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This appendix develops the mathematical machinery of screening and Green’s functions needed for electrostatics and magnetostatics. Starting from the screened Coulomb potential, it computes its Fourier transform, takes the unscreened limit, and thereby derives the standard free-space Green’s function and its representation as a Fourier integral. The appendix then examines convergence issues and the definition of the delta function, showing how to regularize Fourier representations with exponential factors. Translational invariance is used to motivate partial Fourier transforms when only some coordinates are symmetric, reducing Poisson’s equation to an ordinary differential equation in the remaining variable. These methods are applied to construct the Green’s function for half-space bounded by a grounded conducting plane, from which one obtains the induced surface charge, the potential, and the force on a point charge near the conductor.
Screening decisions—choosing a costly action that reveals information about an unknown quality—can be crucial in various situations, such as hiring workers or designing policies. Choosing whether to screen can be difficult because it requires recognizing and trading off the benefits of information with the costs of getting it. We investigate whether people recognize when the benefits of screening dominate its costs and what causes them to choose otherwise. Our online experiment simulates a hiring scenario with an initial trial task. Participants can first reveal candidates’ quality at a small cost and then choose which candidate to hire. Most participants choose the dominated task that does not reveal the candidates’ quality, and this mistake persists even with experience and feedback. We show that this insufficient screening is driven by failures to anticipate inference and plan the full strategy.
Malnutrition is prevalent among community-dwelling older adults (OAs), particularly those using healthcare services, and the number of affected individuals is expected to increase with ongoing population ageing. Early and systematic identification of OAs at risk of malnutrition is recommended as a key first step in prevention and management. However, a significant gap exists between recommended nutritional practices and their implementation in routine care.
Aim:
This article aims to describe the development process of a complex intervention for early detection of malnutrition risk among community-dwelling OAs (≥65 years) in a Danish homecare setting.
Methods:
The development process was overall framed by the Medical Research Council (MRC) framework and guided by the IdentifyiNg and assessing different approaches to DEveloping compleX intervention framework. Eleven iterative actions were undertaken, including systematic consideration of contextual conditions, key uncertainties, stakeholder engagement, review of published evidence, and development of the intervention’s programme theory.
Findings:
The development process resulted in an intervention comprising four activities:
A. An interprofessional workgroup.
B. Learning activities for homecare staff.
C. Conversations with OAs and their informal caregivers.
D. Systematic and continuous screening followed by an action guide.
Activities C and D covered the screening procedure, and activities A and B the implementation strategy for this procedure.
The developed intervention was designed to support nutritional self-care among OAs and facilitate early identification of malnutrition risk in homecare settings. Subsequent feasibility testing of the intervention was conducted between August 2024 and December 2025. It is reported elsewhere.
Despite more than 90% of cases arising in the community, malnutrition is under-recognised in UK primary care. Current screening tools such as the Malnutrition Universal Screening Tool identify malnutrition once it is already established and are inconsistently implemented. As a result, malnutrition is detected late, after functional decline and avoidable harm have already occurred. Our narrative review highlights that existing malnutrition prediction tools were largely developed in hospital populations, show variable accuracy, and have not been validated for community use. Emerging machine-learning models demonstrate feasibility but are similarly limited. We outline the urgent need for automated, data-driven prediction models drawing on routinely collected primary-care data – such as weight trajectories, comorbidities, medications, and biochemistry markers – to identify individuals at future risk of malnutrition. A proactive, electronic health record-embedded approach could shift practice from reactive diagnosis to early intervention, with the potential to improve outcomes and reduce inequalities.
Workshops with Primary Health Care (PHC) practitioners aimed to (1) identify and prioritise key features to include in a child health behaviour screening tool, and (2) understand prioritised supports needed to implement screening in PHC.
Background:
PHC is a key setting for monitoring and promoting child health behaviours including dietary intake, physical activity, sedentary behaviour and sleep. Screening tools to monitor children’s health behaviours in PHC are needed.
Methods:
South Australian practitioners were recruited to participate in virtual workshops. The four-step Nominal Group Technique method was followed including individual brainstorming, round robin, group discussion, and voting. Collaborative recording of participant ideas and discussions, including workshop transcripts and live notes, enabled collection of qualitative quotes. Quantitative voting data were analysed to determine the relative importance of ideas.
