Publications by authors named "Stuart William Jarvis"
Article Synopsis
- - The study reviews the outcomes of social transitioning for children and adolescents experiencing gender dysphoria, highlighting that it's increasingly common for these youths to transition before professional assessment.
- - Eleven studies were analyzed, mostly of low quality, focusing on mental health and gender identity outcomes, showing generally no significant differences in mental health for children who socially transitioned, while adolescent results were mixed.
- - The authors emphasize a lack of robust research, particularly longitudinal studies, making it challenging to determine the effects of social transition on mental health and gender-related outcomes for children and adolescents.
Article Synopsis
- National and international guidelines emphasize that psychosocial support is vital for children and adolescents with gender dysphoria, but specific interventions aren't defined.
- A systematic review identified ten studies on the outcomes of psychosocial support for youth experiencing gender dysphoria, revealing that many studies were of low quality and mostly showed either benefits or no impact on mental health.
- The study highlights a need for better-defined interventions and core outcomes to improve the quality of research and evidence on the effectiveness of psychosocial support in this area.
Objective: To assess trends in place of death for children with a life-limiting condition and the factors associated with death at home or hospice rather than hospital.
Design: Observational cohort study using linked routinely collected data.
Setting: England.
Introduction: Neurological conditions are a major and increasing cause of hospitalisation among children and young people, but little is known about the impact of neurological conditions on hospital services in England, nor the factors that influence length of stay and bed days per year.
Objectives: To quantify the hospital usage in children and young people related to neurological conditions, trends over time and variation by ethnicity and deprivation status.
Methods: An ICD10 coding framework identified a cohort of individuals aged 0-19 years with neurological conditions from linked routinely collected healthcare data from England (The Hospital Episode Statistics Admitted Patient Care dataset), from 1 April 2003 to 31 March 2015.