Acute Kidney Injury in Hematopoietic Stem Cell Transplantation: A Review

被引:28
|
作者
Krishnappa, Vinod [1 ]
Gupta, Mohit [2 ]
Manu, Gurusidda [3 ]
Kwatra, Shivani [1 ]
Owusu, Osei-Tutu [4 ]
Raina, Rupesh [5 ]
机构
[1] Akron Nephrol Associates, Akron Gen Cleveland Clin, Akron, OH USA
[2] Akron Gen Cleveland Clin, Dept Internal Med, Akron, OH USA
[3] Beth Israel Deaconness Med Ctr, Boston, MA USA
[4] Akron Gen Cleveland Clin, Dept Hematol Med Oncol, Akron, OH USA
[5] Akron Gen Cleveland Clin, Dept Nephrol Internal Med, Akron, OH 44307 USA
关键词
D O I
10.1155/2016/5163789
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
Hematopoietic stem cell transplantation (HSCT) is a highly effective treatment strategy for lymphoproliferative disorders and bone marrow failure states including aplastic anemia and thalassemia. However, its use has been limited by the increased treatment related complications, including acute kidney injury (AKI) with an incidence ranging from 20% to 73%. AKI after HSCT has been associated with an increased risk of mortality. The incidence of AKI reported in recipients of myeloablative allogeneic transplant is considerably higher in comparison to other subclasses mainly due to use of cyclosporine and development of graft-versus-host disease (GVHD) in allogeneic groups. Acute GVHD is by itself a major independent risk factor for the development of AKI in HSCT recipients. The other major risk factors are sepsis, nephrotoxic medications (amphotericin B, acyclovir, aminoglycosides, and cyclosporine), hepatic sinusoidal obstruction syndrome (SOS), thrombotic microangiopathy (TMA), marrow infusion toxicity, and tumor lysis syndrome. The mainstay of management of AKI in these patients is avoidance of risk factors contributing to AKI, including use of reduced intensity-conditioning regimen, close monitoring of nephrotoxic medications, and use of alternative antifungals for prophylaxis against infection. Also, early identification and effective management of sepsis, tumor lysis syndrome, marrow infusion toxicity, and hepatic SOS help in reducing the incidence of AKI in HSCT recipients.
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页数:13
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