(
11
)
|
2017/ Brazil |
To understand the management of emotions involved in the relationship between doctors, mothers, and children in the experience of sharing difficult news in a pediatric and hematological oncology service. |
Descriptive qualitative. P: 9 doctors and 5 mothers. |
2
|
(
12
)
|
2007/ USA and Japan |
To describe patterns of communication at diagnosis between pediatric oncologists and children with cancer and to compare cultural differences in these practices in the US and Japan. |
Cross-sectional quantitative. P: 350 US and 362 Japanese pediatric oncologists. |
4
|
(
13
)
|
2010/ Israel |
To assess parents' experiences with receiving the bad news of the detection of their child's hearing loss. |
Descriptive qualitative. P: 14 families/parents. |
2
|
(
14
)
|
2003/ Australia |
To explore parents' experience of being told that their child had a condition, such as bone dysplasia, that would result in significant short stature. |
Descriptive qualitative. P: 11 family members. |
2
|
(
15
)
|
2010/ Sweden |
To describe the main concern of physicians facing malignant disorders, psychosocial issues and existential provocation; and strategies for handling these challenges. |
Qualitative, Grounded Theory. P: 10 physicians. |
2
|
(
16
)
|
2014/ USA
|
To examine primary care provider experiences with the initial parental disclosure of cystic fibrosis newborn screening results in order to identify methods to improve parent-provider communication during the process. |
Descriptive qualitative. P: 10 primary care providers. |
2
|
(
17
)
|
2014/ Iran |
To explore Iranian mothers' experiences to receive bad news about childhood cancer and to summarize suggestions for improving the delivery of bad news by healthcare providers. |
Descriptive qualitative. P: 14 mothers. |
2
|
(
18
)
|
2000/ Australia |
To investigate the level of parent satisfaction with the first communication of a diagnosis of developmental disability in their child and the determinants of this satisfaction. |
Descriptive qualitative. P: 23 parents. |
2
|
(
19
)
|
2008/ Canada |
To assess how well parents recall discussing the diagnosis of cancer and to summarize suggestions for improvement. |
Cross-sectional quantitative. P: 116 parents. |
4
|
(
20
)
|
2010/ Uganda |
To explore the challenges of providing HIV counselling and testing services to children in Uganda. |
Descriptive qualitative. P: 60 health workers. |
2
|
(
21
)
|
1994/ Australia |
To assess the receptiveness of parents to information given about their child's life threatening illness. |
Descriptive qualitative. P: 25 parents. |
2
|
(
22
)
|
2000/ USA |
To report on parental response to the disclosure and realization that their child has neurofibromatosis 1. |
Descriptive qualitative. P: 18 family members. |
2
|
(
23
)
|
2015/ Malawi |
To explore the experiences of children (10-14 years) living with HIV following the diagnosis disclosure. |
Descriptive qualitative. P: 10 children and 7 caregivers. |
2
|
(
24
)
|
2014/ Brazil |
To learn the experiences of nurses in communicating difficult news to families of hospitalized children in serious condition or process of terminality. |
Descriptive qualitative. P: 9 nursing team professionals. |
2
|
(
25
)
|
2015/ Tanzania |
To assess the determinants and processes of HIV status disclosure to HIV-infected children aged 4 to 17 years receiving HIV care services at the Baylor College of Medicine Children's Foundation Tanzania, Centre of Excellence in Mbeya. |
Cross-sectional quantitative. P: 334 caregivers. |
4
|
(
26
)
|
2012/ South Africa |
To identify beliefs about disclosing HIV diagnosis to HIV-infected children among caregivers, health-care providers, and HIV-positive children who knew their diagnosis. |
Descriptive qualitative. P: 51 caregivers, 24 health-care providers and 5 children. |
4
|
(
27
)
|
2005/ United Kingdom |
To identify the child's reactions and behavior following diagnosis, the parents' views about what to tell their child and factors influencing parents' communication with the child. |
Descriptive qualitative. P: 55 parents. |
2
|
(
28
)
|
2016/ Romania |
To explore children's involvement from the perspective of parents and oncologists. |
Descriptive qualitative. P: 18 caregivers and 10 physicians. |
2
|
(
29
)
|
2015/ Australia and Israel |
To examine the relationship between the diagnosis experience and the disclosure experience for parents of children with developmental disorders of a genetic etiology known as 22q11.2 deletion syndrome. |
Cross-sectional quantitative. P: 559 parents and caregivers. |
4
|
(
30
)
|
2011/ Jordan |
