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If emotions constitute a central part of teachers’ professional lives (Hargreaves, 1998), it is plausible to hypothesize that becoming and being a language teacher educator could be a highly emotional process as well. To date, while research on teacher emotions has been highly vibrant and fruitful, scant attention has been paid to teacher educators’ emotions, particularly in the field of second language education (Yuan et al., 2022). As documented by existing literature (e.g., Izadinia, 2014; Yuan & Yang, 2022), teacher educators often face various challenges (e.g., a heavy workload and the research-practice divide) in their daily work, and they may struggle with the emotional and intellectual distance between their current professionalism and the expected performance in teacher education (Intrator & Kunzman, 2009; Nazari et al., 2024). Nevertheless, the emotional state of teacher educators is interconnected with their personal well-being, as well as the motivation and quality of teachers, ultimately influencing classroom instruction and student learning (Day & Leitch, 2001). Scholars (e.g., Hagenauer & Volet, 2014; Johnson & Golombek, 2020) have thus argued that teacher educators need to foster and maintain a sense of control over their emotions to facilitate their teaching of teachers.
Background: Electronic surveillance for hospital-onset sepsis using CDC’s Adult Sepsis Event definition could provide an efficient and objective method to identify a broad array of serious healthcare-associated infections, many of which are missed through current reporting processes. We developed risk adjustment models of varying complexity to support facility-level comparison of hospital-onset sepsis rates, evaluated trade-offs between model performance and feasibility, and quantified residual inter-facility variation that may reflect gaps in care. Methods: We conducted a retrospective study of adults hospitalized for <3 days within 113 community hospitals between 2022-2023. Hospital-onset Adult Sepsis Events (HO-ASEs) occurring on day 4 or later were identified using updated CDC surveillance criteria. We used logistic regression to develop three risk adjustment models of increasing complexity using covariates from administrative and electronic health record data: basic model (hospital and aggregate patient descriptors), intermediate model (replacing aggregate patient descriptors with patient-level descriptors), and maximal model (adding detailed physiologic and clinical data from hospital days 1-3; Figure 1). We evaluated model performance using Area Under Receiver Operating Curve (AUROC), calculated hospital-level Standardized Infection Ratios (SIRs) for each model and assessed concordance in hospital rankings using Kendall’s tau coefficient (τ). Results: The cohort included 1,557,252 hospitalizations of <3 days, of which 24,169 (1.6%) met HO-ASE criteria and 8,500 (35.2%) died in-hospital. The basic model had limited discrimination (AUROC 0.589, 95% CI, 0.585-0.593). Adding patient-level characteristics to form the intermediate model markedly improved performance (AUROC 0.839, 95% CI 0.836-0.841), with further inclusion of detailed clinical data in the maximal model yielding modest additional improvement (AUROC 0.850, 95% CI 0.848-0.853). Concordance between hospital rankings derived from the crude or basic risk-adjusted HO-ASE rates versus rankings derived from the intermediate or maximal models was moderate (τ 0.40-0.51) whereas concordance between rankings derived from the intermediate vs. maximal models was high (τ 0.86). There was a wide distribution of HO-ASE SIRs across facilities even after risk adjustment using the maximal model (Figure 2), with high signal-to-noise ratios and good calibration. Conclusions: Risk adjustment models incorporating hospital characteristics and patient-level data perform well and might explain substantial variability in HO-ASE rates between facilities. The persistence of residual variability after highly detailed adjustment may reflect differences in care processes, suggesting that risk-adjusted HO-ASE comparisons can help identify gaps and opportunities in the prevention of severe healthcare-associated infections. Our findings support the use of HO-ASE as an electronic, scalable, risk-adjusted metric for facility-level benchmarking to inform quality improvement initiatives.
Anxiety disorders are associated with disrupted amygdala connectivity; however, resting-state functional MRI studies have reported heterogeneous findings. To clarify these inconsistencies, we conducted a meta-analysis of amygdala-based connectivity studies.
