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Managing Agitation in Managing Agitation in Traumatic Brain Injury Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC
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Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Dec 19, 2015

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Page 1: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Managing Agitation in Managing Agitation in Traumatic Brain InjuryTraumatic Brain Injury

Jennifer E. Marks, D.O.

Department of PM&R

LSUHSC

Page 2: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

TBITBI

#1 cause of TBI is MVAMales at higher risk in all age groupsPeak risk 18-25 years

Page 3: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

TBITBI

Severe TBI estimated to be only 6% of all hospitalized brain injury cases

However,the health care costs and residual deficits are much greater than with mild/moderate TBI

Page 4: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

TBITBI

Mechanisms of injury:PRIMARY: Occur at the moment of impactSECONDARY: Triggered by primary

mechanisms, cause more damage to the brain

Page 5: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Primary Injury Mechanisms-Primary Injury Mechanisms-TBITBI

Most brain damage caused by acceleration-deceleration

Diffuse axonal injury: Widespread stretching of axons caused by the rotation of the brain around its axis

DAI may be seen on brain MRI

Page 6: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Diffuse axonal injuryDiffuse axonal injury

Aka Shear injury Occurs in 50% of all head

trauma cases Characterized clinically

by LOC at time of impact Multiple b/l focal lesions

throughout white matter Most commonly seen in

the corpus collosum, brain stem, and frontal/temporal lobes

Page 7: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Secondary TBI Injury Secondary TBI Injury MechanismsMechanisms

ICH (ex. SDH)Brain edemaOxidant injuryHypoxia secondary to cerebral perfusion

pressureExcitotoxicity: Neuronal damage caused by

accelerated release of excitatory neurotransmitters by injured neurons

Page 8: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Glasgow Coma Scale Glasgow Coma Scale

No direct way to measure the severity of brain injury

The Glasgow Coma Scale is used to measure TBI severity

The GCS evaluates the patient’s eye, motor, and verbal response

The lowest score obtainable is 3, the highest is 15 The lowest post resuscitation score is the preferred

value

Page 9: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

GCS PitfallsGCS Pitfalls

Score can be affected by intoxicationIntubation can obscure the difference

between a mild and moderate TBIAlso unscorable if patient cannot

understand the examiner’s language

Page 10: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Mild TBIMild TBI

GCS 13 or greater Equivalent to concussion

Page 11: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Moderate TBIModerate TBI

GCS 9-12Follows commandsDoes not answer questions appropriately

Page 12: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Severe TBISevere TBI

GCS < or = to 8Patient was in a comaPermanent neurological sequelae and

functional disabilityAt least one year for maximal return to

functioningLarge majority of patients in rehab units

Page 13: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.
Page 14: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

TBI patient issuesTBI patient issues

Spasticity Hetereotopic ossification Posttraumatic epilepsy Postraumatic hydrocephalus Cranial nerve damage Sleep disorders Dysphagia DVT Skin breakdown Post traumatic amnesia/AGITATION

Page 15: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Definition of agitation in TBIDefinition of agitation in TBI

A consensus at this time has not been reached on the exact definition of agitation.

“Subtype of delirium occurring during the period of post traumatic amnesia, characterized by excessive behaviors including some combination of aggression, disinhibition, akathisia, and emotional lability.”

A 1996 literature review featured in the Archives of PM&R by Sandel &Mysiw, 77:617-623

Page 16: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Etiology of agitationEtiology of agitation

Brain trauma disrupts the catecholamine/neurotransmitter pathways: surges of norepinephrine and epinephrine have been documented in the plasma and CSF.

TBI patients can also have hypothalamic dysfunction affecting temperature, blood pressure, etc.

Page 17: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Diagnosing agitation Diagnosing agitation

A diagnosis of exclusion after medical and neurological conditions have been ruled out

Must rule out metabolic derangement, hypothyroidism, infection/sepsis, hypoglycemia , hypoxemia, medications such as anticholinergics

Drug withdrawal (ex. Sedatives, hypnotics)

Page 18: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Diagnosing agitation Diagnosing agitation continued…continued…

Neurologic complications such as seizures, hydrocephalus, IC mass lesions, and migraine are possibilities that must be investigated

NEVER FORGET THAT THE PATIENT COULD BE IN PAIN ALSO!!!

Page 19: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Tests suggested to evaluate Tests suggested to evaluate the agitated patientthe agitated patient

CMP, Thyroid function, CBC with differential, UA, B12/folate, tox screen, Brain CT/MRI, EEG, XR (see if occult fractures/heterotopic ossification causing pain)

Page 20: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Agitation Behavior ScaleAgitation Behavior Scale

Plan for ABS to be instituted at Charity in the near future

Patient given a rating of 1(absent) to 4 (severe) on 14 subcategories

Subcategories include distractibility, impulsivity, violence, alterations of mood

High inter-rater reliability

Page 21: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Rancho Los Amigos Scale of Rancho Los Amigos Scale of Cognitive FunctioningCognitive Functioning

Developed at the California Hospital of the same name

Rancho I: No response to any stimulation; appears to be sleeping

Rancho II: Generalized Response Rancho III: Localized response

Page 22: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Rancho Los Amigos scale Rancho Los Amigos scale (continued)(continued)

