1
40
10
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Dublin Core
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Title
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June 2023 List
Text
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June 2022 List
URL Address
<a href="https://www.mdpi.com/2227-9067/10/3/482">https://www.mdpi.com/2227-9067/10/3/482</a>
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Title
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Palliative care education in an Australian undergraduate pharmacy curriculum: an exploratory descriptive study
Publisher
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International Journal of Pharmacy Practice
Date
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2023
Subject
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Palliative Care; Education; Adolescence; Adult; Female; Human; Male; Questionnaires; Surveys; Australia; Clinical Reasoning; Communication; Confidence; Curriculum; Descriptive Research; Descriptive Statistics; Education Pharmacy; Empathy; Exploratory Research; Mann-Whitney U Test; Prospective Studies; Qualitative Studies; Reflection; Self Concept; Students Undergraduate; Thematic Analysis
Creator
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Ong JA; Rego J; Ung T; Kumar S; Ash K; Saini B; Yates P
Rights
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Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Identifier
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<a href="https://www.mdpi.com/2227-9067/10/3/482"><span>10.1093/ijpp/riac093</span></a>
2023
Adolescence
Adult
Ash K
Australia
clinical reasoning
Communication
Confidence
Curriculum
Descriptive Research
Descriptive Statistics
Education
Education Pharmacy
Empathy
Exploratory Research
Female
Human
International Journal of Pharmacy Practice
June 2022 List
Kumar S
Male
Mann-Whitney U Test
Ong JA
Palliative Care
Prospective Studies
Qualitative Studies
Questionnaires
Reflection
Rego J
Saini B
Self Concept
Students Undergraduate
surveys
Thematic Analysis
Ung T
Yates P
-
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
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April 2023 List
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
April List 2023
URL Address
<a href="https://www.proquest.com/openview/38170f14f1589d8cbe54d1a6a9df9395/1?pq-origsite=gscholar&cbl=33099" target="_blank" rel="noreferrer noopener">https://www.proquest.com/openview/38170f14f1589d8cbe54d1a6a9df9395/1?pq-origsite=gscholar&cbl=33099 http://doi.org/</a>
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Title
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It Was a Shared Duty': Bereaved Fathers' Perspectives, Experiences and Practices in Relation to their Partner's Lactation after Infant Death
Publisher
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Breastfeeding Review
Date
A point or period of time associated with an event in the lifecycle of the resource
2022
Subject
The topic of the resource
Male; Bereavement; Infant; Palliative Care; Intensive Care Units Neonatal; Interpersonal Relations; Australia; Purposive Sample; Qualitative Studies; Health Policy; Data Analysis Software; Exploratory Research; Human; Descriptive Statistics; Phenomenological Research; Life Experiences; Thematic Analysis; Perinatal Death; Psychosocial Factors; Semi-Structured Interview; Milk Human; Donor Milk; Infant Death; Lactates; Lactation; Lactic Acid; Open-Ended Questionnaires; Paternal Attitudes; Paternal Role
Creator
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Noble-Carr D; Carroll K; Copland S; Waldby C
Description
An account of the resource
This exploratory study targets a significant gap in the lactation and bereavement literature by exploring bereaved fathers' experiences, perspectives and practices in relation to their partner's lactation after stillbirth, neonatal or infant death. Semi-structured interviews were conducted with seven bereaved fathers in two Australian state/ territory jurisdictions. Purposive sampling ensured the partners of five of the fathers had been involved in bereaved breastmilk donation to a human milk bank. Thematic data analysis identified key themes that drew attention to the significant grief experienced by fathers and highlighted: (i) breastmilk and infant feeding holding significant meaning for some fathers especially within the neonatal intensive care or palliative care settings, (ii) the impact of diverse lactation management options on the awareness and involvement of fathers in their partner's lactation after infant death, (iii) fathers' provision of significant care and support for partners participating in bereaved breastmilk donation, (iv) bereaved breastmilk donation positively impacting some fathers' grief and meaning- making, and (v) bereaved families' requirement for enhanced lactation care, information and support. Results indicate the need for an enhanced focus on family-centred bereaved lactation care and acknowledgement of the positive role that bereaved breastmilk donation may have for both mothers and fathers following infant loss.