Findings:
Nine workshops were facilitated with two practitioner groups: 1) General Practice and Allied Health (n = 21) and 2) Child and Family Health (n = 8) . Ten practitioner-generated features of a screening tool and 10 supports to facilitate implementation of a screening tool were identified. Top ranked features included ‘Clear results and next steps’ and ‘Question design and response format’. ‘Practitioner training’ and ‘Practitioner resources’ were key supports for implementation. Consistent findings across practitioner groups demonstrate tool features and implementation strategies that are likely to be widely accepted. Unique findings demonstrate context specific tool features and implementation strategies. This study provides important insight to guide the development of an acceptable child health behaviour screening tool to facilitate a supportive prevention environment in PHC.
This chapter reviews the most common clinical presentations of abusive head trauma (AHT) and associated indications for imaging. The presentation of AHT is highly variable, and may include a history of accidental trauma, acute neurologic or constitutional symptoms, sentinel non-central nervous system (CNS) injuries, macrocephaly or chronic neurologic dysfunction or asymptomatic high-risk contacts of a child abuse victim. The indications for screening neuroimaging depend on clinical presentation and level of concern. Some patients warrant evaluation based on acute neurological presentation. In others the clinical history, physical examination, laboratory and non-CNS radiologic findings indicate the need for screening. This chapter reviews the available evidence and outlines an approach to screening neuroimaging followed by diagnostic evaluation. Cranial ultrasound, CT or MRI are used depending on presentation and clinical setting. If screening neuroimaging is suspicious for AHT then full diagnostic neuroimaging evaluation with brain and often spine MRI is essential. Strengths and limitations of the modalities used are discussed.
Human papillomavirus (HPV), particularly high-risk types such as HPV 16 and 18, is a major cause of cervical cancer and other cancers. Despite the United Kingdom’s (UK’s) commitment to cervical cancer elimination by 2040, participation in HPV screening is declining, disproportionately affecting underserved groups, including those experiencing poverty, people from minoritized racial, ethnic, gender, or sexual identity groups, and people living with HIV.
Methods
We conducted a mixed-methods study to explore awareness, barriers, and facilitators to HPV self-sampling from clinician and public perspectives. A multi-stakeholder survey (n = 105) and two online focus groups with clinicians (n = 4) and members of the public (n = 5) were undertaken.
Results
Survey respondents identified accuracy, cost-free availability, ease of use, accessibility, clear instructions, and adequate follow-up as critical test features. Participants emphasized that disability, cultural context, language, and socioeconomic status strongly influence barriers and facilitators to uptake. Focus groups provided contextual depth, illustrating how privacy, logistical and emotional impacts, and supportive follow-up pathways shaped acceptability and trust. Clinicians highlighted the need for integration into healthcare infrastructure to maintain trust and ensure support. Public participants recommended community-driven engagement, including multilingual instructions and tailored communication to encourage adoption among diverse groups. Concerns were raised about unintended consequences, such as anxiety following asymptomatic HPV diagnoses and challenges in managing clinical pathways after positive results. Suggestions included leveraging community organizations to reduce hesitancy.
Conclusions
Findings highlight policy and implementation considerations for embedding HPV self-sampling within care pathways to improve uptake and reduce inequalities.
In low-prevalence settings, the epidemiological yield of screening strategies for controlling vancomycin-resistant enterococci (VRE) outbreaks has not been fully established. We retrospectively analysed a prolonged VRE outbreak at a 536-bed tertiary-care hospital in Japan from 2010 to 2021 to evaluate sequential screening strategies across epidemic phases and to identify risk factors for VRE acquisition. Hospital-wide, admission-based, antimicrobial exposure-based, passive, and haemodialysis-targeted screening strategies were implemented over time. Screening yields were compared longitudinally, and a retrospective case–control study was performed using data from the initial hospital-wide screening phase. Molecular epidemiology was assessed by pulsed-field gel electrophoresis (PFGE). In total, 169 VRE-positive patients were identified, including seven infections and 162 asymptomatic carriers. Hospital-wide screening in the early epidemic phase showed the highest positivity rate (0.91%), whereas targeted strategies consistently yielded lower rates (0.09–0.34%). Haemodialysis, specific oral care practices, and prior exposure to carbapenems, glycopeptides, and piperacillin/tazobactam were independently associated with VRE acquisition. PFGE revealed substantial genetic diversity, suggesting sustained nosocomial transmission with repeated introductions. Early broad-based screening may be epidemiologically efficient in the initial phase of VRE outbreaks in low-prevalence settings, followed by adaptive refinement for long-term control.
