Delayed Versus Early Enoxaparin Prophylaxis After Traumatic Brain Injury (TBI)
| Status: | Completed |
|---|---|
| Conditions: | Cardiology, Hospital, Neurology |
| Therapuetic Areas: | Cardiology / Vascular Diseases, Neurology, Other |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 4/2/2016 |
| Start Date: | November 2009 |
| End Date: | November 2010 |
| Contact: | Herb A Phelan, MD |
| Email: | herb.phelan@utsouthwestern.edu |
| Phone: | 214-648-6841 |
The Delayed vs Early Enoxaparin Prophylaxis (DEEP) Study After Traumatic Brain Injury: A Randomized, Double-Blinded, Placebo Controlled Pilot Trial
Brain injured patients are at high risk for forming blood clots in the legs and lungs. For
non-brain injured trauma patients, we decrease the chances of these blood clots forming by
placing the patients on a low dose of the blood thinner enoxaparin. Starting patients with a
brain injury on the blood thinner is problematic, however, as this can theoretically cause
the brain injury to worsen. Trauma surgeons wait a variable period of time before starting
this blood thinner because waiting too long can result in the formation of these blood clots
in the legs and lungs. Previous research has shown that some brain injuries which are of
lower severity can have enoxaparin started at 24 hours after injury if the brain injury is
stable on a repeated computed tomography (CT) scan of the head. This is a pilot study
designed to look at the rates of worsening of brain injury if the low dose blood thinner is
started at 24 versus 96 hours post-injury.
non-brain injured trauma patients, we decrease the chances of these blood clots forming by
placing the patients on a low dose of the blood thinner enoxaparin. Starting patients with a
brain injury on the blood thinner is problematic, however, as this can theoretically cause
the brain injury to worsen. Trauma surgeons wait a variable period of time before starting
this blood thinner because waiting too long can result in the formation of these blood clots
in the legs and lungs. Previous research has shown that some brain injuries which are of
lower severity can have enoxaparin started at 24 hours after injury if the brain injury is
stable on a repeated computed tomography (CT) scan of the head. This is a pilot study
designed to look at the rates of worsening of brain injury if the low dose blood thinner is
started at 24 versus 96 hours post-injury.
We propose to conduct a placebo-controlled non-inferiority pilot study to evaluate the rate
of worsening of intracranial injury patterns after initiation of enoxaparin in TBI patients.
Patient enrollment will occur at ETMC, blinded re-reading of CTs will occur at PMH, and
administrative/analytical support will occur at UTSW. The study design will be a
double-blind, randomized controlled trial in the ETMC Surgical Intensive Care Unit (SICU)
consisting of 40 patients per arm. The decision for 80 patients was resource-based, as this
is a pilot study. Further, we anticipate the need to contact 3 patients in order to obtain 1
successful recruitment.
Each arm will consist of low-risk TBI patients (defined as patients with a subdural or
epidural hematoma < 8mm, intraparenchymal contusion < 2 cm, and/or single contusion per
lobe) who have had a CT scan of the head without contrast at 24 hours post-injury which
documents a stable injury pattern. The severity of neurologic deficit will have no bearing
on their suitability for participation, and will not be considered in inclusion/exclusion
criteria. After documentation of a stable intracranial injury pattern at this time interval,
patients will be randomized to receive either enoxaparin 30 mg SQ every 12 hours or placebo
with each regimen being initiated at 24 hours post-injury. A follow-up CT scan of the brain
without contrast will be obtained on all patients 48 hours post-injury (and 24 hours after
the initiation of enoxaparin/placebo). An additional CT scan of the brain without contrast
will be obtained on any patient who experiences an abrupt change in neurologic exam at any
time between the initiation of enoxaparin/placebo and the end of the study's interventional
period at 96 hours post-injury (this time frame was chosen as it is the earliest time point
at which there is universal agreement among both of our group's practitioners that
enoxaparin use is safe from the risks of TBI expansion). Any patient with a worsened CT scan
will have their investigational treatment discontinued at that time. At 96 hours
post-injury, the interventional portion of the study will end, data collection for the
primary endpoint will cease, and all patients will be placed on enoxaparin for the remainder
of their hospital stay as per local standards of care. Patient participation in the study
will last from the time of injury to 96 hours post-injury for the interventional part of the
study, and from 96 hours post-injury until discharge from ETMC for the observational
portion. While this latter time frame is obviously extremely variable, it averages
approximately one to two weeks. During both the interventional and observational time
periods, patients will have Duplex ultrasonography of the lower extremities performed for an
edematous extremity, CT-angiography of the chest for unexplained hypoxia or tachycardia, and
ventilation-perfusion scanning for suspicion of PE in the presence of a contraindication to
IV contrast.
of worsening of intracranial injury patterns after initiation of enoxaparin in TBI patients.
