Abstract

BackgroundTraumatic brain injury (TBI) is a worldwide leading cause of mortality and disability. Among TBI complications, agitation is a frequent behavioural problem. Agitation causes potential harm to patients and caregivers, interferes with treatments, leads to unnecessary chemical and physical restraints, increases hospital length of stay, delays rehabilitation, and impedes functional independence. Pharmacological treatments are often considered for agitation management following TBI. Several types of agents have been proposed for the treatment of agitation. However, the benefit and safety of these agents in TBI patients as well as their differential effects and interactions are uncertain. In addition, animal studies and observational studies have suggested impaired cognitive function with the use of certain antipsychotics and benzodiazepines. Hence, a safe and effective treatment for agitation, which does not interfere with neurological recovery, remains to be identified.Methods/designWith the help of Health Sciences librarian, we will design a search strategy in the following databases: PubMed, Ovid MEDLINE®, EMBASE, CINAHL, PsycINFO, Cochrane Library, Google Scholar, Directory of Open Access Journals, LILACS, Web of Science, and Prospero. A grey literature search will be performed using the resources suggested in CADTH’s Grey Matters. We will include all randomized controlled, quasi-experimental, and observational studies with control groups. The population of interest is all patients, including children and adults, who have suffered a TBI. We will include studies in which agitation, not further defined, was the presenting symptom or one of the presenting symptoms. We will also include studies where agitation was not the presenting symptom but was measured as an outcome variable and studies assessing the safety of these pharmacological interventions in TBI patients. We will include studies evaluating all pharmacological interventions including beta-adrenergic blockers, typical and atypical antipsychotics, anticonvulsants, dopamine agonists, psychostimulants, antidepressants, alpha-2-adrenergic agonists, hypnotics, and anxiolytics.DiscussionAlthough agitation is frequent following TBI and pharmacological agents that are often used, there is no consensus on the most efficacious and safest strategy to treat these complications. There is a need for an updated systematic review to summarize the evidence in order to inform practice and future research.Systematic review registrationPROSPERO CRD42016033140 Electronic supplementary materialThe online version of this article (doi:10.1186/s13643-016-0374-6) contains supplementary material, which is available to authorized users.

Highlights

  • DiscussionAgitation is frequent following Traumatic brain injury (TBI) and pharmacological agents that are often used, there is no consensus on the most efficacious and safest strategy to treat these complications

  • Traumatic brain injury (TBI) is a worldwide leading cause of mortality and disability

  • There is a need for an updated systematic review to summarize the evidence in order to inform practice and future research

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Summary

Discussion

Agitation is frequent following TBI and pharmacological agents that are often used, there is no consensus on the most efficacious and safest strategy to treat these complications. Published systematic reviews on agitation and behaviour disorders following TBI by the French society of physical and rehabilitation medicine evaluated studies between 1990 and 2015 [48, 49]. These recent systematic reviews identified studies solely through a MEDLINE search, restricted languages to English and French, and did not search grey literature. Adding the grey literature to a systematic review has been shown to increase studies in Cochrane reviews. As there are possible unidentified studies, there is a need for an updated systematic review evaluating all the possible sources including the grey literature, all major databases, and to summarize the evidence in order to inform practice and future research.

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Methods/design
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