Editorial Type:
Article Category: Research Article
 | 
Online Publication Date: 08 Nov 2021

Postconcussion Dizziness, Sleep Quality, and Postural Instability: A Cross-Sectional Investigation

PT, DPT,
MD,
BA,
BA,
BS, and
PhD, ATC
Page Range: 1072 – 1078
DOI: 10.4085/1062-6050-0470.21
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Context

Dizziness, poor sleep quality, and postural instability are all commonly reported postconcussion and individually relate to poor outcomes.

Objective

To examine sleep quality and postural stability among adolescents who did and those who did not report dizziness within 2 weeks of concussion.

Design

Cross-sectional study.

Setting

Research laboratory.

Patients or Other Participants

Participants were individuals 12 to 18 years old and either within 14 days of concussion (n = 58; girls = 29, boys = 29, age = 15.2 ± 1.8 years, time postinjury = 7.1 ± 3.1 days) or uninjured control recruits (n = 73, girls = 31, boys = 42, age = 15.8 ± 1.3 years).

Main Outcome Measure(s)

Participants rated preinjury and current dizziness using the Post-Concussion Symptom Inventory (PCSI) and current sleep quality using the Pittsburgh Sleep Quality Index. They also completed postural stability assessments (single-task and dual-task tandem gait and modified Balance Error Scoring System[mBESS]).

Results

We divided patients with concussion into dizzy (n = 21) or not-dizzy (n = 37) groups based on PCSI dizziness ratings (difference between current and preinjury dizziness rating: dizzy = >3, not dizzy = <3). The dizzy and not-dizzy groups both reported worse sleep quality compared with the control group (Pittsburgh Sleep Quality Index score: dizzy = 9.6 ± 3.7 versus not dizzy = 7.2 ± 3.5 versus control = 4.3 ± 2.6; P < .001) via univariable comparison. Similarly, the dizzy group performed slowest, followed by the not-dizzy group, and then the control group on single-task tandem gait (dizzy = 27.2 ± 11.7 seconds versus not dizzy = 21.2 ± 6.3 seconds versus control = 14.7 ± 3.6 seconds, P < .001) and dual-task tandem gait (dizzy = 38.4 ± 16.2 seconds versus not dizzy = 29.9 ± 7.2 seconds versus control = 21.6 ± 7.5 seconds, P < .001). Both concussion groups demonstrated more errors than the control group on the mBESS (dizzy = 9.8 ± 5.1 versus not dizzy = 6.9 ± 5.8 versus control = 3.8 ± 3.5, P < .001). After controlling for total symptom severity in the multivariable model, we observed that tandem gait, but not mBESS score or sleep quality, was associated with dizziness.

Conclusions

Individuals with postconcussion dizziness demonstrated impaired tandem-gait performance, whereas poor sleep quality was associated with total symptom severity. Identifying and treating the underlying dysfunction contributing to dizziness and postural instability may guide customized rehabilitation strategies and facilitate recovery.

A concussion can result in a myriad of symptoms, including physical, cognitive, behavioral, and sleep disturbances.1 Given the heterogeneity of clinical presentation that can exist after a concussion, evaluations can be challenging for health care providers; thus, considerable variability exists in the delivery of care postconcussion.2 Whereas most adolescent athletes report resolution of concussion symptoms within 4 weeks of injury,3 some will develop persistent symptoms lasting >28 days from injury.4 Early detection of postconcussion impairments is necessary to identify appropriate management strategies and rehabilitation protocols that may reduce the risk of developing persistent symptoms.

Among the many symptoms that can occur, dizziness is one of the most commonly reported symptoms postconcussion.5,6 It can negatively affect quality of life7 and is associated with a greater overall concussion symptom burden8 and prolonged recovery.5 Dizziness is a complex symptom that is multifactorial.9 Underlying causes can include vestibular, oculomotor, or cervical spine dysfunction or sensory integration disruptions among these systems.6,9 Given the complexity of dizziness and the many possible underlying causes, understanding how dizziness relates to other common concussion symptoms may facilitate effective concussion-management strategies.

