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Adverse childhood experiences (ACEs) are associated with physical and mental health difficulties in adulthood. This study examines the associations of ACEs with functional impairment and life stress among military personnel, a population disproportionately affected by ACEs. We also evaluate the extent to which the associations of ACEs with functional outcomes are mediated through internalizing and externalizing disorders.
Methods
The sample included 4,666 STARRS Longitudinal Study (STARRS-LS) participants who provided information about ACEs upon enlistment in the US Army (2011–2012). Mental disorders were assessed in wave 1 (LS1; 2016–2018), and functional impairment and life stress were evaluated in wave 2 (LS2; 2018–2019) of STARRS-LS. Mediation analyses estimated the indirect associations of ACEs with physical health-related impairment, emotional health-related impairment, financial stress, and overall life stress at LS2 through internalizing and externalizing disorders at LS1.
Results
ACEs had significant indirect effects via mental disorders on all functional impairment and life stress outcomes, with internalizing disorders displaying stronger mediating effects than externalizing disorders (explaining 31–92% vs 5–15% of the total effects of ACEs, respectively). Additionally, ACEs exhibited significant direct effects on emotional health-related impairment, financial stress, and overall life stress, implying ACEs are also associated with these longer-term outcomes via alternative pathways.
Conclusions
This study indicates ACEs are linked to functional impairment and life stress among military personnel in part because of associated risks of mental disorders, particularly internalizing disorders. Consideration of ACEs should be incorporated into interventions to promote psychosocial functioning and resilience among military personnel.
Patients with posttraumatic stress disorder (PTSD) exhibit smaller regional brain volumes in commonly reported regions including the amygdala and hippocampus, regions associated with fear and memory processing. In the current study, we have conducted a voxel-based morphometry (VBM) meta-analysis using whole-brain statistical maps with neuroimaging data from the ENIGMA-PGC PTSD working group.
Methods
T1-weighted structural neuroimaging scans from 36 cohorts (PTSD n = 1309; controls n = 2198) were processed using a standardized VBM pipeline (ENIGMA-VBM tool). We meta-analyzed the resulting statistical maps for voxel-wise differences in gray matter (GM) and white matter (WM) volumes between PTSD patients and controls, performed subgroup analyses considering the trauma exposure of the controls, and examined associations between regional brain volumes and clinical variables including PTSD (CAPS-4/5, PCL-5) and depression severity (BDI-II, PHQ-9).
Results
PTSD patients exhibited smaller GM volumes across the frontal and temporal lobes, and cerebellum, with the most significant effect in the left cerebellum (Hedges’ g = 0.22, pcorrected = .001), and smaller cerebellar WM volume (peak Hedges’ g = 0.14, pcorrected = .008). We observed similar regional differences when comparing patients to trauma-exposed controls, suggesting these structural abnormalities may be specific to PTSD. Regression analyses revealed PTSD severity was negatively associated with GM volumes within the cerebellum (pcorrected = .003), while depression severity was negatively associated with GM volumes within the cerebellum and superior frontal gyrus in patients (pcorrected = .001).
Conclusions
PTSD patients exhibited widespread, regional differences in brain volumes where greater regional deficits appeared to reflect more severe symptoms. Our findings add to the growing literature implicating the cerebellum in PTSD psychopathology.
Develop and implement a system in the Veterans Health Administration (VA) to alert local medical center personnel in real time when an acute- or long-term care patient/resident is admitted to their facility with a history of colonization or infection with a multidrug-resistant organism (MDRO) previously identified at any VA facility across the nation.
Methods:
An algorithm was developed to extract clinical microbiology and local facility census data from the VA Corporate Data Warehouse initially targeting carbapenem-resistant Enterobacterales (CRE) and methicillin-resistant Staphylococcus aureus (MRSA). The algorithm was validated with chart review of CRE cases from 2010-2018, trialed and refined in 24 VA healthcare systems over two years, expanded to other MDROs and implemented nationwide on 4/2022 as “VA Bug Alert” (VABA). Use through 8/2023 was assessed.
