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Association between traumatic brain injury and suicidality using a mediation approach and MarketScan
  1. Gabrielle F. Miller1,
  2. Hong Zhou1,
  3. Alexis B. Peterson1,
  4. Elizabeth Swedo2,
  5. Kristin Holland3,
  6. Marcie-jo Kresnow1
  1. 1 Division of Injury Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia, USA
  2. 2 Division of Violence Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia, USA
  3. 3 Division of Overdose Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia, USA
  1. Correspondence to Dr Gabrielle F. Miller, Division of Injury Prevention, Centers for Disease Control and Prevention, Atlanta, GA 30341, USA; ygm3{at}cdc.gov

Abstract

Introduction Negative outcomes, including suicidal ideation/attempts, are a major public health concern, particularly among individuals who sustain a traumatic brain injury (TBI). TBI is associated with high rates of postinjury substance use, psychiatric disorders, post-traumatic stress disorder and sleep disturbances. This study examines the mediation effects of substance use, psychiatric disorder and sleep disorder on the associations between TBI and suicidal ideation/attempts.

Methods A matched case–control study using data from MarketScan databases for private health insurance and Medicaid from October 2015 to December 2018 estimated the association between TBI and suicidal ideation/attempts using a mediation approach. Individuals less than 65 years of age were included.

Results In the Medicaid sample, psychiatric disorders mediated 22.4% of the total effect between TBI and suicidal ideation/attempt, while substance use disorders other than opioid use disorder mediated 7.47%. In the private health insurance sample, psychiatric disorders mediated 3.97% of the total effect, opioid use disorders mediated 2.08% of the total effect and sleep disorder mediated 1.25% of the total effect.

Conclusions Mediators explained less than 30% of the relationship between TBI and suicidal ideation/attempt. Findings reinforce the importance of primary prevention of TBI and monitoring patients with a TBI for risk of suicide in the first 6–12 months following injury.

  • Traumatic Brain Injury
  • Psychological
  • Case-Control Study

Data availability statement

Data may be obtained from a third party and are not publicly available. Data are available through IBM MarketScan Research.

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Data availability statement

Data may be obtained from a third party and are not publicly available. Data are available through IBM MarketScan Research.

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Footnotes

  • Contributors GM conceptualised the study, conducted the analysis, drafted the manuscript, and reviewed the final manuscript. HZ conceptualised the study, performed data analysis, and revised/reviewed the final manuscript. AP, ES, KH and M-JK drafted the manuscript and reviewed the final manuscript. All authors approved the final manuscript as submitted.

  • 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.

  • Disclaimer The findings and conclusions in this manuscript are those of the author(s) and do not necessarily represent the official position of the Centers for Disease Control and Prevention.

  • Competing interests None declared.

  • Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.

  • Provenance and peer review Not commissioned; externally 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.