Antiepileptic drugs—best practice guidelines for therapeutic drug monitoring: A position paper by the subcommission on therapeutic drug monitoring, ILAE Commission on Therapeutic Strategies

Summary Although no randomized studies have demonstrated a positive impact of therapeutic drug monitoring (TDM) on clinical outcome in epilepsy, evidence from nonrandomized studies and everyday clinical experience does indicate that measuring serum concentrations of old and new generation antiepilep...

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Published in:Epilepsia (Copenhagen) Vol. 49; no. 7; pp. 1239 - 1276
Main Authors: Patsalos, Philip N., Berry, David J., Bourgeois, Blaise F. D., Cloyd, James C., Glauser, Tracy A., Johannessen, Svein I., Leppik, Ilo E., Tomson, Torbjörn, Perucca, Emilio
Format: Journal Article
Language:English
Published: Malden, USA Blackwell Publishing Inc 01.07.2008
Blackwell
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ISSN:0013-9580, 1528-1167, 1528-1167
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Abstract Summary Although no randomized studies have demonstrated a positive impact of therapeutic drug monitoring (TDM) on clinical outcome in epilepsy, evidence from nonrandomized studies and everyday clinical experience does indicate that measuring serum concentrations of old and new generation antiepileptic drugs (AEDs) can have a valuable role in guiding patient management provided that concentrations are measured with a clear indication and are interpreted critically, taking into account the whole clinical context. Situations in which AED measurements are most likely to be of benefit include (1) when a person has attained the desired clinical outcome, to establish an individual therapeutic concentration which can be used at subsequent times to assess potential causes for a change in drug response; (2) as an aid in the diagnosis of clinical toxicity; (3) to assess compliance, particularly in patients with uncontrolled seizures or breakthrough seizures; (4) to guide dosage adjustment in situations associated with increased pharmacokinetic variability (e.g., children, the elderly, patients with associated diseases, drug formulation changes); (5) when a potentially important pharmacokinetic change is anticipated (e.g., in pregnancy, or when an interacting drug is added or removed); (6) to guide dose adjustments for AEDs with dose‐dependent pharmacokinetics, particularly phenytoin.
AbstractList Summary Although no randomized studies have demonstrated a positive impact of therapeutic drug monitoring (TDM) on clinical outcome in epilepsy, evidence from nonrandomized studies and everyday clinical experience does indicate that measuring serum concentrations of old and new generation antiepileptic drugs (AEDs) can have a valuable role in guiding patient management provided that concentrations are measured with a clear indication and are interpreted critically, taking into account the whole clinical context. Situations in which AED measurements are most likely to be of benefit include (1) when a person has attained the desired clinical outcome, to establish an individual therapeutic concentration which can be used at subsequent times to assess potential causes for a change in drug response; (2) as an aid in the diagnosis of clinical toxicity; (3) to assess compliance, particularly in patients with uncontrolled seizures or breakthrough seizures; (4) to guide dosage adjustment in situations associated with increased pharmacokinetic variability (e.g., children, the elderly, patients with associated diseases, drug formulation changes); (5) when a potentially important pharmacokinetic change is anticipated (e.g., in pregnancy, or when an interacting drug is added or removed); (6) to guide dose adjustments for AEDs with dose‐dependent pharmacokinetics, particularly phenytoin.
Although no randomized studies have demonstrated a positive impact of therapeutic drug monitoring (TDM) on clinical outcome in epilepsy, evidence from nonrandomized studies and everyday clinical experience does indicate that measuring serum concentrations of old and new generation antiepileptic drugs (AEDs) can have a valuable role in guiding patient management provided that concentrations are measured with a clear indication and are interpreted critically, taking into account the whole clinical context. Situations in which AED measurements are most likely to be of benefit include (1) when a person has attained the desired clinical outcome, to establish an individual therapeutic concentration which can be used at subsequent times to assess potential causes for a change in drug response; (2) as an aid in the diagnosis of clinical toxicity; (3) to assess compliance, particularly in patients with uncontrolled seizures or breakthrough seizures; (4) to guide dosage adjustment in situations associated with increased pharmacokinetic variability (e.g., children, the elderly, patients with associated diseases, drug formulation changes); (5) when a potentially important pharmacokinetic change is anticipated (e.g., in pregnancy, or when an interacting drug is added or removed); (6) to guide dose adjustments for AEDs with dose-dependent pharmacokinetics, particularly phenytoin.
Although no randomized studies have demonstrated a positive impact of therapeutic drug monitoring (TDM) on clinical outcome in epilepsy, evidence from nonrandomized studies and everyday clinical experience does indicate that measuring serum concentrations of old and new generation antiepileptic drugs (AEDs) can have a valuable role in guiding patient management provided that concentrations are measured with a clear indication and are interpreted critically, taking into account the whole clinical context. Situations in which AED measurements are most likely to be of benefit include (1) when a person has attained the desired clinical outcome, to establish an individual therapeutic concentration which can be used at subsequent times to assess potential causes for a change in drug response; (2) as an aid in the diagnosis of clinical toxicity; (3) to assess compliance, particularly in patients with uncontrolled seizures or breakthrough seizures; (4) to guide dosage adjustment in situations associated with increased pharmacokinetic variability (e.g., children, the elderly, patients with associated diseases, drug formulation changes); (5) when a potentially important pharmacokinetic change is anticipated (e.g., in pregnancy, or when an interacting drug is added or removed); (6) to guide dose adjustments for AEDs with dose-dependent pharmacokinetics, particularly phenytoin.Although no randomized studies have demonstrated a positive impact of therapeutic drug monitoring (TDM) on clinical outcome in epilepsy, evidence from nonrandomized studies and everyday clinical experience does indicate that measuring serum concentrations of old and new generation antiepileptic drugs (AEDs) can have a valuable role in guiding patient management provided that concentrations are measured with a clear indication and are interpreted critically, taking into account the whole clinical context. Situations in which AED measurements are most likely to be of benefit include (1) when a person has attained the desired clinical outcome, to establish an individual therapeutic concentration which can be used at subsequent times to assess potential causes for a change in drug response; (2) as an aid in the diagnosis of clinical toxicity; (3) to assess compliance, particularly in patients with uncontrolled seizures or breakthrough seizures; (4) to guide dosage adjustment in situations associated with increased pharmacokinetic variability (e.g., children, the elderly, patients with associated diseases, drug formulation changes); (5) when a potentially important pharmacokinetic change is anticipated (e.g., in pregnancy, or when an interacting drug is added or removed); (6) to guide dose adjustments for AEDs with dose-dependent pharmacokinetics, particularly phenytoin.