**RANCHO IV: Confused, Agitated, may be aggressive

Rancho V: Confused, Inapproriate, nonagitated

Rancho VI: Confused, appropriateRancho VII: Automatic, appropriateRanch VIII: Purposeful, appropriate

Page 23: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

ManagementManagement

EnvironmentEducate Staff and FamilyBehaviorMedication

Page 24: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Environmental ManagementEnvironmental Management

Page 25: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Environmental ManagementEnvironmental Management

FIRST REDUCE STIMULI- light, noise, distractions

Patient should have a limited number of visitors at a time

EVERYONE should speak in a low volume, one at a time

Page 26: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Environmental ManagementEnvironmental Management

To reduce patient confusion:Consistent schedule and staffingDon’t move patient to another roomReorient person frequently

Page 27: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Behavioral StrategiesBehavioral Strategies

Tolerate patient’s restlessness as much as possible (ex. Allow patient to pace if ambulatory)

Mobile patients may need a closed unit or sensor unit for their safety

Remove lines tubes ASAPConsider Craig bed or Vail bed

Page 28: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Vail BedVail Bed

Page 29: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Environmental ManagementEnvironmental Management

AVOID RESTRAINTS IF AT ALL POSSIBLE

Padded hand mittens if necessary Soft lap belt in the wheelchairHeavy, stable wheelchair that will not tip

over

Page 30: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

MedicationsMedications

Since 1966, there have only been six randomized controlled trials concerning medication management of TBI agitation!

Almost all studies evaluating medications have been on subjects greater than ten years old.

Page 31: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

RCT studies 1966-presentRCT studies 1966-present

Page 32: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Measurement and Treatment Measurement and Treatment of Agitation following TBI- of Agitation following TBI-

Fugate et al.Fugate et al.Study of 129 physicians divided into

experts or nonexperts surveyed.

Experts either had published two or greater articles on pharmacological interventions for TBI in the last 5 years, or had > or = 70% of their practice devoted to treating TBI

Page 33: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Fugate et al. continuedFugate et al. continued

Experts most frequently prescribed carbamazepine, beta blockers, TCA’s

Nonexperts chose Haldol four times more frequently than experts

Page 34: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

MedicationsMedications

Most commonly utilized Antiepileptics Dopamine agonists (amantadine)Antidepressants (TCA’S)Antipsychotics (Haldol)Beta Blockers(Inderal)

Page 35: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Medications for agitationMedications for agitation

Antiepileptics: Carbamazepine: Commonly utilized by rehab

facilities. Some promise with agitation but only case reports have been published

Phenytoin, Phenobarbitol: Not recommended secondary to interfering with cognitive function and causing excessive sedation

Page 36: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

MedicationsMedications

Benzodiazepines: Not recommended for long term agitation treatment due to interference with cognitive function and sedation

Page 37: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

FOR SEVERE AGITATIONFOR SEVERE AGITATION, , Lorazepam 1-2 mg IM/IV !Lorazepam 1-2 mg IM/IV !

Page 38: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

AntipsychoticsAntipsychotics

Ex. Haldol: The typical agents, in both human and animal studies, have been shown to cause a decline in cognitive performance (verbal ability, memory, learning, attention, spatial ability…..once the medication was stopped, cognition improved)

Stanislav et al, Brain Injury 1997, p335-41

Page 39: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Beta blockersBeta blockers

Two placebo-controlled, blinded studies with propanolol showed decreased agitation in patients with TBI.

Also helps to control tachycardia and hypertension many TBI patients have

Page 40: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Beta BlockersBeta Blockers

Twenty one subjects with TBI Treated with propanolol or placebo in a

double-blind studyIn the treatment group the intensity of

agitation was significantly lower, although the number of episodes was similar. The use of restraints was also significantly lower.

Brooke et al., Arch Phys Med Rehabil 73, Oct 1992, 917-921

Page 41: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

Beta BlockersBeta Blockers

Starting dose of propanolol at 20 mg BIDCan use QID dosingIN ADULTS can titrate up to 60 mg/day Usually max amount 240 mg/day in adults,

but doses as high as 600 mg/day have been reported

As patient improves, can taper off

Page 42: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

MedicationMedication

Dopamine agonists (amantadine, bromocriptine) , SSRIs, methyphenidate, and TCA’s have not been shown to control agitation successfully, but do improve alertness/initiation

Page 43: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

ConclusionConclusion

More RCT studies need to be done to determine the optimum pharmacologic intervention for TBI

Page 44: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.

SourcesSources

As previously stated, and…… Randall L. Braddom. Physical Medicine and

Rehabilitation. Second Edition. W. B Saunders Co. , Pennsylvania. 2000.

Fleminger S., Greenwood RJ, Oliver D.L. Pharmacological management for agitation and aggression in people with acquired brain injury (Cochrane Review). In: The Cochrane Library, Issue 3, 2004. Chichester, UK: John Wiley & Sons, Ltd.

Thank you to Dr. Kiersta Kurtz-Burke, PM&R consult service staff at Charity!

Page 45: Managing Agitation in Traumatic Brain Injury Jennifer E. Marks, D.O. Department of PM&R LSUHSC.