Methods
A systematic search of Embase, PubMed, and Web of Science was performed through December 26, 2025. Studies comparing amygdala-based whole-brain resting-state functional connectivity in patients with anxiety disorders versus healthy controls were included. Meta-analysis was conducted with the latest software – Seed-based d Mapping with Permutation of Subject Images (SDM-PSI), which employs voxel-wise tests and multiple corrections to minimize false positives. Subgroup analyses were performed to examine differences by age and hemisphere.
Results
Fifteen datasets (378 patients, 405 controls) were included. Compared to healthy controls, patients with anxiety disorders had decreased amygdala-anterior cingulate cortex (ACC, g = −0.54, 95% confidence interval [CI]: −0.73 to −0.35) connectivity and increased connectivity with the left superior temporal gyrus (g = 0.46, 95% CI: 0.27–0.65), middle temporal gyrus (g = 0.38, 95% CI: 0.19–0.57), and cuneus (g = 0.35, 95% CI: 0.17–0.53). After threshold-free cluster enhancement correction, only reduced amygdala-ACC connectivity remained significant (g = −0.54, 95% CI: −0.73 to −0.35). Subgroup analyses confirmed this effect was driven mainly by adult patients and the left amygdala.
Conclusions
Reduced connectivity between the left amygdala and the ipsilateral ACC was the most robust neuroimaging marker of anxiety disorders, which suggests a lateralized vulnerability. By applying updated analytic methods, this study refines our understanding of the neuropathology of anxiety disorders and provides a potential primary target for biomarker development and novel interventions.
Nerve growth factor (NGF), which acts on receptors tropomyosin receptor kinase A and p75 neurotrophic receptor, is a member of neurotrophin family and a kind of secretory polypeptides.
Methods
A comprehensive literature search was conducted in the following databases: PubMed and Web of Science. The following search terms were used in various combinations: “NGF,” “nerve growth factor,” “ovarian steroidogenesis,” “follicular development,” “oocyte maturation,” and “ovulation.” Boolean operators (AND, OR) were applied to combine search terms (e.g., “NGF AND PCOS,” “NGF AND follicular development”).
Results
NGF plays important roles in multiple reproductive physiological activities. Its ovarian effects are crucial for oocyte maturation, follicular assembly, early follicle development, ovulation and steroidogenesis. While the ovary is a major target, NGF’s role extends to the broader regulation of the female reproductive system. In particular, the role of NGF in inducing ovulation by acting on the hypothalamus has garnered considerable scholarly attention. Although relatively few studies have examined the direct impact of NGF on hypothalamic gonadotrophin-releasing hormone neurons—the central regulators of the hypothalamic–pituitary–ovary (HPO) axis, extensive evidence demonstrates that NGF can cause an influence on the synthesis and release of follicle-stimulating hormone, luteinizing hormone and steroid hormones, which act downstream in the HPO axis.
Conclusions
Our review outlines the critical role of NGF in female reproductive physiology, with a particular focus on its modulatory influence on induced ovulation. Furthermore, in this review, we aim to provide a more comprehensive perspective on NGF’s role in reproductive disorders, such as polycystic ovary syndrome, diminished ovarian reserve and endometriosis.
We investigate the onset of transient natural convection in fluid layers subject to volumetric radiative heating and surface cooling. Linear stability analysis reveals a non-monotonic evolution of stability in deep layers, where the flow undergoes successive stages of initial destabilisation, intermediate suppression and eventual restabilisation. This complex temporal behaviour necessitates the definition of dual critical Rayleigh numbers: a lower bound marking the onset of initial instability and an upper bound required for sustained convection. To efficiently predict these thresholds, we develop a local Rayleigh number model that depends solely on the instantaneous conductive temperature profile. When the Rayleigh number exceeds the lower bound, the critical time $t_c$ for flow onset is determined through transient linear stability analysis, and scaling laws are derived to characterise the dependence of $t_c$ on the Rayleigh number $\textit{Ra}$, Prandtl number $\textit{Pr}$, cooling parameter $\phi$ and layer depth $H$. Two distinct instability triggering mechanisms are identified: a top-triggered regime, where $t_c \sim [\textit{Ra} \textit{Pr} \phi /(2+\textit{Pr})]^{-1/2}$, and a bottom-triggered regime, where $t_c \sim [\textit{Ra} \textit{Pr} \exp (-H)/(2+\textit{Pr})]^{-1/2}$. All theoretical predictions are rigorously validated against direct numerical simulations, providing a unified predictive framework for convective onset in systems governed by coupled effects of radiation absorption and surface cooling.
