Impact of Protease Inhibitor-Based Anti-Retroviral Therapy on Outcomes for HIV plus Kidney Transplant Recipients

被引:51
|
作者
Sawinski, D. [1 ]
Shelton, B. A. [2 ]
Mehta, S. [2 ]
Reed, R. D. [2 ]
MacLennan, P. A. [2 ]
Gustafson, S. [3 ]
Segev, D. L. [4 ]
Locke, J. E. [2 ]
机构
[1] Univ Penn, Comprehens Transplant Ctr, Philadelphia, PA 19104 USA
[2] Univ Alabama Birmingham, Birmingham Comprehens Transplant Inst, Birmingham, AL 35294 USA
[3] Sci Registry Transplant Recipients, Minneapolis, MN USA
[4] Johns Hopkins Sch Med, Baltimore, MD USA
关键词
health services and outcomes research; kidney transplantation; nephrology; graft survival; infection and infectious agents; viral: human immunodeficiency virus (HIV); acquired immunodeficiency syndrome (AIDS); patient survival; DRUGS; PHARMACOKINETICS; EXPERIENCE; SAFETY; LIVER; HCV;
D O I
10.1111/ajt.14419
中图分类号
R61 [外科手术学];
学科分类号
摘要
Excellent outcomes have been demonstrated among select HIV-positive kidney transplant (KT) recipients with well-controlled infection, but to date, no national study has explored outcomes among HIV+ KT recipients by antiretroviral therapy (ART) regimen. Intercontinental Marketing Services (IMS) pharmacy fills (1/1/01-10/1/12) were linked with Scientific Registry of Transplant Recipients (SRTR) data. A total of 332 recipients with pre- and posttransplantation fills were characterized by ART at the time of transplantation as protease inhibitor (PI) or non-PI-based ART (88 PI vs. 244 non-PI). Cox proportional hazards models were adjusted for recipient and donor characteristics. Comparing recipients by ART regimen, there were no significant differences in age, race, or HCV status. Recipients on PI-based regimens were significantly more likely to have an Estimated Post Transplant Survival (EPTS) score of >20% (70.9% vs. 56.3%, p=0.02) than those on non-PI regimens. On adjusted analyses, PI-based regimens were associated with a 1.8-fold increased risk of allograft loss (adjusted hazard ratio [aHR] 1.84, 95% confidence interval [CI] 1.22-2.77, p=0.003), with the greatest risk observed in the first posttransplantation year (aHR 4.48, 95% CI 1.75-11.48, p=0.002), and a 1.9-fold increased risk of death as compared to non-PI regimens (aHR 1.91, 95% CI 1.02-3.59, p=0.05). These results suggest that whenever possible, recipients should be converted to a non-PI regimen prior to kidney transplantation.
引用
收藏
页码:3114 / 3122
页数:9
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