Combined use of rituximab and plasmapheresis pre-transplant increases post-transplant infections in renal transplant recipients with basiliximab induction therapy
Introduction We investigated the effect of combined use of rituximab (RTX) and plasmapheresis (PP) pre‐transplant on post‐transplant infection. Methods A total of 196 patients undergoing living‐donor kidney transplantation at Seoul St. Mary's Hospital, all of whom underwent basiliximab inductio...
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Published in: | Transplant infectious disease Vol. 15; no. 6; pp. 559 - 568 |
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Main Authors: | , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Denmark
Blackwell Publishing Ltd
01-12-2013
Wiley Subscription Services, Inc |
Subjects: | |
Online Access: | Get full text |
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Summary: | Introduction
We investigated the effect of combined use of rituximab (RTX) and plasmapheresis (PP) pre‐transplant on post‐transplant infection.
Methods
A total of 196 patients undergoing living‐donor kidney transplantation at Seoul St. Mary's Hospital, all of whom underwent basiliximab induction therapy, were included in the study. They were divided into 3 groups: RTX/PP/intravenous immune globulin (IVIG) (the RPI group; n = 53), RTX monotherapy (the RTX group; n = 14), and control (the CONT group; n = 129). We compared the post‐transplant infections in the 3 groups.
Results
The overall prevalence of infection was significantly higher, and the infection‐free survival rate was lower, in the RPI group compared with the RTX or CONT groups (P < 0.05). A trend toward more severe bacterial infections was seen in the RPI group compared with the other groups, and fungal infections developed only in the RPI group. After anti‐rejection therapy, a significantly higher rate of infection developed in the RPI group than in the other groups (P < 0.05). In addition, the RPI group was an independent risk factor for the development of infection.
Conclusion
Our results show that in the setting of basiliximab induction, the use of combined RTX and PP therapy pre‐transplant significantly increases the risk for post‐transplant infection. |
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Bibliography: | Korea Healthcare Technology R&D Project - No. A092258 ArticleID:TID12135 Welfare & Family Affairs istex:0AFB0609A8E3200D23A771E7ADB179852DC8578D Ministry for Health ark:/67375/WNG-XP995741-S Republic of Korea ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1398-2273 1399-3062 |
DOI: | 10.1111/tid.12135 |