Recruitment and retention challenges continue to hinder the success of clinical trials. Artificial intelligence (AI) has emerged as a promising means to optimize various clinical trial processes; however, its impact specifically on recruitment and retention has not been comprehensively evaluated. This scoping review utilized the Joanna Briggs Institute framework and adhered to PRISMA-ScR guidelines, systematically searching literature published between January 2018 and June 2024 across multiple databases. Of the 21,573 records screened, 121 studies were included. A meta-analysis was conducted to quantitatively assess the performance of AI-driven tools. AI applications for patient screening demonstrated strong performance, achieving a pooled sensitivity of 0.91 (95% CI: 0.84–0.95) and an area under the curve (AUC) of 0.79 (95% CI: 0.72–0.85). AI tools employed for eligibility identification and classification also exhibited strong outcomes, with pooled sensitivities of 0.80 (95% CI: 0.76–0.84) and 0.92 (95% CI: 0.84–0.96), respectively, and precisions of 0.84 (95% CI: 0.80–0.88) and 0.91 (95% CI: 0.85–0.95). AI tools aimed at identifying patient cohorts showed moderate effectiveness (pooled sensitivity: 0.70 [95% CI: 0.52–0.84]; AUC: 0.74 [95% CI: 0.61–0.84]). Overall, AI presents significant potential for enhancing clinical trial recruitment and retention, with effectiveness varying across specific applications. These findings underscore AI’s valuable role in improving trial efficiency and data quality.
Discrepancies in iodised salt coverage rate (ISCR) between household salt and that used in catering establishments may significantly compromise the accuracy of dietary iodine intake assessments. To evaluate this impact, we analysed data from the 2023 Shanghai Diet and Health Survey, a cross-sectional study involving 2920 adults. Dietary intake was assessed using three 24-h dietary recalls and an FFQ, while condiment intake was collected using the weighed inventory method. Additionally, salt samples from 960 canteens and restaurants were tested to determine the ISCR in dining establishments. Results showed that the ISCR was 85·9 % in dining establishments, markedly higher than the 53·3 % observed in households. Among employed participants in Shanghai, 51·7 %, 56·1 % and 18·7 % reported consuming breakfast, lunch and dinner outside the home at least once during the 3-d study period, respectively. The estimated daily iodine intake was 101 μg/d when dining-out salt was assumed to have the same ISCR as household salt, but it increased to 118 μg/d after accounting for the ISCR discrepancy. In conclusion, the rising prevalence of eating out has reshaped residents’ dietary habits, rendering traditional household-centric survey methods inadequate for iodine intake estimation in Shanghai. Incorporating ISCR differences between household and dining settings is essential for more accurate dietary iodine assessments.
Clay minerals in the Yishu fault zone, as typical products of hydrothermal activity, carry critical information regarding subsurface geothermal processes. To clarify their hyperspectral remote sensing characteristics and their guiding value for geothermal resource exploration, this study takes the Yishu fault zone and three key subareas (Tangtou, Tongjing and Fangzi) as the research objects. Based on ZY1-02D hyperspectral remote sensing data, combined with principal component analysis and the Crósta method, we analysed the spectral features of typical clay minerals (illite, montmorillonite and chlorite) and extracted their spatial distribution patterns. In addition, ZY1-02E thermal infrared data were used to invert the land surface temperature so as to explore the spatial correlation between clay mineral distribution and geothermal anomalies. The results show that the spatial distribution of clay minerals is closely associated with fault structures, being mainly concentrated along the four major fault belts of the Yishu fault zone and their surrounding areas. High-intensity hydrothermal alteration zones dominated by clay minerals exhibit significant spatial overlap with surface temperature anomalies. The consistent distribution of clay minerals and known geothermal fields further confirms that the hyperspectral characteristics of clay minerals can effectively indicate the upwelling channels and accumulation zones of geothermal fluids. This study provides a rapid and accurate technical method for geothermal resource prospecting in the Yishu fault zone and other tectonically similar regions.
