TY - JOUR
T1 - Blood levels to optimize antipsychotic treatment in clinical practice
T2 - A joint consensus statement of the American society of clinical psychopharmacology and the therapeutic drug monitoring task force of the arbeitsgemeinschaft für neuropsychopharmakologie und pharmakopsychiatrie
AU - Schoretsanitis, Georgios
AU - Kane, John M.
AU - Correll, Christoph U.
AU - Marder, Stephen R.
AU - Citrome, Leslie
AU - Newcomer, John W.
AU - Robinson, Delbert G.
AU - Goff, Donald C.
AU - Kelly, Deanna L.
AU - Freudenreich, Oliver
AU - Piacentino, Daria
AU - Paulzen, Michael
AU - Conca, Andreas
AU - Zernig, Gerald
AU - Haen, Ekkehard
AU - Baumann, Pierre
AU - Hiemke, Christoph
AU - Gründer, Gerhard
AU - Bergemann, Niels
AU - Clement, Hans Willi
AU - Deckert, Jürgen
AU - Eckermann, Gabriel
AU - Egberts, Karin
AU - Gerlach, Manfred
AU - Greiner, Christine
AU - Havemann-Reinecke, Ursula
AU - Hefner, Gudrun
AU - Helmer, Renate
AU - Laux, Gerd
AU - Messer, Thomas
AU - Mössner, Rainald
AU - Müller, Matthias J.
AU - Pfuhlmann, Bruno
AU - Riederer, Peter
AU - Saria, Alois
AU - Schoppek, Bernd
AU - Schwarz, Markus
AU - Gracia, Margarete Silva
AU - Stegmann, Benedikt
AU - Steimer, Werner
AU - Uhr, Manfred
AU - Ulrich, Sven
AU - Unterecker, Stefan
AU - Waschgler, Roland
AU - Zurek, Gabriela
N1 - Publisher Copyright:
© 2020 Copyright Physicians Postgraduate Press Inc.
PY - 2020/6
Y1 - 2020/6
N2 - Objective: The quantification of antipsychotic levels in blood, also known as therapeutic drug monitoring (TDM), is a potentially useful tool of modern personalized therapy that can be applied to augment antipsychotic use and dosing decisions. The application of TDM for antipsychotics can be helpful in numerous challenging clinical scenarios, such as lack of therapeutic response, relapse, or adverse drug reactions (ADRs) related to antipsychotic treatment. The benefits of TDM may be particularly evident in the treatment of highly vulnerable patient subgroups, such as children, adolescents, pregnant women, and the elderly. The main aim of this article is to aid clinicians who routinely prescribe antipsychotics to successfully apply TDM in routine clinical practice in order to help optimize the efficacy and safety of those antipsychotics. Participants: Participants were clinicians and researchers, members of the American Society of Clinical Psychopharmacology, and the Therapeutic Drug Monitoring Task Force of the Arbeitsgemeinschaft für Neuropsychopharmakologie und Pharmakopsychiatrie (Association of Neuropsychopharmacology and Pharmacopsychiatry). Evidence: TDM literature on antipsychotics was critically reviewed to provide a condensed clinical decision-making algorithm with therapeutic reference ranges for blood antipsychotic levels, within which patients are most likely to respond and tolerate treatment, although TDM is not equally recommended/supported for all antipsychotics. Consensus Process: A preliminary draft was prepared and circulated to the writing group members. Consensus was achieved in all cases, and resulting recommendations focused on following areas: steady-state and sampling time, levels of recommendations, indications, therapeutic reference ranges and laboratory alert levels, practical issues, and interpretation, as well as limitations. Conclusions: The utilization of TDM as a tool for problem solving in antipsychotic treatment offers a unique method to improve safety and efficacy. This consensus statement summarizes essential information on the routine use of TDM for antipsychotics and encourages clinicians to perform TDM with the appropriate indications as part of the clinical decision-making process.
AB - Objective: The quantification of antipsychotic levels in blood, also known as therapeutic drug monitoring (TDM), is a potentially useful tool of modern personalized therapy that can be applied to augment antipsychotic use and dosing decisions. The application of TDM for antipsychotics can be helpful in numerous challenging clinical scenarios, such as lack of therapeutic response, relapse, or adverse drug reactions (ADRs) related to antipsychotic treatment. The benefits of TDM may be particularly evident in the treatment of highly vulnerable patient subgroups, such as children, adolescents, pregnant women, and the elderly. The main aim of this article is to aid clinicians who routinely prescribe antipsychotics to successfully apply TDM in routine clinical practice in order to help optimize the efficacy and safety of those antipsychotics. Participants: Participants were clinicians and researchers, members of the American Society of Clinical Psychopharmacology, and the Therapeutic Drug Monitoring Task Force of the Arbeitsgemeinschaft für Neuropsychopharmakologie und Pharmakopsychiatrie (Association of Neuropsychopharmacology and Pharmacopsychiatry). Evidence: TDM literature on antipsychotics was critically reviewed to provide a condensed clinical decision-making algorithm with therapeutic reference ranges for blood antipsychotic levels, within which patients are most likely to respond and tolerate treatment, although TDM is not equally recommended/supported for all antipsychotics. Consensus Process: A preliminary draft was prepared and circulated to the writing group members. Consensus was achieved in all cases, and resulting recommendations focused on following areas: steady-state and sampling time, levels of recommendations, indications, therapeutic reference ranges and laboratory alert levels, practical issues, and interpretation, as well as limitations. Conclusions: The utilization of TDM as a tool for problem solving in antipsychotic treatment offers a unique method to improve safety and efficacy. This consensus statement summarizes essential information on the routine use of TDM for antipsychotics and encourages clinicians to perform TDM with the appropriate indications as part of the clinical decision-making process.
UR - http://www.scopus.com/inward/record.url?scp=85090277332&partnerID=8YFLogxK
U2 - 10.4088/JCP.19cs13169
DO - 10.4088/JCP.19cs13169
M3 - Article
AN - SCOPUS:85090277332
SN - 0160-6689
VL - 81
JO - Journal of Clinical Psychiatry
JF - Journal of Clinical Psychiatry
IS - 3
M1 - 19cs13169
ER -