Identifier
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<a href="http://doi.org/" target="_blank" rel="noreferrer noopener"></a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
2022
April List 2023
Australia
Bereavement
Breastfeeding Review
Carroll K
Copland S
Data Analysis Software
Descriptive Statistics
Donor Milk
Exploratory Research
Health Policy
Human
Infant
Infant Death
Intensive Care Units Neonatal
Interpersonal Relations
Lactates
lactation
Lactic Acid
Life Experiences
Male
Milk Human
Noble-Carr D
Open-Ended Questionnaires
Palliative Care
Paternal Attitudes
Paternal Role
Perinatal Death
Phenomenological Research
Psychosocial Factors
Purposive Sample
Qualitative Studies
Semi-Structured Interview
Thematic Analysis
Waldby C
-
Dublin Core
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Title
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July 2020 List
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
July 2020 List
URL Address
<a href="http://doi.org/10.1016/j.nedt.2020.104417" target="_blank" rel="noreferrer noopener">http://doi.org/10.1016/j.nedt.2020.104417</a>
Dublin Core
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Title
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Educational needs and preferred learning approaches of the paediatric palliative care workforce: A qualitative exploratory study
Publisher
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Nurse education today
Date
A point or period of time associated with an event in the lifecycle of the resource
2020
Subject
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education; exploratory research; learning; pediatric palliative care; pediatric palliative care workforce; qualitative study
Creator
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Malcolm C; McGirr D
Identifier
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<a href="http://doi.org/10.1016/j.nedt.2020.104417" target="_blank" rel="noreferrer noopener">10.1016/j.nedt.2020.104417</a>
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Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
2020
Education
Exploratory Research
July 2020 List
Learning
Malcolm C
McGirr D
Nurse Education Today
Pediatric Palliative Care
pediatric palliative care workforce
Qualitative Study
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Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
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March 2020 List
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
March 2020 List
URL Address
<a href="http://doi.org/10.1590/2177-9465-EAN-2019-0030" target="_blank" rel="noreferrer noopener">http://doi.org/10.1590/2177-9465-EAN-2019-0030</a>
Dublin Core
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Title
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Mothers of angels: (re)living the death of the child as a coping strategy
Publisher
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Anna Nery School Journal of Nursing / Escola Anna Nery Revista de Enfermagem
Date
A point or period of time associated with an event in the lifecycle of the resource
2020
Subject
The topic of the resource
Adult; Attitude to Death; Child; Coping; Data Analysis Software; Death -- In Infancy and Childhood; Descriptive Research; Exploratory Research; Focus Groups; Hardiness; Human; Mother-Child Relations; Mothers -- Psychosocial Factors; Qualitative Studies; Thematic Analysis
Creator
An entity primarily responsible for making the resource
Gramazio Soares L; Kuchla É; de Azevedo Mazza V; Gramazio Soares L; Raimondo Ferraz M I; Padilha Mattei A
Description
An account of the resource
Objective: To describe the experiences lived by mothers facing the death of their children. Method: A qualitative, exploratory and descriptive research conducted in Guarapuava-PR, with six participants of the "Marias" group that brings together mothers who lost their children and share their experiences to spontaneously help other women in the process of mourning. Data collection took place from May to August 2017, through a focus group. The speeches were organized by the Iramuteq® software and analyzed according to Creswell. Results: Age ranged from 28 to 40 years old, and most participants were married and catholic. The categories express the need to strengthen bonds and to create ways in which women can express themselves; the importance of the social network to accommodate mourning; the relevance of ethical and humanized care; and group identity as an element to promote resilience. Conclusion and implications for practice: Describing the potentialities and weaknesses in the process of loss and grief enables a qualifying