好色先生

好色先生

Explore the latest content from across our publications

Log In

Forgot Password?
Create New Account

Loading... please wait

Abstract Details

Tobacco, Marijuana, and Antidepressant Use Prior to Concussion Are Associated with Increased Depression Risk in Post-concussive Syndrome Patients
Neuro Trauma and Critical Care
P2 - Poster Session 2 (11:45 AM-12:45 PM)
14-015

This study aims to assess alcohol, tobacco, marijuana, and antidepressant use pre- and post-mild traumatic brain injury (mTBI) as potential risk factors for depression in the context of PCS (DPCS).

Post-Concussion Syndrome (PCS) describes symptoms which persist beyond the typical recovery time frame for mTBI. Although there is a confirmed correlation between mTBI and depression risk, there is a paucity of literature investigating risk factors for DPCS. Associations between tobacco or marijuana use and DPCS have not been previously demonstrated.
This single-center, retrospective study included 297 patients diagnosed with PCS between January 2020 and January 2023. Data comprised Patient Health Questionnaire (PHQ)-2/PHQ-9 surveys, substance use pre- and post-PCS diagnosis, and antidepressant use pre- and post-PCS diagnosis. P-values were calculated using Fisher’s exact tests and Pearson’s Chi-squared tests.

Of the initial 297 patients identified, 82% received depression screening, and 31% were at risk of DPCS based on PHQ-2 scores. Tobacco use pre-mTBI (p=0.027) and marijuana use pre- (p=0.002) and post-mTBI (p=0.004) were associated with increased risk of DPCS. Elevated DPCS risk was seen in patients who used selective serotonin reuptake inhibitors (SSRIs) (p=0.003), serotonin-norepinephrine reuptake inhibitors (SNRIs) (p=0.010), or atypical antidepressants (p=0.032), pre-mTBI or SNRIs (p=0.047) or atypical antidepressants (p=0.003) post-mTBI. Combining all antidepressants into one variable, the use of any antidepressant pre-mTBI was associated with increased DPCS risk (p<0.001). Patients who didn't use antidepressants pre or post-mTBI demonstrated lower risk of DPCS than patients who used antidepressants pre-mTBI and post-mTBI and patients who used antidepressants pre- but not post-mTBI.

This study highlights several risk factors for DPCS which may inform improved PCS patient management and emphasizes the need to develop standardized screening protocols for DPCS. Future prospective studies including PHQ-2/PHQ-9 scores pre- and post-mTBI may better elucidate relationships between DPCS and substance and medication use.

Authors/Disclosures
Sarah E. Bellatti
PRESENTER
Ms. Bellatti has nothing to disclose.
Eli Snyder Eli Snyder has nothing to disclose.
Ryan Nakamura Mr. Nakamura has received personal compensation for serving as an employee of Hawaii Health & Harm Reduction Center.
Miriya Ogawa No disclosure on file
Kaylin Bersamin No disclosure on file
Edward Weldon (John A. Burns School of Medicine) Edward Weldon has nothing to disclose.
Julia Jahansooz Julia Jahansooz has nothing to disclose.
Anson Lee (University of Hawaii John A. Burns School of Medicine) Anson Lee has nothing to disclose.
Kyle Ishikawa (University of Hawai'i) Kyle Ishikawa has nothing to disclose.
Janette Abramowitz, MD (Queens University Medical Center) Dr. Abramowitz has nothing to disclose.
Enrique Carrazana (Neurelis, Inc.) Enrique Carrazana has received personal compensation for serving as an employee of Neurelis. Enrique Carrazana has received personal compensation in the range of $10,000-$49,999 for serving as an officer or member of the Board of Directors for Hawaii-Biotech, CND Life Sciences, Apex Labs. Enrique Carrazana has stock in Neurelis, CND, Apex.
Jason Viereck, MD, PhD (Adventist Health Castle Hospital) Dr. Viereck has nothing to disclose.
Kore K. Liow, MD, FACP (University of Hawaii, John Burns School of Medicine) The institution of Dr. Liow has received research support from UCB. The institution of Dr. Liow has received research support from Livanova. The institution of Dr. Liow has received research support from Biogen. The institution of Dr. Liow has received research support from Novartis. The institution of Dr. Liow has received research support from Eisai. The institution of Dr. Liow has received research support from Engage Therapeutics. The institution of Dr. Liow has received research support from SK Lifescience. The institution of Dr. Liow has received research support from Cerevel. The institution of Dr. Liow has received research support from Xenon. The institution of Dr. Liow has received research support from NeuroDerm. The institution of Dr. Liow has received research support from Avanir. The institution of Dr. Liow has received research support from Annovis. The institution of Dr. Liow has received research support from Acadia. The institution of Dr. Liow has received research support from Prothena. The institution of Dr. Liow has received research support from SAGE. The institution of Dr. Liow has received research support from Annovis. The institution of Dr. Liow has received research support from Cyclerion.