Elsevier

Sleep Medicine

Volume 16, Issue 8, August 2015, Pages 926-932
Sleep Medicine

Original Article
Sleep difficulties one year following mild traumatic brain injury in a population-based study

https://doi.org/10.1016/j.sleep.2015.04.013Get rights and content

Highlights

  • Forty-one per cent of people had sleep difficulties 1 year following a mild brain injury.

  • There is a link between sleep and other outcomes following brain injury.

  • Sleep quality does not spontaneously recover in many cases after brain injury.

Abstract

Background

Sleep quality affects all aspects of daily functioning, and it is vital for facilitating recovery from illness and injury. Sleep commonly becomes disrupted following moderate to severe brain injury, yet little is known about the prevalence of sleep disruption over time and how it impacts on recovery following mild injury.

Methods

This was a longitudinal study of 346 adults who experienced a mild brain injury (aged ≥16 years) identified within a population-based incidence sample in New Zealand. The prevalence of sleep difficulties was assessed at baseline (within two weeks), one, six and 12 months, alongside other key outcomes.

Results

One year post injury, 41.4% of people were identified as having clinically significant sleep difficulties, with 21.0% at a level indicative of insomnia. Poor sleep quality at baseline was significantly predictive of poorer post-concussion symptoms, mood, community integration, and cognitive ability one year post injury. The prevalence of insomnia following mild traumatic brain injury (TBI) was more than three times the rate found in the general population. Of those completing a sleep assessment at six and 12 months, 44.9% of the sample showed improvements in sleep quality, 16.2% remained stable, and 38.9% worsened.

Conclusions

Screening for sleep difficulties should occur routinely following a mild brain injury to identify adults potentially at risk of poor recovery. Interventions to improve sleep are needed to facilitate recovery from injury, and to prevent persistent sleep difficulties emerging.

Introduction

Traumatic brain injury (TBI) is the leading cause of disability in young adults worldwide [1], and the personal, societal, and economic costs of sustaining a TBI are substantial [2], [3]. The effects of TBI are wide ranging and disabling, with symptoms persisting for many years after injury, even following a mild TBI [4], [5]. The most common symptoms following a mild TBI include memory difficulties, fatigue, and poor sleep [6]. In the general population, rates of sleep problems can vary considerably based on how sleep is measured. Based on the Diagnostic and Statistical Manual of Mental Disorder (DSM) criteria [7], around 6% of people experience insomnia, with 34.5% found to be classified as poor sleepers [8]. Within the general population, poor sleep has been associated with an increased risk of poor health [9], absenteeism from work, and increased risk of accidents [10], [11], [12]. Following a TBI, the effects of poor sleep can be even more profound, exacerbating symptoms and impeding the ability to perform well at work or engage in rehabilitation [13], [14], [15], [16], [17]. Indeed, following moderate and severe TBI, poor sleep has been found to be associated with lower mood and poorer functional status [15]. Yet, despite its impact, sleep is one of the least explored symptoms following a mild TBI [17]. Understanding the role of sleep in recovery from injury and its impact on other symptoms is important to informing treatment and improving patient outcomes [18].

Sleep difficulties can occur as a direct result of the injury (eg, due to biochemical changes post TBI and injury to areas of the brain responsible for sleep) or as a secondary consequence in response to increased fatigue, lower mood, and changes in lifestyle following injury [17], [18]. Current evidence suggests that the most common sleep difficulties experienced are falling asleep (sleep-onset latency), poorer sleep efficiency, longer sleep duration, increased used of napping [18], [19], and increased sleep disruptions [20]. Whilst some cases of poor sleep post TBI resolve spontaneously, evidence suggests that sleep difficulties can become persistent for several years after injury [17]. In moderate and severe TBI, increased age, reduced cognitive ability, and being female have been identified as predisposing risk factors of poor sleep [21], yet it remains unclear if these factors are also risk factors of poor sleep following mild TBI.