and humanizing care, overcoming care gaps, stimulating the creation of creative and dialogical spaces in maternal care. These results may guide the professional approach by considering the sociocultural context and the risk factors experienced by the mothers, by supporting the development of resilient skills and enabling a humanized and individualized care. Objetivo: Describir las experiencias vivenciadas por las madres frente a la muerte de sus hijos. Método: Investigación descriptiva, exploratoria y cualitativa realizada en Guarapuava-PR, con seis participantes del grupo "Marías" que reúne a madres que perdieron a sus hijos y comparten sus vivencias además de ayudar a otras mujeres espontáneamente en el proceso de duelo. Los datos se recolectaron entre mayo y agosto de 2017, por medio de un grupo focal. Las conversaciones se organizaron por medio del software Iramuteq® y se analizaron según Creswell. Resultados: La edad varió entre 28 y 40 años, y la mayoría de las participantes estaban casadas y eran católicas. Las categorías expresan la necesidad de fortalecer vínculos y de crear medios con los que las mujeres puedan expresarse; la importancia de la red social para sobrellevar el duelo; la relevancia de una atención ética y humanizada y la identidad grupal como elemento promotor de la resiliencia. Conclusión e implicaciones para la práctica: Describir las potencialidades y debilidades en el proceso de pérdida y duelo permite calificar y humanizar el cuidado, superando las lagunas asistenciales y estimulando la creación de espacios creativos y de diálogo en el cuidado materno. Estos resultados pueden orientar el enfoque profesional al considerar el contexto sociocultural y los factores de riesgo que experimentan las madres, apoyando el desarrollo de habilidades resilientes y haciendo posible un cuidado humanizado e individualizado. Objetivo: Descrever as experiências vivenciadas pelas mães frente à morte do filho. Método: Pesquisa descritiva exploratória qualitativa realizada em Guarapuava-PR, junto a seis participantes do grupo "Marias" que reúne mães que perderam seus filhos e compartilham suas vivências além de ajudar outras mulheres espontaneamente no processo de luto. A coleta de dados ocorreu de maio e agosto/2017, por meio de grupo focal. As falas foram organizadas pelo software Iramuteq® e analisada segundo Creswell. Resultados: Idade variou entre 28 a 40 anos, maioria casadas e católicas. As categorias expressam a necessidade fortalecer vínculos e criar meios em que possam se expressar; importância da rede social para acolher o luto; relevância do atendimento ético e humanizado e a identidade grupal como elemento promotor da resiliência. Conclusão e implicações para a prática: Descrever as potencialidades e fragilidades no processo de perda e luto possibilita qualificar e humanizar o cuidado, com a superação de lacunas assistenciais estimulando a criação de espaços criativos e dialógicos no acolhimento materno. Estes resultados podem orientar a abordagem profissional ao considerar o contexto cultural, social e fatores de risco em que as mães vivenciam, ao apoiar o desenvolvimento de habilidades resilientes e possibilitando um cuidado humanizado e individualizado.
Identifier
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<a href="http://doi.org/10.1590/2177-9465-EAN-2019-0030" target="_blank" rel="noreferrer noopener">10.1590/2177-9465-EAN-2019-0030</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
2020
Adult
Anna Nery School Journal of Nursing / Escola Anna Nery Revista de Enfermagem
Attitude To Death
Child
Coping
Data Analysis Software
de Azevedo Mazza V
Death -- In Infancy and Childhood
Descriptive Research
Exploratory Research
Focus Groups
Gramazio Soares L
Hardiness
Human
Kuchla É
March 2020 List
Mother-child Relations
Mothers -- Psychosocial Factors
Padilha Mattei A
Qualitative Studies
Raimondo Ferraz M I
Thematic Analysis
-
Dublin Core
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Title
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2019 Oncology List
Text
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Citation List Month
Oncology 2019 List
URL Address
<a href="http://doi.org/10.1089/jayao.2018.0154" target="_blank" rel="noreferrer noopener">http://doi.org/10.1089/jayao.2018.0154</a>
Dublin Core
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Title
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An Exploratory Study into the Experience of Health Care Professionals Caring for Adolescents and Young Adults with Incurable Cancer
Publisher
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Journal of adolescent and young adult oncology.