This study examined the incidence, type of electrocardiogram abnormalities, and associated risk factors in healthy paediatric athletes. A single-centre retrospective cohort study was conducted on a local male youth competitive soccer programme, ages 11–18. The primary outcome was the incidence of electrocardiogram abnormalities. The secondary outcomes were recurrence and the type of electrocardiogram abnormalities. Covariables were age, race, family history, and current medications. Statistical analysis program was used for analysis. There was a total of 368 electrocardiograms reviewed from 2021–2024, of which 68 (18.5%) had at least one abnormality. 182 unique athletes were screened. A higher proportion of multi-racial and African American athletes had electrocardiogram abnormalities (p-value 0.02). In our sample of healthy paediatric athletes, electrocardiogram abnormality incidence was similar to that noted in other studies. There were no significant cardiac findings noted after further evaluation on any of the athletes with abnormal electrocardiogram findings. Our data support that universal electrocardiogram screening of healthy paediatric athletes is not beneficial.
People with severe mental illness (SMI) die 10–20 years earlier than the general population, largely due to non-communicable diseases (NCDs) such as hypertension and diabetes and risk factors such as hypercholesterolaemia. This cross-sectional study gathered data from people with SMI from three national mental health institutions in South Asia. Data was collected based on the WHO Stepwise approach to NCD risk factor surveillance and the prevalence of screening, diagnosis and treatment for diabetes, hypertension, and hypercholesterolaemia was assessed. Logistic regression models assessed the associations of sociodemographic characteristics with NCD screening. Three thousand nine hundred and eighty nine participants were recruited. Screening prevalence varied by country and disease, with hypertension being the most commonly screened NCD (Bangladesh = 52.5% [50.0–55.1], India = 43.1% [40.3–45.9], Pakistan = 60.9% [58.2–63.5]), and cholesterol was the least common (Bangladesh = 4.1% [3.2–5.2], India = 14.8% [12.9–17.0], Pakistan = 9.6% [8.1–11.3]). Characteristics such as BMI, age and education level were positively associated with screening, and females were more likely to be screened than males. There are low levels of screening for NCDs among individuals with SMI accessing tertiary institutions in South Asia, with significant sociodemographic disparities. Standardised screening protocols tailored to South Asian populations could mitigate the increased risk of NCDs in this population.
Identifying studies for inclusion in realist syntheses using title and abstract screening is challenging given the need to unearth explanatory insights to build context–mechanism–outcome configurations. Such insights may only be uncovered through full-text paper reading. To address this issue, a novel approach for identifying studies has been developed called Reverse Chronology Quota Record Screening (RCQRS). Results of database searches are screened in reverse chronology, and in stages, to fill quotas matching the requirements of the review. RCQRS may be beneficial in any of the following circumstances: (a) the timeframe to complete the synthesis is short; (b) the scope of inquiry is not fully defined, (c) the availability of suitable literature is beyond the screening capacity of the reviewers; or (d) the availability of literature is sparse and reviewers seek to extrapolate insights from other areas. In contrast to RCQRS, exhaustive title and abstract screening (i.e., screening entire database results) may hamper study selection due to being overwhelming in volume and time-intensive, resulting in a causally thin cohort of papers for analysis. RCQRS used in stages, and in conjunction with other search strategies (e.g., hand searching, backward citation tracking, and expert solicitation) can support creative, robust analytical insights with causally rich extrapolations. Using the Horizon-EU funded SERENITY study on deprescribing in palliative care as a case example, the benefits and limitations of RCQRS are explored. Finally, a checklist template is offered for teams who wish to reflect on, and transparently report, the use of RCQRS in their realist synthesis.
Developing and sustaining ICU follow-up clinics to address PICS in survivors of critical illness and their loved ones pose significant challenges, and clinics need to be tailored to the physical, personnel, and financial resources available at a given institution. Although no standard recipe guarantees a successful ICU aftercare program, emerging clinics need to address a common set of hurdles, including securing an adequate space; assembling an invested, multidisciplinary staff; and procuring the necessary equipment, technological, and financial support to be successful. Although certain risk factors for the development of PICS are defined, there remains no consensus on screening tools to determine which patients would derive most benefit, and recruitment strategies for clinic participants remain institution-dependent. Although there is expert consensus on some screening tools to detect PICS, significant additional investigation is needed to refine these recommendations. Benefits derived by patients and their families, feedback mechanisms to improve in-ICU care at the organizational and clinician level, and the general lack of awareness of PICS among the critical care, medical, and lay communities demand that motivated clinicians with a commitment to interprofessional teamwork, defined operational processes, and creative problem-solving skills continue their efforts to further refine the promise of ICU follow-up clinics.
