Journal of Child Health Care最新文献

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Exploring the implementation of child life services with facility dogs. 探索利用设施犬实施儿童生活服务。
IF 1.3 4区 医学
Journal of Child Health Care Pub Date : 2024-09-01 Epub Date: 2022-12-16 DOI: 10.1177/13674935221146382
Emily Goldstein, Sherwood Burns-Nader, Deborah Casper, Julie Parker
{"title":"Exploring the implementation of child life services with facility dogs.","authors":"Emily Goldstein, Sherwood Burns-Nader, Deborah Casper, Julie Parker","doi":"10.1177/13674935221146382","DOIUrl":"10.1177/13674935221146382","url":null,"abstract":"<p><p>Many children's hospitals around the United States have programs in which a trained facility dog goes to work daily with a psychosocial healthcare worker, typically a Certified Child Life Specialist (CCLS). CCLSs help children and their families cope with the stress of a healthcare experience by utilizing evidence-based, developmentally appropriate interventions. The purpose of this study was to explore how CCLSs incorporate facility dogs into their treatments and gain their perspectives on handling a facility dog. Participants, four CCLSs, completed a checklist, which assessed patients seen by facility dogs for 10 workdays, and a semi-structured interview. Participants primarily saw patients of ages three to five years and aided with general anxiety and coping support. Findings indicated the dog's specific training, therapeutic value, and ability to bond with patients allowed these interactions to be successful and impactful. This study provides information about the benefits of facility dogs for child life programs and presents data for programs that are considering incorporating this therapeutic modality into their services offered.</p>","PeriodicalId":54388,"journal":{"name":"Journal of Child Health Care","volume":" ","pages":"501-513"},"PeriodicalIF":1.3,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10706653","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Why are we still doing sucrose trials for newborns? 我们为什么还要对新生儿进行蔗糖试验?
IF 1.3 4区 医学
Journal of Child Health Care Pub Date : 2024-09-01 Epub Date: 2024-09-09 DOI: 10.1177/13674935241280854
Denise Harrison, Melinda Cruz, Stephen McKeever
{"title":"Why are we still doing sucrose trials for newborns?","authors":"Denise Harrison, Melinda Cruz, Stephen McKeever","doi":"10.1177/13674935241280854","DOIUrl":"10.1177/13674935241280854","url":null,"abstract":"","PeriodicalId":54388,"journal":{"name":"Journal of Child Health Care","volume":" ","pages":"453-456"},"PeriodicalIF":1.3,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142156655","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Community paediatric clinics and their role in supporting developmental outcomes and services for children living in disadvantaged communities. 社区儿科诊所及其在支持弱势社区儿童发展成果和服务方面的作用。
IF 1.3 4区 医学
Journal of Child Health Care Pub Date : 2024-09-01 Epub Date: 2022-12-21 DOI: 10.1177/13674935221146008
Lynn Buckley, Louise Gibson, Katherine Harford, Nicola Cornally, Margaret Curtin
{"title":"Community paediatric clinics and their role in supporting developmental outcomes and services for children living in disadvantaged communities.","authors":"Lynn Buckley, Louise Gibson, Katherine Harford, Nicola Cornally, Margaret Curtin","doi":"10.1177/13674935221146008","DOIUrl":"10.1177/13674935221146008","url":null,"abstract":"<p><p>Children living in disadvantaged communities have substantially increased risk for deleterious health and developmental outcomes. A considerable proportion of developmental delay is avoidable; however if children do not receive appropriate treatment within this critical period, damage can be irreparable. Community paediatric clinics provide medical and developmental assessment; deliver health promotion services, counselling, and advice to caregivers; and referral to services. The aim of this study was to systematically search, appraise, and synthesise the literature exploring the role of community paediatric clinics in supporting developmental outcomes and services for children living in disadvantaged communities. Electronic databases were searched using a carefully developed search strategy. Validated tools and appropriate guidelines assessed quality and confidence in evidence. Data analysis and mixed-methods synthesis was guided by the Segregated Framework for Mixed-Method Systematic Reviews. Eighteen studies were selected for inclusion. Areas of emphasis in the literature include the identification and monitoring of developmental delay; engagement of vulnerable families; relational working with children, families, and local services; referral to early intervention services; parental empowerment, practitioner capacity building; and tackling barriers to healthcare access. Through use of a child and family-centred model of care, community paediatric clinics can better meet the needs of vulnerable populations.</p>","PeriodicalId":54388,"journal":{"name":"Journal of Child Health Care","volume":" ","pages":"658-674"},"PeriodicalIF":1.3,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11457470/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10402565","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Children and young people's participation in decision-making within healthcare organisations in New Zealand: An integrative review. 新西兰儿童和青少年参与医疗机构决策的情况:综合评述。
IF 1.3 4区 医学
Journal of Child Health Care Pub Date : 2024-09-01 Epub Date: 2023-02-21 DOI: 10.1177/13674935231153430
Mandie Foster, Julie Blamires, Chris Moir, Virginia Jones, Jagamaya Shrestha-Ranjit, Brie Fenton, Annette Dickinson