To examine mothers' accounts of communication about cancer diagnosis to their children, how much children knew about their illnesses and how satisfied the mothers were with the method they used in communicating the diagnosis. |
Descriptive qualitative. P: 51 mothers. |
4
|
(
31
)
|
2011/ Saudi Arabia |
To elicit the preferences of Saudi mothers about breaking bad news concerning newborns. |
Randomized clinical trial. P: 402 mothers. |
4
|
(
32
)
|
2013/ Brazil |
To study the meanings that difficult news assumes when transmitted by health professionals to relatives of young cystic fibrosis patients. |
Descriptive qualitative. P: 10 family members. |
2
|
(
33
)
|
2005 Thailand |
To assess diagnosis disclosure status of perinatally acquired HIV-infected Thai children. |
Cross-sectional quantitative. P: 96 primary caregivers |
4
|
(
34
)
|
2016/ Sweden |
To explore how children with cancer want to receive bad news about their disease, such as when no more treatment options are available. |
Descriptive qualitative. P: 10 children |
2
|
(
35
)
|
2015/ Colombia |
To evaluate the effects of the "DIRE" clinical model of disclosing the diagnosis of HIV in children under the age of 17. |
Validation study. P: 41 health professionals, 31 caregivers and 33 children. |
2
|
(
36
)
|
1996/ Netherlands |
To test the hypothesis that being openly informed about the diagnosis and prognosis benefits the emotional well-being of children with cancer. |
Cross-sectional quantitative. P: 56 children and their parents. |
6
|
(
37
)
|
2013/ USA |
To learn about the experience of receiving a diagnosis from parents of children with Williams syndrome. |
Descriptive qualitative. P: 600 families. |
2
|
(
38
)
|
2000/ Germany, Italy, Netherlands, Portugal, Spain, Switzerland, United Kingdom |
To describe the extent to which disclosure of infection status and planning for the future occurs in families with children affected by HIV in seven European countries. |
Cross-sectional quantitative. P: 182 family members. |
4
|
(
39
)
|
2014/ France |
To explore lay people's and professionals' views on breaking bad news to children. |
Cross-sectional quantitative. P: 170 lay persons, 33 nurses and 6 physicians. |
4
|
(
40
)
|
2010/ Democratic Republic of Congo |
To explore the events before, during, and after disclosure to generate a narrative of Congolese children's experiences with being told their HIV status. |
Descriptive qualitative. P: 8 families (7 children and 9 caregivers). |
2
|
(
41
)
|
2013/ USA |
To assess parental perceptions of physicians' interpersonal behaviors and their role in communication of bad news. |
Descriptive qualitative. P: 13 parents. |
2
|
(
42
)
|
2012/ England |
To explore the experiences of the 'feedback session' with nine sets of parents in a community Child and Adolescent Mental Health Service in North East England. |
Descriptive qualitative. P: 9 families. |
2
|
(
43
)
|
2009/ Ireland |
To describe the way that parents are told that their child has disabilities. |
Mixed method. P: 1588 professionals and 584 families. |
4
|
(
44
)
|
2006/ USA |
To determine parent preferences for prognostic information about their children with cancer and the results of receiving such information. |
Cross-sectional quantitative. P: 194 parents. |
4
|
(
45
)
|
2015/ Belgium |
To explore how parents recall circumstances of the cystic fibrosis diagnosis and the information they received; and to investigate their current coping styles. |
Descriptive qualitative. P: 38 parents. |
2
|
(
46
)
|
2012/ Egypt |
To elicit Egyptian mothers' preferences for how to be told the bad news about their child's disability. |
Cross-sectional quantitative. P: 100 mothers. |
4
|
(
47
)
|
2011/ United Kingdom |
To examine parents' views regarding their preadolescent child's presence during discussions about serious illnesses. |
Descriptive qualitative. P: 53 parents. |
2
|
(
48
)
|
2008/ USA |
To describe parents' perceptions of their conversations with physicians regarding their child's terminal illness and death in the pediatric intensive care unit. |
Descriptive qualitative. P: 56 parents. |
2
|
(
49
)
|
2007/ USA |
To identify the aspects of physician communication that children with life-limiting illnesses and their parents perceived to be facilitative or obstructive in pediatric palliative care. |
Descriptive qualitative. P: 20 parents. |
2
|
(
50
)
|
2002/ United Kingdom |
To describe how findings about four preschool children, with difficulties suspected to lie within the autistic spectrum, were negotiated with parents. |
Descriptive qualitative. P: 2 multiprofessional groups. |
2
|