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BACKGROUND CONTEXTPositive psychosocial factors early after surgery, such as resilience and self-efficacy, may be important characteristics for informing individualized postoperative care.PURPOSETo examine the association of early postoperative resilience and self-efficacy on 12-month physical function, pain interference, social participation, disability, pain intensity, and physical activity after lumbar spine surgery.STUDY DESIGN/SETTINGPooled secondary analysis of prospectively collected trial data from two academic medical centers.PATIENT SAMPLETwo hundred and forty-eight patients who underwent laminectomy with or without fusion for a degenerative lumbar condition.OUTCOME MEASURESPhysical function, pain inference, and social participation (ability to participate in social roles and activities) were measured using the Patient Reported Outcomes Measurement Information System. The Oswestry Disability Index, Numeric Rating Scale, and accelerometer activity counts were used to measure disability, pain intensity, and physical activity, respectively.METHODSParticipants completed validated outcome questionnaires at 6 weeks (baseline) and 12 months after surgery. Baseline positive psychosocial factors included resilience (Brief Resilience Scale) and self-efficacy (Pain Self-Efficacy Questionnaire). Multivariable linear regression analyses were used to assess the associations between early postoperative psychosocial factors and 12-month outcomes adjusting for age, sex, study site, randomized group, fusion status, fear of movement (Tampa Scale for Kinesiophobia), and outcome score at baseline. This study was funded by Patient-Centered Outcomes Research Institute and Foundation for Physical Therapy Research. There are no conflicts of interest.RESULTSResilience at 6 weeks after surgery was associated with 12-month physical function (unstandardized beta=1.85 [95% confidence interval [CI]: 0.29; 3.40]), pain interference (unstandardized beta=?1.80 [95% CI: ?3.48; ?0.12]), social participation (unstandardized beta=2.69 [95% CI: 0.97; 4.41]), and disability (unstandardized beta=?3.03 [95% CI: ?6.04; ?0.02]). Self-efficacy was associated with 12-month disability (unstandardized beta=?0.21 [95% CI: ?0.37; ?0.04].CONCLUSIONSPostoperative resilience and pain self-efficacy were associated with improved 12-month patient-reported outcomes after spine surgery. Future work should consider how early postoperative screening for positive psychosocial characteristics can enhance risk stratification and targeted rehabilitation management in patients undergoing spine surgery.  相似文献   
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URO-Telegramm     
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High‐risk neuroblastoma (NB) patients with 11q deletion frequently undergo late but consecutive relapse cycles with fatal outcome. To date, no actionable targets to improve current multimodal treatment have been identified. We analyzed immune microenvironment and genetic profiles of high‐risk NB correlating with 11q immune status. We show in two independent cohorts that 11q‐deleted NB exhibits various immune inhibitory mechanisms, including increased CD4+ resting T cells and M2 macrophages, higher expression of programmed death‐ligand 1, interleukin‐10, transforming growth factor‐beta‐1, and indoleamine 2,3‐dioxygenase 1 (P < 0.05), and also higher chromosomal breakages (P ≤ 0.02) and hemizygosity of immunosuppressive miRNAs than MYCN‐amplified and other 11q‐nondeleted high‐risk NB. We also analyzed benefits of maintenance treatment in 83 high‐risk stage M NB patients focusing on 11q status, either with standard anti‐GD2 immunotherapy (n = 50) or previous retinoic acid‐based therapy alone (n = 33). Immunotherapy associated with higher EFS (50 vs. 30, P = 0.028) and OS (72 vs. 52, P = 0.047) at 3 years in the overall population. Despite benefits from standard anti‐GD2 immunotherapy in high‐risk NB patients, those with 11q deletion still face poor outcome. This NB subgroup displays intratumoral immune suppression profiles, revealing a potential therapeutic strategy with combination immunotherapy to circumvent this immune checkpoint blockade.

Abbreviations

11q‐del
11q‐deleted
ADCC
antibody‐dependent cellular cytotoxicity
CDC
complement‐dependent cytotoxicity
COJEC
chemotherapeutic agents cisplatin, vincristine, carboplatin, etoposide, and cyclophosphamide
CTLA‐4
cytotoxic T lymphocyte antigen 4
EFS
event‐free survival
FISH
fluorescence in situ hybridization
HR
hazard ratio
ICI
immune checkpoint inhibitor
IDO1
indoleamine 2,3‐dioxygenase 1
IFN‐γ
interferon‐γ
IL‐10
interleukin 10
INRG
International Neuroblastoma Risk Group
miR
microRNA
MLPA
multiplex ligation‐dependent probe amplification
MMR
mismatch repair
MNA
MYCN amplification
MS
metastatic special stage
MSI
microsatellite instability
NB
neuroblastoma
NCA
numerical chromosome aberrations
NOS
nitric oxide synthase
OS
overall survival
PD‐1
programmed cell death protein 1
PD‐L1
programmed death‐ligand 1
SCA
segmental chromosome aberrations
TAM
tumor‐associated macrophages
Tfh
follicular helper T cells
TGF‐β
tumor growth factor‐β
TMB
tumor mutational burden
TME
tumor microenvironment
TNF‐α
tumor necrosis factor‐α
Treg
regulatory T cells
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Eclampsia, a clinical syndrome classically defined by the occurrence of seizures and/or coma in pregnant women with hypertension and proteinuria, is often presented as a posterior reversible encephalopathy syndrome (PRES), a clinical-radiological entity characterized by headache, visual disturbances, seizures and/or alteration of consciousness, besides a radiological pattern of reversible vasogenic cerebral edema located in posterior territory.  相似文献   
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