Infectious Disease Research Program, Center for Bone Marrow Transplantation and Department of Pediatric Hematology and Oncology, University Children's Hospital Münster, Münster, Germany.
Department of Pediatric Hematology and Oncology, Children's Hospital, University Medicine Greifswald, Greifswald, Germany.
Mycoses. 2020 Feb;63(2):172-180. doi: 10.1111/myc.13029. Epub 2019 Nov 24.
Epidemiology and management practices of invasive fungal diseases (IFD) after allogeneic haematopoietic stem cell transplantation (HSCT) are a subject of constant change. We investigated the contemporary incidence, diagnostics, antifungal management and outcome at a major paediatric transplant centre in Germany.
The single-centre retrospective observational study included all paediatric allogeneic HSCT patients (pts) transplanted between 2005 and 2015. Patient-related data were assessed up to 365 days post-transplant. The primary endpoint was the incidence of possible, probable and proven IFDs. Secondary endpoints included diagnostics and antifungal treatment; analysis of risk factors; and overall survival with the last follow-up in January 2017.
A total of 221 first (196), second (21) or third (4) procedures were performed in 200 pts (median age: 9 years, range, 0.5-22) for leukaemia/lymphoma (149) and non-malignant disorders (72). Prophylaxis was administered in 208 HSCT procedures (94%; fluconazole, 116, mould-active agents, 92). At least one computed tomography scan of the chest was performed in 146, and at least one galactomannan antigen assay in 60 procedures. There were 15 cases of proven (candidemia, 4; aspergillosis, 4) or probable (aspergillosis, 7) IFDs, accounting for an incidence rate of 6.8%. Overall mortality at last follow-up was 30%; the occurrence of proven/probable IFDs was associated with a reduced survival probability (P < .001).
Morbidity and mortality from IFDs at our institution were consistent with data reported from other centres. Utilisation of healthcare resources for prevention, diagnosis and management of IFDs was considerable.
异基因造血干细胞移植(HSCT)后侵袭性真菌病(IFD)的流行病学和管理实践是一个不断变化的主题。我们在德国的一个主要儿科移植中心调查了当代发病率、诊断、抗真菌管理和结果。
这项单中心回顾性观察研究纳入了 2005 年至 2015 年间接受异基因 HSCT 的所有儿科患者(pts)。对患者相关数据进行了评估,直至移植后 365 天。主要终点是可能、可能和确诊 IFD 的发病率。次要终点包括诊断和抗真菌治疗;危险因素分析;以及截至 2017 年 1 月的最后一次随访的总生存率。
共对 200 名患者(中位年龄:9 岁,范围:0.5-22 岁)的 221 次首次(196 次)、第二次(21 次)或第三次(4 次)手术进行了评估,这些患者患有白血病/淋巴瘤(149 例)和非恶性疾病(72 例)。208 次 HSCT 手术中进行了预防治疗(94%;氟康唑 116 例,霉菌活性药物 92 例)。146 例患者至少进行了一次胸部计算机断层扫描,60 例患者至少进行了一次半乳甘露聚糖抗原检测。确诊(念珠菌血症 4 例,曲霉病 4 例)或疑似(曲霉病 7 例)IFD 共 15 例,发病率为 6.8%。最后一次随访时的总死亡率为 30%;确诊/疑似 IFD 的发生与生存率降低相关(P<.001)。
本机构 IFD 的发病率和死亡率与其他中心报告的数据一致。用于 IFD 的预防、诊断和管理的医疗资源的利用相当可观。