Understanding fluid-elastic instabilities in slender bodies is crucial for predicting and controlling flow-induced vibration (FIV) in engineering and biological systems. The FIV of a prolate spheroid with an aspect ratio of $\epsilon = 3$, a mass ratio of $m^* = 3$ and a damping ratio of $\zeta = 0$, elastically mounted in a uniform flow at ${\textit{Re}} = 600$, are investigated using direct numerical simulations and a reduced-order model (ROM). As reduced velocity $U_r$ increases, five vibration states emerge: quasi-steady (QS), periodic (PM), large-amplitude chaotic (LAC), quasi-periodic (QP) and small-amplitude chaotic (SAC) modes. These mode regimes form two categories of response branches, namely synchronised branches (SB) and desynchronised branches (DB). In SB, three synchronisation mechanisms are identified, i.e. conventional lock-in (CLI), secondary-component lock-in (SCLI) and superharmonic lock-in (SHLI), corresponding to PM, LAC and QP modes, respectively. In contrast, DB comprises two types. The flow-dominated desynchronised (FDD) branch corresponds to QS mode, where flow instability dominates while structural vibrations remain weak. The dual-mode competition desynchronised (DMCD) branch corresponds to the SAC mode, where fluid and structural instabilities coexist but fail to synchronise. Analysis of wake dynamics identifies spanwise, transverse and high-frequency spanwise shedding patterns that are closely correlated with vibration regimes. The overlap of the response branches produces three distinct hysteresis zones, emphasising the sensitivity of spheroidal FIV to initial conditions and its inherently path-dependent behaviour. Dynamic mode decomposition (DMD) and an ERA-based ROM, which together resolve mode-specific spatial structures and frequency evolution, show that the vibration dynamics is governed by a persistently unstable wake mode (WM) and a structural mode (SM) whose stability alternates across branches. This clarifies the resulting sequence of vibration modes and provides insight into how different branches compete and transition.
Histone lysine-specific demethylase 4A (KDM4A) plays a critical role in the embryonic development of mammals such as mouse and goat, however its function in zebrafish (Danio rerio) embryogenesis remains poorly understood, due to the existence of two kdm4a paralogs (kdm4aa and kdm4ab) in zebrafish. The current study revealed that kdm4aa–/– embryos exhibited dramatically increased mortality during gastrulation. RT-qPCR showed that RNA-binding motif protein 46 (rbm46) was downregulated after kdm4aa knockout. CUT&Tag-qPCR revealed that kdm4aa knockout significantly decreased H3K4me3, while increasing H3K9me3 and H3K36me3 at rbm46 promoter. kdm4aa–/– embryos displayed elevated reactive oxygen species (ROS) and reduced adenosine triphosphate (ATP). And rbm46 mRNA injection alleviated ROS accumulation and increased ATP level, thereby rescuing the lethal phenotype in kdm4aa–/– embryos. Our findings demonstrate that kdm4aa knockout disturbs zebrafish embryogenesis by suppressing rbm46 mRNA expression.
Persistent affective disturbance is a core, disabling feature of major depressive disorder (MDD), thought to stem from a dysfunctional interaction between emotional bias and cognitive control. However, the underlying neural dynamics are debated, with studies reporting both hyper- and hypoactivation. This study utilized high-temporal-resolution electroencephalogram (EEG) to resolve this discrepancy by examining distinct stages of emotional information processing.
Methods
We recruited 175 medication-free patients with MDD (Hamilton Depression Rating Scale-17 ≥ 14) and 101 healthy controls (HCs) who completed an emotional Stroop task while an EEG was recorded. We analyzed event-related potentials reflecting conflict monitoring (N250), inhibition (N450), and resolution (LSP) using a 2 (group) × 2 (valence) × 2 (congruency) analysis of variance.
Results
Results revealed a stage-specific neural cascade. Compared to HCs, the MDD group showed: (1) hypoactivation during initial conflict monitoring (attenuated N250 amplitude); (2) compensatory hyperactivation during conflict inhibition (a significant N450 interaction revealed generalized conflict activity in MDD, unlike the context-specific response in HCs); and (3) subsequent hypoactivation during conflict resolution (reduced LSP amplitude for negative stimuli). Crucially, altered N450 correlated with depression severity, and the entire neural cascade predicted behavioral performance.
