Halverson Colin M E, Wang Jackie Y, Poulson Michael, Karlin Jennifer, Crowley-Matoka Megan, Ross Lainie F
Georgetown University School of Medicine, Washington D.C., USA.
Am J Nephrol. 2016;43(6):389-96. doi: 10.1159/000446161. Epub 2016 May 25.
Psychosocial data about living kidney donors have been collected for almost 5 decades now. To date, however, no study has provided any psychosocial follow-up of donors who developed a serious health problem such as end-stage renal disease (ESRD).
Donors who developed ESRD were invited to participate in a qualitative interview if they met one or both of the inclusion criteria: (1) developed ESRD within 10 years of donating and/or (2) lacked health insurance at the time of donation. We contacted 38 individuals who met these criteria, and 22 participated (58%). Two were subsequently excluded from analysis.
Twenty qualitative interviews were analyzed. Five findings are described: (1) donors describe the decision-making process as spontaneous and fast; (2) donors describe lack of appreciation for the need for post-donation self-care; (3) donors do not regret donating despite the adverse outcome; (4) donors advise future donors to have in place emotional and physical support post donation; and (5) donors appreciate the opportunity to tell their story from being a living donor to living with ESRD, which virtually all perceive as 2 separate unrelated events.
Most donors are positive about their donation decision and experience and would donate again, despite developing ESRD themselves. They propose some important changes to the decision-making and informed-consent processes. Our data are reassuring regarding lack of donor regret, but highlight the need for living donor transplant programs to ensure that living donors understand their long-term risks and receive appropriate life-long follow-up care to minimize these risks.
关于活体肾供者的社会心理数据收集至今已有近50年。然而,迄今为止,尚无研究对出现诸如终末期肾病(ESRD)等严重健康问题的供者进行任何社会心理随访。
若符合以下一项或两项纳入标准,即邀请出现ESRD的供者参与定性访谈:(1)在捐献后10年内出现ESRD和/或(2)捐献时缺乏健康保险。我们联系了38名符合这些标准的个体,22人参与(58%)。随后有2人被排除在分析之外。
对20次定性访谈进行了分析。描述了五项发现:(1)供者将决策过程描述为自发且迅速;(2)供者表示对捐献后自我护理的必要性缺乏认识;(3)尽管出现不良后果,供者并不后悔捐献;(4)供者建议未来的供者在捐献后要有情感和身体上的支持;(5)供者感激有机会讲述从活体供者到患ESRD患者的经历,几乎所有人都将这视为两个独立且不相关的事件。
大多数供者对他们的捐献决定和经历持积极态度,即使自身患了ESRD也会再次捐献。他们提议对决策和知情同意过程进行一些重要改变。我们的数据显示供者没有后悔,这让人安心,但也凸显了活体供者移植项目需要确保活体供者了解其长期风险并接受适当的终身随访护理,以将这些风险降至最低。