Assessment of the effects of dexmedetomidine on outcomes of traumatic brain injury using propensity score analysis.

BMC Anesthesiol

Critical Care Medicine Department, Lianyungang Second People's Hospital, No. 161, Xingfu Road, Lianyungang City, 222000, Jiangsu Province, China.

Published: September 2022

Background: Dexmedetomidine was found to be protective against traumatic brain injury (TBI) in animal studies and safe for use in previous clinical studies, but whether it improves TBI patient survival remains to be determined. We sought to answer this question by analyzing data from the MIMIC clinical database.

Methods: Data for TBI patients from the MIMIC III and MIMIC IV databases were extracted and divided into a dexmedetomidine group and a control group. In the former group, dexmedetomidine was used for sedation, while in the latter, it was not used. Parameters including patient age, the Acute Physiology score III, the Glasgow Coma Scale, other sedatives used, and pupillary response within 24 h were employed in propensity score matching to achieve a balance between groups for further analysis. In-hospital survival and 6-month survival were analyzed by Kaplan-Meier survival analysis and compared by log-rank test. Cox regression was used repeatedly for the univariate analysis, the multivariate analysis, the propensity score-matched analysis, and the inverse probability of treatment weighted analysis of survival data. Meanwhile, the influences of hypotension, bradycardia, infection, and seizure on outcome were also analyzed.

Results: Different types of survival analyses demonstrated the same trend. Dexmedetomidine significantly improved TBI patient survival. It caused no more incidents of hypotension, infection, and seizure. Hypotension was not correlated with in-hospital mortality, but was significantly correlated with 6-month mortality.

Conclusions: Dexmedetomidine may improve the survival of TBI patients. It should be used with careful avoidance of hypotension.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9438148PMC
http://dx.doi.org/10.1186/s12871-022-01822-2DOI Listing

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