Literature DB >> 10346419

Fosphenytoin. Pharmacoeconomic implications of therapy.

S M Holliday1, P Benfield, G L Plosker.   

Abstract

Advantages and disadvantages of Fosphenytoin. Advantages. More rapid intravenous administration than phenytoin and no need for an in-line filter. May be administered by intramuscular injection. Lower potential for local tissue and cardiac toxicity than phenytoin. Associated with less pain and phlebitis at the injection site, fewer reductions in infusion rate and fewer changes of administration site because of injection site complications than phenytoin. Benefits in terms of ease of administration and improved tolerability vs phenytoin have pharmacoeconomic implications which may translate into an overall cost advantage. Disadvantages. Approximately 10-fold higher acquisition cost vs phenytoin. Fosphenytoin is a parenterally administered prodrug of phenytoin, used in the treatment of patients with seizures. Advantages of fosphenytoin over phenytoin include more rapid intravenous administration, no need for an intravenous filter, and a lower potential for local tissue and cardiac toxicity. Unlike phenytoin, fosphenytoin may also be administered by intramuscular injection. Pharmacoeconomic data from a small study of patients with acute seizures in a US emergency department showed an overall cost advantage of fosphenytoin over phenytoin, despite a considerably greater acquisition cost of fosphenytoin. The main cost drivers for phenytoin therapy were treatment costs associated with adverse events. In view of the limited pharmacoeconomic data currently available, it is in the interests of individual institutions to conduct their own formal pharmacoeconomic studies applying local cost data and patterns of clinical practise to determine whether fosphenytoin should replace phenytoin on their formularly list.

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Year:  1998        PMID: 10346419     DOI: 10.2165/00019053-199814060-00008

Source DB:  PubMed          Journal:  Pharmacoeconomics        ISSN: 1170-7690            Impact factor:   4.981


  15 in total

1.  A pharmacoeconomic evaluation of intravenous fosphenytoin (Cerebyx) versus intravenous phenytoin (Dilantin) in hospital emergency departments.

Authors:  A Marchetti; R Magar; J Fischer; E Sloan; P Fischer
Journal:  Clin Ther       Date:  1996 Sep-Oct       Impact factor: 3.393

2.  The cardiocirculatory changes caused by intravenous Dilantin and its solvent.

Authors:  S Louis; H Kutt; F McDowell
Journal:  Am Heart J       Date:  1967-10       Impact factor: 4.749

Review 3.  Fosphenytoin (Cerebyx).

Authors:  T R Browne
Journal:  Clin Neuropharmacol       Date:  1997-02       Impact factor: 1.592

4.  Pharmacokinetics and safety of a phenytoin prodrug given i.v. or i.m. in patients.

Authors:  I E Leppik; B A Boucher; B J Wilder; V S Murthy; C Watridge; N M Graves; R J Rangel; C A Rask; P Turlapaty
Journal:  Neurology       Date:  1990-03       Impact factor: 9.910

5.  Plasma diphenylhydantoin values after oral and intramuscular administration of diphenylhydantoin.

Authors:  E E Serrano; D B Roye; R H Hammer; B J Wilder
Journal:  Neurology       Date:  1973-03       Impact factor: 9.910

6.  Absolute bioavailability of phenytoin after 3-phosphoryloxymethyl phenytoin disodium (ACC-9653) administration to humans.

Authors:  B D Jamerson; K H Donn; G E Dukes; J A Messenheimer; K L Brouwer; J R Powell
Journal:  Epilepsia       Date:  1990 Sep-Oct       Impact factor: 5.864

7.  Severe soft-tissue injury following intravenous infusion of phenytoin. Patient and drug administration risk factors.

Authors:  R F Spengler; J B Arrowsmith; D J Kilarski; C Buchanan; L Von Behren; D R Graham
Journal:  Arch Intern Med       Date:  1988-06

8.  The safety, tolerability, and pharmacokinetics of fosphenytoin after intramuscular and intravenous administration in neurosurgery patients.

Authors:  B A Boucher; C A Feler; J C Dean; D D Michie; B K Tipton; K R Smith; R E Kramer; B Young; B R Parks; A R Kugler
Journal:  Pharmacotherapy       Date:  1996 Jul-Aug       Impact factor: 4.705

9.  Venous irritation related to intravenous administration of phenytoin versus fosphenytoin.

Authors:  B D Jamerson; G E Dukes; K L Brouwer; K H Donn; J A Messenheimer; J R Powell
Journal:  Pharmacotherapy       Date:  1994 Jan-Feb       Impact factor: 4.705

10.  Phenytoin prodrug 3-phosphoryloxymethyl phenytoin (ACC-9653): pharmacokinetics in patients following intravenous and intramuscular administration.

Authors:  B A Boucher; A M Bombassaro; S N Rasmussen; C B Watridge; R Achari; P Turlapaty
Journal:  J Pharm Sci       Date:  1989-11       Impact factor: 3.534

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  2 in total

Review 1.  Fosphenytoin: clinical pharmacokinetics and comparative advantages in the acute treatment of seizures.

Authors:  James H Fischer; Tejal V Patel; Patricia A Fischer
Journal:  Clin Pharmacokinet       Date:  2003       Impact factor: 6.447

Review 2.  Levetiracetam for Status Epilepticus in Adults: A Systematic Review.

Authors:  Carly A Webb; Richard Wanbon; Erica D Otto
Journal:  Can J Hosp Pharm       Date:  2022
  2 in total

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