Citation

Hammond FMC, Zafonte RD, Tang Q, Jang JH. J. Neurotrauma 2021; ePub(ePub): ePub.

Copyright

(Copyright © 2021, Mary Ann Liebert Publishers)

DOI

10.1089/neu.2020.7530

PMID

unavailable

Abstract

This study tested the hypothesis that carbamazepine (CBZ) reduces irritability/aggression among individuals > 6 months post-traumatic brain injury (TBI). 70 individuals were enrolled in a parallel-group, randomized, double-blind, placebo-controlled, forced-titration trial of CBZ (n=35) versus placebo (n=35). Participants were randomly assigned to receive CBZ or placebo 42 days with outcome assessed at baseline and day-42. Dose was titrated up to 400 mg CBZ or placebo equivalent two times daily. Symptoms of irritability and aggression were measured using the Neuropsychiatric Inventory Irritability (NPI-I) and Aggression (NPI-A) Domains as a composite measure (NPI-I/A). Global impression of change was recorded from participant, observer, and study clinician. The CBZ group did not differ significantly from the placebo group (p=0.60 and 0.59 for NPI-I/A observer and participant ratings respectively). High placebo effects were observed with Minimal Clinically Important Difference in observer NPI-I/A 57% in CBZ group and 77% in placebo group (p=0.09).

FINDINGS were similar for participant ratings. 18 of 35 had therapeutic CBZ level > 4. Therapeutic sample analysis revealed similar high placebo response and non-significant differences except clinician ratings favoring CBZ. Non-serious adverse events occurred more frequently in the CBZ group with greater nervous system effects. CBZ up to 400 mg two times daily was not superior to placebo at reducing irritability/aggression according observers and participants. Large placebo effects may have masked the detection of differences. Clinician rating metrics suggest benefit, and thus, CBZ should remain a treatment option for the experienced brain injury clinician; data are provided that may aid treatment decisions.

Language: en

Keywords

ADULT BRAIN INJURY; HEAD TRAUMA; HUMAN STUDIES; TRAUMATIC BRAIN INJURY