Guidelines for nonemergency use of parenteral phenytoin products -: Proceedings of an expert panel consensus process

被引:26
作者
Meek, PD
Davis, SN
Collins, M
Gidal, BE
Rutecki, PA
Burstein, AH
Fischer, JH
Leppik, IE
Ramsay, RE
机构
[1] Univ Wisconsin, Sch Pharm, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Neurol, Madison, WI 53706 USA
[3] Univ Wisconsin Hosp & Clin, Ctr Drug Policy & Clin Econ, Madison, WI 53792 USA
[4] Univ Wisconsin Hosp & Clin, Dept Pharm, Madison, WI 53792 USA
[5] Univ Maryland, Dept Pharm Practice & Sci, Baltimore, MD 21201 USA
[6] Univ Illinois, Dept Pharm Practice, Chicago, IL 60680 USA
[7] Univ Minnesota, MINCEP Epilepsy Care, Minneapolis, MN USA
[8] Univ Miami, Int Ctr Epilepsy, Miami, FL 33152 USA
关键词
D O I
10.1001/archinte.159.22.2639
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This document summarizes the proceedings of an expert panel consensus process addressing the nonemergency use of parenteral phenytoin products for management of seizures in pediatric and adult patients. The algorithm and consensus statements developed by the expert panel emphasize strategies for lowering the probability of adverse events associated with the use of parenteral phenytoin products. Specific patient characteristics are defined to guide administration and monitoring of parenteral phenytoin therapy. The algorithm provides a decision pathway for the selection of the product and the route of administration of phenytoin sodium or fosphenytoin sodium after it has been determined that a parenteral phenytoin product is appropriate. Key factors covered in the algorithm include a list of patient characteristics and considerations necessary to prevent parenteral phenytoin adverse effects during selection of administration route and recommendations for monitoring of parenteral phenytoin therapy once it has been initiated. Situations requiring rapid attainment of high phenytoin concentrations, such as in the management of acute seizures, are not addressed in these guidelines.
引用
收藏
页码:2639 / 2644
页数:6
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