{"title":"Children and young people's participation in decision-making within healthcare organisations in New Zealand: An integrative review.","authors":"Mandie Foster, Julie Blamires, Chris Moir, Virginia Jones, Jagamaya Shrestha-Ranjit, Brie Fenton, Annette Dickinson","doi":"10.1177/13674935231153430","DOIUrl":"10.1177/13674935231153430","url":null,"abstract":"<p><p>There is a paucity of literature on children and young people's participation in decision-making within healthcare organisations in New Zealand. This integrative review examined child self-reported peer-reviewed manuscripts and published guidelines, policy, reviews, expert opinion and legislation to explore how New Zealand children and young people participate in discussions and decision-making processes within healthcare settings and what are barriers and benefits to such participation. Four child self-reported peer-reviewed manuscripts and twelve expert opinion documents were retrieved from four electronic databases including academic, government and institutional websites. Inductive content thematic analysis generated one theme (a discourse in children and young people's participation within healthcare settings), four sub-themes, 11 categories, 93 codes and 202 findings. It is evident within this review that there is a discourse between what expert opinion are stating is required to promote children and young people's participation in discussions and decision-making processes within healthcare settings and what is occurring in practice. Despite literature reporting on how children and young people's participation and voice were essential for healthcare provision, there was sparse literature published on children and young people's participation in discussions and decision-making processes in healthcare delivery in New Zealand.</p>","PeriodicalId":54388,"journal":{"name":"Journal of Child Health Care","volume":" ","pages":"675-692"},"PeriodicalIF":1.3,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11528880/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10809565","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Experiences of siblings and parents of children with congenital heart disease and exploration of siblings' support needs. 先天性心脏病患儿的兄弟姐妹和父母的经历以及对兄弟姐妹支持需求的探索。
IF 1.3 4区 医学
Journal of Child Health Care Pub Date : 2024-08-14 DOI: 10.1177/13674935241273982
Alice Sarah Schamong, Ümran Sema Seven, Ann-Kristin Folkerts, Konrad Brockmeier, Elke Kalbe
{"title":"Experiences of siblings and parents of children with congenital heart disease and exploration of siblings' support needs.","authors":"Alice Sarah Schamong, Ümran Sema Seven, Ann-Kristin Folkerts, Konrad Brockmeier, Elke Kalbe","doi":"10.1177/13674935241273982","DOIUrl":"https://doi.org/10.1177/13674935241273982","url":null,"abstract":"<p><p>Research with siblings of children with congenital heart disease (CHD) is scarce, although more than one-third of them experience limitations on their quality of life. This interview study aims to explore the diagnosis-associated experience of German siblings of children with CHD, their interest in a potential intervention, and potential key topics and contextual conditions of such an intervention. Interviews with 10 siblings aged 10 to 21 and a respective parent were conducted from August to October 2021, resulting in 20 interviews. Negative experiences associated with CHD included concerns regarding hospitalization, health deterioration, and the death of the child with CHD, as well as burdens including reduced family activities, less parental attention and support, and extended family meals. Positive experiences included perceived positive consequences of CHD, such as strong family cohesion and empathy toward people with chronic illnesses. Furthermore, siblings experienced enhanced coping mechanisms, such as having conversations with friends and family about the high prevalence of CHD and successful treatment or using distractions such as entertainment or study. Siblings' reported interest in a future intervention included empathy, peer support, and studying medical information on CHD. These findings should be used for counseling and developing tailored interventions to support these siblings.</p>","PeriodicalId":54388,"journal":{"name":"Journal of Child Health Care","volume":" ","pages":"13674935241273982"},"PeriodicalIF":1.3,"publicationDate":"2024-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141977232","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mothers' experience seeking healthcare advice for their unsettled infants in Victoria, Australia. 澳大利亚维多利亚州母亲为躁动不安的婴儿寻求医疗建议的经历。
IF 1.3 4区 医学
Journal of Child Health Care Pub Date : 2024-08-08 DOI: 10.1177/13674935241271954
Bridget Kenny, Sarah McTaggart, Rachel O'Loughlin, Branavie Ranjithakumaran, Rachel Pelly, Harriet Hiscock
