keyword
https://read.qxmd.com/read/38589261/caregiving-experiences-of-family-caregivers-of-patients-with-schizophrenia-in-a-community-a-qualitative-study-in-beijing
#21
JOURNAL ARTICLE
Zhaolu Pan, Ting Li, Guanghui Jin, Xiaoqin Lu
OBJECTIVES: This study aims to understand the caregiving experiences of family caregivers of people with schizophrenia in a community. DESIGN: A qualitative study based on phenomenological analysis was conducted through in-depth interviews. SETTING: This study was carried out from May to June 2023 in two community health service centres in urban Beijing, China. PARTICIPANTS: We selected 16 family caregivers for interviews using purposive sampling method...
April 8, 2024: BMJ Open
https://read.qxmd.com/read/38589039/parental-stress-depression-anxiety-and-participation-in-care-in-neonatal-intensive-care-unit-a-cross-sectional-study-in-italy-comparing-mothers-versus-fathers
#22
JOURNAL ARTICLE
Jenny Bua, Paolo Dalena, Ilaria Mariani, Martina Girardelli, Maddalena Ermacora, Ursula Manzon, Sabrina Plet, Laura Travan, Marzia Lazzerini
BACKGROUND: This study aimed at documenting the levels of stress, depression, anxiety and participation in care among mothers versus fathers of newborns hospitalised in a third-level neonatal intensive care unit (NICU) in Northern Italy. METHODS: Parental stress, depression and anxiety were assessed by the Parental Stressor Scale in NICU (PSS:NICU), the Edinburgh Postnatal Depression Scale (EPDS) and the State-Trait Anxiety Inventory (STAI). Participation in care was evaluated with the Index of Parental Participation...
April 8, 2024: BMJ Paediatrics Open
https://read.qxmd.com/read/38587469/end-of-life-care-at-home-dignity-of-family-caregivers
#23
JOURNAL ARTICLE
Katrine Staats, Kristin Jeppestøl, Bente Egge Søvde, Bodil Aarmo Brenne, Anett Skorpen Tarberg
BACKGROUND: Healthcare services are increasingly being shifted to home settings for patients nearing end-of-life. Consequently, the burden on family caregivers is significant. Their vulnerable situation remains poorly understood and there is little information available regarding their experiences of dignity. AIM: This study seeks to understand the experiences of family caregivers related to dignity and loss of dignity, aiming to provide a deeper insight into their situation when caring for a home-dwelling family member nearing end-of-life...
April 8, 2024: Nursing Ethics
https://read.qxmd.com/read/38586593/preliminary-development-of-a-measure-of-parental-behavioral-responses-to-everyday-pains-in-young-children-the-prep
#24
JOURNAL ARTICLE
Perri R Tutelman, Christine T Chambers, Jennifer A Parker, Samantha J Eisen, Melanie Noel
INTRODUCTION: Everyday pains are experienced frequently by young children. Parent responses shape how young children learn about and experience pain. However, research on everyday pains in toddlers and preschoolers is scarce, and no self-report measures of parent responses to their child's pain exist for this age group. OBJECTIVES: The objective of this study was to develop a preliminary self-report measure of parent behavioral responses to everyday pains in the toddler and preschool years (the PREP) and examine its relationship with child age, sex, and parent and child distress...
June 2024: Pain Reports
https://read.qxmd.com/read/38578477/the-performance-of-the-eq-hwb-s-as-a-measure-of-quality-of-life-of-caregivers-in-families-that-have-experienced-adverse-events
#25
JOURNAL ARTICLE
Cate Bailey, Kim Dalziel, Leanne Constable, Nancy J Devlin, Harriet Hiscock, Helen Skouteris, Tessa Peasgood
PURPOSE: The recently developed EQ Health and Wellbeing Instrument (EQ-HWB) is a broad, generic measure of quality-of-life designed to be suitable for caregivers. The aim of this study was to investigate performance and validity of the 9-item version (EQ-HWB-S) for caregivers where families had experienced adverse-life-events. METHODS: Using survey data from caregivers of children aged 0-8 years attending a community-health centre in 2021-2022, the general performance, feasibility, convergent and known-group validity, responsiveness-to-change, and test-retest reliability of the EQ-HWB-S was assessed...
