Epidemiology and Outcomes of Acute Respiratory Distress Syndrome Following Isolated Severe Traumatic Brain Injury.
Abstract
Patients with traumatic brain injury (TBI) are at risk for extra-cranial complications,
such as the acute respiratory distress syndrome (ARDS). We conducted an analysis of
risk factors, mortality, and healthcare utilization associated with ARDS following
isolated severe TBI. The National Trauma Data Bank (NTDB) dataset files from 2007-2014
were used to identify adult patients who suffered isolated [other body region-specific
Abbreviated Injury Scale (AIS) < 3] severe TBI [admission total Glasgow Coma Scale
(GCS) from 3 to 8 and head region-specific AIS >3]. In-hospital mortality was compared
between patients who developed ARDS and those who did not. Utilization of healthcare
resources (ICU length of stay, hospital length of stay, duration of mechanical ventilation,
and frequency of tracheostomy and gastrostomy tube placement) was also examined. This
retrospective cohort study included 38,213 patients with an overall ARDS occurrence
of 7.5%. Younger age, admission tachycardia, pre-existing vascular and respiratory
diseases, and pneumonia were associated with the development of ARDS. Compared to
patients without ARDS, patients that developed ARDS experienced increased in-hospital
mortality (OR 1.13, 95% CI 1.01-1.26), length of stay (p = <0.001), duration of mechanical
ventilation (p = < 0.001), and placement of tracheostomy (OR 2.70, 95% CI 2.34-3.13)
and gastrostomy (OR 2.42, 95% CI 2.06-2.84). After isolated severe TBI, ARDS is associated
with increased mortality and healthcare utilization. Future studies should focus on
both prevention and management strategies specific to TBI-associated ARDS.
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https://hdl.handle.net/10161/23869Published Version (Please cite this version)
10.1177/0885066620972001Publication Info
Komisarow, Jordan M; Chen, Fangyu; Vavilala, Monica S; Laskowitz, Daniel; James, Michael
L; & Krishnamoorthy, Vijay (2020). Epidemiology and Outcomes of Acute Respiratory Distress Syndrome Following Isolated
Severe Traumatic Brain Injury. Journal of intensive care medicine. pp. 885066620972001. 10.1177/0885066620972001. Retrieved from https://hdl.handle.net/10161/23869.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Michael Lucas James
Associate Professor of Anesthesiology
I have an extensive background in neuroanesthesia and neurointensive care and a special
research interest in translational and clinical research aspects of intracerebral
hemorrhage.
After completing residencies in neurology and anesthesiology with fellowships in neurocritical
care, neuroanesthesia, and vascular neurology, I developed a murine model of intracerebral
hemorrhage in the Multidisciplinary Neuroprotection Laboratories at Duke University.
After optimization of the model, I h
Jordan Komisarow
Assistant Professor of Neurosurgery
Vijay Krishnamoorthy
Associate Professor of Anesthesiology
Daniel Todd Laskowitz
Professor of Neurology
Our laboratory uses molecular biology, cell culture, and animal modeling techniques
to examine the CNS response to acute injury. In particular, our laboratory examines
the role of microglial activation and the endogenous CNS inflammatory response in
exacerbating secondary injury following acute brain insult. Much of the in vitro work
in this laboratory is dedicated to elucidating cellular responses to injury with the
ultimate goal of exploring new therapeutic interventions in the clinical settin
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