Søk på norsk i Svemed+, eksempel KOLS - finn engelske søkeord fra treff
Se i bøker/artikler og oppslagsverk, feks ordnett.no
Kreft
|
Livets slutt | Påørende |
Hjemmebaserte
|
Palliativ pleie Terminal pleie |
Erfaringer Opplevelser |
Neoplasm* oncology oncologic "Oncologic Nurs*" "Cancer Patient*" |
"end of life" terminal terminally death dying |
Caregiver* "next of kin*" parent*
Barn som pårørende: "child* of Impaired Parent*" ... |
"Home Care" Flere, se emnet Hjemmesykepleie |
"Palliative care" "end of life" terminal terminally death dying
|
experience* ... Søkeord for
...
|
Palliativ plan: ("care plan*" OR "Individual plan" OR "care pathway*") AND (palliative OR "end of life" OR terminal*")
Forhåndssamtaler: "advance care planning" OR "advance directiv*"
Bøker finner du via søk i ORIA
Ta en kikk på våre hyller for å lete etter aktuelle bøker - se hylle-plasseringer nedenfor. Klikk for oppslag i ORIA
sørg for å være tilkoblet UiA nettet med VPN se informasjon her
Norsk elektronisk legehåndbok
UpToDate (krever eduVPN også på campus)
"Child, Hospitalized" "Childhood Neoplasms"¨ |
child* pediatric* |
"quality of life" psychosocial*
"self care" play* ... |
cancer* neoplams* leukemi* tumor tumors |
Chemotherap* Cytostatic* "Antineoplastic Agent*" "Antitumor Agent*"
Nausea vomiting symtom*
prevent* control* management* assess* measure* |
parent* mother* father* sibling* "parent-child relations" family
|
Oversiktsartikkel: Alya, F. P., Sri, H. & and Mediani, H. S. (2025). Factors Associated with Psychological Well-Being Among Children Under 18 Years Old with Cancer: A Scoping Review. Psychology Research and Behavior Management, 18(null), 39-53. https://doi.org/10.2147/PRBM.S488905
Linder, L. A., Bratton, H., Nguyen, A., Parker, K., & Wawrzynski, S. E. (2018). Symptoms and Self-Management Strategies Identified by Children With Cancer Using Draw-and-Tell Interviews. Oncology Nursing Forum, 45(3), 290–300. https://doi.org/10.1188/18.ONF.290-300
Larsen, M. H., Hansson, K. E., Larsen, E. H., Fridh, M. K., Petersen, N. N., Mellblom, A. V., Ruud, E., Larsen, H. B., & Lie, H. C. (2022). The gap between expectations and reality: A qualitative study of psychosocial challenges of young childhood cancer survivors from the PACCS study. European Journal of Cancer Care, 31(6), 1–11. https://doi.org/10.1111/ecc.13696
Braam, K. I., van Dijk-Lokkart, E. M., Kaspers, G. J. L., Takken, T., Huisman, J., Buffart, L. M., Bierings, M. B., Merks, J. H. M., van den Heuvel-Eibrink, M. M., Veening, M. A. & van Dulmen-den Broeder, E. (2018). Effects of a combined physical and psychosocial training for children with cancer: a randomized controlled trial. BMC Cancer, 18(1), 1289. https://doi.org/10.1186/s12885-018-5181-0
Dijk, L. E. M., Braam, K. I., Dulmen, den B. E., Kaspers, G. J. L., Takken, T., Grootenhuis, M. A., Streng, I. C., Bierings, M., Merks, J. H., den Heuvel, E. M. M., Veening, M. A., & Huisman, J. (2016). Effects of a combined physical and psychosocial intervention program for childhood cancer patients on quality of life and psychosocial functioning: results of the QLIM randomized clinical trial. Psycho-Oncology, 25(7), 815–822. https://doi.org/10.1002/pon.4016