Results:
VABA performed well for CRE with recall of 96.3%, precision of 99.8%, and F1 score of 98.0%. At the 24 trial sites, feedback was recorded for 1,011 admissions with a history of CRE (130), MRSA (814), or both (67). Among Infection Preventionists and MDRO Prevention Coordinators, 338 (33%) reported being previously unaware of the information, and of these, 271 (80%) reported they would not have otherwise known this information. By fourteen months after nationwide implementation, 113/130 (87%) VA healthcare systems had at least one VABA subscriber.
Conclusions:
A national system for alerting facilities in real-time of patients admitted with an MDRO history was successfully developed and implemented in VA. Next steps include understanding facilitators and barriers to use and coordination with non-VA facilities nationwide.
Community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) causes skin and soft-tissue infection (SSTI) in military recruits.
Objective.
To evaluate the effectiveness of 2% Chlorhexidine gluconate (CHG)-impregnated cloths in reducing rates of SSTI and S. aureus colonization among military recruits.
Design.
A cluster-randomized (by platoon), double-blind, controlled effectiveness trial.
Application of CHG-impregnated or control (Comfort Bath; Sage) cloths applied over entire body thrice weekly.
Measurements.
Recruits were monitored daily for SSTI. Baseline and serial nasal and/or axillary swabs were collected to assess S. aureus colonization.
Results.
Of 1,562 subjects enrolled, 781 (from 23 platoons) underwent CHG-impregnated cloth application and 781 (from 21 platoons) underwent control cloth application. The rate of compliance (defined as application of 50% or more of wipes) at 2 weeks was similar (CHG group, 63%; control group, 67%) and decreased over the 6-week period. The mean 6-week SSTI rate in the CHG-impregnated cloth group was 0.094, compared with 0.071 in the control group (analysis of variance model rate difference, 0.025 ± 0.016; P = .14). At baseline, 43% of subjects were colonized with methicillin-susceptible S. aureus (MSSA), and 2.1% were colonized with MRSA. The mean incidence of colonization with MSSA was 50% and 61% (P = .026) and with MRSA was 2.6% and 6.0% (P = .034) for the CHG-impregnated and control cloth groups, respectively.
Conclusions.
CHG-impregnated cloths applied thrice weekly did not reduce rates of SSTI among recruits. S. aureus colonization rates increased in both groups but to a lesser extent in those assigned to the CHG-impregnated cloth Intervention. Antecedent S. aureus colonization was not a risk factor for SSTI. Additional studies are needed to identify effective measures for preventing SSTI among military recruits.
A-Z of Musculoskeletal and Trauma Radiology is an invaluable reference to the key aspects of imaging for all conditions of bones, muscles, tendons and ligaments. It provides the clinician with practical guidance on the key presenting characteristics, clinical features, diagnosis and management. The description of each condition is provided in a standard template of Characteristics, Clinical Features, Radiology and Management, enabling the reader to find the relevant information quickly. All diagnostic modalities are included and a separate section is dedicated to musculoskeletal trauma. Written by a multidisciplinary team of radiologists and an orthopaedic surgeon, A-Z of Musculoskeletal and Trauma Radiology is an invaluable resource for radiologists, orthopaedic surgeons, rheumatologists and all clinicians managing musculoskeletal conditions.
True incidence unknown but increasingly recognised by health-care staff.
Classified into physical, sexual, psychological abuse and neglect.
Prevalent in all ethnic and socio-economic classes.
No sex preponderance seen in physical abuse.
Can occur at any age. Infants are more vulnerable to fatal head trauma than older age group.
Up to one-third of fractures in children may be non-accidental.
Clinical features
Spectrum of physical injuries from mild soft tissue to fatal trauma seen.
Usually present with an obvious injury but beware the non-specific presentation. Observe the child's behaviour and parental interaction.
History suggestive if injuries are not consistent with history; changing or incomplete history; delay in seeking help.
Beware the infant with head injuries or injuries suggestive of significant abdominal trauma.
Look for characteristic soft-tissue injuries such as circular burns (cigarette), linear weals, ‘finger-print’ bruises and immersion-burn injuries.
Accidental bruising is unusual in the non-ambulant child.
Radiological features
The location and developmental age of the child are better indicators than shape of long-bone fracture.
Metaphyseal fractures are characteristic but less commonly seen than shaft fractures (low specificity). Other highly specific fractures include scapular, posterior rib, spinal, sternal, multiple fracture of differing ages and complex skull fractures. Epiphyseal separations are suspicious.