Patient enrollment will occur at ETMC, blinded re-reading of CTs will occur at PMH, and
administrative/analytical support will occur at UTSW. The study design will be a
double-blind, randomized controlled trial in the ETMC Surgical Intensive Care Unit (SICU)
consisting of 40 patients per arm. The decision for 80 patients was resource-based, as this
is a pilot study. Further, we anticipate the need to contact 3 patients in order to obtain 1
successful recruitment.
Each arm will consist of low-risk TBI patients (defined as patients with a subdural or
epidural hematoma < 8mm, intraparenchymal contusion < 2 cm, and/or single contusion per
lobe) who have had a CT scan of the head without contrast at 24 hours post-injury which
documents a stable injury pattern. The severity of neurologic deficit will have no bearing
on their suitability for participation, and will not be considered in inclusion/exclusion
criteria. After documentation of a stable intracranial injury pattern at this time interval,
patients will be randomized to receive either enoxaparin 30 mg SQ every 12 hours or placebo
with each regimen being initiated at 24 hours post-injury. A follow-up CT scan of the brain
without contrast will be obtained on all patients 48 hours post-injury (and 24 hours after
the initiation of enoxaparin/placebo). An additional CT scan of the brain without contrast
will be obtained on any patient who experiences an abrupt change in neurologic exam at any
time between the initiation of enoxaparin/placebo and the end of the study's interventional
period at 96 hours post-injury (this time frame was chosen as it is the earliest time point
at which there is universal agreement among both of our group's practitioners that
enoxaparin use is safe from the risks of TBI expansion). Any patient with a worsened CT scan
will have their investigational treatment discontinued at that time. At 96 hours
post-injury, the interventional portion of the study will end, data collection for the
primary endpoint will cease, and all patients will be placed on enoxaparin for the remainder
of their hospital stay as per local standards of care. Patient participation in the study
will last from the time of injury to 96 hours post-injury for the interventional part of the
study, and from 96 hours post-injury until discharge from ETMC for the observational
portion. While this latter time frame is obviously extremely variable, it averages
approximately one to two weeks. During both the interventional and observational time
periods, patients will have Duplex ultrasonography of the lower extremities performed for an
edematous extremity, CT-angiography of the chest for unexplained hypoxia or tachycardia, and
ventilation-perfusion scanning for suspicion of PE in the presence of a contraindication to
IV contrast.
Inclusion Criteria:
1. Male and female patients admitted to the ETMC SICU with TBI who speak English or
Spanish.
Exclusion Criteria:
1. Epidural or subdural hematoma > 8mm.
2. Intraparenchymal contusion >2 cm
3. Multiple contusions w/in one lobe
4. Subarachnoid hemorrhage in basilar or supracellar cistern and positive CTA
5. Increased TBI on 24 hr post-injury CT
6. Spinal canal hematoma
7. Nonoperative mgmt of American Association for the Surgery of Trauma (AAST) Grade IV
or higher organ injury
8. Gastrointestinal hemorrhage
9. Ongoing bleeding from a pelvic fracture
10. Anticipated open reduction of long bone or pelvic fracture within study period.
11. Intracranial pressure (ICP) >20 mmHg
12. Coagulopathy consisting of International Normalized Ratio (INR)>1.5 or platelet count
<50,000
13. Expect brain death/discharge in 48 hrs
14. Pre-existing dialysis dependence
15. Documented DVT at time of admission
16. Prisoners
17. Pregnancy
18. Age <18 years
19. Terminally ill patients
20. Anticoagulant use at time of injury
21. Inability to gain consent from patient or legal next-of-kin in instance of TBI,
intoxication, or psychiatric diagnoses
22. Documented history of heparin allergy
23. Initial head CT >6 hours post-injury
We found this trial at
2
sites
Click here to add this to my saved trials
U.T. Southwestern Medical Center The story of UT Southwestern Medical Center is one of commitment...
Click here to add this to my saved trials