Cargando…

SWK-07. Family mental health screening early after a diagnosis of pediatric brain tumor

INTRODUCTION: A new diagnosis of a brain tumor in a child has significant emotional consequences for every member of the family. Nevertheless, early phases of oncologic care rarely provide formal mental health screening. METHODS: We implemented a mental health screening protocol for families and pat...

Descripción completa

Detalles Bibliográficos
Autores principales:	Rodemann, Ashley, Hartmann, Mary, Limbrick, David, Abdelbaki, Mohamed, Cluster, Andrew
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2022
Materias:	Social Work/Patient Support/Palliative Care
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9165156/ http://dx.doi.org/10.1093/neuonc/noac079.679

Ejemplares similares

SWK-10. TELEHEALTH IN OUTPATIENT PEDIATRIC NEURO-ONCOLOGY CARE
por: Raber, Shannon, et al.
Publicado: (2020)

SWK-07. A MULTINATIONAL SURVEY OF PAEDIATRIC NEURO-ONCOLOGY SERVICES: A EUROPEAN RESEARCH NETWORK (ERN) PAEDCAN PROJECT
por: Cooper, Katherine, et al.
Publicado: (2020)

SWK-03. CAREGIVER EXPERIENCES FOR PEDIATRIC BRAIN TUMOR PATIENTS AND THEIR FAMILIES AT A DEDICATED MEDICAL SPECIALTY CAMP
por: Brownfield, Ryan, et al.
Publicado: (2020)

SWK-05. EDUCATIONAL APPROACH TO GRIEF MANAGEMENT
por: DeRosa, Veronica, et al.
Publicado: (2020)

SWK-02. WEAVING COMFORT AND SUPPORT FOR CHILDREN WITH BRAIN TUMORS AND THEIR FAMILIES IN AN OUTPATIENT CLINIC
por: Hawks, Ria, et al.
Publicado: (2020)

SWK-08. Implementing awareness practice in Neuro-Oncology
por: DeRosa, Veronica
Publicado: (2022)

SWK-03. Neuroimaging in CNS tumours: To GA , or not to GA, that is the question.
por: Ryles, Jade, et al.
Publicado: (2022)

SWK-12. PEDIATRIC NEURO-ONCOLOGY PARENT PERSPECTIVE ON ASPECTS OF SOCIAL AND EMOTIONAL SUPPORT FOR ONLINE APPLICATION
por: Koch, Kendra, et al.
Publicado: (2020)

SWK-10. Survivorship: Education, Clinical Guidelines, and Transition to Adult Care
por: Hemenway, Molly, et al.
Publicado: (2022)

SWK-02. Palliative sedation in pediatric patients suffering from brain tumors: choosing the best drugs to improve end of life
por: Podda, Marta, et al.
Publicado: (2022)

SWK-05. Clinical social work in pediatric neuro-oncology – A research project on the social dimension using social diagnostics
por: Krottendorfer, Kerstin, et al.
Publicado: (2022)

SWK-04. Investigation on Anxiety and Depression of Parents of Children with Central Nervous System Tumors
por: Yang, Huajun, et al.
Publicado: (2022)

SWK-06. Structured transition from pediatric neuro-oncology to adult survivorship follow-up care - Can we close the gap?
por: Krottendorfer, Kerstin, et al.
Publicado: (2022)

SWK-01. Partnership between caregivers, patients and healthcare professionals: promoting collaboration in a complex care pathway in pediatric neuro-oncology
por: Granero, Anita, et al.
Publicado: (2022)

SWK-04. A MOBILE AUGMENTED REALITY APP FOR SURGICAL PREPARATION FOR CHILDREN WITH BRAIN TUMORS
por: Granville, Sharon, et al.
Publicado: (2020)

SWK-08. DELAYED DIAGNOSIS OF CENTRAL NERVOUS SYSTEM (CNS) TUMORS IN CHILDREN: PERSPECTIVE FROM THE FRONTLINE
por: Jogendran, Manisha, et al.
Publicado: (2020)

SWK-06. ANSWERING 900 VOICES: A NATIONAL NONPROFIT ORGANIZATION RESPONDS TO A NATIONWIDE COMMUNITY HEALTH NEEDS ASSESSMENT THAT ELUCIDATED KEY CHALLENGES FACED BY PEDIATRIC BRAIN TUMOR FAMILIES
por: Riley, Kathy
Publicado: (2020)

SWK-11. ASSESSMENT OF THE INDIRECT COSTS ASSOCIATED WITH PROTON THERAPY TREATMENT FOR ALBERTA PATIENTS REFERRED OUT OF COUNTRY
por: Black, Karina, et al.
Publicado: (2020)

