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1 e been developed to reduce morbidity for the living renal donor.
2 ucted a prospective multicenter study of 172 living liver donors.
3 of the psychosocial evaluation for eligible living organ donors.
4 ursed by Program for Reimbursing Expenses of Living Organ Donors.
5 n current psychosocial screening programs of living organ donors.
6 adient-echo MRA with surgical findings in 15 living renal donors.
7 ography and angiography in the assessment of living renal donors.
8 ample that is not representative of all U.S. living kidney donors.
9 isparities in medical conditions occur among living kidney donors.
10 genetic testing in the screening process for living kidney donors.
11 can lead to misclassification of many older living kidney donors.
12 to increase the use of genetically unrelated living kidney donors.
13 because of the short waiting time and use of living kidney donors.
14 lomerular filtration rate (GFR) in potential living kidney donors.
15 rams minimize some of the financial loss for living kidney donors.
16 to increase the use of genetically unrelated living kidney donors.
17 of well-being and a boost in self-esteem for living kidney donors.
18 phy in determining renal vascular anatomy in living kidney donors.
19 ant centers are opposed to using children as living kidney donors.
20 sing body composition-related kidney risk in living kidney donors.
21 ies remain to remove the financial burden of living kidney donors.
22 rmed consent and varies substantially across living kidney donors.
23 ay predict long-term renal outcomes in white living kidney donors.
24 l cortex volume [RCV]) were performed in 101 living kidney donors.
25 perceptions of current voters toward paying living kidney donors.
26 ation rate, eGFR) of the remaining kidney in living kidney donors.
27 ow pilot studies of financial incentives for living kidney donors.
28 e, which might be alleviated by compensating living kidney donors.
29 he relatively benign renal outcomes for most living kidney donors.
30 tioning at 5 years as that of a graft from a living related donor.
31 ted, or nonhuman leukocyte antigen identical living-related donor.
32 fts were from a cadaver, and 14% were from a living-related donor.
33 similar concerns are important to potential living related donors.
34 nt of both transplant patients and potential living related donors.
35 We performed six SPKs from living-related donors.
36 apse and received a kidney transplant from a living-unrelated donor.
37 d in recipients of 50% segmental grafts from living, related donors?
38 health, we matched living pancreas donors to living kidney donors (1:3) by demographic traits and yea
41 tabase linking U.S. registry identifiers for living kidney donors (1987-2007) to billing claims from
44 king for their views and practices regarding living kidney donors; 44% of these organizations respond
46 leukocyte antigen-mismatched, haploidentical living-related donors after modified nonmyeloablative co
47 most to the variation in willingness to be a living related donor, although race contributed most to
50 of APOL1 risk alleles among African American living kidney donors and for living-related donors for A
51 ey function is critical in the evaluation of living kidney donors and higher donor glomerular filtrat
55 (SEP) may influence hypothetical and actual living kidney donors and where appropriate, summarizes t
57 stimated waiting time, the availability of a living kidney donor, and previous hematological treatmen
59 KTRs) (together: CKD population), and in 447 living kidney donors, and 385 healthy controls (together
60 increased risk of ESRD has been reported for living kidney donors, and appears to be higher for those
62 to prevent acquisition of HIV by prospective living organ donors, and to conduct HIV antibody testing
63 rgans, 29 were ex vivo reduced size, 33 were living-related donor, and 36 were in situ split-liver al
64 ence up to 50%, an increased recurrence with living-related donors, and the rarity of graft loss due
68 While cautious criteria for selection of living kidney donors are credited for favorable outcomes
72 The motives and decision making of potential living liver donors are critical areas for transplant cl
78 regarding the actual change in the number of living kidney donors associated with voucher programs an
80 ransplant physicians should inform potential living kidney donors at risk for APOL1-associated nephro
83 es regarding the evaluation and selection of living kidney donors based on metabolic, cardiovascular,
84 FR], urine protein, and microalbumin) in 148 living kidney donors before and 6 to 12 months after nep
87 higher (P < 0.01) for cadaveric donor versus living related donor, blacks versus whites, age >12 vers
88 e called for more comprehensive follow-up of living kidney donors, both for the donor's benefit and t
89 increased 'hypothetical' willingness to be a living kidney donor but with marked heterogeneity in the
90 y cancer as the leading cause of death among living kidney donors, but information on the burden of c
