Shannon B. B Juengst

Dr. Shannon B. B Juengst

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Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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2 October 2019 in JAMA Network Open
Verified
Journal Article
Open access
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SJShannon B. B Juengst
Shannon B. B Juengst
ARAlexa Royston
Alexa Royston
IHIsabel Huang
Isabel Huang
BWBrittany Wright
Brittany Wright
Nearly all physicians find achieving work-life integration difficult because of long work hours and uncompromising schedules.1,2 With substantial growth in the proportion of women graduating from medical school,3 factors surrounding maternity/family leave require particular attention. Current family medical leave policies in the United States are inadequate and often difficult to put into effective practice in medicine.4 Physician mothers frequently stitch together a patchwork of sick days, vacation, and unpaid time off to recover, provide care, and bond with their child before returning to work, often leading to career dissatisfaction and burnout.1,2,5,6

1 September 2017 in Journal of Head Trauma Rehabilitation
Verified
Journal Article
Closed access
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JBJennifer A. Bogner
Jennifer A. Bogner
GWGale G. Whiteneck
Gale G. Whiteneck
JMJessica MacDonald
Jessica MacDonald
SJShannon B. B Juengst
Shannon B. B Juengst
ABAllen W. Brown
Allen W. Brown
JCJohn D. Corrigan
John D. Corrigan
Objective: Evaluate the test-retest reliability of measures that comprise the Traumatic Brain Injury Model Systems follow-up data set. Participants: A total of 224 persons with a moderate-severe traumatic brain injury (TBI) enrolled in the Traumatic Brain Injury Model Systems National Database. Design: Following standard administration of the follow-up interview, a second interview was administered 14 to 28 days later using the same interviewer and the same mode of administration. Main Measures: Traumatic Brain Injury Model Systems follow-up interview that includes 66 variables comprised (a) single item measures of demographics; employment; general health as well as specific health conditions; rehospitalization; tobacco, alcohol, and other drug use; transportation; and mental health and (b) multi-item instruments: FIM; Participation Assessment With Recombined Tools-Objective; Disability Rating Scale; Glasgow Outcome Scale—Extended; Supervision Rating Scale; Satisfaction With Life Scale; TBI Quality of Life Anxiety and Depression items; and The Ohio State University TBI Identification Method. Results: Intraclass correlation coefficient values ranged from 0.65 to 0.99, weighted kappa values ranged from 0.54 to 0.99, and kappa values ranged from 0.43 to 1.00. Four kappa/weighted kappa estimates fell below 0.60: arrested, psychiatric hospitalization, number of days not in good physical health, and rating of general emotional health. Conclusions: With few exceptions, good to excellent test-retest reliability estimates were obtained. The findings support the use of these measures in prior and future studies and indicate that persons with moderate-severe TBI can provide reliable self-report.

1 June 2017 in Psychology Research and Behavior Management
Verified
Journal Article
Open access
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SJShannon B. B Juengst
Shannon B. B Juengst
RKRaj G Kumar
Raj G Kumar
AWAmy K Wagner
Amy K Wagner
Depression is one of the most common conditions to emerge after traumatic brain injury (TBI), and despite its potentially serious consequences it remains undertreated. Treatment for post-traumatic depression (PTD) is complicated due to the multifactorial etiology of PTD, ranging from biological pathways to psychosocial adjustment. Identifying the unique, personalized factors contributing to the development of PTD could improve long-term treatment and management for individuals with TBI. The purpose of this narrative literature review was to summarize the prevalence and impact of PTD among those with moderate to severe TBI and to discuss current challenges in its management. Overall, PTD has an estimated point prevalence of 30%, with 50% of individuals with moderate to severe TBI experiencing an episode of PTD in the first year after injury alone. PTD has significant implications for health, leading to more hospitalizations and greater caregiver burden, for participation, reducing rates of return to work and affecting social relationships, and for quality of life. PTD may develop directly or indirectly as a result of biological changes after injury, most notably post-injury inflammation, or through psychological and psychosocial factors, including pre injury personal characteristics and post-injury adjustment to disability. Current evidence for effective treatments is limited, although the strongest evidence supports antidepressants and cognitive behavioral interventions. More personalized approaches to treatment and further research into unique therapy combinations may improve the management of PTD and improve the health, functioning, and quality of life for individuals with TBI.