The 7-item Dysmorphic Concern Questionnaire (DCQ; Oosthuizen et al., 1998) is designed to screen for, and quantify the degree of, dysmorphic concern in an individual. Dysmorphic concern describes an individual’s preoccupation with certain features of their physical appearance (e.g., hair, skin, nose, genitalia). Excessive levels may cause clinically significant distress and functional impairment, leaning to a diagnosis of body dysmorphic disorder (BDD). However, the DCQ is not a diagnostic tool for BDD; rather, it is a dimensional measure of dysmorphic concern and a screening tool with validated cut-offs for both clinically relevant appearance concern and BDD. The DCQ can be administered online or in-person to adolescents and adults and is free to use. This chapter first discusses the development of the DCQ and then provides evidence of its psychometrics. More specifically, the DCQ has a unidimensional factor structure within exploratory and confirmatory factor analyses. Internal consistency reliability, convergent validity, discriminant validity, and structural validity support the use of the DCQ. Next, this chapter provides the DCQ items in their entirety, instructions for administration and scoring, and the item response scale. Links to available translations are included. Logistics of use, such as permissions, copyright, and contact information, are available for readers.
The prevalence, morbidity and mortality of youth substance misuse should mandate public health prioritisation worldwide. Roots in multiple adversity and child mental health problems point to substance misuse as an indicator of the underlying vulnerability of populations, in which case young people in the developed world are not doing so well. Child services should screen and assess all youth for substance use. Investment in the development of new treatments has shown that interventions can be moderately effective, likely to share core characteristics, and given will, training and resources are readily deployable. However, all studies show a substantial subset had not improved following intervention, so that enormous scientific and cultural challenges persist.
Social disadvantage can result in healthcare gaps and primary care may be a suitable healthcare context to identify unmet social needs. A variety of screening tools exists but none of them is consolidated in clinical practice. After reviewing the available instruments, we conducted a rigorous translation and trans-cultural adaptation into Italian language of the EveryONE social need screening tool questionnaire of the American Academy of Family Physicians. The translated questionnaire was piloted among 45 patients consecutively recruited in two general practices in the northern Italian city of Modena in 2023 and obtained excellent scores in comprehension and acceptability. The cross-cultural adaptation presented in this study is a first step towards a complete validation. A full validation study is needed to safely adopt EveryONE in routine general practice and to evaluate its effects on health provision.
Introduction: Hundreds of millions of patients worldwide are infected with Healthcare-Associated Infections (HAIs) each year causing deaths and significant financial losses to health systems. HAIs incidence in Indonesia (2021) reached 15.74%, far above in developed countries (4.8-15.5%). At Premier Bintaro Hospital (RSPB), the number of High Care Unit (HCU) patients at risk of HAIs reached 51% in the January - June 2023 period. The aim of this research is to reduce the risk of HAIs in HCU patients at RSPB. Methods: The HAIs risk identification was conducted on all HCU patients when first admitted using the SIRS (Systemic Inflammatory Response Syndrome) and REDS (Risk Emergency Department Scoring) criteria. Based on the screening results, interventions were applied through environmental modifications, implementation of HAIs care bundle, and nurse allocation based on colour codes: At risk of infection as RED, and no risk of infection as GREEN. The risk monitoring was conducted using HAIs scoring. Results: The research was conducted in the January - June 2023 period on 206 patients. It was found that 51% of the patients were at risk of HAIs. After interventions, the number reduced to 39%. In addition, there were zero incidents of HAIs during that period. Conclusions: To control the risk of HAIs in HCUs, the implementation of risk screening & scoring and interventions such as environmental modifications, nurse allocation, and HAIs care bundle, have shown to be effective strategies. This is evident from the decrease in the number of patients at risk of HAIs.
Recommendations for hospital is to continue implementing risk control of HAIs by regularly assessing the risk, applying interventions, and consistently monitoring the risk as efforts in continuously reducing the HAIs risks. For future research, it is recommended to expand the sample of patients and extend the period to implement risk control of HAIs even further.
Acknowledgements: We are very grateful to all members of CCU team at Premier Bintaro Hospital for their contribution in implementing the methods and strategies of HAIs risk control in this study.
