Every year, over 6000 healthy individuals donate a kidney in the United States to benefit a loved one or even a stranger. Currently, approximately 100,000 individuals are living post-nephrectomy. Live kidney donors gain no medical benefit from donation, nor do they expect to. However, live donors do expect the medical community to understand the long-term risks of kidney donation, for the purposes of donor selection, informed consent, and post-donation care. For African American kidney donors, we have thus far failed in this regard. The largest cohort study of kidney donors, from which the transplant community's assessment of the safety of kidney donation has been primarily derived, was comprised of less than 1% African American donors. Yet 13% of live donors in the US are African American, and our preliminary findings suggest that rates of death, hypertension, chronic kidney disease, and end-stage renal disease following donation are significantly higher in African Americans. It is critical to not only estimate the risk of these diseases, but to understand the risk attributable t donation; however, no study to date has captured appropriate non-donor controls that are necessary for this estimation. Furthermore, many African American donors, particularly young donors, have limited access to healthcare, and it is important to elucidate potential disparities i the management of post- donation consequences such as hypertension and decline in kidney function. In light of a significant knowledge gap regarding long-term outcomes and medical care following kidney donation in African Americans, we propose to estimate the incidence and consequences of hypertension and kidney disease in African American versus Caucasian donors. More importantly, we will determine how much of that risk is attributable to donating a kidney (rather than population-based differences in underlying risk) by comparing donors to healthy non-donors. We will also evaluate the reliability of administrative data sources in capturing and studying post-donation morbidity, and seek to better understand racial differences in treatment patterns for donors who develop hypertension or chronic kidney disease. We will accomplish these goals by recruiting the largest primary cohort of African American donors (over 4000 donors from the top 13 centers in the US), a comparison cohort of Caucasian donors, and healthy non-donors who met eligibility criteria for donation but did not actually donate. We will supplement these cohort with linkage of national registry data to Medicare, Medicaid, and private payer claims and pharmacy data. Our findings will have a direct impact on the practice of live kidney donation among African Americans in the US, informing critical aspects of donor selection, informed consent for donation, and post-donation care. In addition, this research will create an important resource from which several future ancillary projects are foreseeable, including genotyping to risk stratify potential donors, evaluating the effects of acut kidney injury and nephrotoxic drugs after donation, and estimating lifetime healthcare costs and utilization for kidney donors.
Every year, over 6000 healthy individuals donate a kidney to benefit a loved one or even a stranger, but the long-term consequences of donating a kidney, particularly in African Americans, are poorly understood. In this study, we will study high blood pressure, chronic kidney disease, and post-donation treatment patterns in largest ever primary cohort of African American donors, Caucasian American donors, matched healthy non-donor controls (who were cleared for donation but did not ultimately donate because of recipient factors), and other matched healthy individuals (who participated in large cohort studies and were deemed healthy enough to have likely passed a donor evaluation). Our findings will influence the practice of live kidney donation in the United States, particularly among African Americans, informing critical aspects of donor selection, informed consent for donation, and post-donation care.
| Ruck, Jessica M; Holscher, Courtenay M; Purnell, Tanjala S et al. (2018) Factors associated with perceived donation-related financial burden among living kidney donors. Am J Transplant 18:715-719 |
| Holscher, Courtenay M; Ishaque, Tanveen; Garonzik Wang, Jacqueline M et al. (2018) Living donor postnephrectomy kidney function and recipient graft loss: A dose-response relationship. Am J Transplant 18:2804-2810 |
| Eno, Ann K; Thomas, Alvin G; Ruck, Jessica M et al. (2018) Assessing the Attitudes and Perceptions Regarding the Use of Mobile Health Technologies for Living Kidney Donor Follow-Up: Survey Study. JMIR Mhealth Uhealth 6:e11192 |
| Ruck, Jessica M; Zhou, Sheng; Thomas, Alvin G et al. (2018) Electronic messaging and communication with living kidney donors. Clin Transplant 32: |
| Holscher, Courtenay M; Kmd, Sunjae Bae; Thomas, Alvin G et al. (2018) Early Hypertension and Diabetes after Living Kidney Donation: A National Cohort Study. Transplantation : |
| Haugen, Christine E; Mountford, Alexandra; Warsame, Fatima et al. (2018) Incidence, Risk Factors, and Sequelae of Post-kidney Transplant Delirium. J Am Soc Nephrol 29:1752-1759 |
| Ruck, Jessica M; Van Pilsum Rasmussen, Sarah E; Henderson, Macey L et al. (2018) Interviews of living kidney donors to assess donation-related concerns and information-gathering practices. BMC Nephrol 19:130 |
| Holscher, Courtenay M; Leanza, Joseph; Thomas, Alvin G et al. (2018) Anxiety, depression, and regret of donation in living kidney donors. BMC Nephrol 19:218 |
| DiBrito, Sandra R; Olorundare, Israel O; Holscher, Courtenay M et al. (2018) Surgical approach, cost, and complications of appendectomy in kidney transplant recipients. Clin Transplant 32:e13245 |
| Henderson, Macey L; Adler, Joel T; Van Pilsum Rasmussen, Sarah E et al. (2018) How Should Social Media Be Used in Transplantation? A Survey of The American Society of Transplant Surgeons. Transplantation : |
Showing the most recent 10 out of 49 publications