Date
A point or period of time associated with an event in the lifecycle of the resource
2019
Subject
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adolescent; adult; article; Australia; cancer center; challenges; enablers; exploratory research; health care personnel; health care professionals; human; incurable disease; multidisciplinary; semi structured interview; young adult
Creator
An entity primarily responsible for making the resource
Berger I; Thompson K; Joubert L
Description
An account of the resource
Adolescents and young adults 15 to 25 years of age with incurable cancer are a unique patient group. There is growing evidence of the emotionally taxing nature of this work, yet limited understanding of the health care professional experience across professional disciplines. This exploratory study, comprising in-depth semistructured interviews, undertaken at a major cancer center in Melbourne, Australia, describes the challenges facing health care professionals and the factors enabling them to deliver care with greater confidence. The findings provide a platform for further research with key recommendations to enhance the delivery of care to young people with a life-limiting cancer diagnosis.
Identifier
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<a href="http://doi.org/10.1089/jayao.2018.0154" target="_blank" rel="noreferrer noopener">10.1089/jayao.2018.0154</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
2019
Adolescent
Adult
Article
Australia
Berger I
cancer center
challenges
enablers
Exploratory Research
Health Care Personnel
Health care professionals
Human
incurable disease
Joubert L
Journal of adolescent and young adult oncology.
multidisciplinary
Oncology 2019 List
Semi Structured Interview
Thompson K
Young Adult
-
Dublin Core
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Title
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2018 Oncology List
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Oncology 2018 List
URL Address
<a href="http://doi.org/10.1007/s00431-018-3170-6" target="_blank" rel="noreferrer noopener">http://doi.o
rg/10.1007/s00431-018-3170-6</a>
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Title
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The timing and circumstances of the implementation of pediatric palliative care in Hungarian pediatric oncology
Publisher
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European Journal of Pediatrics
Date
A point or period of time associated with an event in the lifecycle of the resource
2018
Subject
The topic of the resource
child death; parent; family; terminal care; priority journal; psychologist; doctor patient relation; constructive feedback; childhood cancer; cancer palliative therapy; cohort analysis; oncologist; structured interview; human; article; female; male; adult; exploratory research; time to treatment; ambivalence; data analysis software; Hungarian (citizen); Hungary
Creator
An entity primarily responsible for making the resource
Nyiro J; Zorgo S; Eniko F; Hegedus K; Hauser P
Description
An account of the resource
Despite the continuous improvement of pediatric palliative care, medical professionals still face various barriers regarding its implementation; our aim was to investigate this question in Hungarian pediatric oncology practice. Structured interviews were carried out in person with physicians from the Hungarian Pediatric Oncology Group (n = 22). Codes were generated inductively with the aid of Atlas.ti 6.0 software. Most physicians placed the palliative care discussion at the end of curative treatment (n = 21) and preferred to conduct it in a team setting (n = 18), mainly in the presence of a psychologist. Preparing parents for the child's death can occur during the palliative care discussion (n = 3), in the child's final days/h (n = 6), gradually (n = 10), or never (n = 3). There are words consciously utilized and avoided during this discussion, with the word "death" proving to be the most ambivalent (utilized n = 5, avoided n = 6). Conclusions: There is no widely accepted unified practice among pediatric oncologists concerning the implementation of palliative care in Hungary. Despite the international recommendation, the common practice of timing is still at the end of curative treatment. Physicians rely on multidisciplinary teamwork, where the psychologist's role is the most prominent in this discussion.What is Known:* There is an international consensus that palliative care should commence at the diagnosis of a pediatric malignant disease regardless of illness outcome.* Barriers to the early implementation of palliative care in pediatric oncology involve resource-based and attitudinal factors.What is New:* In Hungary, where pediatric oncologists are sole decision-makers, early implementation of palliative care is rare.* There is a strong preference among physicians for working within a team, while also asserting that presence of team members may decrease the level of intimacy.
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/%2010.1007/s00431-018-3170-6" target="_blank" rel="noreferrer noopener">10.1007/s00431-018-3170-6</a>
2018
Adult
ambivalence
Article
Cancer Palliative Therapy
Child Death
Childhood Cancer
Cohort Analysis
constructive feedback
Data Analysis Software
Doctor Patient Relation
Eniko F
European Journal of Pediatrics
Exploratory Research
Family
Female
Hauser P
Hegedus K
Human
Hungarian (citizen)
Hungary
Male
Nyiro J
Oncologist
Oncology 2018 List
Parent
Priority Journal
Psychologist
Structured Interview
Terminal Care
time to treatment
Zorgo S
-
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
2018 Oncology List
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Oncology 2018 List
URL Address
<a href="http://doi.org/10.1002/pbc.27455" target="_blank" rel="noreferrer noopener">http://doi.o
rg/10.1002/pbc.27455</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
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Family experiences and viewpoints of palliative and supportive care for children with cancer: Can we do better?