What are the consequences of selective emigration from a closed regime? To answer this question, I focus on socialist East Germany and leverage an emigration reform in 1983 that led to the departure of about 65,200 citizens. Analyzing panel data on criminal activity in a difference-in-differences framework, I demonstrate that emigration can be a double-edged sword in contexts where it is restricted. Emigration after the reform had benefits in the short run and came with an initial decline in crime. However, it created new challenges for the regime as time passed. Although the number of ordinary crimes remained lower, border-related political crimes rose sharply in later years. Analysis of emigration-related petitioning links this result to a rise in demand for emigration after the initial emigration wave. These findings highlight the complexities of managing migration flows in autocracies and reveal a key repercussion of using emigration as a safety valve.
Having relevant indicator(s) of students’ school adjustment is the basis for making educational decisions with regard to an enormous scope of topics that refer to either individual students, a specific class, or even the entire school level. Thus, a major cornerstone in the effort to promote students’ school adjustment is the ability to correctly and accurately measure it. The problem of defining a given student’s state is a multi-aspect and multi-level challenge that is shaped by the local authorities’ guidelines, cultural norms, economic circumstances, and the student’s intellectual qualifications and personal characteristics. The existing literature suggests a rich list of measurements of the student’s feelings and the teacher’s evaluation of the student’s academic achievements, but parental and peer reflections are relatively underrepresented. This chapter advocates the priority of students’ subjective evaluations. Such measurements appear under various titles: students’ belonging, engagement, attitude, feelings, satisfaction, well-being, liking, burnout, sentiment, and more. In order to conduct routine evaluations of students’ school adjustment there is a need for a short and easily administered scale. For this end, the School Adjustment Questionnaire (SAQ) is presented as a possible example.
We analysed the early results of a screening and management protocol of imported female genital schistosomiasis (FGS) among migrant women from endemic countries. In total we screened 136 women, from which 39 had suspicion of FGS (serology-positive test and clinical signs and symptoms compatible). Median age was of 42.7 years [interquartile range (IQR 35–45)], median time living in the Europe (EU) was of 14 years (IQR 10–19) and all of them were coming from a West African country, mainly Senegal (17 out of 39; 43.6%). All of them had 1 or more clinical genitourinary findings [median 5 (IQR 2–6)], being the most prevalent pelvic pain, vaginal discharge and menstrual disorders. According to the protocol, colposcopy and cytology examination was performed in 11 participants, from whom 7 had findings compatible with FGS and 5 had low-grade cervical dysplasia with human papillomavirus (HPV)-negative results. After specific treatment with praziquantel (PZQ), we observed a high rate of resolution of clinical signs and symptoms, serology clearance at the 12th month of follow-up. Colposcopy lesions of 3 women assessed at the end of follow-up were fully resolved. Our findings and previous research support the implementation of management protocols of FGS in non-endemic countries, in spite of the knowledge gaps that still remain. Clinical trials need further assessment to determine the efficacy of PZQ, new diagnostic tools and the interaction between FGS, HPV and cervical cancer.
Peripartum depression (PPD) is a prevalent mental health disorder in the peripartum period. However, a recent systematic review of clinical guidelines relating to PPD has revealed a significant inconsistency in recommendations.
Aims
This study aimed to collect up-to-date evidence on the effectiveness of interventions and provide recommendations for prevention, screening and treating PPD.
Method
A series of umbrella reviews on the effectiveness of PPD prevention, screening and treatment interventions was conducted. A search was performed in five databases from 2010 until 2023. The guidelines were developed according to the GRADE framework and AGREE II Checklist recommendations. Public stakeholder review was included.
Results
One hundred and forty-five systematic reviews were included in the final analysis and used to form the guidelines. Forty-four recommendations were developed, including recommendations for prevention, screening and treatment. Psychological and psychosocial interventions are strongly recommended for preventing PPD in women with no symptoms and women at risk. Screening programmes for depression are strongly recommended during pregnancy and postpartum. Cognitive–behavioural therapy is strongly recommended for PPD treatment for mild to severe depression. Antidepressant medication is strongly recommended for treating severe depression in pregnancy. Electroconvulsive therapy is strongly recommended for therapy-resistant and life-threatening severe depression during pregnancy. Other recommendations are offered to healthcare professionals, stakeholders and researchers in managing PPD in different contexts.
Conclusion
Treatment recommendations should be implemented after carefully considering clinical severity, previous history, risk–benefit for mother and foetus/infant and women’s values and preferences. Implementation of evidence-based clinical practice guidelines within country-specific contexts should be facilitated.