Conclusions
The apparent contradiction in the literature reflects a multistage process. MDD is characterized by an inefficient neural cascade: an initial deficit in conflict monitoring is followed by compensatory overactivation during inhibition, which ultimately proves insufficient, leading to impaired late-stage resolution. This temporally specific model advances our understanding of the pathophysiology of depression and identifies potential stage-specific targets for intervention.
This study aimed to determine the optimal Biological Effective Dose (BED)-based compensation strategy for treatment interruptions in left-sided breast cancer radiotherapy, with a focus on evaluating cardiac substructures to address a previously unmet clinical need.
Methods:
Twenty patients with left-sided breast cancer who had received radiotherapy were retrospectively enrolled.
Simulations assumed treatment interruptions (number of interruption days) occurred after the first week, ranging from 1 to 10 days. Three BED-based compensation strategies were evaluated: (A) maintaining total fractions and days while delivering twice-daily treatments; (B) maintaining total days while increasing the dose per fraction; and (C) keeping the dose per fraction constant while extending the overall treatment course. Original uninterrupted plans served as the baseline. BEDs for the planning target volume (PTV), simultaneous integrated boost (SIB), cardiac substructures and other organs at risk (OARs) were calculated. Physical and BED differences among the schemes were systematically compared.
Results:
Compared to the original scheme, physical doses to PTV and SIB were lower in Scheme B but higher in Scheme C. As interruptions increased from 1 to 10 days, PTV and SIB doses in Scheme B decreased to minimum values of 42.71 Gy and 50.58 Gy, respectively, while Scheme C resulted in maximum values of 58.60 Gy and 67.15 Gy. Analysis of BED changes (ΔBED) in OARs revealed that the left anterior descending artery (LAD) was the most affected cardiac substructure, with ΔBED values of 0.41, –1.20 and 0.60 for Schemes A, B and C, respectively, at 10 interruption days. Among other OARs, the left lung showed the highest ΔBED changes (0.39, –0.30 and 0.32, respectively). Most OAR comparisons reached statistical significance (ANOVA, p < 0.05).
Conclusion:
Compensation strategies for radiotherapy interruptions significantly influence the BED of OARs, particularly in the LAD and left lung. Scheme B most effectively reduced the BED of OARs but requires replanning. Schemes A and C offer clinical convenience at the cost of a higher BED of OARs. The choice of compensation strategy should be individualised based on clinical priorities and patient-specific anatomy.
Structural brain alterations in bipolar disorder (BD) have been widely reported, yet the hierarchical organization of cortical morphometric networks and their molecular and cognitive underpinnings remain unclear.
Methods
We applied the morphometric inverse divergence (MIND) network approach to structural MRI data from 49 BD patients and 119 healthy controls. Principal MIND gradients were derived using diffusion map embedding, followed by multiscale analyses linking gradient alterations to neurotransmitter systems, cognitive-behavioral domains, and transcriptomic profiles from the Allen Human Brain Atlas. Validation was performed in three independent, cross-scanner, cross-race, and cross-age validation datasets.
Results
Bipolar disorder patients showed significant principal gradient alterations in the left rostral middle frontal and lateral occipital cortices, with network-level decreases in the ventral attention and motor networks and increases in frontoparietal and visual networks. Gradient alterations spatially correlated with acetylcholine (VAChT) and GABA (GABAA/BZ) systems, and were associated with cognitive processes involving executive control and visual attention. Transcriptomic analyses identified gene sets enriched for BD-related GWAS loci, expressed predominantly in excitatory and inhibitory neurons, astrocytes, and oligodendrocytes, with preferential enrichment in cortical layers III-IV and developmental windows spanning early fetal to young adulthood.
Conclusions
These findings reveal disrupted hierarchical cortical organization in BD and link macroscale morphometric alterations to specific neurotransmitter systems and transcriptional architectures. The MIND gradient emerges as a potential biomarker bridging structural disruptions with molecular and cognitive mechanisms in BD.