Publisher
An entity responsible for making the resource available
Pediatric Blood and Cancer
Date
A point or period of time associated with an event in the lifecycle of the resource
2018
Subject
The topic of the resource
oncology; South Africa; grounded theory; basic needs; sibling; conference abstract; financial management; psychosocial care; human; child; female; male; interview; clinical article; awareness; palliative therapy; qualitative research; staff; exploratory research; error
Creator
An entity primarily responsible for making the resource
Du Plessis J; Stones D; Meiring M
Description
An account of the resource
Background/Objectives: Palliative and supportive care needs of children with cancer and their families are unique and require special attention. Development of appropriate services sensitive to the needs of families and based on observed evidence has become more and more recognized. As an introduction to develop and improve supportive and palliative care services for children with cancer, families were questioned regarding their experiences and suggestions for improvements. Design/Methods: In this exploratory, qualitative study using a grounded theory approach, sixteen family members of children with cancer and treated at Universitas Academic Hospital, Bloemfontein, South Africa were interviewed regarding their children's standard oncology and supportive/palliative care. Their responses were studied and repeating themes were identified. Results: A number of areas of need were identified: erratic psychosocial support, minimal financial support, poor parental access to basic needs and food provision, preventable errors in procedures and lack of sibling support. Staff were also not always sufficiently equipped to attend to palliative care patients. Conclusions: Supportive and palliative care for children with cancer need to be improved. Family members are a valuable resource and the interviews identified a number of themes, valuable to consider in the expansion of a supportive/palliative service. The intension of the study were to create the awareness that by making small and affordable changes the quality of care the children and families receive can be improved.
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/%2010.1002/pbc.27455" target="_blank" rel="noreferrer noopener">10.1002/pbc.27455</a>
2018
Awareness
Basic Needs
Child
Clinical Article
conference abstract
Du Plessis J
error
Exploratory Research
Female
financial management
Grounded Theory
Human
Interview
Male
Meiring M
Oncology
Oncology 2018 List
Palliative Therapy
Pediatric Blood and Cancer
psychosocial care
Qualitative Research
Sibling
South Africa
Staff
Stones D
-
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
2018 Developing World List
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Developing World 2018 List
URL Address
<a href="http://doi.org/10.1097/JPN.0000000000000361" target="_blank" rel="noreferrer noopener">http://doi.o
rg/10.1097/JPN.0000000000000361</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Brazilian Neonatal Nurses' Palliative Care Experiences
Publisher
An entity responsible for making the resource available
The Journal of perinatal & neonatal nursing
Date
A point or period of time associated with an event in the lifecycle of the resource
2018
Subject
The topic of the resource
quality of life; infant; grief; newborn; Brazil; vulnerable population; education; palliative therapy; thematic analysis; human experiment; genetic transcription; neonatal intensive care unit; human; article; female; male; controlled study; interview; clinical article; neonatal nurse; convenience sample; exploratory research; quality of nursing care; registered nurse; teaching hospital
Creator
An entity primarily responsible for making the resource
de Castro de Oliveira F; Cleveland LM; Darilek U; Borges Silva AR; Carmona EV
Identifier
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<a href="http://doi.org/10.1097/JPN.0000000000000361" target="_blank" rel="noreferrer noopener">10.1097/JPN.0000000000000361</a>
2018
Article
Borges Silva AR
Brazil
Carmona EV
Cleveland LM
Clinical Article
Controlled Study
Convenience Sample
Darilek U
de Castro de Oliveira F
Developing World 2018 List
Education
Exploratory Research
Female
genetic transcription
Grief
Human
Human Experiment
Infant
Interview
Male
Neonatal Intensive Care Unit
Neonatal Nurse
Newborn
Palliative Therapy
Quality Of Life
quality of nursing care
registered nurse
teaching hospital
The Journal Of Perinatal & Neonatal Nursing
Thematic Analysis
vulnerable population
-
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
April 2018 List
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
April 2018 List
URL Address