April 5, 2024: European Journal of Health Economics: HEPAC: Health Economics in Prevention and Care
https://read.qxmd.com/read/38576586/effects-of-family-dignity-interventions-combined-with-standard-palliative-care-on-family-adaptability-cohesion-and-anticipatory-grief-in-adult-advanced-cancer-survivors-and-their-family-caregivers-a-randomized-controlled-trial
#26
JOURNAL ARTICLE
Nannan Wang, Kun Wang, Xinyu Lu, Shuyu Zhang, Xuhan Sun, Yuxi Zhang
BACKGROUND: Family involvement and comfort are equally important in palliative care. Dignity undertook a new meaning and novel challenges as a result of restrictions on visits and companionship during the pandemic. Family-centered family dignity interventions have been shown to be effective in increasing patients' sense of dignity, increasing levels of hope, and reducing psychological distress; however, the effectiveness in enhancing family adaptability and intimacy in the survivor-caregiver binary and reducing expected grief have been inconclusive...
April 15, 2024: Heliyon
https://read.qxmd.com/read/38561909/experiences-of-caring-for-women-with-cervical-cancer-a-qualitative-study-among-male-partners-in-dar-es-salaam-tanzania
#27
JOURNAL ARTICLE
Rashid A Gosse, Emanueli Amosi Msengi, Emmanuel Z Chona, Joel S Ambikile
BACKGROUND: More than three-fourths of cervical cancer cases occur in low- and middle-income countries, with sub-Saharan Africa (SSA) accounting for approximately 25% of global mortality. The significant rise in the prevalence of cervical cancer in SSA amplifies the burden on caregivers, contributing to elevated rates of mental illness, particularly among spouses who provide care. Men who assume the role of caregivers for their partners with cervical cancer encounter unique challenges and substantial adjustments across multiple facets of life, impacting both their own quality of life and that of their partners...
April 2024: Health Expectations: An International Journal of Public Participation in Health Care and Health Policy
https://read.qxmd.com/read/38559816/facilitating-childbirth-choice-for-positive-postnatal-mental-health-well-being-among-women-a-namibian-case-study
#28
JOURNAL ARTICLE
S Mlambo, H J Amukugo
Childbirth affects women in a myriad of ways including feelings of tiredness, being overwhelmed, stressed, and having baby blues, and if not attended to, this can lead to postpartum depression, which is a mental condition that can have disastrous effects. Childbirth can affect the mental and physical status of a woman and having supportive midwives who guide women by giving adequate information is an issue of critical concern for a positive birth experience. The World Health Organisation (WHO) has emphasised the need to facilitate childbirth choices for women as a means of having a safe and memorable experience as the experience in childbirth affects the psychological status of a woman...
2024: Frontiers in global women's health
https://read.qxmd.com/read/38558082/profiling-the-medical-functional-cognitive-and-psychosocial-care-needs-of-adults-assessed-for-home-care-in-ontario-canada-the-case-for-long-term-life-care-at-home
#29
JOURNAL ARTICLE
Margaret E Saari, Justine L Giosa, Paul Holyoke, George A Heckman, John P Hirdes
Calls to leverage routinely collected data to inform health system improvements have been made. Misalignment between home care services and client needs can result in poor client, caregiver, and system outcomes. To inform development of an integrated model of community-based home care, grounded in a holistic definition of health, comprehensive clinical profiles were created using Ontario, Canada home care assessment data. Retrospective, cross-sectional analyses of 2017-2018 Resident Assessment Instrument Home Care (RAI-HC) assessments (n = 162,523) were completed to group home care clients by service needs and generate comprehensive profiles of each group's dominant medical, functional, cognitive, and psychosocial care needs...
2024: PloS One
https://read.qxmd.com/read/38555100/systematic-review-of-clinical-manifestations-management-and-outcome-following-accidental-ingestion-of-liquid-mosquito-repellent-vaporiser-in-children
#30
JOURNAL ARTICLE
Babar Naeem, Junaid Saleem, Agha Syed Ali Haider Naqvi, Sidra Kausar, Aqdas Arshad, Kantash Kumar, Aashar Khalid, Parkash Kumar
BACKGROUND: Pyrethroid-based mosquito repellents are widely used to control mosquito-borne diseases. Liquid mosquito-repellent vaporisers are effective modes of pyrethroid delivery but can also pose significant health risks if ingested or used improperly. OBJECTIVE: This systematic review was performed to assess the demographic distribution, clinical presentation, management strategies and outcomes in children resulting from accidental ingestion of liquid mosquito repellent vaporiser...
