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1 is critical for the selection of a potential kidney donor.
2 daveric waiting list have a prospective live kidney donor.
3 s said they would accept a close friend as a kidney donor.
4 these centers had actually used a child as a kidney donor.
5 ith KTx recipients regardless of the type of kidney donor.
6 hat is not representative of all U.S. living kidney donors.
7 but needs to be tested in healthy potential kidney donors.
8 ssential in the risk evaluation of potential kidney donors.
9 eGFR is a poor predictor of true GFR in kidney donors.
10 ies in medical conditions occur among living kidney donors.
11 the appropriateness of accepting obese live kidney donors.
12 t option for patients with incompatible live kidney donors.
13 based equations for estimating GFR in former kidney donors.
14 members, spouses, or friends to become live kidney donors.
15 828 patients had CKD and 457 were potential kidney donors.
16 hronic kidney disease (CKD) and in potential kidney donors.
17 ad to misclassification of many older living kidney donors.
18 ctron microscopy in 83 living and 53 cadaver kidney donors.
19 ssues derived from normal living and cadaver kidney donors.
20 ease the use of genetically unrelated living kidney donors.
21 my (LDN) is the procedure of choice for live kidney donors.
22 of the short waiting time and use of living kidney donors.
23 ar filtration rate (GFR) in potential living kidney donors.
24 mal arterial branches were present in 46% of kidney donors.
25 ease the use of genetically unrelated living kidney donors.
26 -being and a boost in self-esteem for living kidney donors.
27 determining renal vascular anatomy in living kidney donors.
28 lic permeability by 66% compared with normal kidney donors.
29 ters are opposed to using children as living kidney donors.
30 ions of 132 kidneys in 66 healthy, potential kidney donors.
31 tically unrelated) people (e.g., spouses) as kidney donors.
32 isk variants were genotyped in additional AA kidney donors.
33 d prevent adverse outcomes in living related kidney donors.
34 in RTRs compared with 85 +/- 25 mmol/24 h in kidney donors.
35 nsent and varies substantially across living kidney donors.
36 idates and to inform acceptance criteria for kidney donors.
37 ict long-term renal outcomes in white living kidney donors.
38 ult was consistent across different types of kidney donors.
39 x volume [RCV]) were performed in 101 living kidney donors.
40 R: 1.9-12.0 y) after transplantation and 253 kidney donors.
41 tions of current voters toward paying living kidney donors.
42 ate, eGFR) of the remaining kidney in living kidney donors.
43 t studies of financial incentives for living kidney donors.
44 h might be alleviated by compensating living kidney donors.
45 PCCs were studied in 42 normal adrenals from kidney donors.
46 cept for 1A, different from those in healthy kidney donors.
47 tively benign renal outcomes for most living kidney donors.
48 on might increase the cardiovascular risk in kidney donors.
49 we matched living pancreas donors to living kidney donors (1:3) by demographic traits and year of do
50 linking U.S. registry identifiers for living kidney donors (1987-2007) to billing claims from a priva
53 r their views and practices regarding living kidney donors; 44% of these organizations responded.
55 based GFR prediction equations in 187 former kidney donors against iohexol GFR for measuring GFR.
57 aged 18 to 59 years with a hypothetical live kidney donor aged 50 years and four HLA mismatches, the
58 they would offer life insurance to a healthy kidney donor and only one believed it might raise the pr
59 terquartile range [IQR], 3.9-11.5 years) for kidney donors and 15.0 years (IQR, 13.7-15.0 years) for
60 n was 30.8 per 10,000 (95% CI, 24.3-38.5) in kidney donors and 3.9 per 10,000 (95% CI, 0.8-8.9) in th
61 1 risk alleles among African American living kidney donors and for living-related donors for African
62 ival data were compared with those from live kidney donors and healthy participants of the National H
63 tion is critical in the evaluation of living kidney donors and higher donor glomerular filtration rat
64 niques is often present in excellent cadaver kidney donors and is not detected by dipstick testing.
65 liver donors was comparable to that of live kidney donors and NHANES participants (1.2%, 1.2%, and 1
67 lant registry to select a cohort of deceased kidney donors and the corresponding transplant recipient
72 upernumerary arteries were present in 49% of kidney donors and were bilateral in approximately 17%.