{"title":"Mothers' experience seeking healthcare advice for their unsettled infants in Victoria, Australia.","authors":"Bridget Kenny, Sarah McTaggart, Rachel O'Loughlin, Branavie Ranjithakumaran, Rachel Pelly, Harriet Hiscock","doi":"10.1177/13674935241271954","DOIUrl":"https://doi.org/10.1177/13674935241271954","url":null,"abstract":"<p><p>Unsettled infant behaviours are highly prevalent in the postnatal period and constitute a significant proportion of visits to healthcare services. Unsettled infant behaviours can be highly distressing for parents and are identified as a significant risk factor for postnatal depression. Understanding parents' experiences is paramount to reducing the gap between consumer expectations and service delivery. This study employed a qualitative descriptive approach to explore parents' experiences seeking healthcare advice for their infant with unsettled behaviours. Semi-structured interviews were conducted with 20 mothers. Inductive thematic analysis yielded two overarching themes: (1) 'the journey for answers', consisting of five sub-themes, and (2) 'parents' knowledge and behaviours', consisting of six sub-themes. Despite some positive interactions with healthcare services, mothers generally spoke negatively of their overall experience seeking answers and receiving care for their infant, and they felt the healthcare services they attended were not equipped to meet their needs. To address the gap between service delivery and consumer expectations, mothers relied on online communities for advice and emotional support. The findings of this study highlight several discrepancies between mothers' expectations and service delivery in the context of unsettled infant behaviours, and this paper makes recommendations to address identified shortcomings in approaches to care.</p>","PeriodicalId":54388,"journal":{"name":"Journal of Child Health Care","volume":" ","pages":"13674935241271954"},"PeriodicalIF":1.3,"publicationDate":"2024-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141908319","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Factors that support children and young people to express their views and to have them heard in healthcare: An inductive qualitative content analysis. 支持儿童和青少年在医疗保健中表达意见并使其意见得到倾听的因素:归纳式定性内容分析。
IF 1.9 4区 医学
Journal of Child Health Care Pub Date : 2024-06-04 DOI: 10.1177/13674935241258515
Clare Davies, Donna Waters, Jennifer Fraser
{"title":"Factors that support children and young people to express their views and to have them heard in healthcare: An inductive qualitative content analysis.","authors":"Clare Davies, Donna Waters, Jennifer Fraser","doi":"10.1177/13674935241258515","DOIUrl":"https://doi.org/10.1177/13674935241258515","url":null,"abstract":"<p><p>Despite development of healthcare charters supporting Article 12 of The United Nations Convention on the Rights of the Child, children and young people remain largely silenced in discussions about their healthcare. This article is based on the premise that children and young people should be able to exercise their right to express their views and be heard in all matters that affect their lives. This study examined children's and young people's experiences of expressing their views and having them heard in an Australian healthcare context. Using child-centred inquiry and 'draw, write, and tell' methods, data were collected from 20 children and young people. Five factors that supported children and young people to express their views and have their views heard were identified: time, relationships with health professionals, communication, teamwork, and family support. By paying attention to these factors, clinicians and others in health settings can better facilitate child-centred practices and support children and young people to express their views and have those views heard.</p>","PeriodicalId":54388,"journal":{"name":"Journal of Child Health Care","volume":" ","pages":"13674935241258515"},"PeriodicalIF":1.9,"publicationDate":"2024-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141238832","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Goals of Morbidity and Mortality meetings in paediatric acute care. A qualitative case study. 儿科急症护理中发病率和死亡率会议的目标。定性案例研究。
IF 1.9 4区 医学
Journal of Child Health Care Pub Date : 2024-06-04 DOI: 10.1177/13674935241249597
Emma Jeffs, Fiona Newall, Clare Delany, Sharon Kinney
{"title":"Goals of Morbidity and Mortality meetings in paediatric acute care. A qualitative case study.","authors":"Emma Jeffs, Fiona Newall, Clare Delany, Sharon Kinney","doi":"10.1177/13674935241249597","DOIUrl":"https://doi.org/10.1177/13674935241249597","url":null,"abstract":"<p><p>Morbidity and Mortality meetings are conducted in varied clinical contexts including paediatrics. Widely cited as an educational or quality improvement tool, the reality is more complex. In this qualitative study, the aim was to explore the perceived goals of the paediatric acute care Morbidity and Morbidity meeting. This study used semi-structured interviews and observation within a qualitative case study methodology. Data were collected in a large paediatric quaternary hospital. Analysis generated themes related to meeting observations and the participant's interpretation of meeting goals. A total of 44 interviews were conducted with 14 nurses, 29 doctors, and 1 allied health professional. Thirty-two meetings in six clinical departments were observed. Two themes were developed: complex and nuanced goals; and tensions and contest between and within goals. Meeting goals to evaluate care, learn, support, adhere, and change and respond were sometimes in competition and had varied interpretations. Morbidity and Mortality meetings in this setting are valued and occupy a complex role which reaches beyond identification of measurable patient safety interventions. Understanding goals more fully can lead to optimised conduct and meaningful measurement of efficacy. The strength in these meetings may be the way they promote an embedded safety culture, and an informed and skilled workforce.</p>","PeriodicalId":54388,"journal":{"name":"Journal of Child Health Care","volume":" ","pages":"13674935241249597"},"PeriodicalIF":1.9,"publicationDate":"2024-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141238833","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Are we at risk of commodifying lived experience in childhood disability research? 在儿童残疾研究中,我们是否面临着生活经验商品化的风险?
