TY - JOUR
T1 - Use of psychotropic medications among glioma patients in Denmark, Norway, Sweden, and Wales
AU - Baxter, Sarah M.
AU - Bjørge, Tone
AU - Bjerkvig, Rolf
AU - Cardwell, Christopher
AU - Engeland, Anders
AU - Eriksson, Julia
AU - Habel, Laurel
AU - Igland, Jannicke
AU - Klungsøyr, Kari
AU - Lunde, Astrid
AU - Miletic, Hrvoje
AU - Olesen, Morten
AU - Pottegård, Anton
AU - Reutfors, Johan
AU - Sharifian, Mohammad Jalil
AU - Linder, Marie
AU - Hicks, Blánaid
PY - 2025
Y1 - 2025
N2 - Purpose: Glioma patients often suffer from psychiatric and neurological conditions. However, little is known about the patterns of use of psychotropic drugs pre- and post-glioma diagnosis. Therefore, we assessed temporal patterns of psychotropic prescriptions among glioma patients, compared to an age and sex matched comparison cohort in four European countries. Methods: Incident gliomas were identified in Wales from the Secured Anonymized Information Linkage Databank (2005–2016) and population-based registries in Denmark (2001–2016), Norway (2006–2019), and Sweden (2008–2018). From each data source, a cancer-free comparison cohort was matched to the glioma cases by age and sex. We calculated rates of new psychotropic prescriptions and any psychotropic prescriptions during the 2 years prior to and post glioma diagnosis. Analyses were stratified by histological subtypes and subclasses of psychotropic medications. Results: We identified 16,007 glioma patients. The rate of new psychotropic drug use increased from 7 months before diagnosis, peaking around the month of glioma diagnosis (with peak rates ranging from 227 to 753 new psychotropic drugs per 1000 person-months). New use remained substantially higher among glioma patients than comparators throughout the 2-year follow-up period after glioma diagnosis, though rates of new use continued to decline throughout. New use was largely driven by antiepileptics, anxiolytics, hypnotics, and sedatives. Patterns were similar when analyses were stratified by histological subtype. Conclusion: Psychotropic drug use among glioma patients was high, and elevations observed around the time of cancer diagnosis, largely driven by antiepileptics, anxiolytics, hypnotics, and sedatives, are likely associated with the consequences of the disease.
AB - Purpose: Glioma patients often suffer from psychiatric and neurological conditions. However, little is known about the patterns of use of psychotropic drugs pre- and post-glioma diagnosis. Therefore, we assessed temporal patterns of psychotropic prescriptions among glioma patients, compared to an age and sex matched comparison cohort in four European countries. Methods: Incident gliomas were identified in Wales from the Secured Anonymized Information Linkage Databank (2005–2016) and population-based registries in Denmark (2001–2016), Norway (2006–2019), and Sweden (2008–2018). From each data source, a cancer-free comparison cohort was matched to the glioma cases by age and sex. We calculated rates of new psychotropic prescriptions and any psychotropic prescriptions during the 2 years prior to and post glioma diagnosis. Analyses were stratified by histological subtypes and subclasses of psychotropic medications. Results: We identified 16,007 glioma patients. The rate of new psychotropic drug use increased from 7 months before diagnosis, peaking around the month of glioma diagnosis (with peak rates ranging from 227 to 753 new psychotropic drugs per 1000 person-months). New use remained substantially higher among glioma patients than comparators throughout the 2-year follow-up period after glioma diagnosis, though rates of new use continued to decline throughout. New use was largely driven by antiepileptics, anxiolytics, hypnotics, and sedatives. Patterns were similar when analyses were stratified by histological subtype. Conclusion: Psychotropic drug use among glioma patients was high, and elevations observed around the time of cancer diagnosis, largely driven by antiepileptics, anxiolytics, hypnotics, and sedatives, are likely associated with the consequences of the disease.
KW - Anticonvulsants
KW - Brain tumor
KW - Glioma
KW - Hypnotics
KW - Psychotropics
U2 - 10.1007/s11060-025-04996-0
DO - 10.1007/s11060-025-04996-0
M3 - Journal article
C2 - 40208515
AN - SCOPUS:105002238489
SN - 0167-594X
JO - Journal of Neuro-Oncology
JF - Journal of Neuro-Oncology
ER -