73 may influence hypothetical and actual living kidney donors and where appropriate, summarizes the quan
74 ed risk of ESRD has been reported for living kidney donors, and appears to be higher for those donati
75 ine protein excretion in 23 "normal" cadaver kidney donors, and correlated results with urine protein
76 mpacting allograft survival from deceased AA kidney donors, APOL1 renal-risk variants were genotyped
77 l and the risk of ESRD in carefully screened kidney donors appear to be similar to those in the gener
79 e profound organ shortages, the use of older kidney donors appears to be an equivalent or beneficial
81 le cautious criteria for selection of living kidney donors are credited for favorable outcomes, recen
82 Data regarding health outcomes among living kidney donors are lacking, especially among nonwhite per
85 einuria, reduced GFR, and ESRD in 3956 white kidney donors, assessed the contribution of postdonation
86 Societal plight driving caution about living kidney donor assessment was emphasized in the context of
88 es genetic testing in the evaluation of live kidney donors at risk for ADPKD whose disease status can
91 mated the number of potential imminent death kidney donors at the University of Wisconsin Hospital an
92 ine protein, and microalbumin) in 148 living kidney donors before and 6 to 12 months after nephrectom
95 One thousand six hundred sequential living kidney donor biopsies were performed between 2001 and 20
96 d for more comprehensive follow-up of living kidney donors, both for the donor's benefit and to estab
97 ed 'hypothetical' willingness to be a living kidney donor but with marked heterogeneity in the absolu
98 r as the leading cause of death among living kidney donors, but information on the burden of cancer o
100 mon in young, otherwise healthy, prospective kidney donor candidates with persistent, asymptomatic, m
101 of GFR, required in the evaluation of living kidney donor candidates, is now receiving increasing emp
103 rojected long-term risk of ESRD among living kidney-donor candidates and to inform acceptance criteri
105 11 patients from Birmingham, United Kingdom, kidney donor CC genotype at C3435T (rs1045642) within AB
108 psychologically screened unspecified living kidney donors completed the Symptom Checklist before and
109 ties for long-term costs generated by living kidney donors contributes to the problem was examined by
111 During this same time period, 102 previous kidney donors developed kidney failure and were listed f
112 6 nonobese (body mass index<27 kg/m2) living kidney donors donating at a single institution between 1
113 d have been available from the OPTN deceased kidney donors during 2002 to 2004 were investigated.
115 compare the outcomes of the first 60 living kidney donors enrolled in our enhanced recovery program
116 id (DTPA) renal studies as part of a routine kidney donor evaluation at either Brigham and Women's Ho
119 past few years, the implementation of paired kidney donor exchange programs and the development of pr
120 o undergo nephrectomy or adults who serve as kidney donors exhibit little difference in renal functio
123 who underwent blood typing as potential live kidney donors for recipients being evaluated for transpl
124 ped DNA from 1805 recipients and 1038 living kidney donors for TL to determine the association of TL
125 ped DNA from 1805 recipients and 1038 living kidney donors for TL to determine the association of TL
128 tation Network registrations for 4650 living kidney donors from 1987 to 2007 with administrative data
130 status and development of ESRD in 143 living kidney donors from 1994 to 2007 with predonation impaire
132 he study population consisted of 3074 living kidney donors from 28 centers during 2004 and 2005.
134 prospective cohort study involving deceased kidney donors from five organ procurement organizations.
135 ve study of 4650 persons who had been living kidney donors from October 1987 through July 2007 and wh
137 Compared with matched healthy nondonors, kidney donors had an increased risk of ESRD over a media
138 Risk of end-stage renal disease (ESRD) in kidney donors has been compared with risk faced by the g
141 show that attitudes toward unrelated living kidney donors have gradually become much more liberal.
144 The overall evidence suggests that living kidney donors have survival similar to that of nondonors
147 ntation Network identifiers for 4,650 living kidney donors in 1987 to 2007 were linked to administrat
148 antation Network identifiers for 4650 living kidney donors in 1987 to 2007 were linked to administrat
149 etwork (OPTN) registry data for 4,007 living kidney donors in 1987 to 2008 with Medicare billing clai
150 umbilicus) outcomes justify application for kidney donors in experienced centers and may motivate ad
151 viewed the predonation charts for all living kidney donors in Ontario, Canada between 1992 and 2010 a
153 e records of all patients who were cadaveric kidney donors in the state of Louisiana between Septembe
154 scopic donor nephrectomies in 2006, two live kidney donors in the United States and one in India have
155 a mandated national registry of 80 347 live kidney donors in the United States between April 1, 1994
156 TTINGS, AND PARTICIPANTS: A cohort of 96,217 kidney donors in the United States between April 1994 an
158 15-year observed risks after donation among kidney donors in the United States were 3.5 to 5.3 times
159 ata on all African-American and white living kidney donors in the United States who were registered i
160 average risk of postdonation ESRD for living kidney donors in the United States, but personalized est
162 d to provide this follow-up of former living kidney donors, including concerns that donor insurance w
164 ucted a retrospective cohort study of living kidney donors involving 85 women (131 pregnancies after
165 candidate's only medically-acceptable living kidney donor is ABO incompatible, the most common practi
166 eutic options for patients whose only living kidney donor is ABO incompatible, with a specific emphas
