Low-dose prophylactic intravenous immunoglobulin does not prevent HLA sensitization in left ventricular assist device recipients

被引:14
作者
Drakos, Stavros G.
Kfoury, Abdallah G.
Long, James W.
Stringham, James C.
Fuller, Thomas C.
Nelson, Karl E.
Campbell, Beverly K.
Gilbert, Edward M.
Renlund, Dale G.
机构
[1] Univ Utah, LDS Hosp, Sch Med, Salt Lake City, UT 84143 USA
[2] Utah Transplantat Affiliated Hosp, Cardiac Transplant Program, George E Wahlen Vet Affairs Med Ctr, Salt Lake City, UT USA
关键词
PANEL-REACTIVE-ANTIBODY; RISK-FACTORS; CROSS-MATCH; TRANSPLANTATION; HISTOCOMPATIBILITY; IMPLANTATION; REJECTION; SURVIVAL; ALLOSENSITIZATION; TRANSFUSIONS;
D O I
10.1016/j.athoracsur.2006.04.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. The use of left ventricular assist devices is associated with human leukocyte antigen ( HLA) allosensitization. We investigated whether prophylactic treatment with low-dose intravenous immunoglobulin ( IVIG), analogous to the use of IgG anti-D ( anti-Rh) in preventing Rh immunization, can abrogate HLA allosensitization after left ventricular assist device implantation. Methods. We retrospectively reviewed the data from 84 consecutive heart failure patients who underwent implantation of a left ventricular assist device as a bridge to transplantation. After implantation, panel reactive antibody ( PRA) was measured biweekly to assess sensitization ( defined by PRA > 10%). Patients who were sensitized before left ventricular assist device implantation were excluded from further analysis ( n = 12). Patients who either did not require perioperatively transfusions of cellular blood products or received other immunomodifying regimens were also excluded from further analysis ( n = 21). The rest of the patients were divided into two groups based on whether they received IVIG, 10 g daily for 3 days ( IVIG group, n = 26; non-IVIG group, n = 25). The decision as to whether patients received IVIG was not randomized but was based on surgeon preference. Results. The sensitization rates ( expressed as ratio of sensitized patients to total patients at risk) in the two groups were similar at consecutive time points ( 2, 4, 6, 8, 12, 20 weeks) after left ventricular assist device implantation. Also, mean PRA at the same time points did not differ between the two groups. Overall, 34.6% ( 9 of 26) of the IVIG group became sensitized during mechanical support, compared with 32% ( 8 of 25) of the non-IVIG group ( p = 1.0). A PRA of 90% or greater ( high-degree sensitization) occurred in 15.3% ( 4 of 26) of the IVIG group and 12.0% ( 3 of 25) of the non-IVIG group ( p = 0.5). Conclusions. The use of low-dose prophylactic IVIG after left ventricular assist device implantation affects neither the incidence nor the severity of HLA allosensitization.
引用
收藏
页码:889 / 894
页数:7
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