94 ss practices used to assess kidney health in living kidney donor candidates in 2017; the response rat
96 uation of GFR, required in the evaluation of living kidney donor candidates, is now receiving increas
99 essment is a key aspect in the evaluation of living kidney donor candidates; however, data on perform
100 e the projected long-term risk of ESRD among living kidney-donor candidates and to inform acceptance
104 lly and psychologically screened unspecified living kidney donors completed the Symptom Checklist bef
105 facilities for long-term costs generated by living kidney donors contributes to the problem was exam
106 ut how well postoperative pain is managed in living liver donors, despite pain severity being the str
107 and 116 nonobese (body mass index<27 kg/m2) living kidney donors donating at a single institution be
108 ective cohort study of 924 standard-criteria living kidney donors enrolled before surgery and a concu
109 sis, we compare the outcomes of the first 60 living kidney donors enrolled in our enhanced recovery p
110 retrospective data analysis of all potential living liver donors evaluated at our center from 1998 to
112 gh genetic testing can be a valuable tool in living kidney donor evaluation, its overall benefit in d
113 roviding an overview of current practices in living kidney donor evaluation, our study highlights the
116 any jurisdictions have programs to reimburse living kidney donors for expenses, few programs have bee
117 genotyped DNA from 1805 recipients and 1038 living kidney donors for TL to determine the association
119 frican American living kidney donors and for living-related donors for African American recipients.
120 We report here on two cases in which the living-related donors for children with Alagille's syndr
121 y system of family members who are potential living-related donors for patients with this condition.
123 reimbursement from insurance providers for a living kidney donor from 47% to 85% of the amount billed
124 ansplantation Network registrations for 4650 living kidney donors from 1987 to 2007 with administrati
126 vital status and development of ESRD in 143 living kidney donors from 1994 to 2007 with predonation
131 ospective study of 4650 persons who had been living kidney donors from October 1987 through July 2007
132 ared 24 h before and after nephrectomy in 38 living kidney donors from the REnal Protection Against I
134 the first report of the successful use of a living-related donor graft for an orthotopic liver trans
139 wn "reduced" livers, split liver grafts, and living-related donors has provided more organs for pedia
142 d-stage renal disease (ESRD) risks for young living kidney donors have conflicted with the knowledge
144 se data show that attitudes toward unrelated living kidney donors have gradually become much more lib
151 ransplantation Network identifiers for 4,650 living kidney donors in 1987 to 2007 were linked to admi
152 Transplantation Network identifiers for 4650 living kidney donors in 1987 to 2007 were linked to admi
153 ation Network (OPTN) registry data for 4,007 living kidney donors in 1987 to 2008 with Medicare billi
154 We reviewed the predonation charts for all living kidney donors in Ontario, Canada between 1992 and
159 with data on all African-American and white living kidney donors in the United States who were regis
160 ed the average risk of postdonation ESRD for living kidney donors in the United States, but personali
163 atients who received kidney transplants from living unrelated donors in the United States from 1995 t
164 entified to provide this follow-up of former living kidney donors, including concerns that donor insu
167 antation of the right lobe of a liver from a living adult donor into an adult recipient has been perf
168 We conducted a retrospective cohort study of living kidney donors involving 85 women (131 pregnancies
169 splant candidate's only medically-acceptable living kidney donor is ABO incompatible, the most common
170 therapeutic options for patients whose only living kidney donor is ABO incompatible, with a specific
172 technique in the preoperative evaluation of living renal donors is accurate even when images are rea
174 t and demographic characteristics with HL in living kidney donors (LD), living donor kidney transplan
175 s demonstrate that graft survival from older living kidney donors (LD; age>60 years) is worse than yo
176 nt may serve as a primary motivating factor, living kidney donors (LDs) also may expect to accrue som
178 Two hundred thirty-one programs performing living kidney donor (LKD) and/or living liver donor (LLD
183 performing living kidney donor (LKD) and/or living liver donor (LLD) transplantation were contacted
186 ently, we make thorough attempts to locate a living related donor (LRD) or a living unrelated donor (
188 sies were obtained from cadaveric (n=23) and living-related donor (LRD) (n=10) liver transplants befo
189 , we embarked on a study of DBMC infusion in living-related donor (LRD) kidney transplant recipients.
