Published online Sep 19, 2026. doi: 10.5498/wjp.116579
Revised: March 12, 2026
Accepted: May 8, 2026
Published online: September 19, 2026
Processing time: 205 Days and 22.3 Hours
Given the current insufficiency of effective prevention and treatment methods for post-ischemic stroke depression (PISD), the exploration of improved management strategies is essential.
To analyze the efficacy and influencing factors of the 3-N-Butylphthalide (NBP)-Trazodone (TRZ) combination in the management of PISD.
A total of 122 patients with PISD (March 2023-March 2025) were enrolled. According to the treatment regimens they actually received, 56 cases receiving TRZ alone were assigned to the reference group, while 66 cases administered NBP + TRZ were allocated to the research group. The following parameters were comparatively analyzed: Therapeutic efficacy; safety (nausea, celialgia, headache, and drowsiness); National Institutes of Health Stroke Scale (NIHSS); Barthel Index; 17-item Hamilton Depression Rating Scale; and serum neurotransmitters [5-hydroxytryptamine (5-HT), dopamine (DA), and norepinephrine (NE)]. Sub
Compared with the reference group, the research group demonstrated: (1) A markedly higher overall treatment effectiveness rate; (2) A comparable total incidence of adverse reactions; (3) Significantly reduced NIHSS and HAMD-17 scores after intervention; and (4) Improved Barthel Index and higher 5-HT, DA, and NE levels after treatment. Comorbid hyperlipidemia, 5-HT, DA, and me
The NBP-TRZ combination is effective in the management of PISD. Ineffective treatment is associated with clinical features such as hyperlipidemia, 5-HT < 60 ng/mL, DA < 122 ng/mL, and TRZ monotherapy.
Core Tip: For the optimization of treatment for post-ischemic stroke depression, this study verified the efficacy of the 3-N-Butylphthalide (NBP)-Trazodone (TRZ) combination and explored efficacy-associated determinants. Without increasing the total incidence of adverse reactions, the NBP-TRZ combination was significantly superior to TRZ monotherapy in therapeutic efficacy, while also significantly improving patients’ neurological function and daily living ability, alleviating depression, and regulating serum neurotransmitters. Comorbid hyperlipidemia, low 5-hydroxytryptamine, reduced dopamine, and TRZ monotherapy were associated with treatment ineffectiveness in such patients.