Şenol, F. B., & Şenol, Y. (2024). The effect of drama on psychosocial problems and emotional states of hospitalized children with cancer. Journal of Pediatric Nursing, 77, e276–e282. https://doi.org/10.1016/j.pedn.2024.04.041
søk på ord i tittel: TI (nurs* AND child* AND (cancer* OR leukem* OR neoplasm* OR tumor*)) - limit: 2005- Språk; norsk,dansk,svensk,engelsk link til søk
Bøker
Varre, P. (2017). Sykepleieutfordringer ved kjemoterapi. I A. M. Reitan & T. K. Schjølberg (Red.), Kreftsykepleie : pasient, utfordring, handling (4. utg.). Oslo: Cappelen Damm akademisk. Søk i ORIA
Artikler
Og videre
Se også bøker - tips på emnesiden Hjemmesykepleie
Lersveen Gunhild, L. & Devik Siri, A. Opplevelse av trygghet i hjemmebasert palliativ omsorg: pasienters og pårørendes perspektiv. Tidsskrift for omsorgsforskning, 7(3), 1-15. https://doi.org/10.18261/issn.2387-5984-2021-03-05
Aamold, K., Grov, K. & Rostad Hanne, M. Hjemmesykepleieres erfaringer når kreftpasienter ønsker å dø hjemme. Klinisk Sygepleje, 34(1), 3-15. https://doi.org/10.18261/issn.1903-2285-2020-01-02
Røgenes, G. K., Moen, A. & Grov, E. K. (2013). Heimesjukepleiarens perspektiv på forhold som fremjar palliasjon i heimen. Klinisk Sygepleje, 27(1), 64-76. Hentet fra Idunn.no
Drageset, I. (2009). Forholdet mellom avhengighet og autonomi i hjemmesykepleien. Klinisk Sygepleje, 23(2), 15-23. Hentet fra Idunn.no
Hov, R., Bjørsland, B., Kjøs, B. Ø. & Wilde-Larsson, B. (2021). Pasienters opplevelse av trygghet med palliativ omsorg i hjemmet. Tidsskrift for omsorgsforskning, 7(1), 1-19. https://doi.org/10.18261/issn.2387-5984-2021-01-05
Midlöv, E. M., & Lindberg, T. (2019). District nurses’ experiences of providing palliative care in the home: An interview study. Nordic Journal of Nursing Research. https://doi.org/10.1177/2057158519857002
Molnes, S. I. (2014). Sykepleieres erfaringer med smertelindring til hjemmeboende kreftpasienter. Nordisk sygeplejeforskning 4
(2), 142-155. https://doi.org/10.18261/ISSN1892-2686-2014-02-06
Sønning, H. E. & Fossum, M. (2020). "Jeg gråter noen tårer hver dag". En fenomenologisk studie av hjemmeboende kreftpasienters beskrivelse av deres livvsituasjon i palliativ fase. Nordisk tidsskrift for helseforskning, 16(1), 16. https://doi.org/10.7557/14.4319
Lersveen, G. L. & Devik, S. A. (2021). Opplevelse av trygghet i hjemmebasert palliativ omsorg: pasienters og pårørendes perspektiv. Tidsskrift for omsorgsforskning, 7(3), 1-15. https://doi.org/10.18261/issn.2387-5984-2021-03-05
hjemmesykepleie - se emnet hjemmesykepleie - feks "home care" OR homebased OR "home based" OR "home health*" OR "home nurs'" OR "district* nurs*" OR "Community Health*"
palliativ*
terminal*
"end of life" OR "last day*" OR death OR dying
cancer OR neoplasm*
dignit*
hope*
uncertain*
stress
anxity
cope OR coping OR adapt*
experience* OR attitude* OR perception* OR satisfact* OR opinion* OR view* OR belie* OR perspective*
qualitative OR interview* OR phenomenolog* OR thematic OR themes
Pårørende: caregiver* OR "care giver*" OR famil* OR relatives OR "next of kin*" OR spous* OR ...