March 30, 2024: BMJ Paediatrics Open
https://read.qxmd.com/read/38553902/impact-of-dental-sedation-treatment-on-the-oral-health-related-quality-of-life-of-distressed-young-children-a-secondary-analysis-of-a-randomized-clinical-trial
#31
JOURNAL ARTICLE
Patrícia Corrêa-Faria, Saul Martins Paiva, Luciane Rezende Costa
INTRODUCTION: Little is known regarding the impact of dental treatment under sedation on distressed young children's oral health-related quality of life (OHRQoL). AIM: To evaluate the impact of dental treatment under sedation on the OHRQoL of children and their families. METHODS: Caregivers of two-to-six-year-old children answered the Brazilian version of the Early Childhood Oral Health Impact Scale (B-ECOHIS): (1) before treatment under sedation (T0), (2) two weeks (T1) and (3) 3 months after the completion of treatment (T2)...
March 30, 2024: Special Care in Dentistry
https://read.qxmd.com/read/38551845/psychological-wellbeing-among-parents-of-a-child-living-with-a-serious-chronic-illness-a-cross-sectional-survey-study
#32
JOURNAL ARTICLE
Eden G Robertson, Lauren Kelada, Robert Ilin, Elizabeth Emma Palmer, Ann Bye, Adam Jaffe, Sean E Kennedy, Chee Y Ooi, Donna Drew, Claire E Wakefield
Parents of a child with a chronic illness can experience greater distress than the average population, yet little is understood about differences between illness groups. This cross-sectional survey study aimed to compare parents' psychological distress and perceived wellbeing across five chronic illnesses. Parents from one Australian pediatric hospital completed the Kessler Psychological Distress Scale and seven purpose-designed items about their wellbeing. Data from 106 parents (cancer = 48, cystic fibrosis [CF] = 27, kidney disease = 12, gastrointestinal condition/disorder = 9, developmental and epileptic encephalopathy [DEE] = 10) was analysed using bivariate Pearson's Correlation and linear mixed-effects models...
March 29, 2024: Journal of Child Health Care: for Professionals Working with Children in the Hospital and Community
https://read.qxmd.com/read/38551644/developing-and-implementing-a-web-based-branching-logic-survey-to-support-psychiatric-crisis-evaluations-of-individuals-with-developmental-disabilities-qualitative-study-and-evaluation-of-validity
#33
JOURNAL ARTICLE
Deborah A Bilder, Mariah Mthembu, Whitney Worsham, Patricia Aguayo, Jacob R Knight, Steven W Deng, Tejinder P Singh, John Davis
BACKGROUND: Individuals with developmental disabilities (DD) experience increased rates of emotional and behavioral crises that necessitate assessment and intervention. Psychiatric disorders can contribute to crises; however, screening measures developed for the general population are inadequate for those with DD. Medical conditions can exacerbate crises and merit evaluation. Screening tools using checklist formats, even when designed for DD, are too limited in depth and scope for crisis assessments...
March 29, 2024: JMIR Mental Health
https://read.qxmd.com/read/38549352/advancing-the-care-experience-for-patients-receiving-palliative-care-as-they-transition-from-hospital-to-home-acepath-codesigning-an-intervention-to-improve-patient-and-family-caregiver-experiences
#34
JOURNAL ARTICLE
Madeline McCoy, Taylor Shorting, Vinay Kumar Mysore, Edward Fitzgibbon, Jill Rice, Meghan Savigny, Marianne Weiss, Daniel Vincent, Meaghen Hagarty, Krystal Kehoe MacLeod, Natalie C Ernecoff, Rex Pattison, Mona Kornberg, Adrianna Bruni, Shirley H Bush, Kerry Kuluski, Valerie Fiset, Cecilia Li, Henrique A Parsons, Geneviève Lalumière, Tara Connolly, Colleen Webber, Sarina R Isenberg
BACKGROUND: Returning home from the hospital for palliative-focused care is a common transition, but the process can be emotionally distressing and logistically challenging for patients and caregivers. While interventions exist to aid in the transition, none have been developed in partnership with patients and caregivers. OBJECTIVE: To undergo the initial stages of codesign to create an intervention (Advancing the Care Experience for patients receiving Palliative care as they Transition from hospital to Home [ACEPATH]) to improve the experience of hospital-to-home transitions for adult patients receiving palliative care and their caregiver(s)...
