Supplementing living kidney transplantees’ medical records with donor- and recipient-narratives
Author:
Funder
EkstraStiftelsen Helse og Rehabilitering
Publisher
Springer Science and Business Media LLC
Subject
Health Policy,Education,Health(social science)
Link
http://link.springer.com/article/10.1007/s11019-017-9822-x/fulltext.html
Reference46 articles.
1. Alnæs, Anne Hambro 2001. Minding Matter. Medical Modernity’s Difficult Decisions. Anthropological thesis, Oslo University, Oslo.
2. Bailey, P.K., Y. Ben-Shlomo, C.R. Tomson, and A. Owen-Smith. 2016. Socioeconomic deprivation and barriers to live-donor kidney transplantation: A qualitative study of deceased-donor kidney transplant recipients. British Medical Journal Open 6 (3): e010605. https://doi.org/10.1136/bmjopen-2015-010605 .
3. Boulware, L.E., F. Hill-Briggs, E.S. Kraus, J.K. Melancon, M. Senga, K.E. Evans, M.U. Troll et al. 2011. Identifying and addressing barriers to African American and non-African American families’ discussions about preemptive living related kidney transplantation. Progress in Transplantation 21 (2):97–104; quiz 105.
4. Boulware, L.E., L.E. Ratner, J.A. Sosa, A.H. Tu, S. Nagula, C.E. Simpkins, R.W. Durant, and N.R. Powe. 2002. The general public’s concerns about clinical risk in live kidney donation. American Journal of Transplantation 2 (2): 186–193.
5. Brown, J.B., M.L. Karley, N. Boudville, R. Bullas, A.X. Garg, and N. Muirhead. 2008. The experience of living kidney donors. Health and Social Work 33 (2): 93–100.
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