Background Image
Table of Contents Table of Contents
Previous Page  83 / 162 Next Page
Information
Show Menu
Previous Page 83 / 162 Next Page
Page Background

non-biased, and of acceptable quality. This datasheet and an online

questionnaire were then emailed to 384 patients with chronic trau-

matic SCI. The chi-square test was used to analyze responses.

Results:

77 patients completed our questionnaire (20.1%). 65 of the

77 patients (84.4%) report arriving to the hospital within the 8 hour

MPSS treatment window. Only 6 patients (7.8%) reported that they

were given the chance to decide whether they would receive MPSS or

not. Only 11 patients (15.3%) know whether they received MPSS or

not.

59.4% of respondents rated the small neurological benefits associ-

ated with MPSS as being very important to them (10 on a 10 point

Likert scale, p

<

0.0001). Patients had little concern for potential side-

effects of MPSS (49.3% chose 1–3 on a 10 point Likert scale,

p

<

0.0001). The majority of patients (53.2% or 41/77) ‘‘felt strongly’’

that MPSS should be a treatment option for SCI patients (p

<

0.0001).

Only 1.4% of respondents felt that MPSS should not be given to SCI

patients (p

<

0.0001).

Conclusion:

Communication surrounding MPSS administration

was poor. Patients with SCI favor the administration of MPSS for

acute SCI, however very few had input into whether or not it was

administered. Conscious patients should be given greater opportunity

to decide how they are treated; the results of this study provide some

guidance regarding MPSS administration in patients who are unable to

communicate.

Keywords: methylprednisolone, spinal cord injury, patient prefer-

ence, communication

C3-09

IMPLEMENTATION OF UNIQUE PROCESS FOR CERE-

BRAL MICRODIALYSIS AT A LEVEL I TRAUMA CENTER

Kathryn D’Aquila

, Kathy Cosimano, Lori Csenscics, Terry Rattigan-

Davis, Linda McGinnis, Patricia Wrobbel

Westchester Medical Center, Neuroscience/ Trauma, Valhalla, USA

Objectives:

To create an efficient and reliable process for cerebral

microdialysis (CMD) promoting rapid speciment turnaround and op-

timal utilization of multidisciplinary organizational roles.

Background:

Industry implementation of cerebral microdialysis

includes point of care bedside analysis of hourly microdialysis spec-

imens. Establishing a unique process using a collaborative multidis-

ciplinary team approach at our level I trauma hospital, microdialysis

specimen analysis is processed in the clinical laboratory. This unique

process promotes nurses’ role to focus on vigilant patient assessment,

monitoring, and implementation of therapies to prevent secondary

brain injury.

Methods:

Planning initiated in the third quarter 2012 with im-

plementation in April 2013. Specific roles and process steps were

established for team members. Handoff of microdialysis specimens in

the trauma intensive care unit reflects time of patient specimen re-

moval to courier handoff for hand delivery to the STAT clinical

laboratory for immediate analysis. Handoff tools provide quality im-

provement data for monitoring and team communication.

Results:

The process improved teamwork, communication and

resource utilization. The mean delivery to lab time

=

5.5 minutes for

98 CMD patients since initiation of the process. Successful process

eliminated need for nurses to perform point of care lab analysis on

microdialysis specimens. Process demonstrates effective communi-

cation and matches team member roles according to training and

expertise.

Conclusions:

Creating a process with specific roles matched to

organizational roles improved specific process, efficiency, and com-

munication. Clarifying roles and responsibilities can reduce time to

interventions and improve outcomes.

Keywords: Microdialysis, Specimen processing, Multidisciplinary

implementation

C4 Poster Session V - Group C: Neurotoxicity/

Neuroexcitation

C4-01

NEUROLOGICAL COMPLICATIONS DUE TO A SUB-

ARACHNOID INJECTION OF HYPERTONIC CONTRAST

MEDIA IN RAT

Kazuhiko Kibayashi

, Ryo Shimada, Jiro Ezaki

School of Medicine, Tokyo Women’s Medical University, Department

of Legal Medicine, Tokyo, Japan

Myelography is routinely performed using a non-ionic contrast media.

However, the inadvertent administration of ionic hypertonic contrast

media into the subarachnoid space results in convulsions and acute

respiratory failure, and can lead to death if not treated immediately.

The mechanisms underlying the adverse effects of hypertonic contrast

media on the central nervous system are unclear. We examined the

effects of a subarachnoid injection of hypertonic contrast media (60%

Urografin ; osmotic pressure 6) on the central nervous system in the

rat. Under general anesthesia, rats were administered a subarachnoid

injection of 20.0, 10.0, 7.5, or 5.0

l

L of Urografin or saline. The rats

that received 20.0 or 10.0

l

L of Urografin immediately developed

severe convulsions and died within 42 minutes of the injection. The

rats that received 7.5 or 5.0

l

L of Urografin exhibited delayed-onset

convulsions that subsided within 240 minutes. Immunohistological

examinations of the brain and spinal cord two days after the 7.5

l

L

Urografin injection revealed microglial activation and decreased

expression of transient receptor potential vanilloid 4 (TRPV4), a

protein related to osmoregulation, in the brain stem. Neither convul-

sions nor histological changes were observed in rats that received the

saline injection. These findings indicate that the extent and duration of

convulsions and fatality depend on the volume of hypertonic contrast

media. Furthermore, brain stem injury is the mechanism underlying

the acute respiratory failure that occurs following the subarachnoid

injection of hypertonic contrast media. This study also suggests that

high cerebrospinal fluid osmolality affects the central nervous system.

Keywords: cerebrospinal fluid, osmotic pressure, microglia, tran-

sient receptor potential vanilloid 4 (TRPV4), contrast media, myelo-

graphy

C4-02

ALTERED TRYPTOPHAN METABOLISM IN BLAST-

INDUCED TRAUMATIC BRAIN INJURY

Peethambaran Arun

, Donna Wilder, William Rittase, Meghan

Mccuistion, Samuel Oguntayo, Ying Wang, Irene Gist, Joseph Long

Walter Reed Army Institute of Research, Blast-Induced Neurotrauma/

Center for Military Psychiatry & Neurosciences, Silver Spring, USA

Blast-induced traumatic brain injury (bTBI) is one of the major dis-

abilities in service members returning from recent military operations.

The neurobiological underpinnings of bTBI, which is associated with

acute and chronic neuropathological and neurobehavioral deficits, are

uncertain. The role of the essential amino acid, tryptophan, in the

A-83