TY - JOUR
T1 - Central Nervous System-Active Medications and Risk of Hospital Readmission in Older Multimorbid Adults
AU - Stuber, Mirah J.
AU - Brockhus, Lara A.
AU - Spinewine, Anne
AU - O'Mahony, Denis
AU - Jennings, Emma
AU - Dalleur, Olivia
AU - Knol, Wilma
AU - Koek, Huiberdina L.
AU - Baggio, Stéphanie
AU - Rodondi, Nicolas
AU - Aubert, Carole E.
N1 - Publisher Copyright:
© 2025 The Author(s). Journal of the American Geriatrics Society published by Wiley Periodicals LLC on behalf of The American Geriatrics Society.
PY - 2025
Y1 - 2025
N2 - Background: Polypharmacy is associated with adverse outcomes, particularly in older multimorbid adults. However, little is known about the negative outcomes associated with multiple central nervous system (CNS)-active medications that are commonly prescribed to these patients. Objective: To assess the association between the number of CNS-active medications at discharge and the risk of 1-year all-cause hospital readmission, drug-related hospital readmission (DRA), death, quality of life (QoL) and functional status in older multimorbid adults. Methods: Among 2008 older multimorbid inpatients with polypharmacy, we assessed the association between the number of CNS-active medications and 1-year all-cause hospital readmission, DRA, and death by Cox proportional hazard models. We further assessed the association of the number of CNS-active medications with QoL (measured with EQ-5D-VAS) and functional status (measured with Barthel Index) using binary and quantile regression models. Analyses were adjusted for age, sex, discharge location, Charlson Comorbidity Index, depression/anxiety, and randomization arm. Additional sensitivity analyses were adjusted for the number of non-CNS active medications, neurological and psychiatric comorbidities, alcohol or tobacco use, education level, and living arrangements. Results: The risk of all-cause hospital readmission and DRA increased by 7% with each additional CNS-active medication (multivariable-adjusted hazard ratio (HR) 1.07 (95% confidence interval 1.03 to 1.12) for all-cause hospital readmission and 1.07 (1.01 to 1.14) for DRA). HR for death was 1.14 (1.07 to 1.23) for each additional CNS-active medication. The mean differences in EQ-5D-VAS and Barthel Index after 1 year were −2.13 (−2.82 to −1.44) and −1.6 (−2.16 to −1.04) respectively, per additional CNS-active medication. Conclusion: The presence of CNS-active medications at discharge is associated with a higher risk for 1-year all-cause hospital readmission and DRA in older multimorbid adults with polypharmacy. Additionally, CNS-active medications were associated with lower QoL and functional status. Trail Registration: ClinicalTrials.gov NCT02986425.
AB - Background: Polypharmacy is associated with adverse outcomes, particularly in older multimorbid adults. However, little is known about the negative outcomes associated with multiple central nervous system (CNS)-active medications that are commonly prescribed to these patients. Objective: To assess the association between the number of CNS-active medications at discharge and the risk of 1-year all-cause hospital readmission, drug-related hospital readmission (DRA), death, quality of life (QoL) and functional status in older multimorbid adults. Methods: Among 2008 older multimorbid inpatients with polypharmacy, we assessed the association between the number of CNS-active medications and 1-year all-cause hospital readmission, DRA, and death by Cox proportional hazard models. We further assessed the association of the number of CNS-active medications with QoL (measured with EQ-5D-VAS) and functional status (measured with Barthel Index) using binary and quantile regression models. Analyses were adjusted for age, sex, discharge location, Charlson Comorbidity Index, depression/anxiety, and randomization arm. Additional sensitivity analyses were adjusted for the number of non-CNS active medications, neurological and psychiatric comorbidities, alcohol or tobacco use, education level, and living arrangements. Results: The risk of all-cause hospital readmission and DRA increased by 7% with each additional CNS-active medication (multivariable-adjusted hazard ratio (HR) 1.07 (95% confidence interval 1.03 to 1.12) for all-cause hospital readmission and 1.07 (1.01 to 1.14) for DRA). HR for death was 1.14 (1.07 to 1.23) for each additional CNS-active medication. The mean differences in EQ-5D-VAS and Barthel Index after 1 year were −2.13 (−2.82 to −1.44) and −1.6 (−2.16 to −1.04) respectively, per additional CNS-active medication. Conclusion: The presence of CNS-active medications at discharge is associated with a higher risk for 1-year all-cause hospital readmission and DRA in older multimorbid adults with polypharmacy. Additionally, CNS-active medications were associated with lower QoL and functional status. Trail Registration: ClinicalTrials.gov NCT02986425.
KW - hospital readmission
KW - multimorbid
KW - polypharmacy
KW - psychotropic medications
UR - https://www.scopus.com/pages/publications/105014592026
U2 - 10.1111/jgs.70049
DO - 10.1111/jgs.70049
M3 - Article
AN - SCOPUS:105014592026
SN - 0002-8614
JO - Journal of the American Geriatrics Society
JF - Journal of the American Geriatrics Society
ER -