SWK-09. SELF-CARE OUTCOMES AND INTERVENTIONS FOR CHILDREN WHO HAVE HAD A BRAIN TUMOUR: EVIDENCE AND HYPOTHESES. WHAT SHOULD SELF-CARE INTERVENTIONS FOR CHILDREN WITH PAST OR PRESENT BRAIN TUMOUR BE?
por: Rowen, Elizabeth, et al.
Publicado: (2020)

IMPACT OF COVID-19 PANDEMIC ON DELAY OF CHILDHOOD CANCER DIAGNOSIS AND THE OUTCOMES IN A PEDIATRIC HEMATOLOGY/ONCOLOGY DEPARTMENT
por: CAKMAKCI, Selma, et al.
Publicado: (2022)

Development of a screening tool for the need of specialist palliative care in oncologic inpatients: study protocol for the ScreeningPALL Study
por: Müller, Evelyn, et al.
Publicado: (2022)

Understanding care when cure is not likely for young adults who face cancer: a realist analysis of data from patients, families and healthcare professionals
por: Kenten, Charlotte, et al.
Publicado: (2019)

Cultural adaptation of meaning-centered psychotherapy for latino families: a protocol
por: Torres Blasco, Normarie, et al.
Publicado: (2022)

Protocol for an integrative review: patient and families’ perspectives on telehealth in palliative care
por: Bauer, Eithne Hayes, et al.
Publicado: (2022)

Effects of the Namaste Care Family programme on quality of life of nursing home residents with advanced dementia and on family caregiving experiences: study protocol of a cluster-randomised controlled trial
por: Smaling, Hanneke J A, et al.
Publicado: (2018)

Financial interventions for family caregivers of individuals with chronic illness: a scoping review protocol
por: Thomas Hebdon, Megan C, et al.
Publicado: (2022)

Family physicians supporting patients with palliative care needs within the patient medical home in the community: an appreciative inquiry study
por: Tan, Amy, et al.
Publicado: (2021)

End-of-life care for people with severe mental illness: mixed methods systematic review and thematic synthesis of published case studies (the MENLOC study)
por: Coffey, Michael, et al.
Publicado: (2022)

Private or shared room? A nationwide questionnaire survey on bereaved family members’ perceptions of where patients spend their last days
por: Otani, Hiroyuki, et al.
Publicado: (2022)

Preferences about place of end-of-life care and death of patients with life-threatening illnesses and their families: a protocol for an umbrella review
por: Pinto, Sara, et al.
Publicado: (2023)

Care needs of dying patients and their family caregivers in hospice and palliative care in mainland China: a meta-synthesis of qualitative and quantitative studies
por: Zhu, Shuqin, et al.
Publicado: (2021)

Pandemic impact on patients with advanced non-COVID-19 illness and their family carers receiving specialised palliative home care: a qualitative study
por: Nyblom, Stina, et al.
Publicado: (2022)

Impact of patient-centred and family-centred care meetings on intensive care and resource utilisation in patients with terminal illness: a single-centre retrospective observational study in Taiwan
por: Hsu, Nin-Chieh, et al.
Publicado: (2019)

Nurse-led, screening-triggered, early specialised palliative care intervention programme for patients with advanced lung cancer: study protocol for a multicentre randomised controlled trial
por: Fujisawa, Daisuke, et al.
Publicado: (2020)

Challenges and facilitators of hospice decision-making: a retrospective review of family caregivers of home hospice patients in a rural US–Mexico border region—a qualitative study
por: Ko, Eunjeong, et al.
Publicado: (2020)

Timely short-term specialised palliative care service intervention for frail older people and their family carers in primary care: study protocol for a pilot randomised controlled trial
por: de Nooijer, Kim, et al.
Publicado: (2021)

Prevalence of Anxiety, Depression, and Perceived Stress Among Family Caregivers of Patients Diagnosed With Oral Cancer in a Tertiary Care Hospital in Central India: A Cross-Sectional Study
por: Belapurkar, Parth, et al.
Publicado: (2023)

Practitioners’ perceptions of acceptability of a question prompt list about palliative care for advance care planning with people living with dementia and their family caregivers: a mixed-methods evaluation study
por: van der Steen, Jenny T, et al.
Publicado: (2021)

The journey through care: study protocol for a longitudinal qualitative interview study to investigate the healthcare experiences and preferences of children and young people with life-limiting and life-threatening conditions and their families in the West Midlands, UK
por: Mitchell, Sarah, et al.
Publicado: (2018)

Comparison of attitudes towards five end-of-life care interventions (active pain control, withdrawal of futile life-sustaining treatment, passive euthanasia, active euthanasia and physician-assisted suicide): a multicentred cross-sectional survey of Korean patients with cancer, their family caregivers, physicians and the general Korean population
por: Yun, Young Ho, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_2kbkhs0j9bjmh5jshmg6hf1g7s