Eksempeler på søk- og lenker til treff
Noen treff
Borstrand, I. & Berg, L. (2009). Närståendes erfarenheter av ett palliativt hemsjukvårdsteam. Vård i Norden, 29(4), 15-19. http://dx.doi.org/10.1177/010740830902900404
Brazil, K., Bainbridge, D., Poloeg, J., Krueger, P., Taniguchi, A. & Marshall, D. (2012). Family caregiver views on patient-centred care at the end of life. Scandinavian Journal of Caring Sciences, 26(3), 513-518. http://dx.doi.org/10.1111/j.1471-6712.2011.00956.x
Eilertsen, I. & Kiik, R. (2016). Nurses’ emotional challenges in providing home care in Norway. Nordic Journal of Nursing Research, 36(2), 82-87. http://dx.doi.org/10.1177/2057158515623406
Grov, E. K. (2012). Hjemmet som lindrende enhet for gamle döende. Geriatrisk Sykepleie, 4(3), 26-33. Hentet fra https://www.nsf.no/Content/1012049/Geriatrisk%20hjemmet_som_lindrende_enhet_541.pdf
Molnes, S. I. (2014). Sykepleieres erfaringer med smertelindring til hjemmeboende kreftpasienter. Nordisk Sygeplejeforskning, 4(2), 142-155. Hentet fra https://www.idunn.no/nsf/2014/02/sykepleieres_erfaringer_medsmertelindring_til_hjemmeboende
Mousing, C. A., Timm, H., Kirkevold, M. & Lomborg, K. (2018). Receiving home care and communicating about COPD-related concerns and palliative care. A qualitative study of the patient perspectives. Nordisk Sygeplejeforskning, 8(2), 107-121. https://doi.org/10.18261/issn.1892-2686-2018-02-03
Neergaard, M. A., Bonde Jensen, A., Sondergaard, J., Sokolowski, I., Olesen, F. & Vedsted, P. (2011). Preference for place-of-death among terminally ill cancer patients in Denmark. Scandinavian Journal of Caring Sciences, 25(4), 627-636. http://dx.doi.org/10.1111/j.1471-6712.2011.00870.x
Nordsveen, H. & Andershed, B. (2015). Pasienter med kreft i palliativ fase på vei hjem - Sykepleieres erfaringer av samhandling. Nordisk Sygeplejeforskning, 5(3), 239-252. Hentet fra https://www.idunn.no/nsf/2015/03/pasienter_med_kreft_i_palliativ_fase_paa_vei_hjem_-_sykeplei
Pusa, S., Hägglund, K., Nilsson, M. & Sundin, K. (2015). District nurses' lived experiences of meeting significant others in advanced home care. Scandinavian Journal of Caring Sciences, 29(1), 93-100. http://dx.doi.org/10.1111/scs.12134
Rögenes, G. K., Moen, A. & Grov, E. K. (2013). Heimesjukepleiarens perspektiv på forhold som fremjar palliasjon i heimen. Klinisk Sygepleje, 27(1), 64-76. Hentet fra http://www.idunn.no/klinisk_sygepleje/2013/01/heimesjukepleiarens_perspektiv_paa_forhold_som_fremjar_palli
Saarnio, L., Boström, A.-M., Gustavsson, P. & Öhlen, J. (2016). Meanings of at-homeness at end-of-life among older people. Scandinavian Journal of Caring Sciences, 30(2), 312-319. http://dx.doi.org/ 10.1111/scs.12246
Smedman, A., Gustafsson, K. & Flesner, G. (2015). Att vårda äldre personer på särskilt boende under livets slutskede - Undersköterskornas. Nordisk Sygeplejeforskning, 5(2), 87-92. Hentet fra https://www.idunn.no/nsf/2015/02/att_vaarda_ldre_personer_paasrskilt_boende_under_livetssl
Sörhus, G. S., Landmark, B. T. & Grov, E. K. (2016). Ansvarlig og avhengig - Pårörendes erfaringer med forestående död i hjemmet. Klinisk Sygepleje, 30(2), 87-100. http://dx.doi.org/10.18261/issn.1903-2285-2016-02-03
Eksempel
TI ((home OR homebased OR home-based OR district*) NOT "nursing home*" ) AND TI (palliative OR terminal* OR "end of life")) - lenke til søk
(TI ((home OR homebased OR home-based OR district*) NOT "nursing home*" ) AND TI cancer) NOT "nursing home" Lenke til søk
TI foran søkeord = ordene må stå i artikkelens tittel
Söderman, A., Werkander Harstäde, C., Östlund, U., & Blomberg, K. (2021). Community nurses’ experiences of the Swedish Dignity Care Intervention for older persons with palliative care needs – A qualitative feasibility study in municipal home health care. International Journal of Older People Nursing, 16(4), 1–12. https://doi.org/10.1111/opn.12372
Staats, K., Grov, E. K., Husebø, B. S., & Tranvåg, O. (2021). Dignity of older home-dwelling women nearing end-of-life: Informal caregivers’ perception. Nursing Ethics, 28(3), 444–456. https://doi.org/10.1177/0969733020956372
