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PHARMACOKINETIC BASIS OF INTRAVENOUS DRUG DELIVERY
被引:5
|
作者
:
GLASS, PSA
论文数:
0
引用数:
0
h-index:
0
GLASS, PSA
DOHERTY, D
论文数:
0
引用数:
0
h-index:
0
DOHERTY, D
JACOBS, JR
论文数:
0
引用数:
0
h-index:
0
JACOBS, JR
QUILL, TJ
论文数:
0
引用数:
0
h-index:
0
QUILL, TJ
机构
:
来源
:
BAILLIERES CLINICAL ANAESTHESIOLOGY
|
1991年
/ 5卷
/ 03期
关键词
:
D O I
:
10.1016/S0950-3501(05)80050-9
中图分类号
:
R614 [麻醉学];
学科分类号
:
100217 ;
摘要
:
We have seen in recent years the release of numerous intravenous anaesthetic agents whose duration of action is relatively short, thus lending themselves to administration via continuous infusion. Clinical studies have clearly demonstrated the advantages of continuous infusion over repeated bolus dosing. These two factors have prompted pump manufacturers to produce devices that simplify the administration of intravenous anaesthetics by continuous infusion. It is concentration rather than dose that results in the desired effect. Utilizing pharmacokinetic principles, it is possible to provide automated drug delivery systems whereby the device can produce a clinician-specified drug concentration. In addition, where there is an easily measurable end-point, closed-loop feedback control can be implemented automatically to control the desired parameter within a very narrow range. With this rapid development in intravenous drug delivery, it becomes imperative that clinicians familiarize themselves with these new drug delivery devices so that they can use them optimally to care for their patients. © 1991 Baillière Tindall.
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收藏
页码:735 / 775
页数:41
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