Fine-grained mortality forecasting has gained momentum in actuarial research due to its ability to capture localized, short-term fluctuations in death rates. This paper introduces MortFCNet, a deep-learning method that predicts weekly death rates using region-specific weather inputs. Unlike traditional Serfling-based methods and gradient-boosting models that rely on predefined fixed Fourier terms and manual feature engineering, MortFCNet automatically learns patterns from raw time-series data without needing explicitly defined Fourier terms or manual feature engineering. Extensive experiments across over 200 NUTS-3 regions in France, Italy, and Switzerland demonstrate that MortFCNet consistently outperforms both a standard Serfling-type baseline and XGBoost in terms of predictive accuracy. Our ablation studies further confirm its ability to uncover complex relationships in the data without feature engineering. Moreover, this work underscores a new perspective on exploring deep learning for advancing fine-grained mortality forecasting.
Timely dissemination of clinical trial results is essential to advance knowledge, guide practice, and improve outcomes, yet many trials remain unpublished, limiting impact. We examine what drives publication and timelines across three major clinical domains.
Methods:
We analyzed study design and factors associated with dissemination of interventional trials, focusing on cardiovascular disease (CVD), cancer, and COVID-19. A total of 10,785 trials (CVD: 5929; cancer: 4210; COVID-19: 646) were linked to PubMed publications using National Clinical Trial identifiers. Study design, operational, and transparency-related features were assessed as predictors of time to publication, defined as the interval from study completion to first publication, using Cox proportional hazards model.
Results:
COVID-19 trials had the highest publication rate (49.6%), followed by CVD (42.3%) and cancer (32.9%), likely reflecting pandemic-related prioritization. Faster publication was associated with larger enrollment, more sites, result posting, randomization, DMC presence, and higher blinding levels (all p < 0.05). Slower publication was linked to supportive care or diagnostic trials (CVD), basic science (cancer), and later COVID-19 trial completion. In subgroups, U.S. facility presence (CVD) and phase 3 design (cancer) predicted faster publication, while healthy volunteer inclusion (CVD) predicted slower publication. Among DMC trials, more secondary outcomes were linked to faster publication across all disease areas.
Conclusions:
Key study design and operational factors consistently predict whether and when trials are published. Strengthening methodological rigor, result reporting, and multi-site collaboration may accelerate timely dissemination into peer-reviewed literature.
Accurate mortality forecasting is crucial for actuarial pricing, reserving, and capital planning, yet the traditional Lee-Carter model struggles with non-linear age and cohort patterns, coherent multi-population forecasting, and quantifying prediction uncertainties. Recent advances in deep learning provide a range of tools that can address these limitations, but actuarial surveys have not kept pace. This paper provides the first concise view of deep learning in mortality forecasting. We cover six deep network architectures, namely Recurrent Neural Networks, Convolutional Neural Networks, Transformers, Autoencoders, Locally Connected Networks, and Multi-Task Feed-Forward Networks. We discuss how these architectures tackle cohort effects, population coherence, interpretability, and uncertainty in mortality forecasting. Evidence from the literature shows that carefully calibrated deep learning models can consistently outperform the Lee-Carter baselines; however, no single architecture resolves every challenge, and open issues remain with data scarcity, interpretability, uncertainty quantification, and keeping pace with the advances of deep learning. This review is also intended to provide actuaries with a practical roadmap for adopting deep learning models in mortality forecasting.
Non-ventilator hospital-acquired pneumonia (NV-HAP) is common and deadly. Guidelines recommend improving oral care and mobility performance to prevent NV-HAP but data on their impact are limited. We therefore evaluated associations between oral care and mobility performance with NV-HAP and mortality rates in a large hospital network.
Design:
Retrospective cohort study
Setting:
144 acute care hospitals
Patients:
Adults hospitalized for ≥4 days between May 2021 and July 2023
Methods:
We extracted daily data on oral care performance (yes, no) and patient mobility (bed-bound, upright, walking) and used time-varying Cox proportional hazards models to evaluate associations between oral care and mobility performance with NV-HAP and in-hospital mortality risk, adjusting for patients’ demographics, comorbidities, hospital service, daily vital signs, and daily laboratory measures.