After concussion, sleep impairments may also disrupt recovery or other functional abilities.10 Similar to dizziness, impaired sleep is associated with a greater symptom burden and longer duration of symptom recovery.1113 Independent of concussion, vestibular dysfunction has been reported to disrupt sleep,14 and greater symptom provocation with vestibular-oculomotor testing has been observed in those with poor sleep quality postconcussion.15 Taken together, this body of evidence suggests that both dizziness and impaired sleep postconcussion may result in a poor recovery trajectory, and vestibular dysfunction may be implicated in both symptoms. Therefore, further understanding how dizziness and sleep quality relate postconcussion may provide insight into effective and timely concussion-management strategies.

Another common impairment postconcussion that frequently accompanies dizziness is postural instability, which is associated with a prolonged return to sport postconcussion.16 Maintaining standing balance requires accurate sensory information from the cervical spine and vestibular and oculomotor systems in addition to appropriate motor and postural corrections.17 Dizziness and imbalance may both be caused by dysfunction in the same sensory systems, so the assessment of these symptoms in tandem postconcussion may provide a more complete picture of impairments than assessing either symptom in isolation.

Dizziness, impaired sleep, and postural instability individually relate to poor outcomes postconcussion.7,8,1113,16 Given the overlap in systems implicated in the presence of each symptom, we sought to examine associations among dizziness, sleep impairment, and postural instability after concussion. Specifically, the 2 purposes of this study were to examine the association of self-reported postconcussion dizziness with sleep quality and postural stability among adolescents with concussion and uninjured adolescents. To achieve this purpose, we used a measurement battery to assess sleep quality and postural stability between 2 concussion subgroups (those with and those without postinjury dizziness versus baseline) and a group of uninjured control individuals. We hypothesized that the concussion group with dizziness would report worse sleep quality and perform worse on postural stability tests than the concussion group without dizziness and uninjured control individuals.

METHODS

Participants and Study Design

We performed a cross-sectional study of pediatric and adolescent participants who were evaluated at Children's Hospital Colorado Sports Medicine Center, Aurora. We recruited, enrolled, and assessed participants with concussion within 14 days of injury. Concussion was diagnosed in these participants by one of the Sports Medicine Center's board-certified sports medicine physicians in line with current consensus definitions,1 independent of the study. Control participants were recruited to complete the assessments during a sport preparticipation physical evaluation performed by the Sports Medicine Center's medical team.

Patients with concussion were included if they still had symptoms at the time of enrollment, defined as a Post-Concussion Symptom Inventory (PCSI) score >9, to ensure they had not recovered before assessment.8 This cutoff threshold was selected because concussion symptoms are nonspecific and many high school athletes without a recent concussion history commonly report concussion symptoms at baseline (eg, headache, fatigue, difficulty concentrating).18 Athletes were included as healthy, uninjured control participants if they were cleared during their sport preparticipation physical evaluation for full sport participation by the Sports Medicine Center's physicians at the time of enrollment, confirming their healthy status. All participants were 12 to 18 years of age. We excluded athletes if they had a coexisting lower extremity injury affecting balance at the time of assessment, a concussion within the year before the study, a preexisting learning disability or a documented structural brain injury or had sustained their concussion during a high-velocity mechanism (eg, motor vehicle accident). All participants and parents or guardians, if participants were <18 years of age, provided written informed assent and consent, respectively, and the study was approved by the Colorado Multiple Institutional Review Board.

Symptom Ratings

Patients completed symptom ratings using the PCSI.19 The PCSI was validated in a youth population and demonstrated strong test-retest reliability (intraclass correlation coefficient [ICC] = 0.79) and internal consistency (r = 0.79–0.90).19 At the time of the assessment, participants rated 21 concussion symptoms at 2 time points: preinjury severity (asked as Before the Injury/Preinjury) and current severity (asked as Current Symptoms Yesterday and Today). Responses for each symptom ranged from 0 (not a problem) to 6 (severe problem), with a score of 3 indicating the symptom was a moderate problem. We calculated total symptom severity as the total PCSI score (current symptoms) excluding dizziness, as dizziness was used for our primary grouping variable.