A meta-analysis of prevalence studies on sleep difficulties following TBI [22] revealed that 49% of people experience clinically significant sleep disturbance post TBI, with 25–29% experiencing a specific sleep disorder. Whilst previous evidence has highlighted that sleep is highly problematic following TBI, estimates of the number of people affected vary widely. Variations may be due to differences in clinical definitions of sleep difficulties and sleep disorders, severity of TBI included, follow-up time points studied, and sample sizes used [17], [22], [23], [24]. A further limitation of the evidence is that few studies have recruited participants who did not seek hospital treatment following injury. Non-identification of cases is particularly problematic when studying the prevalence of symptoms following mild TBI, as injuries may be overshadowed by other more obvious or severe injuries and/or people may not be aware of the need to seek medical treatment following a mild TBI [25]. Indeed, about 30% of cases seek treatment from community practitioners such as physiotherapists or general practitioners [26]; thus, findings from hospital-based studies may not be generalisable to the whole mild TBI population. This study aims to determine the prevalence of sleep difficulties in a population-based sample of adults who experienced mild TBI, and to identify their trajectory for recovery over the year following injury.

Section snippets

Study population

This study was conducted as part of a longitudinal, population-based TBI incidence cohort study known as Brain Injury Incidence and Outcomes in the New Zealand Community (BIONIC). Complete details of the methodology and TBI incidence findings have been published separately [26], [27]. Within the main BIONIC study, all cases of TBI that occurred during a 1-year period (1 March 2010 through 28 February 2011) in the Hamilton and Waikato Districts of New Zealand (NZ) were identified. TBI was

Results

There were 346 adults included in the analysis who met the inclusion criteria (Fig. 1). There were no differences in age, gender, ethnicity, seeking of medical treatment following injury, additional injuries sustained, and mechanism of injury, between adults who consented to participate in the outcome assessments (N = 346) and those who did not participate (N = 529) (p > 0.05). At the 12-month follow-up, assessment data were available for 68.5% of the sample. Over 77% of the sample had multiple

Discussion

Sleep difficulties are highly problematic following mild TBI, with one in five of participants experiencing sleep difficulties at a level equivalent to insomnia one year following injury. Although sleep problems prior to injury were predictive of poorer sleep quality post injury, it should be noted that <10% of the sample reported experiencing sleep difficulties pre injury, suggesting that the TBI directly contributes to a decline in sleep quality, although recall bias cannot be ruled out.

Conclusions

Sleep difficulties are highly problematic following mild TBI, and they can have a detrimental impact on recovery from injury in the longer term. Whilst some sleep difficulties may resolve spontaneously over time, this study highlights that for over half of the sample, their sleep quality remained the same or deteriorated when assessed at six and 12 months post injury. The findings highlight the need for early screening of sleep difficulties to inform treatment and to identity those potentially

Conflict of interest

The ICMJE Uniform Disclosure Form for Potential Conflicts of Interest associated with this article can be viewed by clicking on the following link: http://dx.doi.org/10.1016/j.sleep.2015.04.013.

. ICMJE Form for Disclosure of Potential Conflicts of Interest form.

BIONIC Research Group Members

Valery Feigin, Alice Theadom, Kelly Jones, Kathryn McPherson, Amy Jones, Braden Te Ao, Paul Brown and Peggy Fairbairn-Dunlop (Auckland University of Technology); Rob Kydd, P. Alan Barber, Varsha Parag, Shanthi Ameratunga and Suzanne Barker-Collo (University of Auckland); Nicola Starkey (University of Waikato); Tony Dowell (University of Otago); Michael Kahan and Grant Christey (Waikato Distract Health Board); and Natalie Hardaker (Accident Compensation Corporation).

Acknowledgements

This study was funded by the Health Research Council of New Zealand (09/063A, 11/192). We thank the research team for their dedication and performance, in addition to staff at the Coroner's office in Hamilton; New Zealand Accident Compensation Corporation, New Zealand Health Information Service; Waikato District Health Board; Spring Hill Correctional Facility, Waikato University Staff. We thank the many doctors, nurses and rehabilitation professionals and service providers such as ABI

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