Effects of anti-hypertensive treatment on graft function and proteinuria in a kidney transplant from an elderly hypertensive donor

被引:0
作者
Kobayashi, Akimitsu [1 ]
Yamamoto, Hiroyasu
Matsuoka, Kentaro [2 ]
Ito, Hideyuki
Yamamoto, Izumi
Kawamura, Yoshimi
Tanno, Yudo
Yaginuma, Tatsuhiro
Mitome, Jun
Hayakawa, Hiroshi
Miyazaki, Yoichi
Utsunomiya, Yasunori
Yamaguchi, Yutaka [3 ]
Hosoya, Tatsuo
机构
[1] Jikei Univ, Sch Med, Dept Internal Med, Div Kidney & Hypertens,Minato Ku, Tokyo 1058471, Japan
[2] Natl Ctr Child Hlth & Dev, Dept Clin Lab, Div Pathol, Tokyo, Japan
[3] Jikei Univ, Kashiwa Hosp, Sch Med, Dept Pathol, Chiba, Japan
关键词
angiotensin II type 1 receptor blocker; angiotensin-converting enzyme inhibitor; arteriolosclerosis; hypertension; kidney transplantation; marginal donor; renal autoregulation;
D O I
10.1111/j.1399-0012.2008.00853.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Hypertension is a common complication after kidney transplantation and adversely affects graft and patient survival. Strategies for anti-hypertensive therapy in an allograft from a hypertensive donor with arteriolosclerosis and the target blood pressure have not been clearly defined. Here, we report the case of deteriorating transplanted kidney function after anti-hypertensive treatment. A 40-yr-old man had received a kidney transplant from a living relative donor (his 69-yr-old father), who was hypertensive and had severe arteriolosclerosis. The recipient showed good allograft function immediately (s-Cr 1.8 mg/dL); however, blood pressure and proteinuria increased markedly two wk after transplantation (blood pressure 180/90, urinary protein 3.4 g/d). We then started anti-hypertensive agents (a calcium channel blocker and an angiotensin II receptor blocker). Blood pressure and proteinuria were corrected to the normal range within two wk of starting the treatment (blood pressure 130/80, urinary protein 0.3 g/d). However, his kidney function continued to deteriorate (s-Cr 2.7 mg/dL). A biopsy, performed at that time, revealed glomerular collapse, advanced interstitial fibrosis and severe arteriolosclerosis, with no evidence of rejection. These findings could have been the result of renal allograft hypoperfusion. We then reduced the anti-hypertensive agents on day 45 after transplantation and observed improved allograft function within a week (s-Cr 1.6 mg/dL). This case suggests that renal hemodynamic responses may be impaired and renal perfusion may not be appropriately maintained in an allograft with severe arteriolosclerosis at a blood pressure level suitable for the recipient. Anti-hypertensive treatment should be performed carefully when the allograft is from an elderly hypertensive donor.
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页码:68 / 71
页数:4
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