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Pneumocystis pneumonia occurrence and prophylaxis duration in kidney transplant recipients according to perioperative treatment with rituximabopen access

Authors
Kim, Young HoonKim, Jee YeonKim, Dong HyunKo, YoungminCHOI, JI YOONShin, SungJung, Joo HeePark, Su-KilKim, Sung-HanKwon, HyunwookHan, Duck, Jong
Issue Date
Mar-2020
Publisher
BMC
Keywords
Kidney transplantationRituximabPneumocystis
Citation
BMC NEPHROLOGY, v.21, no.1, pp.1 - 9
Indexed
SCIE
SCOPUS
Journal Title
BMC NEPHROLOGY
Volume
21
Number
1
Start Page
1
End Page
9
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/190728
DOI
10.1186/s12882-020-01750-8
ISSN
14712369
Abstract
Background Pneumocystis pneumonia (PCP) is a life-threatening fungal infection that can occur in kidney transplantation (KT) recipients. A growing number of KT recipients are receiving perioperative treatment with rituximab, which is associated with prolonged B-cell depletion and possible risk of PCP occurrence; however, the optimal prophylaxis duration according to rituximab treatment is yet unknown. We compared the occurrence of PCP and the duration of prophylaxis in KT recipients according to rituximab treatment. Methods We retrospectively analyzed 2110 patients who underwent KT between January 2009 and December 2016, who were divided into non-Rituximab group (n = 1588, 75.3%) and rituximab group (n = 522, 24.7%). Results In the rituximab group, the estimated number needed to treat (NNT) for prophylaxis prolongation from 6 to 12 months was 29.0 with a relative risk reduction of 90.0%. In the non-rituximab group, the estimated NNT value was 133.3 and the relative risk reduction was 66.4%. Rituximab treatment (hazard ratio (HR) = 3.09; P < 0.01) and acute rejection (HR = 2.19; P = 0.03) were significant risk factors for PCP in multivariate analysis. Conclusions Our results suggest that maintaining PCP prophylaxis for 12 months may be beneficial in KT recipients treated with rituximab for desensitization or acute rejection treatment.
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CHOI, JI YOON
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