Gold Jeremy A W, Benedict Kaitlin, Sajewski Elizabeth, Chiller Tom, Lyman Meghan, Toda Mitsuru, Little Jessica S, Ostrosky-Zeichner Luis
Mycotic Diseases Branch, CDC, Atlanta, Georgia, USA.
Division of Infectious Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Transpl Infect Dis. 2025 Jul 8:e70077. doi: 10.1111/tid.70077.
Updated benchmark data on invasive fungal disease (IFD) in solid organ transplantation (SOT) and hematopoietic cell transplantation (HCT) recipients are necessary to increase clinical recognition and inform treatment and prevention strategies. We estimated IFD incidence and potential risk factors in transplant recipients in a large US commercial health insurance database.
We observed patients who received SOT or HCT during 2018-2022 until IFD development, disenrollment, or database end date (July 31, 2023). We calculated incidence (per 1000 person-years) and time to IFD development, comparing demographic features and underlying conditions for IFD versus non-IFD patients.
Overall, 9143 patients received an SOT (5667 kidney, 2025 liver, 759 heart, 650 lung, 39 pancreas, 3 intestine), and 5693 patients received an HCT (3519 autologous, 2114 allogeneic, 60 unspecified type). Among SOT patients, 360 developed an IFD (incidence: 21.0 [per 1000 person-years]). Mold infections had the highest incidence (7.1), followed by unspecified mycoses (3.9) and endemic mycoses (3.3). Among HCT patients, 292 developed an IFD (incidence: 28.5), with higher incidence among allogeneic (58.4) versus autologous (12.8) HCT recipients; among all HCT recipients, unspecified mycoses had the highest incidence (8.3), then pneumocystosis (7.6), and mold infections (6.7). Median time to IFD was 173.5 days for SOT recipients and 197.5 days for HCT recipients. IFD risk varied substantially by transplant type, region, and certain underlying conditions.
Our results suggest that IFDs remain an important cause of infection among SOT and HCT recipients, particularly later in the posttransplant period, and highlight the need for prevention strategies.
更新实体器官移植(SOT)和造血细胞移植(HCT)受者侵袭性真菌病(IFD)的基准数据对于提高临床认知并为治疗和预防策略提供依据十分必要。我们在美国一个大型商业健康保险数据库中估算了移植受者的IFD发病率及潜在风险因素。
我们观察了2018年至2022年期间接受SOT或HCT的患者,直至发生IFD、退出研究或数据库截止日期(2023年7月31日)。我们计算了发病率(每1000人年)和发生IFD的时间,比较了IFD患者与非IFD患者的人口统计学特征和基础疾病。
总体而言,9143例患者接受了SOT(5667例肾移植、2025例肝移植、759例心脏移植、650例肺移植、39例胰腺移植、3例肠移植),5693例患者接受了HCT(3519例自体移植、2114例异体移植、60例未明确类型)。在SOT患者中,360例发生了IFD(发病率:21.0[每1000人年])。霉菌感染发病率最高(7.1),其次是未明确的真菌病(3.9)和地方性真菌病(3.3)。在HCT患者中,292例发生了IFD(发病率:28.5),异体HCT受者(58.4)的发病率高于自体HCT受者(12.8);在所有HCT受者中,未明确的真菌病发病率最高(8.3),其次是肺孢子菌病(7.6)和霉菌感染(6.7)。SOT受者发生IFD的中位时间为173.5天,HCT受者为197.5天。IFD风险因移植类型、地区和某些基础疾病而有很大差异。
我们的结果表明,IFD仍然是SOT和HCT受者感染的重要原因,尤其是在移植后期,并强调了预防策略的必要性。