Preliminary report on cardiac dysfunction after isolated traumatic brain injury.

Published

Journal Article

OBJECTIVE: The aim of this study was to examine cardiac dysfunction during the first 2 weeks after isolated traumatic brain injury and its association with in-hospital mortality. DESIGN: Retrospective. SETTING: Level 1 regional trauma center. PATIENTS: Adult patients with severe traumatic brain injury. METHODS: After institutional review board approval, data from adult patients with isolated traumatic brain injury who underwent echocardiography during the first 2 weeks after traumatic brain injury between 2003 and 2010 were examined. Patients with preexisting cardiac disease were excluded. Clinical characteristics and echocardiogram reports were abstracted. Cardiac dysfunction was defined as left ventricular ejection fraction less than 50% or presence of regional wall motion abnormality. INTERVENTIONS: None. MEASUREMENT AND MAIN RESULTS: We examined data from 139 patients with isolated traumatic brain injury who underwent echocardiographic evaluation. Patients were 58 ± 20 years old, 66% were male patients, and 62.6% had subdural hematoma; admission Glasgow Coma Scale score was 3 ± 1 (3-15) and head Abbreviated Injury Scale was 4 ± 1 (2-5). Of this cohort, 22.3% had abnormal echocardiogram: reduced left ventricular ejection fraction was documented in 12% (left ventricular ejection fraction, 43% ± 8%) and 17.5% of patients had a regional wall motion abnormality. Hospital day 1 was the most common day of echocardiographic exam. Abnormal echocardiogram was independently associated with all cause in-hospital mortality (9.6 [2.3-40.2]; p = 0.002). CONCLUSIONS: Cardiac dysfunction in the setting of isolated traumatic brain injury occurs and is associated with increased in-hospital mortality. This finding raises the question as to whether there are uncharted opportunities for a more timely recognition of cardiac dysfunction and subsequent optimization of the hemodynamic management of these patients.

Full Text

Duke Authors

Cited Authors

  • Prathep, S; Sharma, D; Hallman, M; Joffe, A; Krishnamoorthy, V; Mackensen, GB; Vavilala, MS

Published Date

  • January 2014

Published In

Volume / Issue

  • 42 / 1

Start / End Page

  • 142 - 147

PubMed ID

  • 23963125

Pubmed Central ID

  • 23963125

Electronic International Standard Serial Number (EISSN)

  • 1530-0293

Digital Object Identifier (DOI)

  • 10.1097/CCM.0b013e318298a890

Language

  • eng

Conference Location

  • United States