Nursing care satisfaction from school‐aged children's perspective: An integrative review

Loureiro, Fernanda; Figueiredo, María Henriqueta; Charepe, Zaida Borges

doi:10.1111/ijn.12764

Cited by 20 publications

(31 citation statements)

References 41 publications

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“…Children tended to prioritize the qualities of the nurse rather than specific elements of the role, so for example someone who listened, understood their needs, was kind and would stand up for them. Personal characteristics of nurses are consistently described by children when asked about their experiences of care; the nurse as a person is the most important factor (Loureiro, Figueiredo, & Charepe, 2019).…”

Section: Discussionmentioning

confidence: 99%

Supporting families of children with an undiagnosed genetic condition: Using co‐design to ensure the right person is in the right post doing the right job

Oulton

Williams

Geoghegan

et al. 2021

Child

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Background Families and professionals caring for a child without a definitive diagnosis face unique challenges, particularly in relation to managing uncertainty; access to healthcare; obtaining relevant information and support; and trying to navigate a healthcare system that is often fragmented. We used co‐design to inform the establishment of the first UK specialist nursing post dedicated to working with children with undiagnosed genetic conditions and their families. Objectives: (1) To understand what families and hospital staff want from the service; (2) To understand how the post should be operationalized in practice; (3) To develop the job description and person specification for the postholder. Methods A range of approaches were used to collect data: interviews (nine parents and 10 hospital staff); a focus group (three parents); a creative workshop (six patients and siblings); and an online forum (81 parents). Data were analyzed using framework and thematic analysis. The strands of data were brought together and reviewed as a whole to formulate the postholder's job description and person specification. Results Stakeholders identified nine key elements to the role which were incorporated into the job description: practical support; point of contact; community liaison; signposting to other services; care coordination; supporting families; advocacy; raising awareness; and emotional support. Conclusions Highlighted in this paper are the practical aspects of engaging and involving all relevant stakeholders in the process of co‐designing a new post and subsequent staff recruitment. The flexibility employed in the setting and methods of data collection were instrumental in ensuring that the views of a diverse range of participants were ascertained. A major consideration is the resources required to undertake co‐design, in terms of time and finances. We believe that the resources required for the co‐design are offset by the advantages of having the right person in the right post, doing the right job.

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Section: Discussionmentioning

confidence: 99%

Supporting families of children with an undiagnosed genetic condition: Using co‐design to ensure the right person is in the right post doing the right job

Oulton

Williams

Geoghegan

et al. 2021

Child

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“…This review examined eligible studies using a two-criterion scale of research quality (high, moderate, or low) and data relevance (yes or no), which is suggested by Whittemore and Knafl (2005). For research rigor, a quality scoring system was adapted from a past integrative review (Loureiro, Figueiredo, & Charepe, 2019) supplemented by new items including ethical issues, rigor of data collection, and analysis, interpretation, and research implications (see Table S1). Quality scores ranged from 0 to 7 ("Yes" = 1 and "Unclear/No" = 0) and were summarized into three categories: low quality (0-3); moderate quality (4-5);…”

Section: Data Examinationmentioning

confidence: 99%

Coping with multiple chronic conditions: An integrative review

Cheng

Inder

Chan

2020

Nursing & Health Sciences

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There is a paucity of summarized evidence concerning coping with multiple chronic conditions. An integrative review approach was used to synthesize current evidence on: (i) coping in forms of perceptions and strategies, (ii) relationship between coping and health‐related outcomes, and (iii) factors related to coping. Five electronic databases were searched without time limitation. Thirty‐two studies met inclusion criteria and were included for full‐text review: 24 qualitative, seven quantitative, and one mixed‐methods study. Studies were assessed for quality using an appraisal system of rigor and relevance. A constant comparison method was used to synthesize findings from eligible studies. This review synthesized perceptions of multiple chronic conditions involving negative moods and physical limitations, and strategies of coping with multiple chronic conditions including problem‐ and emotion‐focused strategies. Findings suggested that coping is a promising path to manage multiple chronic conditions and emphasized that appropriate coping might have positive impacts on health‐related outcomes. Five impact factors including age, gender, clusters of multiple chronic conditions, social support, and ethnicity and culture were associated with people's coping. Future healthcare plans should address the physical and psychological needs of people with multiple chronic conditions and highlight the importance of modifying their illness perceptions and enhancing appropriate coping strategies.

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“…It is considered a care outcome and an important indicator of the quality of care. In pediatric hospitalization, which is a difficult event that disturbs the family and causes anguish, satisfaction is usually measured with the help of the parents as representatives of the child's interests (Loureiro et al, 2019). Moreover, in this context, parents see themselves as recipients of nursing care, so the dominant care philosophy, which is widely accepted as the best practice in pediatrics, is the philosophy of family-centered care (Shevell et al, 2019).…”

Section: Introductionmentioning

confidence: 99%

Validação da Escala de Satisfação do Cidadão com Cuidados de Enfermagem para pais de crianças hospitalizadas

Loureiro¹,

Araújo²,

Charepe³

2021

Rev. Enf. Ref.

Self Cite

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Background: The level of satisfaction of parents of hospitalized with nursing care has been used to measure nursing care quality. Objective: To adapt and validate the Citizen Satisfaction with Nursing Care Scale (CSNCS) for parents of hospitalized children. Methodology: Methodological study using a nonprobability sample of 251 parents of hospitalized children aged 7 to 11 years. The psychometric properties of reliability and validity were examined. Reliability was assessed by calculating Cronbach's alpha coefficient. Construct validity was assessed through an exploratory factor analysis with principal components and orthogonal Varimax rotation. Results: The CSNCS has adequate psychometric characteristics for the Portuguese population of parents of hospitalized children (Cronbach's alpha of 0.92), ensuring its reliability and validity for measuring satisfaction with nursing care. Conclusion: The CSNCS is a reliable and useful tool to assess the level of satisfaction of parents of hospitalized children.

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Nursing care satisfaction from school‐aged children's perspective: An integrative review

Cited by 20 publications

References 41 publications

Supporting families of children with an undiagnosed genetic condition: Using co‐design to ensure the right person is in the right post doing the right job

Supporting families of children with an undiagnosed genetic condition: Using co‐design to ensure the right person is in the right post doing the right job

Coping with multiple chronic conditions: An integrative review

Validação da Escala de Satisfação do Cidadão com Cuidados de Enfermagem para pais de crianças hospitalizadas

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