745 related articles for article (PubMed ID: 27383635)
1. Communication and support from health-care professionals to families, with dependent children, following the diagnosis of parental life-limiting illness: A systematic review.
Fearnley R; Boland JW
Palliat Med; 2017 Mar; 31(3):212-222. PubMed ID: 27383635
[TBL] [Abstract][Full Text] [Related]
2. Health and social care professionals' experiences of supporting parents and their dependent children during, and following, the death of a parent: A qualitative review and thematic synthesis.
Franklin P; Arber A; Reed L; Ream E
Palliat Med; 2019 Jan; 33(1):49-65. PubMed ID: 30371147
[TBL] [Abstract][Full Text] [Related]
3. Healthcare users' experiences of communicating with healthcare professionals about children who have life-limiting conditions: a qualitative systematic review protocol.
Ekberg S; Bradford N; Herbert A; Danby S; Yates P
JBI Database System Rev Implement Rep; 2015 Nov; 13(11):33-42. PubMed ID: 26657462
[TBL] [Abstract][Full Text] [Related]
4. The experiences of family members in the year following the diagnosis of a child or adolescent with cancer: a qualitative systematic review.
Mu PF; Lee MY; Sheng CC; Tung PC; Huang LY; Chen YW
JBI Database System Rev Implement Rep; 2015 Jun; 13(5):293-329. PubMed ID: 26455612
[TBL] [Abstract][Full Text] [Related]
5. Parenting experiences of living with a child with attention deficit hyperactivity disorder: a systematic review of qualitative evidence.
Laugesen B; Groenkjaer M
JBI Database System Rev Implement Rep; 2015 Nov; 13(11):169-234. PubMed ID: 26657468
[TBL] [Abstract][Full Text] [Related]
6. The death of patients with terminal cancer: the distress experienced by their children and medical professionals who provide the children with support care.
Otani H; Ozawa M; Morita T; Kawami A; Sharma S; Shiraishi K; Oshima A
BMJ Support Palliat Care; 2019 Jun; 9(2):183-188. PubMed ID: 26847034
[TBL] [Abstract][Full Text] [Related]
7. A family matter--when a parent is diagnosed with multiple sclerosis. A qualitative study.
Boström K; Nilsagård Y
J Clin Nurs; 2016 Apr; 25(7-8):1053-61. PubMed ID: 26868176
[TBL] [Abstract][Full Text] [Related]
8. Providing care to parents dying from cancer with dependent children: Health and social care professionals' experience.
Hanna JR; McCaughan E; Beck ER; Semple CJ
Psychooncology; 2021 Mar; 30(3):331-339. PubMed ID: 33091180
[TBL] [Abstract][Full Text] [Related]
9. [Experiences and needs of parents of hospitalised children with disabilities and the health professionals responsible for the child’s health-care – A systematic review].
Seliner B; Wattinger A; Spirig R
Pflege; 2015 Oct; 28(5):263-76. PubMed ID: 26412679
[TBL] [Abstract][Full Text] [Related]
10. Talking to children about parental mental illness: The experiences of well parents.
Ballal D; Navaneetham J
Int J Soc Psychiatry; 2018 Jun; 64(4):367-373. PubMed ID: 29536794
[TBL] [Abstract][Full Text] [Related]
11. The support needs of parent caregivers of children with a life-limiting illness and approaches used to meet their needs: A scoping review.
Gill FJ; Hashem Z; Stegmann R; Aoun SM
Palliat Med; 2021 Jan; 35(1):76-96. PubMed ID: 33103579
[TBL] [Abstract][Full Text] [Related]
12. Parental Life-Limiting Illness: What Do We Tell the Children?
Fearnley R; Boland JW
Healthcare (Basel); 2019 Mar; 7(1):. PubMed ID: 30897857
[TBL] [Abstract][Full Text] [Related]
13. Parent participation in the care of hospitalized children: a systematic review.
Power N; Franck L
J Adv Nurs; 2008 Jun; 62(6):622-41. PubMed ID: 18503645
[TBL] [Abstract][Full Text] [Related]
14. Different priorities: a comparison of parents' and health professionals' perceptions of quality of life in quadriplegic cerebral palsy.
Morrow AM; Quine S; Loughlin EV; Craig JC
Arch Dis Child; 2008 Feb; 93(2):119-25. PubMed ID: 17932123
[TBL] [Abstract][Full Text] [Related]
15. Healthcare Users' Experiences of Communicating with Healthcare Professionals About Children Who Have Life-Limiting Conditions: A Qualitative Systematic Review.
Ekberg S; Bradford NK; Herbert A; Danby S; Yates P
J Palliat Med; 2018 Oct; 21(10):1518-1528. PubMed ID: 29762072
[TBL] [Abstract][Full Text] [Related]
16. Communication with children and adolescents about the diagnosis of a life-threatening condition in their parent.
Dalton L; Rapa E; Ziebland S; Rochat T; Kelly B; Hanington L; Bland R; Yousafzai A; Stein A;
Lancet; 2019 Mar; 393(10176):1164-1176. PubMed ID: 30894272
[TBL] [Abstract][Full Text] [Related]
17. Going against patients' will? A qualitative study of how palliative health-care professionals handle competing considerations when children are excluded from parental illness and death.
Hogstad IJ; Leer-Salvesen K
Eur J Oncol Nurs; 2020 Dec; 49():101839. PubMed ID: 33120221
[TBL] [Abstract][Full Text] [Related]
18. Challenges, Coping, and Resilience Among Immigrant Parents Caring for a Child With a Disability: An Integrative Review.
Alsharaydeh EA; Alqudah M; Lee RLT; Chan SW
J Nurs Scholarsh; 2019 Nov; 51(6):670-679. PubMed ID: 31637861
[TBL] [Abstract][Full Text] [Related]
19. Exploring risk for abuse of children with chronic conditions or disabilities--parent's perceptions of stressors and the role of professionals.
Svensson B; Eriksson UB; Janson S
Child Care Health Dev; 2013 Nov; 39(6):887-93. PubMed ID: 23461758
[TBL] [Abstract][Full Text] [Related]
20. Negotiating lay and professional roles in the care of children with complex health care needs.
Kirk S
J Adv Nurs; 2001 Jun; 34(5):593-602. PubMed ID: 11380727
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]