Devik, S. A., Enmarker, I., & Hellzen, O. (2020). Nurses’ experiences of compassion when giving palliative care at home. Nursing Ethics, 27(1), 194–205. https://doi.org/10.1177/0969733019839218
Midlöv, E. M., & Lindberg, T. (2020). District nurses’ experiences of providing palliative care in the home: An interview study. Nordic Journal of Nursing Research, 40(1), 15–24. https://doi.org/10.1177/2057158519857002
Becqué, Y. N., Rietjens, J. A. C., van Driel, A. G., van der Heide, A. & Witkamp, E. (2019). Nursing interventions to support family caregivers in end-of-life care at home: A systematic narrative review. International Journal of Nursing Studies, 97, 28-39. https://doi.org/10.1016/j.ijnurstu.2019.04.011
Alvariza, A., Mjörnberg, M., & Goliath, I. (2020). Palliative care nurses’ strategies when working in private homes—A photo‐elicitation study. Journal of Clinical Nursing (John Wiley & Sons, Inc.), 29(1/2), 139–151. https://doi.org/10.1111/jocn.15072
Bolt, S. R., van der Steen, J. T., Schols, J. M. G. A., Zwakhalen, S. M. G., Pieters, S. & Meijers, J. M. M. (2019). Nursing staff needs in providing palliative care for people with dementia at home or in long-term care facilities: A scoping review. International Journal of Nursing Studies, 96, 143-152. https://doi.org/10.1016/j.ijnurstu.2018.12.011
Danielsen, B. V., Sand, A. M., Rosland, J. H. & Førland, O. (2018). Experiences and challenges of home care nurses and general practitioners in home-based palliative care – a qualitative study. BMC Palliative Care, 17(1), N.PAG-N.PAG. https://doi.org/10.1186/s12904-018-0350-0
Devik, S. A., Enmarker, I. & Hellzen, O. (2020). Nurses' experiences of compassion when giving palliative care at home. Nursing Ethics, 27(1), 194-205. https://doi.org/10.1177/0969733019839218
Griffiths, J., Ewing, G. & Rogers, M. (2010). 'Moving swiftly on.' Psychological support provided by district nurses to patients with palliative care needs. Cancer Nursing, 33(5), 390-397. https://doi.org/10.1097/NCC.0b013e3181d55f9b
Hemberg, J. & Bergdahl, E. (2019). Cocreation as a Caring Phenomenon: Nurses' Experiences in Palliative Home Care. Holistic Nursing Practice, 33(5), 273-284. https://doi.org/10.1097/HNP.0000000000000342
Holmdahl, S., Sävenstedt, S. & Imoni, R. (2014). Parenteral nutrition in home-based palliative care: Swedish district nurses experiences. Scandinavian Journal of Caring Sciences, 28(1), 89-96. https://doi.org/10.1111/scs.12038
Hunstad, I. & Svindseth, M. F. (2011). Challenges in home-based palliative care in Norway: a qualitative study of spouses' experiences. International Journal of Palliative Nursing, 17(8), 398-404. Hentet fra http://search.ebscohost.com/login.aspx?direct=true&db=cin20&AN=104688935&site=ehost-live
Karlsson, M., Karlsson, C., Barbosa da Silva, A., Berggren, I. & Söderlund, M. (2013). Community nurses' experiences of ethical problems in end-of-life care in the patient's own home. Scandinavian Journal of Caring Sciences, 27(4), 831-838. https://doi.org/10.1111/j.1471-6712.2012.01087.x
LeeAi, C. & Abdullah, A. (2017). Community Palliative Care Nurses' Challenges and Coping Strategies on Delivering Home-Based Pediatric Palliative Care: A Qualitative Study. American Journal of Hospice & Palliative Medicine, 34(2), 125-131. https://doi.org/10.1177/1049909115607296
Lima Ribeiro, A., Leite de Almeida, C. S., de Oliveira Reticena, K., Guimarães Maia, M. R. & Aparecida Sales, C. (2014). Nursing in the home palliative care: the view of a family member of a patient with cancer. Rev Rene, 15(3), 499-507. https://doi.org/10.15253/2175-6783.2014000300015
Linderholm, M. & Friedrichsen, M. (2010). A desire to be seen: family caregivers' experiences of their caring role in palliative home care. Cancer Nursing, 33(1), 28-36. https://doi.org/10.1097/NCC.0b013e3181af4f61
