Sleep and adaptation disorders in military personnel with blast injury ====================================================================== * Kateryna Sаrаzhynа * O Ruskykh * I Serbin * Y Solodovnikova * A Son * Neurology * NEUROPATHOLOGY * Anxiety disorders Sleep and adaptation disorders are common in traumatic brain injury (TBI) resulting from blast injuries (BIs) and can significantly complicate the recovery, leading to delayed neurocognitive, psychiatric and behavioural disorders.1 2 Nevertheless, auditory disorders and tinnitus after repeated TBIs significantly worsen and affect daily activity through impaired sleep quality, irritability, anxiety and difficulties with concentration.3–5 We conducted this study to analyse the characteristics of sleep and adaptation disorders in military personnel with BIs. Data were collected from October 2023 to April 2024 among 35 military personnel with BIs aged between 22 and 56 years (mean=31, SD=33.9), undergoing treatment at the University Clinic, with the exclusion of patients who had sleep disorders before the injury and included only military personnel who had sustained a mild TBI and were in the acute phase of their recovery. Sleep quality was assessed using the modified Pittsburgh Sleep Quality Index (PSQI). A sleep quality score of 0–7 points was considered satisfactory, scoring above 7 points was categorised as having poor sleep quality. Adaptation disorders were identified using the Hospital Anxiety and Depression Scale (HADS). On the HADS, scores above 11 were considered significant and indicative of clinical manifestations of adaptation disorder. Participants were divided into three groups: group 1—BI with TBI, barotrauma and tinnitus (n=5, 14.3%); group 2—BI with TBI without tinnitus (n=14, 40%); group 3—control group, BI without TBI (n=16, 45.7%). Table 1 presents summary data from a study involving three separate groups, detailing measures of anxiety, depression and sleep quality. View this table: [Table 1](http://militaryhealth.bmj.com/content/early/2024/09/12/military-2024-002793/T1) Table 1 Descriptive analysis The Shapiro-Wilk test was applied to assess the normality of data distribution to three variables (HADS anxiety, HADS depression, PSQI) across the groups, revealing: group 1: HADS anxiety p=0.502; HADS depression p=0.294; PSQI p=0.421. Group 2: HADS anxiety p=0.192; HADS depression p=0.909; PSQI p=0.091. Group 3: HADS anxiety p=0.114; HADS depression p=0.628; PSQI p=0.896. We used analysis of variance to compare the quality among the groups that fit the normal distribution profile. HADS Anxiety: F-statistic=3.92, p=0.030. HADS Depression: F-statistic=10.85, p=0.00025.PSQI Sleep Quality: F-statistic=29.27, p=5.92e-08. To determine the differences between specific groups, we used post hoc tests, specifically the Tukey test (table 2). View this table: [Table 2](http://militaryhealth.bmj.com/content/early/2024/09/12/military-2024-002793/T2) Table 2 Post hoc tests The results confirm that tinnitus correlates with a significant increase in anxiety and depression with significant differences in sleep quality between the groups (F-statistic=29.27, p<0.001). A potential negative impact of tinnitus on the psychological state of military personnel who have sustained TBI has been identified. Tinnitus can be considered an independent factor in worsening sleep quality and adaptation. The main limitation of our study is the relatively small sample size (n=35) and the inclusion of only men in the study group. This suggests that that should be considered when assessing the condition of patients with various forms of BI.### Supplementary data [[military-2024-002793supp001.pdf]](pending:yes) ## Ethics statements ### Patient consent for publication Not applicable. ### Ethics approval This study involves human participants and was approved by Local Ethics Committee (Odessa National Medical University) N 0842/27 dated 14 March 2024. Participants gave informed consent to participate in the study before taking part. ## Footnotes * X @katjasara * Contributors KS is the main author and guarantor responsible for writing the manuscript. OR performed the calculations and assisted in writing the manuscript. IS conducted data collection and contributed to analysing and interpreting data for the work. YS agreed to be accountable for all aspects of the work, ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. AS provided final approval for the published version. * Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors. * Competing interests None declared. * Provenance and peer review Not commissioned; internally peer reviewed. * Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise. * Received May 26, 2024. * Accepted August 20, 2024. * © Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 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