Preoperative Comorbidities and Outcomes of Medically Complex Living Kidney Donors

被引:14
作者
Hiramitsu, Takahisa [1 ]
Tomosugi, Toshihide [1 ]
Futamura, Kenta [1 ]
Okada, Manabu [1 ]
Tsujita, Makoto [1 ]
Goto, Norihiko [1 ]
Ichimori, Toshihiro [1 ]
Narumi, Shunji [1 ]
Takeda, Asami [2 ]
Watarai, Yoshihiko [1 ]
机构
[1] Nagoya Daini Red Cross Hosp, Dept Transplant & Endocrine Surg, Showa Ku, 2-9 Myoken Cho, Nagoya, Aichi 4668650, Japan
[2] Nagoya Daini Red Cross Hosp, Dept Nephrol, Showa Ku, Nagoya, Aichi, Japan
关键词
baseline biopsy; estimated glomerular filtration rate; kidney transplantation; medically complex living donor; preoperative comorbidities; proteinuria; METABOLIC SYNDROME; RENAL-FUNCTION; RISK-FACTORS; ASSOCIATION; DISEASE; CLASSIFICATION; HYPERTENSION; POPULATION; MORTALITY; DONATION;
D O I
10.1016/j.ekir.2019.10.002
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Recent reports have described an increased risk of renal disease in living kidney donors compared with the general population. However, these reports do not detail the outcomes of medically complex living donors (MCLDs) with preoperative comorbidities (PCs), such as hypertension, dyslipidemia, glucose intolerance, and obesity. Analysis of living donors with end-stage renal disease (ESRD) has shown that these PCs may contribute significantly to the development of ESRD. We aimed to evaluate the effect of PCs on postoperative renal function and mortality in MCLDs. Methods: Between January 2008 and December 2016, 807 living-donor kidney transplants were performed in our unit. Of these, 802 donors completed postoperative follow-up of >5 months. Donors were stratified into 4 groups based on the number of PCs present: healthy living donors (HLDs) with no PCs (n = 214) or MCLDs with 1 PC ( n = 302), 2 PCs (n = 196), or 3 PCs (n = 90) (denoted MCLD [PC 1], MCLD [PC 2], or MCLD [PC 3], respectively). We compared pathology observation data from baseline biopsy, postoperative estimated glomerular filtration rate (eGFR), postoperative urinary protein concentration, and mortality between HLD and MCLD groups. Results: Interstitial fibrosis, tubular atrophy, glomerulosclerosis, and arteriolosclerosis were more frequent in MCLDs (PC 3) than in HLDs. No significant differences were identified between HLDs and MCLDs in terms of postoperative eGFR and short-term mortality. Overt proteinuria and ESRD were not observed. Conclusions: Appropriate postdonation management of MCLDs with PCs may result in similar outcomes as for HLDs.
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页码:13 / 27
页数:15
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