Grouping Variable

We categorized participants into 3 groups: concussion, dizzy; concussion, not dizzy; and controls. To account for preinjury dizziness, we based our categorization on the difference between preinjury and postinjury (current) symptom severity ratings for the dizziness item on the PCSI. Patients with concussion who had a change of ≥3 points between the preinjury and current dizziness ratings were categorized as dizzy, while those with a change of ≤2 points were categorized as not dizzy. This threshold was selected because a 3-point change indicated that dizziness was a moderate to severe problem, consistent with previous research in which participants with concussion were grouped into no/mild or moderate/severe dizziness categories.8 A change of ≥3 points also suggested likely clinical importance in the individual change in preinjury to postinjury dizziness.

Outcome Variables

Our primary outcome variable of interest was the Pittsburgh Sleep Quality Index (PSQI) score. The PSQI is a questionnaire used to assess sleep quality and disturbance over the past month.12,2022 Test-retest reliability for insomnia is 0.87.20 The score range for the PSQI is 0 to 21, and a score >5 has 98.7% sensitivity and 84.4% specificity for identifying clinically important poor sleep quality.20 For initial assessment within 14 days of injury for participants with concussion, the timeframe of the PSQI was modified to reflect sleep quality since the time of injury to the first clinical visit (versus over the past month as in the original timeframe of the PSQI instrument). Control participants were asked to rate their sleep quality over the past month. The PSQI consists of 19 self-rated questions assessing 7 components of sleep: subjective sleep quality, sleep latency, sleep duration, sleep efficiency, sleep disturbances, sleep medication usage, and daytime dysfunction.22

Secondary outcome variables of interest were single-task tandem-gait time, dual-task tandem-gait time, cognitive accuracy during dual-task tandem gait, and modified Balance Error Scoring System (mBESS) errors. Single-task (ICC = 0.86) and dual-task (ICC = 0.84) tandem gait demonstrated high test-retest reliability in youth and adolescent athletes for measuring motor and cognitive function.23 Participants completed single-task and dual-task tandem gait consistent with earlier research.24,25 During both tandem-gait testing conditions, individuals received standardized instructions to walk using an alternating heel-toe pattern along a 3-m line, make a 180° turn beyond the end of the line, and return to the starting position using the same heel-toe gait pattern.24,25 Each person completed 3 timed trials per condition, and the time was averaged across the 3 trials. Instructions for dual-task tandem-gait trials were the same as for the single-task trial with the addition of a simultaneous cognitive task. For each trial, participants were provided with a different cognitive task: (1) spelling a 5-letter word backward, (2) performing serial subtraction by 7 from a randomly selected 2-digit number, and (3) reciting the months in reverse.24,25 Similar to the single-task condition, the primary outcome for dual-task conditions was time to completion, averaged across the 3 trials. During dual-task trials, we also recorded cognitive accuracy for each task, calculated as the number of correct responses divided by total responses.

We assessed static postural stability using the mBESS.2,26 This balance assessment consists of 3 static conditions tested on a solid surface: double-limb stance, nondominant single-limb stance, and tandem-limb stance. For each testing position, participants were instructed to place their hands on their hips and maintain balance for 20 seconds with eyes closed. The number of balance errors for each 20-second trial was the score for the trial. Errors included taking the hands off the hips, opening the eyes, falling out of position, flexing or abducting the hip >30°, lifting the forefoot or heel off the floor, or remaining out of the testing position for >5 seconds.17 The total score was the total number of errors across the 3 conditions, with a higher score indicating worse balance.26 In a systematic review of the BESS, Bell et al26 observed moderate to good reliability, although scores may normalize within 1 week of concussion.27

