Journal of Child Health Care儿童健康照护杂志
Journal of Child Health Care(英文缩写 J CHILD HEALTH CARE),ISSN 1367-4935,eISSN 1741-2889,中文译名:儿童健康照护杂志 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。
发文量统计区间：2025-09-27 至 2026-09-27，按本站收录文献的发表日期统计。
期刊介绍
历年影响因子趋势
| JCR 数据年份 | 影响因子 | JCR 分区 |
|---|---|---|
| 2021 | 1.896 | Q3 |
| 2022 | 1.900 | Q3 |
| 2023 | 1.300 | Q3 |
| 2024 | 1.600 | Q2 |
| 2025 | 1.900 | Q2 |
Journal of Child Health Care 最新收录文献
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1. Breastfeeding experiences of mothers of infants with respiratory tract infection.
PMID:期刊:日期:2026-09-16This study was conducted to determine breastfeeding experiences of mothers of infants with respiratory tract infections. This study is a phenomenological study. Sample of the study consisted of 13 breastfeeding women. Content analysis method was used to evaluate the data. Breastfeeding experiences of mothers participating in the study were determined as two themes: Being Emotionally Affected and Breastfeeding Failure. Being Emotionally Affected theme consists of sub-themes Guilt, Desperation, Inadequacy, and Stress. Under the theme of "Breastfeeding Failure," there were sub-themes of airway obstruction, reluctance to suck, weak sucking, and breast problems. As a result, it was determined that mothers of infant with respiratory tract infections had difficulty breastfeeding and that mothers were emotionally affected by this process. Nurses should be aware that these mothers have problems breastfeeding and their emotional states, and plan nursing care taking these into considerations.
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3. Parent perspectives on family-centered follow-up after pediatric ECMO.
PMID:期刊:日期:2026-09-01The objective of this study was to elicit caregiver perspectives regarding vital components of and challenges to participating in post-extracorporeal membrane oxygenation (ECMO) follow-up care. It was conducted as a single-center electronic survey in a tertiary pediatric hospital with neonatal and pediatric ECMO capabilities. Pediatric survivors less than 18 years of age who survived ECMO between January 2015 and December 2020 were included. An attempt was made to contact 143 eligible families. Fifty of the ninety-three (54%) families who were successfully contacted consented and provided survey responses. Thirty (60%) pediatric ECMO survivors were male, with a median age of 3 months at cannulation and an ECMO duration of 92 h. Eleven (37%) children were categorized as having "fair" or "poor" overall health after ECMO therapy. A majority of respondents were either "extremely likely" or "somewhat likely" to participate in an in-person or virtual multidisciplinary ECMO follow-up (31 (66%) and 36 (77%), respectively). In response to open-ended survey questions, parents expressed need for increased support in three main domains: information/education, psychosocial support, and healthcare coordination. These findings suggest an urgent need to establish a structured, multidisciplinary ECMO follow-up program and to include parents and patients in its development.
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4. A qualitative exploration of child, caregiver, and clinician perspectives on mental health in children with osteogenesis imperfecta.
PMID:期刊:日期:2026-09-01Osteogenesis imperfecta (OI) is a heritable connective disorder with clinical manifestations including bone fragility and short stature. Previous research identified psychosocial themes related to mental health among children with OI and their caregivers, such as independence, social isolation, depression, and anxiety. Several studies have also examined clinicians of individuals with OI for their perspectives on mental health among their patients. However, no known studies have compared psychosocial themes among all three participant groups concurrently. This qualitative study examined mood and anxiety, along with risk and protective factors, from perspectives of youths, parents, and clinicians. Semi-structured interviews were conducted, which were coded independently by two researchers. Codes were analyzed for extraction of themes. Relevant themes include depressed and anxious mood experienced in individuals with OI, as well as risk factors and protective factors for these symptoms. Participants reported functional limitations and social isolation as key risk factors for symptoms of anxious or depressed mood. In contrast, they discussed positive attitudes, social support, multidisciplinary medical groups, and mental health access as key protective factors. Implications for clinical care and future research are discussed. Convergence and divergence of themes across study samples are discussed in detail.
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5. Pediatric tracheostomy education redesign-Impact on length of stay at an academic pediatric center.
PMID:期刊:日期:2026-09-01Pediatric tracheostomy and post-tracheostomy care contribute significantly to total pediatric hospitalization costs and time in hospital. Therefore, we revised our family education methods and reset expectations for post-tracheostomy length of stay (PTLOS), while enabling caregivers to safely manage their children at home with minimal or no professional in-home assistance. At an academic pediatric center, a 14-day tracheostomy education plan, formed by a multidisciplinary team, was enacted. Patient PTLOS and readmission rates were monitored from November 2020 to December 2021 and compared to historical institutional averages for 36 patients. We provided instruction to a total of 184 RNs and RTs on how to teach standardized methods of home tracheostomy care. Following implementation of a new educational curriculum, there was a significant reduction in PTLOS from 78 to 39 days, a decrease of 50% in PTLOS. Post-tracheostomy readmission rate remained stable. Implementation of a multidisciplinary post-tracheostomy education plan which emphasizes preoperative preparedness, efficient family education, and reset expectations of success can reduce PTLOS without increasing hospital readmission rates.
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6. Risk mitigation strategies for children and young people admitted with mental health crisis to acute paediatric care: A systematic review with narrative synthesis.
