Sahbudak Bal Zumrut, Yilmaz Karapinar Deniz, Karadas Nihal, Sen Semra, Onder Sivis Zuhal, Akinci Ayse B, Balkan Can, Kavakli Kaan, Vardar Fadil, Aydinok Yesim
Division of Infectious Diseases, Department of Pediatrics, Faculty of Medicine, Ege University, Izmir, Turkey.
Mycoses. 2015 Apr;58(4):225-32. doi: 10.1111/myc.12303. Epub 2015 Feb 27.
Despite improvements in diagnosis and treatment, invasive fungal infections (IFIs) are still a major cause of morbidity and mortality in immunocompromised patients. The data on IFI among children with acute lymphoblastic leukaemia (ALL) are still scarce, and our aim was to estimate the risk, aetiology and outcome of proven and probable IFIs in children with ALL who did not receive primary prophylaxis over an 8-year period. Between January 2005 and February 2013, 125 children who were treated for ALL at the Pediatric Hematology Department of the Medical School of Ege University were retrospectively reviewed. Proven and probable IFIs were defined according to revised definitions of the European Organization for Research and Treatment of Cancer/Invasive Fungal Infections Cooperative Group and the National Institute of Allergy and Infectious Diseases Mycoses Study Group. The proven and probable IFI incidence was 30/125 (24%). Profound neutropenia was detected in 18 (60%) patients, and prolonged neutropenia was detected in 16 (53.3%) of the patients. The most isolated agents were non-albicans Candida spp. The crude and attributable mortality was 20% and 13.3% respectively. Profound neutropenia was associated with mortality (P < 0.05). The younger patients were especially at risk for proven IFI. Prolonged neutropenia, to be in the induction phase of chemotherapy, and profound neutropenia were found to be the most common predisposing factors for IFI episodes.
尽管在诊断和治疗方面有所改进,但侵袭性真菌感染(IFI)仍是免疫功能低下患者发病和死亡的主要原因。急性淋巴细胞白血病(ALL)患儿中IFI的数据仍然匮乏,我们的目的是评估8年间未接受一级预防的ALL患儿确诊和疑似IFI的风险、病因及预后。2005年1月至2013年2月,对在伊兹密尔大学医学院儿科血液科接受ALL治疗的125名儿童进行了回顾性研究。确诊和疑似IFI根据欧洲癌症研究与治疗组织/侵袭性真菌感染协作组以及美国国立过敏和传染病研究所真菌病研究组的修订定义来确定。确诊和疑似IFI的发生率为30/125(24%)。18名(60%)患者检测到严重中性粒细胞减少,16名(53.3%)患者检测到持续性中性粒细胞减少。分离出最多的病原体是非白色念珠菌属。粗死亡率和归因死亡率分别为20%和13.3%。严重中性粒细胞减少与死亡率相关(P<0.05)。年龄较小的患者尤其有确诊IFI的风险。持续性中性粒细胞减少、处于化疗诱导期以及严重中性粒细胞减少被发现是IFI发作最常见的诱发因素。