Mousing, C. A., Timm, H., Lomborg, K. & Kirkevold, M. (2018). Barriers to palliative care in people with chronic obstructive pulmonary disease in home care: A qualitative study of the perspective of professional caregivers. Journal of Clinical Nursing (John Wiley & Sons, Inc.), 27(3-4), 650-660. https://doi.org/10.1111/jocn.13973
McWilliam, C. L., Ward-Griffin, C., Oudshoorn, A. & Krestick, E. (2008). Living While Dying/Dying While Living. Older Clients' Sociocultural Experience of Home-Based Palliative Care. Journal of Hospice and Palliative Nursing, 10(6), 338-349. https://doi.org/10.1097/01.NJH.0000319190.93906.7d
Offen, J. (2015). The role of UK district nurses in providing care for adult patients with a terminal diagnosis: a meta-ethnography. International Journal of Palliative Nursing, 21(3), 134-141. https://doi.org/10.12968/ijpn.2015.21.3.134
Rabbetts, L., Harrington, A. & Breaden, K. (2020). Nurses' experience of providing home‐based palliative care in the country setting: An integrated literature review. International Journal of Nursing Practice (John Wiley & Sons, Inc.), 26(1), N.PAG-N.PAG. https://doi.org/10.1111/ijn.12773
Reid, F. (2013). Grief and the experiences of nurses providing palliative care to children and young people at home. Nursing Children and Young People, 25(9), 31-36. https://doi.org/10.7748/ncyp2013.11.25.9.31.e366
Rogenes, G. K., Moen, A. & Grov, E. K. (2013). Home care nurses' perspectives of factors of importance for their ability to care for patients requiring palliative care at home. Klinisk Sygepleje, 27(1), 65-76. Hentet fra http://search.ebscohost.com/login.aspx?direct=true&db=cin20&AN=108002690&site=ehost-live
Rydé, K. & Hjelm, K. (2016). How to support patients who are crying in palliative home care: an interview study from the nurses' perspective. Primary Health Care Research & Development (Cambridge University Press / UK), 17(5), 479-488. https://doi.org/10.1017/S1463423616000037
Schou‐Andersen, M., Ullersted, M. P., Jensen, A. B. & Neergaard, M. A. (2016). Factors associated with preference for dying at home among terminally ill patients with cancer. Scandinavian Journal of Caring Sciences, 30(3), 466-476. https://doi.org/10.1111/scs.12265
Svensson, G. (2018). Patient perceptions of specialised hospital-based palliative home care: a qualitative study using a phenomenographical approach. International Journal of Palliative Nursing, 24(1), 22-32. https://doi.org/10.12968/ijpn.2018.24.1.22
Walshe, C. & Luker, K. A. (2010). District nurses’ role in palliative care provision: A realist review. International Journal of Nursing Studies, 47(9), 1167-1183. https://doi.org/10.1016/j.ijnurstu.2010.04.006
Og videre kreft i tittelen ...
Appleyard, S. E. & Clarke, C. (2018). An interpretative phenomenological analysis of the experiences of older people self-managing cancer pain at home. Journal of Psychosocial Oncology, 36(3), 333-349. https://doi.org/10.1080/07347332.2017.1417949
Dunne, K., Sullivan, K. & Kernohan, G. (2005). Palliative care for patients with cancer: district nurses' experiences. Journal of Advanced Nursing (Wiley-Blackwell), 50(4), 372-380. https://doi.org/10.1111/j.1365-2648.2005.03402.x
Griffiths, J., Ewing, G. & Rogers, M. (2013). Early support visits by district nurses to cancer patients at home: A multi-perspective qualitative study. Palliative Medicine, 27(4), 349-357. https://doi.org/10.1177/0269216312451949
Heydari, H., Hojjat-Assari, S., Almasian, M. & Pirjani, P. (2019). Exploring health care providers' perceptions about home-based palliative care in terminally ill cancer patients. BMC Palliative Care, 18(1), N.PAG-N.PAG. https://doi.org/10.1186/s12904-019-0452-3
Lima Ribeiro, A., Leite de Almeida, C. S., de Oliveira Reticena, K., Guimarães Maia, M. R. & Aparecida Sales, C. (2014). Nursing in the home palliative care: the view of a family member of a patient with cancer. Rev Rene, 15(3), 499-507. https://doi.org/10.15253/2175-6783.2014000300015