IF 1.3 4区 医学
Journal of Child Health Care Pub Date : 2024-06-01 Epub Date: 2024-05-05 DOI: 10.1177/13674935241253919
Jim Reeder
{"title":"Are we at risk of commodifying lived experience in childhood disability research?","authors":"Jim Reeder","doi":"10.1177/13674935241253919","DOIUrl":"10.1177/13674935241253919","url":null,"abstract":"","PeriodicalId":54388,"journal":{"name":"Journal of Child Health Care","volume":" ","pages":"217-220"},"PeriodicalIF":1.3,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140871929","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An Australian survey of health professionals' perceptions of use and usefulness of electronic medical records in hospitalised children's pain care. 澳大利亚关于医疗专业人员对住院儿童疼痛护理中电子病历的使用和实用性的看法调查。
IF 1.9 4区 医学
Journal of Child Health Care Pub Date : 2024-05-29 DOI: 10.1177/13674935241256254
Nicole Pope, Janelle Keyser, Dianne Crellin, Greta Palmer, Mike South, Denise Harrison
{"title":"An Australian survey of health professionals' perceptions of use and usefulness of electronic medical records in hospitalised children's pain care.","authors":"Nicole Pope, Janelle Keyser, Dianne Crellin, Greta Palmer, Mike South, Denise Harrison","doi":"10.1177/13674935241256254","DOIUrl":"https://doi.org/10.1177/13674935241256254","url":null,"abstract":"<p><p>Pain in hospitalised children is common, yet inadequately treated. Electronic medical records (EMRs) can improve care quality and outcomes during hospitalisation. Little is known about how clinicians use EMRs in caring for children with pain. This national cross-sectional survey examined the perceptions of clinician-EMR users about current and potential use of EMRs in children's pain care. One hundred and ninety-four clinicians responded (<i>n</i> = 81, 74% nurses; <i>n</i> = 21, 19% doctors; <i>n</i> = 7, 6% other); most used Epic (<i>n</i> = 53/109, 49%) or Cerner (<i>n</i> = 42/109, 38%). Most (<i>n</i> = 84/113, 74%) agreed EMRs supported their initiation of pharmacological pain interventions. Fewer agreed EMRs supported initiation of physical (<i>n</i> = 49/113, 43%) or psychological interventions (<i>n</i> = 41/111, 37%). Forty-four percent reported their EMR had prompt reminders for pain care. Prompts were perceived as useful (<i>n</i> = 40/51, 78%). Most agreed EMRs supported pain care provision (<i>n</i> = 94/110, 85%) and documentation (<i>n</i> = 99/111, 89%). Only 39% (<i>n</i> = 40/102) agreed EMRs improved pain treatment, and 31% (<i>n</i> = 32/103) agreed EMRs improved how they involve children and families in pain care. Findings provide recommendations for EMR designs that support clinicians' understanding of the multidimensionality of children's pain and drive comprehensive assessments and treatments. This contribution will inform future translational research on harnessing technology to support child and family partnerships in care.</p>","PeriodicalId":54388,"journal":{"name":"Journal of Child Health Care","volume":" ","pages":"13674935241256254"},"PeriodicalIF":1.9,"publicationDate":"2024-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141176663","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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