April 2024: Health Expectations: An International Journal of Public Participation in Health Care and Health Policy
https://read.qxmd.com/read/38547962/a-digital-acceptance-and-commitment-therapy-and-education-intervention-targeting-stress-of-parents-and-caregivers-with-preterm-babies-in-the-neonatal-intensive-care-unit-a-randomised-controlled-cluster-trial-protocol
#35
JOURNAL ARTICLE
Kristin H Ginsberg, Jane Alsweiler, Jen Rogers, Alana Cavadino, Meihana Douglas, Anna Serlachius
BACKGROUND: Parents with babies in the neonatal intensive care unit (NICU) experience high levels of stress, anxiety, and depression. The NICU experience may also lead to impaired parenting and early childhood socio-emotional problems. Psychosocial interventions can reduce NICU parent distress. Yet many are time-intensive and costly to deliver. Acceptance and Commitment Therapy (ACT), an evidence-based psychological therapy, may address these needs. ACT has been shown to be effective in reducing distress of parents of children with chronic illnesses, particularly when combined with parent education...
March 27, 2024: Contemporary Clinical Trials
https://read.qxmd.com/read/38541368/autism-stigma-and-south-asian-immigrant-families-in-canada
#36
JOURNAL ARTICLE
Fariha Shafi, Amirtha Karunakaran, Farah Ahmad
Considerable empirical evidence suggests early recognition of autism and access to support result in long-term positive outcomes for children and youth on the spectrum and their families. However, children of racialized families are often diagnosed at later ages, are more likely to be misdiagnosed, and experience many barriers to service access. There is also a paucity of research exploring the experiences of parents from specific immigrant groups caring for their children on the spectrum in Canada, many of whom identify as members of racialized communities...
March 19, 2024: International Journal of Environmental Research and Public Health
https://read.qxmd.com/read/38537107/exploring-psychosocial-distress-in-caregivers-of-children-and-youth-with-special-health-care-needs
#37
JOURNAL ARTICLE
Régine Placide Reaves, Giovanna De Oliveira, Angel Johann Solorzano Martinez
PURPOSE: Caring for a child or youth with special health care needs (CYSHCN) can be overwhelming. Parents and caregivers may experience psychosocial distress, such as depression, frustration, and hopelessness. The purpose of the current study was to gain further insight into families' perspectives on the psychosocial impacts of caring for CYSHCN to identify gaps in health care systems and strengthen systems of support. METHOD: A qualitative descriptive design was used in 16 parents and caregivers...
April 1, 2024: Journal of Psychosocial Nursing and Mental Health Services
https://read.qxmd.com/read/38531386/complications-and-psychological-impact-of-pressure-ulcers-on-patients-and-caregivers
#38
JOURNAL ARTICLE
Li Qian, Song Yan, Shen Ting Ting, Zhang Meng Han, Tian Qi
Pressure ulcers are persistent skin lesions that have substantial detrimental effects on the physical well-being of patients. Moreover, their psychological ramifications for both patients and their caregivers are becoming more widely acknowledged. This research was conducted to examine the psychological ramifications of pressure ulcers and ascertain efficacious approaches to mitigate these effects and improve overall well-being. A cross-sectional study was conducted from March 2022 to December 2023 across tertiary care centres located in Beijing...
April 2024: International Wound Journal
https://read.qxmd.com/read/38530589/abbreviated-dialectical-behavior-therapy-virtual-skills-group-for-caregivers-of-adolescents-an-exploratory-study-of-service-user-and-clinical-outcomes
#39
JOURNAL ARTICLE
Megan Hare, Kristina Conroy, Christopher Georgiadis, Ashley M Shaw
Prior work emphasizes involving caregivers in youth mental health services. To support youth with emotion dysregulation, dialectical behavior therapy for adolescents (DBT-A) includes a multi-family skills group, wherein adolescents and caregivers learn skills together. However, limited work has examined the impact of caregiver involvement within DBT-A. The current study examines outcomes of two caregiver-only DBT-A skills groups adapted for abbreviated telehealth delivery. We report on caregivers' (N = 11, 100% mothers, 55% Hispanic) service user outcomes (e...
March 26, 2024: Child Psychiatry and Human Development
https://read.qxmd.com/read/38528601/profile-and-burden-of-the-family-caregiver-the-caring-experience-in-multiple-sclerosis-an-observational-study
#40
JOURNAL ARTICLE
Michela Ponzio, Andrea Tacchino, Anna Verri, Mario Alberto Battaglia, Giampaolo Brichetto, Jessica Podda
BACKGROUND: The broad implications of caring for a family member with a chronic medical condition, such as MS, can lead caregivers to experience a high burden of care. The aim of the study was to describe profile of MS caregivers and their burden and to explore potential factors influencing this burden. METHODS: 200 family caregivers of a person with MS completed survey questionnaires across a cross-sectional study. Many information were collected: caregiver socio-demographic and health-related data, caregiving activities, knowledge of MS, coping strategies, mood, social support received and care recipient information...
March 26, 2024: BMC Psychology
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