Request for organ donation without donor registration: a qualitative study of the perspectives of bereaved relatives

被引:31
作者
de Groot, Jack [1 ,2 ]
van Hoek, Maria [1 ]
Hoedemaekers, Cornelia [3 ]
Hoitsma, Andries [4 ]
Schilderman, Hans [5 ]
Smeets, Wim [1 ,2 ]
Vernooij-Dassen, Myrra [1 ,6 ]
van Leeuwen, Evert [1 ]
机构
[1] Radboud Univ Nijmegen, Radboud Inst Hlth Sci, Med Ctr, DGVP 20,POB 91016500, Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Dept Spiritual & Pastoral Care, Med Ctr, Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Dept Intens Care Med, Med Ctr, Nijmegen, Netherlands
[4] Radboud Univ Nijmegen, Dept Nephrol, Med Ctr, Nijmegen, Netherlands
[5] Radboud Univ Nijmegen, Fac Philosophy Theol & Religious Studies, Nijmegen, Netherlands
[6] Kalorama Fdn, Nijmegen, Netherlands
关键词
Decision making by proxies; Donor registration; Ethics; Organ transplantation; Professional-family relations; Informational needs; DECISION-MAKING; FAMILY CONSENT;
D O I
10.1186/s12910-016-0120-6
中图分类号
B82 [伦理学(道德学)];
学科分类号
摘要
Background: In the Netherlands, consent from relatives is obligatory for post mortal donation. This study explored the perspectives of relatives regarding the request for consent for donation in cases without donor registration. Methods: A content analysis of narratives of 24 bereaved relatives (14 in-depth interviews and one letter) of unregistered, eligible, brain-dead donors was performed. Results: Relatives of unregistered, brain-dead patients usually refuse consent for donation, even if they harbour pro-donation attitudes themselves, or knew that the deceased favoured organ donation. Half of those who refused consent for donation mentioned afterwards that it could have been an option. The decision not to consent to donation is attributed to contextual factors, such as feeling overwhelmed by the notification of death immediately followed by the request; not being accustomed to speaking about death; inadequate support from other relatives or healthcare professionals, and lengthy procedures. Conclusion: Healthcare professionals could provide better support to relatives prior to donation requests, address their informational needs and adapt their message to individual circumstances. It is anticipated that the number of consenting families could be enlarged by examining the experience of decoupling and offering the possibility of consent for donation after circulatory death if families refuse consent for donation after brain-death.
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页数:14
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