Statistical Analysis

For purpose 1, sleep quality, we compared descriptive information between concussion and control groups using the 1-way analysis of variance (ANOVA), χ2 test, or Fisher exact test (if cell sizes within the group were <5). Variables that demonstrated a difference between groups (P < .05) were covariates in subsequent regression models. To assess differences between groups on sleep quality, we performed ANOVA. The α level was set at .05. If we observed a main effect, we conducted post hoc Tukey testing to identify between-groups differences. We then calculated a multiple linear regression model to assess the association between postconcussion dizziness and sleep quality while controlling for potential confounding variables (age, height, total symptom severity, concussion history, and migraine history). For purpose 2, postural stability, we repeated the same process using ANOVA and multiple linear regression for the outcome variables of single-task tandem gait, dual-task tandem gait, cognitive accuracy during dual-task tandem gait, and mBESS errors. Statistical analyses were performed using Stata (version 15; StataCorp), and all tests were 2 sided.

RESULTS

A total of 131 participants underwent testing (n = 21 dizzy, n = 37 not dizzy, n = 73 control individuals). The highest preinjury PCSI dizziness rating among participants with concussion was 2, confirming that all participants rated their preinjury dizziness as mild or none. Between-groups differences existed for age, height, total symptom severity, concussion history, and migraine history (Table 1). The control group was older than the not-dizzy group and taller than both concussion groups. A larger proportion of both concussion groups than the control group reported higher total symptom severity and a history of concussion and migraine. We included these variables as covariates in subsequent regression models.

Table 1 Participant Characteristics Stratified By Concussion and Control Groups
Table 1

Dizziness and Sleep Quality

On univariable examination, both concussion groups had worse PSQI scores than the control group (Figure 1). The dizzy group had worse PSQI scores (9.6 ± 3.7) than the not-dizzy group (7.2 ± 3.5) and the control group (4.3 ± 2.6; P < .001). After adjusting for age, height, total symptom severity, concussion history, and migraine history, we observed that the strongest association was between total symptoms and sleep quality, and dizziness was no longer associated with sleep quality (Table 2).

Figure 1Figure 1Figure 1
Figure 1 Violin plot describing the univariable distribution of Pittsburgh Sleep Quality Index scores for those in the concussion, dizzy; concussion, not-dizzy; and control groups. Data are presented as median (center dot) and interquartile range (box around the median). The shaded area represents the probability density of data at each Pittsburgh Sleep Quality Index score (range = 0–21), smoothed using a kernel density estimator. a Indicates difference (P < .05). P values presented are adjusted for multiple comparisons.

Citation: Journal of Athletic Training 57, 11-12; 10.4085/1062-6050-0470.21

Table 2 Multiple Linear Regression Results for Each Outcome Measurea
Table 2

Dizziness and Functional Outcomes

In the univariable analysis, we noted that the dizzy group had slower single-task tandem-gait times than the other 2 groups and the not-dizzy group was slower than the control group (dizzy = 27.2 ± 11.7 seconds versus not dizzy = 21.2 ± 6.3 seconds versus control = 14.7 ± 3.6 seconds, P < .001; Figure 2A). We found the same pattern of differences among the dizzy, not-dizzy, and control groups for dual-task tandem gait (dizzy = 38.4 ± 16.2 seconds versus not dizzy = 29.9 ± 7.2 seconds versus control = 21.6 ± 7.5 seconds, P < .001; Figure 2B). After adjusting for age, height, total symptom severity, concussion history, and migraine history, we determined that single-task and dual-task tandem-gait times were still associated with concussion (for both the dizzy and not-dizzy groups; Table 2). No differences were identified among any of the groups for cognitive accuracy during dual-task tandem gait (Figure 2C). In the univariable analysis of mBESS scores, the dizzy and not-dizzy groups each demonstrated more errors than the control group (dizzy = 9.8 ± 5.1 versus not dizzy = 6.9 ± 5.8 versus control = 3.8 ± 3.5, P < .001), but no difference existed between the dizzy and not-dizzy groups (Figure 2D). After adjusting for potential confounding variables (age, height, total symptom severity, concussion history, and migraine history), we observed that mBESS errors were not associated with group status and total symptom severity was the only variable associated with mBESS errors (Table 2).