167 increased compared with CRT if the cadaveric kidney donor is much younger or with fewer HLA mismatche
170 emographic characteristics with HL in living kidney donors (LD), living donor kidney transplant recip
171 strate that graft survival from older living kidney donors (LD; age>60 years) is worse than younger L
172 serve as a primary motivating factor, living kidney donors (LDs) also may expect to accrue some perso
173 undred thirty-one programs performing living kidney donor (LKD) and/or living liver donor (LLD) trans
174 irical research on informed consent for live kidney donors (LKD) and live liver donors (LLD) for both
181 r diabetes treatments, compared with 5.9% of kidney donors (odds ratio, 4.13; 95% confidence interval
182 e donation are mostly for the recipient, but kidney donors often have improved quality of life as a r
187 w often and the reasons why potential living kidney donors opt out of the donor evaluation process fo
190 ation is an accepted method of expanding the kidney donor pool but there is little analysis of the pr
195 evaluated glomerular dynamics in a cohort of kidney donors prior to, within 1 year of, and several ye
196 ctive antibody > 20%, African American race, Kidney Donor Profile Index > 50%, cold ischemia time > 2
199 sed donor kidney allocation algorithm uses a Kidney Donor Profile Index (KDPI) based on donor charact
201 by someone; the median (interquartile range) Kidney Donor Profile Index (KDPI) of these kidneys was 3
202 han 60 years, accepting a kidney with a high Kidney Donor Profile Index (KDPI) score could enable ear
204 kidney allocation policy that introduces the kidney donor profile index (KDPI), which gives scores of
207 achieved with expanded criteria donor, high Kidney Donor Profile Index or advanced age kidneys are p
208 ed age kidneys, we assessed the value of the Kidney Donor Profile Index policy, preimplantation biops
209 is "framed." Thus, labeling a kidney as high Kidney Donor Profile Index results in higher discard rat
210 eristic curve was approximately 0.87 for all Kidney Donor Profile Index thresholds and timeframes con
211 eive an offer for a deceased-donor kidney at Kidney Donor Profile Index thresholds of 0.2, 0.4, and 0
212 hich allocates kidneys in the top 20% of the kidney donor profile index to candidates in the top 20%
218 e the experiences and expectations of living kidney donors regarding follow-up and self-care after do
220 Evaluation of candidates to serve as living kidney donors relies on screening for individual risk fa
225 gistrants (IRR, 1.01; P < 0.001), and higher kidney donor risk index (IRR, 1.98; P < 0.001) were asso
226 discard risk, for kidneys within a range of kidney donor risk index (KDRI) 1.4-2.1 that included bot
228 TAR files) to investigate the utility of the Kidney Donor Risk Index (KDRI) versus delayed graft func
229 s received higher-quality allografts (median kidney donor risk index 0.67 versus 0.90 for nondonors;
233 n donor age rose from 26 to 43 years; median Kidney Donor Risk Index increased from 1.1 in 1994 to 1.
235 ant dialysis duration, kidney cold ischemia, kidney donor risk index, and recipient hyperlipidemia.
239 sis of the A and H antigen expression on the kidney donor's erythrocytes suggested that this donor di
244 strikingly uniform and indicate that healthy kidney donors should be able to obtain and maintain heal
245 Previous studies concluded that healthy kidney donors should be able to obtain life insurance at
248 or preeclampsia was more common among living kidney donors than among nondonors (occurring in 15 of 1
249 eclampsia was more likely to be diagnosed in kidney donors than in matched nondonors with similar ind
250 cs that were similar to those of age-matched kidney donors, the 15-year projections of the risk of ES
252 ients with a solitary kidney, such as living kidney donors, the surgical treatment of renal tumors ma
253 Even within programs that use unspecified kidney donors, there is a lack of consensus regarding ho
254 Although AAs comprised 14.3% of all living kidney donors, they constituted 44% of donors reaching t
255 In the setting of multiple potential living kidney donors, this quantitative tool may facilitate the
257 mation and obtain informed consent from live kidney donors to assist the transplant community in opti
262 ribution to the ethnic differences in living kidney donor transplantation have not been adequately st
267 recipients bolster public support for living kidney donor transplantation; however, ethical dilemmas
268 ram has helped maintain the volume of living kidney donor transplants in Canada over the past 5 years
269 osocial and physical outcomes in unspecified kidney donors (UKDs) versus specified kidney donors (SKD
270 Lennerling et al.'s finding that prospective kidney donors understood their decisions as "the only op
271 profile of Australian and New Zealand living kidney donors using data from the Australia and New Zeal
272 ing trend in acceptance of very obese living kidney donors, variation across centers is significant.
277 ce companies currently view and treat living kidney donors, we mailed a survey to the medical directo
278 ozocin (STZ) and islets from bone marrow and kidney donor were transplanted without immunosuppression
279 We hypothesized that African Americans (AA) kidney donors were at greater risk for kidney failure.
285 at most bills for follow-up visits of living kidney donors were paid by insurance companies, at a rat
288 of individuals wishing to volunteer to be a kidney donor who have no intended recipient specified.
289 rs Evaluation (RELIVE) Study evaluated 8,951 kidney donors who donated between 1963 and 2007 at three
290 tal status and lifetime risk of ESRD in 3698 kidney donors who donated kidneys during the period from
292 ation of extraordinary altruists: altruistic kidney donors who volunteered to donate a kidney to a st
298 reater magnitude of glomerulopenia in living kidney donors with preexisting hypertension justifies th
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