V Esnault, L Hoisnard, B Peiffer, V Fihman, S Fourati, C Angebault, C Champy, S Gallien, P Attias, A Morel, P Grimbert, G Melica, M Matignon
{"title":"超越第一年:肾移植后晚期机会性感染的流行病学与管理》(Epidemiology and Management of Late-Onset Opportunistic Infections After Kidney Transplantation)。","authors":"V Esnault, L Hoisnard, B Peiffer, V Fihman, S Fourati, C Angebault, C Champy, S Gallien, P Attias, A Morel, P Grimbert, G Melica, M Matignon","doi":"10.3389/ti.2024.12065","DOIUrl":null,"url":null,"abstract":"<p><p>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 (<i>N</i> = 83, 69.2%), mostly herpes zoster (HZ) (<i>N</i> = 36, 43.4%). Pneumocystis represented most late fungal infections (<i>N</i> = 12/25, 48%). Compared to early OI, we reported more pneumocystis (<i>p</i> = 0.002) and less invasive aspergillosis (<i>p</i> = 0.01) among late OI. Patients with late OI were significatively younger at KT (54.0 ± 13.3 vs. 60.2 ± 14.3 years, <i>p</i> = 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.</p>","PeriodicalId":23343,"journal":{"name":"Transplant International","volume":"37 ","pages":"12065"},"PeriodicalIF":2.7000,"publicationDate":"2024-02-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10926380/pdf/","citationCount":"0","resultStr":"{\"title\":\"Beyond the First Year: Epidemiology and Management of Late-Onset Opportunistic Infections After Kidney Transplantation.\",\"authors\":\"V Esnault, L Hoisnard, B Peiffer, V Fihman, S Fourati, C Angebault, C Champy, S Gallien, P Attias, A Morel, P Grimbert, G Melica, M Matignon\",\"doi\":\"10.3389/ti.2024.12065\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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 (<i>N</i> = 83, 69.2%), mostly herpes zoster (HZ) (<i>N</i> = 36, 43.4%). Pneumocystis represented most late fungal infections (<i>N</i> = 12/25, 48%). Compared to early OI, we reported more pneumocystis (<i>p</i> = 0.002) and less invasive aspergillosis (<i>p</i> = 0.01) among late OI. Patients with late OI were significatively younger at KT (54.0 ± 13.3 vs. 60.2 ± 14.3 years, <i>p</i> = 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.</p>\",\"PeriodicalId\":23343,\"journal\":{\"name\":\"Transplant International\",\"volume\":\"37 \",\"pages\":\"12065\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2024-02-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10926380/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Transplant International\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3389/ti.2024.12065\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"SURGERY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Transplant International","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3389/ti.2024.12065","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"SURGERY","Score":null,"Total":0}
引用次数: 0
摘要
肾移植(KT)术后一年后发生的晚期机会性感染(OI)很少被描述,也不是预防策略的目标。我们进行了一项为期十年的回顾性单中心队列研究,描述了肾移植术后一年发生的晚期机会性感染的流行病学、风险因素和影响。除 BK 病毒肾病外,我们还纳入了需要治疗的有临床症状的 OI。对照组包括 KT 术后 1 年内发生的早期 OI,以及 KT 术后未发生 OI 且 1 年后仍存活并有功能性同种异体移植的 KT 受者。在 1066 名 KT 受者中,185 人(19.4%)在 KT 术后 21.0(8.0-45.0)个月首次出现 OI:其中 120 人(64.9%)为晚期 OI,65 人(35.1%)为早期 OI。晚期感染主要是病毒性感染(83 例,占 69.2%),其中大部分是带状疱疹(HZ)(36 例,占 43.4%)。晚期真菌感染以肺孢子菌居多(12/25,48%)。与早期 OI 相比,我们报告的晚期 OI 中肺孢子菌较多(p = 0.002),侵袭性曲霉菌病较少(p = 0.01)。晚期 OI 患者在 KT 时明显更年轻(54.0 ± 13.3 岁 vs. 60.2 ± 14.3 岁,p = 0.05)。晚期OI组和对照组的患者和异体移植存活率相似。只有年龄与死亡率独立相关。虽然晚期OI与较高的死亡率或移植物损失无关,但实施预防性策略可能会避免此类感染。
Beyond the First Year: Epidemiology and Management of Late-Onset Opportunistic Infections After Kidney Transplantation.
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.
期刊介绍:
The aim of the journal is to serve as a forum for the exchange of scientific information in the form of original and high quality papers in the field of transplantation. Clinical and experimental studies, as well as editorials, letters to the editors, and, occasionally, reviews on the biology, physiology, and immunology of transplantation of tissues and organs, are published. Publishing time for the latter is approximately six months, provided major revisions are not needed. The journal is published in yearly volumes, each volume containing twelve issues. Papers submitted to the journal are subject to peer review.