Testing the Differential Access Hypothesis That Black Kidney Transplant Candidates Perceive Social Network Access to Fewer Potential Living Donors Than White Candidates.
Jonathan Daw, Mary Roberts, Avrum Gillespie, Ashton M Verdery, Tanjala S Purnell
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引用次数: 0
Abstract
Introduction: Many studies of Black-White disparities in living donor kidney transplantation hypothesize that they were partially due to Black-White differences in candidate social network access to healthy, willing donors. This differential access hypothesis has not been tested using directly measured social network data.
Research questions: Do black kidney transplant candidates have perceived lower social network access to health and/or willing living donors than white candidates?
Design: A cross-sectional survey that measured the social network members was collected in 2015. Black-White differences in patient counts of perceived healthy and/or willing potential donors in social networks, and individual network members' probability of being perceived healthy and/or willing, were compared using logistic and negative binomial regression models.
Results: The survey included 66 kidney transplant candidates reporting on 1474 social network members at a large Southeastern US transplant center in 2015. Black and White patients had similar access to perceived healthy, likely potential donors (86% vs 87% had 1 or more, P = .92; 5.91 vs 4.13 mean counts, P = .20) and perceived healthy, agreed potential donors (56% vs 48%, P = .54; 1.77 vs 1.74, P = .97). Black patients' network members were individually more likely to be perceived healthy and likely potential donors (26% vs 21%, P = .04), and White patients' network members were more likely to have agreed (13% vs 9%, P = .03), but these differences were statistically insignificant in demographically adjusted models.
Conclusion: Black and White transplant candidates perceived access to similar numbers of potential donors in their social networks. This result does not support the differential access hypothesis.
引言:许多关于活体肾移植中黑人和白人差异的研究假设,部分原因是黑人和白人在获得健康、自愿供体的候选社会网络方面存在差异。这种差异访问假设尚未使用直接测量的社交网络数据进行测试。研究问题:与白人候选人相比,黑人肾脏移植候选人在社会网络中获得健康和/或愿意的活体捐赠者的机会是否更低?设计:2015年收集了一份衡量社交网络成员的横断面调查。使用逻辑回归模型和负二项回归模型比较了社会网络中被认为健康和/或愿意的潜在捐赠者的患者数量和个体网络成员被认为健康和/或愿意的概率的黑白差异。结果:该调查包括66名肾移植候选人,报告了2015年美国东南部一家大型移植中心的1474名社交网络成员。黑人和白人患者有相似的途径获得被认为健康的、可能的潜在供体(86%比87%有1个或更多,P = 0.92;5.91 vs 4.13平均计数,P = 0.20)和认为健康,同意潜在捐赠者(56% vs 48%, P = 0.54;1.77 vs 1.74, P = 0.97)。黑人患者的网络成员个人更有可能被认为是健康的和可能的潜在捐赠者(26%对21%,P = 0.04),白人患者的网络成员更有可能同意(13%对9%,P = 0.03),但这些差异在人口统计学调整模型中统计学上不显著。结论:黑人和白人移植候选人在他们的社会网络中可以接触到相似数量的潜在捐赠者。这一结果不支持差异获取假说。
期刊介绍:
Progress in Transplantation (PIT) is the official journal of NATCO, The Organization for Transplant Professionals. Journal Partners include: Australasian Transplant Coordinators Association and Society for Transplant Social Workers. PIT reflects the multi-disciplinary team approach to procurement and clinical aspects of organ and tissue transplantation by providing a professional forum for exchange of the continually changing body of knowledge in transplantation.