Results:
Among 1,744,811 hospitalizations (9.6 million hospital-days), median patient age was 68 (IQR 55–78) and 50.6% were female. Persistent oral care for ≥3 days was associated with 16% less NV-HAP (hazard ratio (HR) 0.84; 95% CI: 0.82–0.86) and 6% lower mortality (HR 0.94; 95% CI: 0.92–0.96), with stronger effects in the ICU than outside the ICU. Persistent walking for ≥3 days was associated with 18% less NV-HAP (HR 0.82; 95% CI: 0.79–0.85) and 80% lower hospital-mortality (HR 0.20; 95% CI: 0.19–0.21), with stronger effects outside the ICU than in the ICU.
Conclusions:
In a large hospital network, both oral care and mobility were associated with lower risk of NV-HAP and hospital mortality, with differential effects inside and outside of the ICU. Prospective trials are needed to confirm these potential benefits.
This study aimed to explore clinical characteristics and treatment efficacy in patients with posterior canal benign paroxysmal positional vertigo and different sleep qualities.
Methods
Patients with posterior canal benign paroxysmal positional vertigo were divided into high and low sleep quality groups based on Pittsburgh Sleep Quality Index scores.
Results
No significant baseline differences existed between low (n = 53) and high (n = 39) sleep quality groups. However, the proportion of cupulolithiasis was higher in the low sleep quality group (60.38 per cent vs. 35.90 per cent; p < 0.05). Additionally, the low sleep quality group had a longer median duration of upbeat nystagmus during the Dix-Hallpike test (63.50 seconds vs. 26.80 seconds; p < 0.05) and a lower cured rate in initial repositioning (9.43 per cent vs. 56.41 per cent) compared to high sleep quality group. Repositioning therapy significantly improved depressive and anxiety symptoms in all patients with posterior canal benign paroxysmal positional vertigo, with a more pronounced improvement in depressive symptoms in the low sleep quality group.
Conclusion
Poor sleep quality is associated with higher cupulolithiasis prevalence and treatment resistance, with residual symptoms mainly affecting social functioning.
To fully understand resilience and to inform resilience-promoting interventions, it is important to explore how resilience develops and the factors that influence it. Using a multidimensional approach that considers both well-being resilience (higher than expected wellbeing after adversity) and depression resilience (lower than expected depression after adversity), this study examined resilience trajectories among Chinese 0adolescents and the associations of gratitude and perceived stress with resilience trajectories. Data from a four-wave longitudinal study were analyzed from 563 Chinese adolescents (mean age at Time 1 = 12.83 years, 51.87% boys). Parallel-process latent class growth modeling identified four distinct trajectories of resilience development: flourishing resilience (increasing resilience; 21.67%), increasing wellbeing resilience but decreasing depression resilience (28.24%), declining resilience (29.48%), and increasing depression resilience but decreasing wellbeing resilience (20.61%). Gratitude was associated with greater odds of being in the flourishing resilience group. Furthermore, perceived stress was associated with lower odds of being in the flourishing resilience group and higher odds of being in the declining resilience group. The findings suggest that resilience is a dynamic and multidimensional construct with highly heterogeneous developmental trajectories. Gratitude and perceived stress may be effective targets for interventions to enhance adolescent resilience.
This paper introduces a high single-pulse energy, narrow-linewidth mid-infrared self-optical parametric oscillator (mid-IR SOPO) with a cavity length of 120 mm and a Nd:MgO:PPLN crystal. To achieve high single-pulse energy and high peak power in mid-IR light sources, a LiNbO3 electro-optic Q-switch (EOQ) is introduced for the first time in a mid-IR SOPO. A narrow-linewidth EOQ-SOPO rate equation is formulated, and experiments are conducted using a single Fabry–Pérot etalon. At a 500 μs pump pulse width, a 4.71 mJ single-pulse idler light at 3838.2 nm is achieved, with a linewidth of 0.412 nm, single-pulse width of 4.78 ns and peak power of 985 kW. At 200 μs, the idler light at 3845.2 nm exhibits a minimum linewidth of 0.212 nm.