PMID:期刊:日期:2026-09-01Globally, the number of Children and Young People (CYP) that experience mental health crisis and access paediatric acute hospital settings continues to increase. Many of these CYP present with thoughts and behaviours of self-harm and/or suicide and often experience severe and fluctuating emotional states. It is therefore important that the risk of self-harm/suicide is assessed during an inpatient admission and strategies implemented to mitigate risk. This study aimed to identify self-harm and suicidality risk management pathways that have been developed and evaluated for use with CYP admitted to acute hospital settings with mental health crisis. A systematic review was conducted. Eight online academic database were searched up to February 2022. The critical appraisal skills programme tool was used to assess the methodological rigour of included studies. Online searches identified 120 potential studies. Five studies met the predefined inclusion criteria. Six risk mitigation strategies were identified; safety huddles, urgent full mental psychiatric review within 2-h of assessment, feedback on screening responses, motivational and barrier-reducing intervention, 1:1 constant observations and environmental safety. All included strategies targeted environmental, family, and individual CYP involving modifications to equipment, surveillance, and communication to enhance safety.
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7. Experiences of parents caring for more than one child with the same chronic or serious illness in Occupied Palestinian Territory: A qualitative study.
PMID:期刊:日期:2026-09-01In Occupied Palestinian territory (OPT), which is in a complex political situation and has limited access to resources, there is a critical need to deepen the understanding of how children with life-limiting and life-threatening illnesses are cared for. This study explores the experiences of parents caring for more than one child with a chronic or serious illness. A qualitative descriptive method was adopted, with data collected from several paediatric units in two OPT cities, Tulkarm and Ramallah. Semi-structured, face-to-face interviews were conducted with 16 parents (each interview was of an individual parent). Data were analysed using thematic analysis, and the analysis unearthed seven major themes that reflected the parents' experiences. These were as follows: Significant life changes with the first child's illness; the second experience; becoming stronger; support systems; economic difficulties; social stigma; and social isolation. Data analyses suggest that there is a significant need for emotional and physical support to be provided to parents, and culturally salient social service provisions should be implemented to alleviate the burden placed on these parents.
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8. Experiences and insights from parents of children with temporary feeding tubes.
PMID:期刊:日期:2026-09-01This study aimed to describe parents' experiences of children with temporary feeding tubes by surveying parents whose children required tubes. This survey included three sections including; (A) Depression Anxiety Stress Scale (DASS-21); (B) Paediatric Assessment Scale for Severe Feeding Problems (PASSFP); and (C) open-ended questions on satisfaction and experiences. Data were analysed using descriptive statistics and inductive content analysis. A total of 44 parent participants completed the survey. Most participants reported satisfaction with their child's care, although for most, tube removal occurred after ≤5 days (n = 25, 57%). Children who were discharged home with a temporary feeding tube (n = 7, 16%) had more feeding difficulties. Two themes were identified: 1) navigating tube feeding and 2) health service experiences. Although parents were generally positive about their child's care, some described ongoing medical and psychosocial impacts. Many parents desired more involvement in decision-making and tube feeding care. Parents described varied experiences regarding temporary tube feeding both in hospital and after discharge home. Further studies are needed across all spectrums of temporary tube feeding care, especially those discharged home. These findings underscore a need for enhanced support and education for parents, which could improve outcomes for children with temporary feeding tubes.
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9. Influence of spoken language and gender identity on healthcare experiences of transgender and non-binary youth living in Quebec, Canada.
PMID:期刊:日期:2026-09-01Whether spoken language influences experiences of trans and non-binary youth (TNBY) with healthcare systems is unknown. We analyzed Quebec data from the Canadian Trans and Non-Binary Youth Health Survey to illustrate healthcare experiences of predominantly French-speaking TNBY aged 14-25 and influence of gender identity and language on those experiences. We included 220 participants of whom 71% identified as French-speaking. Up to 78% reported a mental health problem and 51% reported foregoing mental health care in the last year. Only 26% of non-binary versus 57% of trans youth were comfortable discussing healthcare needs with providers (OR 0.26; 95% CI [0.13-0.54]). English youth were less likely than French youth to be comfortable discussing healthcare needs (aOR 0.33, 95% CI [0.13-0.83]. They were also more likely to forgo care because of negative experiences (aOR 2.21, 95% CI [1.00, 4.87]) and out of fear (aOR 2.38, 96% CI [1.08, 5.28]). Our study found that TNBY had a high prevalence of foregone health care despite a great need. In Quebec, a predominantly French-speaking area within Canada, language-minority English TNBY were less comfortable than French TNBY discussing healthcare needs and accessing needed resources. Limited availability of language-specific resources may be an additional barrier to healthcare access for TNBY.
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10. Standards of care for pediatric clinical service delivery: A rapid scoping review.
PMID:期刊:日期:2026-09-01When pediatric services are not coordinated, children, youth, and their caregivers cannot always access the right services at the right time. Guidance is needed for how pediatric services should be planned and organized to improve integrated care. The objective of this rapid scoping review was to map and characterize current evidence on standards of care for integrated pediatric levels of service. This rapid scoping review was conducted in accordance with Cochrane Rapid Reviews Interim Guidance. We searched academic databases and gray literature in 2022, published in English from Canada, United States, United Kingdom, Australia, New Zealand, with no date parameter. Fifty-three sources met inclusion criteria and were included in this review. Levels of service frameworks categorized services into three, four, or six distinct levels. Eight sources described integrated levels of service. Most pediatric standards of care frameworks defined levels of service by roles and responsibilities. Differences were defined by transitions between levels of care, planning for services across urban and rural communities, and coordinating integrated levels of service. Future research is required to build evidence base of how levels of service frameworks can be used in practice, adapted to local contexts, and evaluated.