Author Berry, David J.
Bourgeois, Blaise F. D.
Perucca, Emilio
Cloyd, James C.
Johannessen, Svein I.
Leppik, Ilo E.
Glauser, Tracy A.
Tomson, Torbjörn
Patsalos, Philip N.
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  surname: Patsalos
  fullname: Patsalos, Philip N.
– sequence: 2
  givenname: David J.
  surname: Berry
  fullname: Berry, David J.
– sequence: 3
  givenname: Blaise F. D.
  surname: Bourgeois
  fullname: Bourgeois, Blaise F. D.
– sequence: 4
  givenname: James C.
  surname: Cloyd
  fullname: Cloyd, James C.
– sequence: 5
  givenname: Tracy A.
  surname: Glauser
  fullname: Glauser, Tracy A.
– sequence: 6
  givenname: Svein I.
  surname: Johannessen
  fullname: Johannessen, Svein I.
– sequence: 7
  givenname: Ilo E.
  surname: Leppik
  fullname: Leppik, Ilo E.
– sequence: 8
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  surname: Tomson
  fullname: Tomson, Torbjörn
– sequence: 9
  givenname: Emilio
  surname: Perucca
  fullname: Perucca, Emilio
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https://www.ncbi.nlm.nih.gov/pubmed/18397299$$D View this record in MEDLINE/PubMed
http://kipublications.ki.se/Default.aspx?queryparsed=id:117327726$$DView record from Swedish Publication Index (Karolinska Institutet)
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CODEN EPILAK
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ISSN 0013-9580
1528-1167
IngestDate Tue Nov 25 03:35:33 EST 2025
Sun Nov 09 12:41:05 EST 2025
Thu Oct 02 04:53:47 EDT 2025
Thu Apr 03 07:04:29 EDT 2025
Mon Jul 21 09:15:29 EDT 2025
Tue Nov 18 22:08:54 EST 2025
Sat Nov 29 06:04:54 EST 2025
Sun Sep 21 06:28:21 EDT 2025
IsPeerReviewed true
IsScholarly true
Issue 7
Keywords Human
Nervous system diseases
Epilepsy
Anticonvulsant
Cerebral disorder
Pregnancy
Drug compliance
Treatment
Central nervous system disease
Children
Pharmacokinetics
Child
Elderly
Saliva
Monitoring
Language English
License http://onlinelibrary.wiley.com/termsAndConditions#vor
CC BY 4.0
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MergedId FETCHMERGED-LOGICAL-c5321-181a4834b528e70c0b61fc94027a078a3c9ffa8a067b405d0df76affe78386403
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ObjectType-Feature-1
content type line 23
ObjectType-Article-1
ObjectType-Feature-2
ObjectType-Instructional Material/Guideline-3
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crossref_citationtrail_10_1111_j_1528_1167_2008_01561_x
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PublicationDate July 2008
PublicationDateYYYYMMDD 2008-07-01
PublicationDate_xml – month: 07
  year: 2008
  text: July 2008
PublicationDecade 2000
PublicationPlace Malden, USA
PublicationPlace_xml – name: Malden, USA
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PublicationTitle Epilepsia (Copenhagen)
PublicationTitleAlternate Epilepsia
PublicationYear 2008
Publisher Blackwell Publishing Inc
Blackwell
Publisher_xml – name: Blackwell Publishing Inc
– name: Blackwell
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Snippet Summary Although no randomized studies have demonstrated a positive impact of therapeutic drug monitoring (TDM) on clinical outcome in epilepsy, evidence from...
Although no randomized studies have demonstrated a positive impact of therapeutic drug monitoring (TDM) on clinical outcome in epilepsy, evidence from...
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StartPage 1239
SubjectTerms Adolescent
Aged
Anticonvulsants - blood
Anticonvulsants - pharmacokinetics
Anticonvulsants - therapeutic use
Anticonvulsants. Antiepileptics. Antiparkinson agents
Biological and medical sciences
Biological Availability
Child
Child, Preschool
Children
Cooperative Behavior
Drug compliance
Drug Monitoring - methods
Drug Therapy, Combination
Elderly
Epilepsy - drug therapy
Half-Life
Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy
Humans
Infant
Infant, Newborn
Medical sciences
Nervous system (semeiology, syndromes)
Neurology
Neuropharmacology
Pharmacokinetics
Pharmacology. Drug treatments
Pregnancy
Reference Values
Saliva
Title Antiepileptic drugs—best practice guidelines for therapeutic drug monitoring: A position paper by the subcommission on therapeutic drug monitoring, ILAE Commission on Therapeutic Strategies
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1528-1167.2008.01561.x
https://www.ncbi.nlm.nih.gov/pubmed/18397299
https://www.proquest.com/docview/20941911
https://www.proquest.com/docview/69337636
http://kipublications.ki.se/Default.aspx?queryparsed=id:117327726
Volume 49
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