Figure 2Figure 2Figure 2
Figure 2 Violin plot describing the distribution of functional outcomes in the univariable analyses for those in the concussion, dizzy; concussion, not-dizzy; and control groups: A, single-task tandem-gait time; B, dual-task tandem-gait time; C, cognitive accuracy during dual-task tandem gait; and D, modified Balance Error Scoring System errors. Data are presented as median (center dot) and interquartile range (box around the median). The shaded area represents the probability density of data at each outcome measurement, smoothed using a kernel density estimator. a Indicates a difference (P < .05). P values presented are adjusted for multiple comparisons.

Citation: Journal of Athletic Training 57, 11-12; 10.4085/1062-6050-0470.21

DISCUSSION

We examined whether postconcussion dizziness was associated with sleep quality and postural stability in adolescents within 14 days of concussion. Our data did not support our primary hypothesis, indicating that dizziness postconcussion was not independently associated with poor sleep quality. Whereas participants with concussion who reported dizziness also reported the worst sleep quality, after we adjusted for total symptom severity, dizziness and sleep quality were no longer associated. However, our data did support our hypothesis that the dizzy group would perform worse on postural stability measures, suggesting that dizziness may also affect postural stability. Thus, examining objective postural stability measures during initial clinical evaluations in the context of postconcussion dizziness may help guide treatment decisions for adolescent athletes.

Participants in the concussion group, whether they reported dizziness or not, described worse sleep quality compared with control individuals, aligning with past findings.28 However, after we adjusted for potential confounding variables (age, height, total symptom severity, concussion history, and migraine history) in the multivariable model, total symptom severity was the only variable associated with sleep quality. Several possible reasons may explain the lack of an association between dizziness and sleep quality after these adjustments. Consistent with previous research,8 participants in the dizzy group also reported the highest total symptom severity among the 3 groups. Thus, it is possible that when analyzed independently, dizziness simply reflected higher total symptom severity, which may explain why it was no longer different in the multivariable model. Additionally, our measure of dizziness was a single question on the PCSI that only involved a severity rating and, therefore, may not have fully addressed the multifactorial nature of dizziness. A more detailed measure of dizziness, such as the Dizziness Handicap Inventory,29 and functional testing of the systems commonly involved in dizziness (vestibular and oculomotor systems, cervical spine)6,9 may provide insight regarding whether specific impairments have a greater effect on sleep quality. Participants also rated preinjury dizziness after their injury, which may have introduced an element of bias in symptom reporting.

In addition to poor sleep quality, participants with concussion performed worse than control individuals on single-task and dual-task tandem gait, consistent with earlier investigations.24,25 Building on this past work, we observed that the dizzy group had slower single-task and dual-task tandem-gait mean times than the not-dizzy and control groups. This difference remained after we adjusted for total symptom severity, indicating that postconcussion dizziness severity may have been independently related to impaired motor performance. Sensory system impairments contributing to dizziness, including vestibular system dysfunction,30 may have also exacerbated postconcussion postural stability impairments, leading to worse tandem-gait performance among individuals with concussion and dizziness relative to those without dizziness.

Although tandem-gait performance was different between the dizzy and not-dizzy groups, the number of errors committed on the mBESS was not. Both concussion groups demonstrated worse performance on the mBESS compared with the control group, aligning with previous work.25 However, after adjusting for total symptom severity, we did not observe mBESS errors that were different between participants with and those without dizziness, and total symptom severity was the only variable associated with mBESS errors. This suggests that, at an average of 7 days postconcussion, the mBESS may not have been sensitive to subtle deficits between concussion subgroups. Tandem gait, a more challenging and dynamic motor task, may be more sensitive to the effects of dizziness than the mBESS. Accordingly, our data indicate that tandem gait may be a useful and clinically feasible assessment for augmenting self-reported symptom evaluations in the context of postconcussion dizziness.