Luker, K., Cooke, M., Dunn, L., Lloyd-Williams, M., Pilling, M. & Todd, C. (2015). Development and evaluation of an intervention to support family caregivers of people with cancer to provide home-based care at the end of life: A feasibility study. European Journal of Oncology Nursing, 19(2), 154-161. https://doi.org/10.1016/j.ejon.2014.09.006
Mohammed, S., Swami, N., Pope, A., Rodin, G., Hannon, B., Nissim, R., … Zimmermann, C. (2018). "I didn't want to be in charge and yet I was": Bereaved caregivers' accounts of providing home care for family members with advanced cancer. Psycho-Oncology, 27(4), 1229-1236. https://doi.org/10.1002/pon.4657
Ndiok, A. & Ncama, B. (2019). A qualitative study of home visiting as a palliative care strategy to follow‐up cancer patients by nurses in clinical setting in a developing country. Scandinavian Journal of Caring Sciences, 33(1), 185-196. https://doi.org/10.1111/scs.12619
Noot, T., Tassanee, T., Forrester, D. A. & Pimpan, S. (2016). Experiences of People with Advanced Cancer in Home--Based Palliative Care. Pacific Rim International Journal of Nursing Research, 20(3), 238-251. Hentet fra http://search.ebscohost.com/login.aspx?direct=true&db=cin20&AN=116406915&site=ehost-live
Oosterveld-Vlug, M. G., Custers, B., Hofstede, J., Donker, G. A., Rijken, P. M., Korevaar, J. C. & Francke, A. L. (2019). What are essential elements of high-quality palliative care at home? An interview study among patients and relatives faced with advanced cancer. BMC Palliative Care, 18(1), N.PAG-N.PAG. https://doi.org/10.1186/s12904-019-0485-7
Pirschel, C. (2019). No Place Like It: Home Care for Patients With Cancer. ONS Voice, 34(7), 22-26. Hentet fra http://search.ebscohost.com/login.aspx?direct=true&db=cin20&AN=137415878&site=ehost-live
Sijabat, M., Dahlia, D. & Waluyo, A. (2019). Experiences of palliative care nurses in providing home-based care for patient with advanced cancer. Enfermeria Clinica, 29, 413-417. https://doi.org/10.1016/j.enfcli.2019.04.060
Wilson, C., Griffiths, J., Ewing, G., Connolly, M. & Grande, G. (2014). A Qualitative Exploration of District Nurses' Care of Patients With Advanced Cancer. Cancer Nursing, 37(4), 310-315. https://doi.org/10.1097/NCC.0b013e31829a9a56
Wilson, K., Pateman, B., Beaver, K. & Luker, K. A. (2002). Patient and carer needs following a cancer-related hospital admission: the importance of referral to the district nursing service. Journal of Advanced Nursing (Wiley-Blackwell), 38(3), 245-253. https://doi.org/10.1046/j.1365-2648.2002.02173.x
Se også emnesiden Smerter
Populasjon: Nurse* OR nursing – avgrenset til tittel: TI (nurse* OR nursing)
Fenomen av interesse, Erfaringer ... med smerte
Eksempel på treff
og
Oversiktsarikkel, review
Søkeord hjemme... ala her ord i tittel:
TI (home OR homecare OR homebased OR homehealth OR community OR district* OR municipal* OR "primary health*")
Eksempel på treff:
Hofset Larsen, B. & Nortvedt, M. W. (2011). Barns og ungdomsinformasjonsbehov når mor eller far får kreft. Sykepleien Forskning, 6(1), 70-77. https://doi.org/10.4220/sykepleienf.2011.0068
"child* of Impaired Parent*" AND (cancer OR neoplasm* OR oncolog*)
"Parent-Child Relations" AND (cancer OR neoplasm* OR oncolog*)
--
"adptation, Psychological"
bereavement
cancer OR neoplasm* OR oncolog*
child*
coping OR cope OR adapt*
uncertain*
anxiety
stress
death
"family Centered Care"
palliative
parent*
"psychosocial Factor*"
"social support*"
terminal*
"Terminally Ill Patient*"
"end of life"
parent* W2 cancer - eller bredere, og med feltkode for at ordene skal finnes i tittelen: TI (parent* W5 cancer)
(dependent W1 child*) AND (cancer OR neoplasm*) AND (parent* OR mother* OR father* OR famil*)
(child* W2 (relatives OR "next of kin")) AND (cancer OR neoplasm*)
W# = nærhetsoperator EBSCOhost databaser, det første ordet må komme før det andre, # angir antall ord som kan tillates mellom søkeordene, Se filmen:
Hauger, B., Wiker, M., & Hamnes, B. (2020). Sykepleiere strekker ikke til i arbeid med barn som pårørende. Nordisk sygeplejeforskning, 10(4), 266-279. https://doi.org/10.18261/issn.1892-2686-2020-04-05 Bakgrunn: Sykepleier plikter etter Norsk lovverk å ivareta mindreårige barn som pårørende. Studier tyder på at dette arbeidet ikke er tilstrekkelig ivaretatt, og fordi barn som pårørende er et satsningsområde er det behov for mer forskning om hvordan det jobbes med barna, samt hvordan dette arbeidet virker. Hensikt: Å utforske sykepleieres opplevelser med oppfølging av barn som pårørende av kreftpasienter i palliativ fase i sykehjem. Metode: Kvalitativ deskriptiv studie, der datainnsamlingen er gjennom individuelle intervjuer. Kvale & Brinkmanns stadier for intervjuundersøkelse er anvendt. Studien undersøker femten sykepleiere med gjennomsnitt syv års erfaring med barn som pårørende i aldersgruppen 0-18 år på sykehjem. Resultat: Analysen av datamaterialet resulterte i tre temaer som beskrev informantenes opplevelser i møte barn som pårørende, og omhandlet sykepleiers opplevelse av utilstrekkelighet, deres ønske om mer kompetanse samt opplevelse av lite støtte fra ledelsen. Konklusjon: Sykepleierne ønsker å gjøre en god jobb med barna, men opplever at de ikke strekker til i arbeidet med barn som pårørende, og at de har for lite kompetanse til å ivareta barna.
Olesen, P. K., & Thestrup Hansen, S. (2024). Advancing nursing care for relatives of patients diagnosed with colorectal cancer: Insights from a qualitative study. Nordisk sygeplejeforskning, 15(2), 1-15. https://doi.org/10.18261/nsf.15.2.4
Relatives of patients with colorectal cancer (CC) can be psychosocially affected to such an extent that they risk becoming ill themselves. The aim of this study was 1) to investigate how relatives of people with CC experience the need for nursing support during the hospital stay and at home, which can help improve their health; 2) To generate knowledge that advances and contributes to the development of evidence-based clinical nursing for this group of relatives. The study was based on interviews of relatives of people with CC. The data was analyzed using reflexive thematic analysis and discussed from a health-promoting perspective with the theory on the sense of coherence, and ‘family dialogue’. Findings include that relatives express a need for professional nursing support, with disease management, tailored communication, and coping assistance. This study suggests that advancing nursing practice focusing on support of relatives of individuals with CC in future clinical practice may enhance the health of these relatives.
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Hauger, B., Wiker, M. & Hamnes, B. (2020). Sykepleiere strekker ikke til i arbeid med barn som pårørende. Nordisk sygeplejeforskning, 10(4), 266-279. https://doi.org/10.18261/issn.1892-2686-2020-04-05 Link til artikkelen på Idunn.no
Hofset Larsen, B. & Nortvedt, M. W. (2011). Barns og ungdomsinformasjonsbehov når mor eller far får kreft. Sykepleien Forskning, 6(1), 70-77. https://doi.org/10.4220/sykepleienf.2011.0068
Semple, C. J., McCaughan, E., Smith, R., & Hanna, J. R. (2022). Parent’s with incurable cancer: “Nuts and bolts” of how professionals can support parents to communicate with their dependent children. Patient Education & Counseling, 105(3), 775–780. https://doi.org/10.1016/j.pec.2021.06.032
Holmberg, P., Nilsson, J., Elmqvist, C., & Lindqvist, G. (2020). Nurses’ encounters with children as next of kin to parents with a cancer diagnosis on oncology wards. Nordic Journal of Nursing Research, 40(1), 33–40. https://doi.org/10.1177/2057158519868437
Hauken, M. A., & Farbrot, I. M. M. (2022). The Fuelbox “Young Next of Kin”-A Mixed-Methods Study on the Development and Piloting of a Communication Tool for Adolescents Coping With Parental Cancer or Death. Cancer Nursing, 45(2), 148–160. https://doi.org/10.1097/NCC.0000000000000960
Ellis, S. J., Wakefield, C. E., Antill, G., Burns, M., & Patterson, P. (2017). Supporting children facing a parent’s cancer diagnosis: a systematic review of children’s psychosocial needs and existing interventions. European Journal of Cancer Care, 26(1), https://doi.org/10.1111/ecc.12432