1 May 2015 in Journal of Head Trauma Rehabilitation
Verified
Journal Article
Closed access
SJShannon B. B Juengst
Shannon B. B Juengst
RKRaj G Kumar
Raj G Kumar
MFMichelle D Failla
Michelle D Failla
AGAkash Goyal
Akash Goyal
AWAmy Wagner
Amy Wagner
Objective: To examine whether acute inflammation profiles predict posttraumatic depression (PTD) risk 6 and 12 months after traumatic brain injury. Setting: University-affiliated level 1 trauma center and community. Participants: Adults with moderate to severe traumatic brain injury (acute serum levels: n = 50; acute cerebrospinal fluid (CSF) levels: n = 41). Design: Prospective cohort study. Main Measures: Patient Health Questionnaire; inflammatory biomarkers (interleukin [IL]-1β, IL-4, IL-5, IL-6, IL-7, IL-8, IL-10, IL-12, tumor necrosis factor α, soluble vascular adhesion molecule [sVCAM-1], soluble intracellular adhesion molecule [sICAM-1], soluble Fas [sFAS]). Results: Higher levels of acute CSF cytokine surface markers (sVCAM-1, sICAM-1, and sFAS) in an inflammatory biomarker risk (IBR) score were associated with a 3.920-fold increase in the odds of developing PTD at 6 months (95% confidence interval: 1.163-8.672). Having sICAM-1, sVCAM-1, or sFAS above the 75th percentile had a positive predictive value of 85.7% for PTD risk at 6 months. An IBR score including inflammatory biomarkers IL-7 and IL-8 showed a trending association with 12-month PTD risk (odds ratio = 3.166, 95% confidence interval: 0.936-10.708). Conclusion: Acute CSF IBR scores show promise for identifying individuals at risk for PTD. Further research should assess acute CSF inflammatory biomarkers' relationships to chronic inflammation as a mechanism of PTD and should explore anti-inflammatory treatments for PTD, as well as prevention and screening protocols, and link inflammatory biomarkers to symptom tracking.

1 October 2014 in Brain, Behavior, and Immunity
Verified
Journal Article
Closed access
SJShannon B. B Juengst
Shannon B. B Juengst
RKR.G. Kumar
R.G. Kumar
PAP.M. Arenth
P.M. Arenth
AWAmy Wagner
Amy Wagner

7 August 2015 in Brain Injury
Verified
Journal Article
Closed access
PDF file
SJShannon B. B Juengst
Shannon B. B Juengst
KGKristin M. Graham
Kristin M. Graham
IPI. Wayan Pulantara
I. Wayan Pulantara
MMMichael McCue
Michael McCue
EWEllen M. Whyte
Ellen M. Whyte
AWAmy K. Wagner
Amy K. Wagner
Objective: This study assessed pilot feasibility and validity of a mobile health (mHealth) system for tracking mood-related symptoms after traumatic brain injury (TBI). Design: A prospective, repeated measures design was used to assess compliance with daily ecological momentary assessments (EMA) conducted via a smartphone application over an 8-week period. Methods: An mHealth system was developed specifically for individuals with TBI and utilized previously validated tools for depressive and anxiety symptoms (Patient Health Questionnaire-9, Generalized Anxiety Disorder-7). Feasibility was assessed in 20 community-dwelling adults with TBI via an assessment of compliance, satisfaction and usability of the smartphone applications. The authors also developed and implemented a clinical patient safety management mechanism for those endorsing suicidality. Results: Participants correctly completed 73.4% of all scheduled assessments, demonstrating good compliance. Daily assessments took <2 minutes to complete. Participants reported high satisfaction with smartphone applications (6.3 of 7) and found them easy to use (6.2 of 7). Comparison of assessments obtained via telephone-based interview and EMA demonstrated high correlations (r = 0.81–0.97), supporting the validity of conducting these assessments via smartphone application in this population. Conclusions: EMA conducted via smartphone demonstrates initial feasibility among adults with TBI and presents numerous opportunities for long-term monitoring of mood-related symptoms in real-world settings.