Simple linear skull fractures can result from a minor accidental fall from height.
CT head may be required. Look for evidence of brain injury, associated haemorrhage or skull fracture.
Management
ABCs.
Sympathetic and considered approach to child and family.
Treat as you would for accidental injuries but consider all for admission.
Careful and accurate documentation. Photograph injuries if possible.
Involve experienced staff early if suspicious.
Follow local protocol (e.g. referral to paediatric registrar, check ‘At risk’ register, appropriate referral to social/community services).
Idiopathic bone infarcts characteristically occur in long-bone metaphyses.
Histological testing reveals mineralisation of necrotic marrow.
Aetiology is likely to be related to intrinsic/extrinsic vascular compromise such as thrombosis, arteritis, atherosclerosis or external compression (fractures, oedema, tumour, etc).
Clinical features
Classically asymptomatic and discovered as an incidental diagnosis.
Radiological features
Early rarefaction followed by sclerosis, calcification, and ossification parallel to the cortex in the healing phase.
Bone scan – ‘cold spot’ or no increased uptake in the early stages; becomes ‘hot’ as revascularisation occurs.
Management
No treatment is required; however, malignant fibrous histiocytoma has been reported developing in previous bone infarcts.
Bone islands
Characteristics
Histologically these are markedly thickened bony trabeculae.
Seen in all ages.
Unknown aetiology but may represent a developmental anomaly.
Usually solitary, commonest in the proximal femur and ilium.
Clinical features
Asymptomatic – incidental diagnosis, but these are important in the differential diagnosis of more sinister lesions.
Radiological features
Sclerotic areas within bone which are well demarcated from surrounding normal bone (narrow zone transition). Classically the margin appears feathery.
No cortical involvement or periosteal reaction.
Often oval with the long axis parallel to the bone.
Bone scan – if large may show increased uptake.
Management
Exclude more sinister pathology, but no particular treatment is required.
Rare condition occurring secondary to various pathological states such as bronchogenic carcinoma, chronic chest infections, inflammatory bowel and liver disease.
Thought to occur due to release of vasoactive mediators not metabolised by lung.
Clinical features
Patients present with a burning pain associated with soft-tissue swelling and joint stiffness.
Ankles, wrists, knees and elbows are commonly affected.
Clubbing of fingers and toes may be evident. Limb hypertrophy may occur secondary to soft-tissue swelling.
Peripheral neurovascular effects include cyanosis, blanching, flushing, paraesthesia and hyperhydrosis.
Radiological features
Periosteal new bone formation at the diametaphysis. Commonest in the tibia and fibula. Other common sites include radius and ulna, proximal phalanges, femur and pelvis.
Soft tissue swelling around the distal phalanges.
A bone scan demonstrates symmetrical periosteal uptake.
Cross-sectional imaging is performed to identify the underlying cause.
Management
Directed at treatment of the underlying cause.
Regression of the periosteal reaction may be seen after treatment.
Common finding on MRI scans of post-traumatic joints – particularly the knee with ligament injury, e.g. in the lateral femoral condyle in ACL deficiency and posterolateral tibial plateau bruising is a marker of joint derangement at the time of ACL injury.
Also known as marrow oedema syndrome and microfracture syndrome.
Numerous patterns of bruising identified.
Most commonly affects the lateral femoral condyle.
May represent damage to the articular cartilage at the time of injury – hence the use of the term ‘microfracture’.
Clinical features
Symptoms often related to the underlying ligamentous disruption – see ‘Knee injuries’.
Bony pain and tenderness often related to the underlying bone bruising.
Lasts up to 12 months frequently becoming more pronounced at 6–12 weeks following injury.
Long-term outcome is unknown.
Radiological features
Usually normal AP and lateral knee X-ray – occasionally an avulsion fracture of the lateral tibial plateau, at the site of attachment of the lateral capsular ligament, is seen; this is known as a Segond fracture and is frequently associated with an ACL injury.
Bone bruising is manifest as high signal intensity on T2 weighting and STIR MRI.
MRI: assess for ligamentous and meniscal pathology.
Management
Treat as per the underlying ligamentous injury.
Possibly restrict weight bearing.
Persistent pain may require analgesia, e.g. after an MCL injury has settled down.