Purpose: Pediatric rheumatologic diseases (PRDs) are characterized by high rates of anxiety and depression known to impact health-related outcomes. We present guidance statements to assess and manage mental health concerns for youth with PRDs in pediatric rheumatology practice.
Methods: Development of the guidance statements was initiated in 2019 and concluded in November 2023. It included: 1) Formation of a taskforce (including pediatric rheumatologists, pediatric behavioral health providers, patients, and parents), led by two licensed pediatric psychologists and two board-certified pediatric rheumatologists, 2) Iterative drafting of statements and rating of evidence based on the Oxford Centre for Evidence-Based Medicine (OCEBM) levels of evidence, 3) An open comment period followed by revision of statements, 4) A Delphi Panel process to attain consensus on the statements, 5) Review by the ACR Committee on Quality of Care and refinement of statements to an identified list of those with strongest empiric evidence for endorsement by the ACR.
Results: The taskforce drafted 34 statements for addressing mental health concerns in pediatric rheumatology, including identification, management, and clinic environment/education considerations. After two rounds of Delphi panel voting by a random sample of 76 members of the Childhood Arthritis and Rheumatology Research Alliance, 31 statements attained at least 80% consensus. Eleven of those statements had high empirical support and endorsement and were thus selected as the final guidance statements, including recommendations for depression and anxiety screening in youth ages 12 years and older, management of identified symptoms and education of patients about mental health.
Conclusion: It is a goal that these recommendations be used to empower pediatric rheumatology teams to consider how they may better address mental health concerns in their setting, and help improve both mental health- and health-related outcomes for youth with rheumatologic diseases.
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http://dx.doi.org/10.1002/acr.25519 | DOI Listing |
Wellcome Open Res
February 2025
Department of International Public Health, Liverpool School of Tropical Medicine, Liverpool, England, UK.
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March 2025
Department for Gynecology, Campus Virchow-Klinikum, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Introduction: Homologous recombination deficiency (HRD) is a key biomarker in the management of high-grade serous ovarian cancer (HGSOC), guiding treatment decisions, particularly regarding the use of poly(ADP-ribose) polymerase inhibitors (PARPi). As multiple HRD assays are available, each with distinct methodologies and cutoff values, the interpretation and clinical application of HRD testing remain complex. This intergroup statement, endorsed by the German Ovarian Cancer Commission, NOGGO, AGO Austria, and AGO Swiss, aims to provide guidance on the indications, appropriate use, and limitations of HRD testing in ovarian cancer.
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March 2025
NHS Northern Gambling Service, Leeds & York Partnership NHS Foundation Trust, Leeds
Int J Radiat Oncol Biol Phys
March 2025
Department of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.
Introduction: Reirradiation (reRT) has become increasingly prevalent due to an aging population and advancements in cancer detection and treatment. However, the field is still lacking standardized dosimetric evaluation methods and reRT workflows, which leads to difficulty in correlating clinical outcomes with delivered dose. This study reports on the implementation and evolution of a standardized reRT workflow in the Department of Radiation Oncology at [redacted], describing insights gained from nearly 3000 external beam reirradiation courses delivered since 2017.
View Article and Find Full Text PDFBMC Res Notes
March 2025
Department of Medical Education, Medical Education Research Center, Fasa University of Medical Sciences, Fasa, Iran.
Objective: Patient education at the time of discharge using models which aim to improve self-care behaviors can significantly contribute to patients' adoption of a healthy lifestyle and treatment adherence. This is a randomized controlled clinical trial with no blinding in which we tested two groups of intervention control. 90 patients having undergone coronary angioplasty were allocated to an intervention (N = 45) and a control group randomly (N = 45).
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