Dual-task tandem-gait cognitive accuracy was not different among our 3 groups. Earlier examinations of dual-task cognitive accuracy during tandem gait produced mixed results. In 1 recent study,25 researchers reported worse tandem-gait cognitive accuracy among the concussed group compared with the control group, whereas the authors of another study24 noted no difference. The lack of differences in cognitive accuracy among our 3 groups suggests that participants may have prioritized accuracy on the cognitive task rather than speed on the motor task under dual-task conditions, although our work was not designed to address this specific question. The dizzy group, which had the slowest time to completion for dual-task tandem gait, did not show impaired cognitive accuracy compared with the other 2 groups, indicating that its motor performance was affected more than cognitive accuracy under dual-task conditions.

Our investigation has potential applications for clinicians managing patients with concussion. Our results built on previous research24,25 supporting the use of tandem gait for postconcussion postural stability assessments. Tandem gait may be a useful and clinically feasible tool for assessing postural stability in patients with concussion who experience dizziness and may better identify individuals with dizziness than the mBESS. Additionally, whereas both dizziness and poor sleep quality were associated with prolonged concussion recovery,5,15,1113,28 our findings suggested that poor sleep quality should be interpreted in the context of total symptom severity rather than dizziness alone.

Limitations

Our study had limitations that should be considered when interpreting the results. First, the cross-sectional study design constrained our ability to determine causal relationships. Although we demonstrated an association between dizziness and tandem gait, prospective research is needed to understand the direction of this relationship. Second, we did not have a rating of preinjury sleep quality, and sleep impairments before concussion could have contributed to poor postconcussion sleep quality. Additionally, given the observational nature of our study, we did not control for the use of sleep aids or medications preconcussion or postconcussion; thus, the use of sleep aids may have influenced our findings. Third, we recruited participants from a specialty sports medicine clinic, and they may have represented a more symptomatic sample than those presenting to other settings for concussion care. This may have limited the generalizability of our results. Future authors should evaluate the underlying dysfunction contributing to dizziness and postural instability, as this may advance the treatment of individuals experiencing these symptoms postconcussion.

CONCLUSIONS

Postconcussion dizziness was associated with impaired single-task and dual-task tandem-gait performance in pediatric and adolescent athletes. Tandem-gait measures differed between concussion subgroups with and without dizziness at the time of assessment. Therefore, tandem gait may provide relevant clinical information to guide treatment decisions in the context of postconcussion dizziness. Sleep quality, however, was more strongly associated with total symptom severity than with self-reported dizziness in isolation.

FINANCIAL DISCLOSURE

This study was funded by the Children's Hospital Colorado Research Institute Pilot Award Program. Separate from this study, Dr Howell has received research support from the Eunice Kennedy Shriver National Institute of Child Health and Human Development (Award No. R03HD094560), the National Institute of Neurological Disorders and Stroke (Award Nos. R01NS100952, R03HD094560, and R43NS108823), and MINDSOURCE Brain Injury Network.

Copyright: © by the National Athletic Trainers' Association, Inc
Figure 1
Figure 1

Violin plot describing the univariable distribution of Pittsburgh Sleep Quality Index scores for those in the concussion, dizzy; concussion, not-dizzy; and control groups. Data are presented as median (center dot) and interquartile range (box around the median). The shaded area represents the probability density of data at each Pittsburgh Sleep Quality Index score (range = 0–21), smoothed using a kernel density estimator. a Indicates difference (P < .05). P values presented are adjusted for multiple comparisons.


Figure 2
Figure 2

Violin plot describing the distribution of functional outcomes in the univariable analyses for those in the concussion, dizzy; concussion, not-dizzy; and control groups: A, single-task tandem-gait time; B, dual-task tandem-gait time; C, cognitive accuracy during dual-task tandem gait; and D, modified Balance Error Scoring System errors. Data are presented as median (center dot) and interquartile range (box around the median). The shaded area represents the probability density of data at each outcome measurement, smoothed using a kernel density estimator. a Indicates a difference (P < .05). P values presented are adjusted for multiple comparisons.


Contributor Notes

Address correspondence to David R. Howell, PhD, ATC, Sports Medicine Center, Children's Hospital Colorado, Department of Orthopedics, University of Colorado School of Medicine, 13123 E 16th Avenue, B060 Aurora, CO 80045. Address email to David.Howell@CUAnschutz.edu.
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