<a href="http://doi.org/10.1080/07481187.2017.1334011" target="_blank" rel="noreferrer noopener">http://doi.org/10.1080/07481187.2017.1334011</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Use of Facebook in the maternal grief process: An exploratory qualitative study
Publisher
An entity responsible for making the resource available
Death Studies
Date
A point or period of time associated with an event in the lifecycle of the resource
2018
Subject
The topic of the resource
Exploratory Research; Grief; Human; Qualitative Studies; Research Subjects; Social Media; Support; Women; grief; Semi-Structured Interview; human; Thematic Analysis; Maternal Attitudes; Social Networks; Utilization; Psychosocial
Creator
An entity primarily responsible for making the resource
Perluxo D; Francisco R
Description
An account of the resource
This study seeks to explore the potential implications of Facebook use in the process of maternal grief. The participants were 11 women who had lost their children due to accidents or prolonged illness. Semistructured interviews were conducted and subjected to thematic analysis. The participants stated that they used Facebook to receive support, to identify with other mothers, to remember the child who died, to access the child's information, to honor him/her, and to express their feelings. The use of Facebook can play a very important role in the initial phase of grieving due to the functions of this social network.
Identifier
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<a href="http://doi.org/10.1080/07481187.2017.1334011" target="_blank" rel="noreferrer noopener">10.1080/07481187.2017.1334011</a>
Rights
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Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
2018
April 2018 List
Death studies
Exploratory Research
Francisco R
Grief
Human
Maternal Attitudes
Perluxo D
psychosocial
Qualitative Studies
Research Subjects
Semi-Structured Interview
social media
Social Networks
Support
Thematic Analysis
utilization
Women
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Text
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Citation List Month
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URL Address
<a href="http://search.ebscohost.com/login.aspx?direct=true&db=c8h&AN=2001072322&site=ehost-live&scope=site" target="_blank" rel="noreferrer">http://search.ebscohost.com/login.aspx?direct=true&db=c8h&AN=2001072322&site=ehost-live&scope=site</a>
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Title
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Self-concept of siblings of children with cancer
Publisher
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Issues In Comprehensive Pediatric Nursing
Date
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2001
Subject
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Child; Female; Male; Questionnaires; Human; sibling bereavement; Support; Childhood Neoplasms -- Psychosocial Factors; Data Analysis Software; Descriptive Research; Exploratory Research; psychosocial; Purposive Sample; Self Concept -- Evaluation; Self Concept -- In Infancy and Childhood; Siblings -- Psychosocial Factors; Southwestern United States; T-Tests
Creator
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Murray Js
Description
An account of the resource
Childhood cancer can have detrimental effects on the psychosocial well-being of healthy siblings of children with cancer. The limited research done over the past 40 years has identified adjustment difficulties such as poor self-concept, depression, sorrow, anxiety, and feelings of loneliness in children who have a sibling with cancer. To date, clinical research investigating self-concept is scarce as it relates to siblings of children with cancer. The purpose of this study was to examine self-concept in siblings of children with cancer who attended summer camp. A nonprobability purposive sample consisted of 50 school-age siblings of children with cancer. Using the Personal Attribute Inventory for Children (PAIC) to measure children's selfconcept, the researcher found that healthy siblings who attended summer camp scored higher on the PAIL than healthy siblings who did not attend camp. This research suggests that social support such as a camp experience may play an important function in coping with having a brother or sister with childhood cancer.
2001-04
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
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Journal Article
2001
Backlog
Child
Childhood Neoplasms -- Psychosocial Factors
Data Analysis Software
Descriptive Research
Exploratory Research
Female
Human
Issues In Comprehensive Pediatric Nursing
Journal Article
Male
Murray Js
psychosocial
Purposive Sample
Questionnaires
Self Concept -- Evaluation
Self Concept -- In Infancy and Childhood
sibling bereavement
Siblings -- Psychosocial Factors
Southwestern United States
Support
T-Tests