药剂量的输注持续时间通过观察记录。测量12个微型袋的液体量以评估制造商的过量灌装情况。微型袋方法在输注后收集二级静脉输液管中剩余的液体。在每次给药前及给药后的不同时间间隔采集17份血样,通过荧光偏振免疫分析法对妥布霉素含量进行双份分析。对于微型袋方法,在输注结束时,平均每次剂量的10%残留在二级静脉输液管中,而对于SP方法,每次剂量残留在二级输液管中的比例不到1%。(摘要截短于250字)