Beyond the First Year: Epidemiology and Management of Late-Onset Opportunistic Infections After Kidney Transplantation

被引:0
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作者
Esnault, V. [1 ]
Hoisnard, L. [2 ,3 ,4 ]
Peiffer, B. [5 ]
Fihman, V. [6 ]
Fourati, S. [6 ]
Angebault, C. [6 ,7 ]
Champy, C. [8 ]
Gallien, S. [1 ,7 ]
Attias, P. [9 ]
Morel, A. [9 ]
Grimbert, P. [9 ,10 ]
Melica, G. [1 ]
Matignon, M. [9 ,10 ]
机构
[1] Ctr Hosp Univ CHU Henri Mondor, Assistance Publ Hop Paris AP HP, Serv Malad Infect & Immunol Clin, Creteil, France
[2] Federat Hosp Univ TRUE Innovat Therapy Immune Diso, Henri Mondor Hosp, AP HP, Creteil, France
[3] INSERM, Ctr Invest Clin 1430, Creteil, France
[4] Paris Est Creteil Univ UPEC, Epiderme Epidemiol Dermatol & Evaluat Therapeut, EA7379, Creteil, France
[5] Univ Med, CHU Henri Mondor, AP HP, Dept Med, Creteil, France
[6] CHU Henri Mondor, AP HP, Dept Prevent Diagnost & Traitement Infect, Serv Microbiol, Creteil, France
[7] Univ Paris Est Creteil UPEC, Ecole Natl Vet Alfort ENVA, EA DYNAMiC 7380, USC Anses,Fac Sante, Creteil, France
[8] CHU Henri Mondor, AP HP, Serv Urol, Creteil, France
[9] CHU Henri Mondor, Federat Hosp Univ Innovat Therapy Immune Disorders, AP HP, Serv Nephrol & Transplantat Renale, Creteil, France
[10] Univ Paris Est Creteil, Inst Natl Sante & Rech Med INSERM U955, Inst Mondor Rech Biomed, Team 21, Creteil, France
关键词
kidney transplant; herpes zoster; opportunistic infections; transplant infectious disease; pneumocystis; PNEUMOCYSTIS-JIROVECII PNEUMONIA; INVASIVE ASPERGILLOSIS; RECIPIENTS; MORTALITY; TRENDS;
D O I
10.3389/ti.2024.12065
中图分类号
R61 [外科手术学];
学科分类号
摘要
Late opportunistic infections (OI) occurring beyond the first year after kidney transplantation (KT) are poorly described and not targeted by prophylactic strategies. We performed a ten-year retrospective monocentric cohort study describing epidemiology, risk factors and impact of late OI occurring 1 year after KT. We included clinically symptomatic OI requiring treatment besides BK virus nephropathy. Control groups included early OI occurring in the first year after KT, and KT recipients without OI since KT and alive with a functional allograft at 1 year. Among 1066 KT recipients, 185 (19.4%) presented a first episode of OI 21.0 (8.0-45.0) months after KT: 120 late OI (64.9%) and 65 early OI (35.1%). Late OI were mainly viral (N = 83, 69.2%), mostly herpes zoster (HZ) (N = 36, 43.4%). Pneumocystis represented most late fungal infections (N = 12/25, 48%). Compared to early OI, we reported more pneumocystis (p = 0.002) and less invasive aspergillosis (p = 0.01) among late OI. Patients with late OI were significatively younger at KT (54.0 +/- 13.3 vs. 60.2 +/- 14.3 years, p = 0.05). Patient and allograft survival rates between late OI and control groups were similar. Only age was independently associated with mortality. While late OI were not associated with higher mortality or graft loss, implementing prophylactic strategies might prevent such infections.
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页数:9
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