190 ith concomitantly transplanted recipients of living-related donor (LRD) kidneys and donor marrow infu
192 usion after transplantation of 13 CAD and 12 living-related donor (LRD) renal allografts were examine
193 ent of CAN in recipients of cadaveric (CAD), living-related donor (LRD), and living-unrelated donor (
194 ymphocytes and iliac crest bone marrow of 11 living-related-donor (LRD) renal transplant recipients,
195 to locate a living related donor (LRD) or a living unrelated donor (LURD) before proceeding with a c
196 veric (CAD), living-related donor (LRD), and living-unrelated donor (LURD) transplants at their cente
202 arrival rates of candidate/donor pairs and (living) nondirected donors (NDDs), and delay time from e
204 ectal surgery, splenectomy for splenomegaly, living-related donor nephrectomy, and procedures conside
205 on rectopexy), splenectomy for splenomegaly, living-related donor nephrectomy, gastric banding for mo
213 ding how often and the reasons why potential living kidney donors opt out of the donor evaluation pro
218 The Program for Reimbursing Expenses of Living Organ Donors (PRELOD) was launched in the provinc
219 His willing donor (female, aged 53 y) with a Living Kidney Donor Profile Index of 2, donated 2 days l
220 sons received kidneys from donors with lower Living Kidney Donor Profile Index scores than their actu
222 vational studies reporting outcomes in adult living kidney donors published from January 2011 to May
224 allograft recipients with cadaveric (89%) or living (11%) donors received 2 mg of sirolimus (troughs>
225 living unrelated and two HLA haploidentical living-related donor recipient pairs, whereas unidirecti
230 ratios were higher in cadaveric donor versus living related donor recipients (15.7 + 2.8 vs. 8.8 + 1.
233 describe the experiences and expectations of living kidney donors regarding follow-up and self-care a
237 However, genetic testing on asymptomatic living kidney donors remains fraught with many challenge
238 ients of one haplotype matched recipients of living, related donor renal allografts selected to contr
246 ould discuss APOL1 genotyping with potential living kidney donors self-reporting recent African ances
250 significantly more vertebral fractures among living kidney donors than among controls (SIR, 1.42; 95%
251 ension or preeclampsia was more common among living kidney donors than among nondonors (occurring in
252 For patients with a solitary kidney, such as living kidney donors, the surgical treatment of renal tu
255 outperformed the MDRD equation in potential living renal donors; this model could be used to estimat
259 ntrols with baseline good health, we matched living pancreas donors to living kidney donors (1:3) by
262 09 (60.2%) were male, 113 (62.4%) received a living kidney donor transplant, and 40 (22.1%) had a gra
264 ir contribution to the ethnic differences in living kidney donor transplantation have not been adequa
265 ortion of kidney paired donation-facilitated living kidney donor transplantation in the United States
270 ts for recipients bolster public support for living kidney donor transplantation; however, ethical di
271 PD program has helped maintain the volume of living kidney donor transplants in Canada over the past
275 e risk profile of Australian and New Zealand living kidney donors using data from the Australia and N
277 declining trend in acceptance of very obese living kidney donors, variation across centers is signif
280 ey data from NSODAP, willingness to become a living organ donor was associated with knowledge, percep
281 The Program for Reimbursing Expenses of Living Organ Donors was launched in the province of Onta
284 insurance companies currently view and treat living kidney donors, we mailed a survey to the medical
286 find that most bills for follow-up visits of living kidney donors were paid by insurance companies, a
287 one haplotype-matched renal transplants from living related donors were studied to determine the asso
289 age have focused on increasing the number of living organ donors, which in 2001 for the first time ex
296 hort-term and 1- and 5-year renal outcome of living kidney donors with preexistent hypertension.
297 t the greater magnitude of glomerulopenia in living kidney donors with preexisting hypertension justi
299 splants from HLA single-haplotype mismatched living related donors, with the use of a nonmyeloablativ
300 ng transplant candidates and their potential living kidney donors would result in sustained increases