Subanalysis of the CYP-GUIDES Trial: CYP2D6 Functional Stratification and Operational Timeline Selection

•The CYP-GUIDES Trial assessed length of hospitalization in major depressive disorder.•It compared drug treatment guided by CYP2D6 functional status versus standard care.•CYP2D6 guidance reduced hospitalization length of stay and drug utilization.•CYP2D6 functional stratification found guidance effe...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Psychiatry research 2021-03, Vol.297, p.113571-113571, Article 113571
Hauptverfasser: Ruaño, Gualberto, Tortora, Joseph, Robinson, Saskia, Baker, Seth, Holford, Theodore, Winokur, Andrew, Goethe, John W.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:•The CYP-GUIDES Trial assessed length of hospitalization in major depressive disorder.•It compared drug treatment guided by CYP2D6 functional status versus standard care.•CYP2D6 guidance reduced hospitalization length of stay and drug utilization.•CYP2D6 functional stratification found guidance effect to be on sub-normal patients.•Sub-normal CYP2D6 function represents a treatable pharmacogenetic vulnerability. CYP-GUIDES (Cytochrome Psychotropic Genotyping Under Investigation for Decision Support) was a Randomized Controlled Trial comparing 2 outcomes in hospitalized patients with major depressive disorder treated according to the patient's CYP2D6 genotype and functional status versus standard psychotropic therapy. The primary outcome was hospital Length of Stay (LOS) and the secondary was Re-Admission Rate (RAR) 30 days after discharge. Methodology, total results and database of the trial have been published. Here we present a subanalysis that isolated 3 confounders to assess the impact of CYP2D6 therapeutic guidance on LOS: a single Electronic Medical Record, a minimum 3-day LOS, and CYP2D6 functional stratification of patients. CYP2D6 functional stratification enabled subgrouping patients and comparing outcomes according to CYP2D6 functionality within Group G and Group S. Subfunctional patients evidenced a 2-day shorter LOS in Group G compared to Group S. Drug administration for subfunctional patients in Group S evidenced a higher percentage of CYP2D6 substrate psychotropics being prescribed as well as a greater number of prescriptions than in functional patients. We conclude that there was an effect of pharmacogenetic clinical decision support that reduced LOS in patients with CYP2D6 subfunctional status and reduced prescribing of CYP2D6 substrate dependent drugs.
ISSN:0165-1781
1872-7123
DOI:10.1016/j.psychres.2020.113571