Analysis of care and gender stereotypes in nursing scientific research: a scoping review.

Objective: To map evidence about care and gender stereotypes in nursing scientific research.

Method: A scoping review developed under the JBI framework with analysis of gender perspective in care approaches. The searches were carried out on January 31, 2023 in SciELO, Scopus, CINAHL, PubMed, BDENF.

Parents' or legal guardians' beliefs and attitudes about childhood vaccination: a scoping review.

Objective: to map scientific evidence about perceptions, beliefs, knowledge and attitudes of parents or legal guardians of children under 5 years of age regarding routine childhood vaccination.

Methods: a scoping review, conducted in accordance with the JBI framework. The searches were carried out in the PubMed/MEDLINE, Web of Science, Scopus and LILACS databases.

Home visit to premature and low birth weight newborns: nurse's experience report.

Objective: To report the structures of the experience of nurse's home visits to premature and low birth weight newborns.

Method: This is a descriptive study of the experience report type, structured on the experience of the nurse authors in the development of 48 home visits in a city in the state of São Paulo and its microregion between August 2020 and 2021 with eight mothers of premature and low weight newborns.

Results: The guiding documents "Home visit for families with preterm and low birth weight newborns" and "Strategy of guiding questions for home visits" were created and used to promote open narratives from parental caregivers about caring for at-risk newborns, creating a relational space aimed at joint construction.

Factors intervening in the childbirth experience: a mixed-methods study.

Objective: To analyze the childbirth experience focusing on the intervening factors and on the delivery method.

Method: A sequential and explanatory mixed-methods study guided by the World Health Organization document for positive childbirth experiences. The participants were puerperal women in a maternity teaching hospital from inland São Paulo (Brazil).

Parents' hope in perinatal and neonatal palliative care: a scoping review.

Background: The diagnosis of a life-limiting condition of a child in the perinatal or neonatal period is a threat to parental hopes. Hope is an interactional and multidimensional construct, and in palliative care, it is a determinant of quality of life, survival, acceptance and peaceful death.

Objective: To map scientific evidence on parents' hope in perinatal and neonatal palliative care contexts.

Online information related to childhood cancer and COVID-19 pandemic: a thematic analysis.

Objective: To analyze online information available on the internet about COVID-19 and childhood cancer and discuss its reach potential with regard to supporting family functioning.

Method: Documentary research supported by thematic analysis and the concept of family functioning and support. A total of 27 publications available on the websites of reference institutions in pediatric oncology, from March 1 to May 31, 2020, were analyzed.

Family experience of living with children and adolescents with bladder and bowel dysfunction.

Objective: to understand the experience of families of living with children and adolescents with bladder and bowel dysfunction.

Methods: a qualitative phenomenological interpretive research carried out through an in-depth open interview with parents of children and adolescents linked to Advanced Practice Nursing clinic in pediatric urology.

Results: the following representative categories of the families' experiences emerged: Knowledge and learning: building family knowledge; Living with the children's BBD: symbolic representations; Management and adaptation to the children's BBD: reorganizing family life.

(Un)receptiveness in interactions with professionals: experiences of parents of children with retinopathy of prematurity.

Objective: To analyze the influence of health professionals' receptiveness on parental care of children with retinopathy of prematurity (ROP).

Method: A qualitative study developed under the theoretical framework of Symbolic Interactionism and using a narrative research methodology. Six women and three men, being parents of children with retinopathy of prematurity were individually interviewed in depth.

Interaction experience for families who live with their child's disease and hospitalization.

Starting from the research question about the meanings the family attributes to interactions experienced during their child's hospitalization, this study tried to understand the interaction experience of families in pediatric hospitals, as well to identify the interventions considered effective the family's perspective. Symbolic Interactionism was the theoretical framework that supported the data analysis process, and Grounded Theory was the methodological framework. Six families with hospitalized children participated.