Division of Infectious Diseases, Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.
Li Ka Shing Institute of Virology, Edmonton, Alberta, Canada.
Transpl Infect Dis. 2024 Aug;26(4):e14292. doi: 10.1111/tid.14292. Epub 2024 May 10.
Cytomegalovirus (CMV) mismatched, donor IgG-positive/recipient IgG-negative, solid organ transplant recipients (SOTRs) are at high risk of CMV invasive disease. Post-prophylaxis disease is an issue in this population. Some programs employ surveillance after prophylaxis (SAP) to limit the incidence of post-prophylaxis disease.
This was a single-center retrospective cohort study that included all CMV mismatched SOTRs from 2003 to 2017. Patients underwent SAP with weekly CMV plasma viral load for 12 weeks. The subjects were classified into three post-prophylaxis DNAemia patterns: no DNAemia, one episode of DNAemia, and multiple episodes of DNAemia. We calculated the cumulative incidence of each DNAemia pattern. We also determined 5-year mortality based on DNAemia pattern stratified by organ transplant type.
Post-prophylaxis recurrent DNAemia occurred in 63% of lung recipients and 32% of non-lung recipients (p = .003). Tissue invasive CMV disease was diagnosed in 3% of the population and CMV syndrome was diagnosed in 33%. Recurrent DNAemia was not associated with 5-year mortality.
In this cohort, undergoing SAP tissue invasive disease was uncommon and CMV DNAemia recurrence did not have an impact on long-term mortality.
巨细胞病毒(CMV) mismatched、供体 IgG 阳性/受体 IgG 阴性的实体器官移植受者(SOTR)存在 CMV 侵袭性疾病的高风险。预防后疾病是该人群中的一个问题。一些项目采用预防后监测(SAP)来限制预防后疾病的发生率。
这是一项单中心回顾性队列研究,纳入了 2003 年至 2017 年间所有 CMV mismatched SOTR。患者接受 SAP,在 12 周内每周进行一次 CMV 血浆病毒载量检测。受试者被分为三种预防后 DNAemia 模式:无 DNAemia、一次 DNAemia 发作和多次 DNAemia 发作。我们计算了每种 DNAemia 模式的累积发生率。我们还根据器官移植类型对 DNAemia 模式进行分层,确定了 5 年死亡率。
预防后复发性 DNAemia 发生在 63%的肺移植受者和 32%的非肺移植受者中(p = 0.003)。人群中有 3%诊断为组织侵袭性 CMV 疾病,33%诊断为 CMV 综合征。复发性 DNAemia 与 5 年死亡率无关。
在本队列中,SAP 组织侵袭性疾病并不常见,CMV DNAemia 复发对长期死亡率没有影响。