Schöning Stefan, Barnbrock Anke, Bochennek Konrad, Gordon Kathrin, Groll Andreas H, Lehrnbecher Thomas
Pediatric Hematology and Oncology, Hospital for Children and Adolescents, Johann Wolfgang Goethe-University, 60590 Frankfurt, Germany.
Infectious Disease Research Program, Department of Pediatric Hematology and Oncology and Center for Bone Marrow Transplantation, University Children's Hospital Münster, 48149 Münster, Germany.
Antibiotics (Basel). 2022 Jul 5;11(7):900. doi: 10.3390/antibiotics11070900.
Whereas the clinical approach in pediatric cancer patients with febrile neutropenia is well established, data on non-neutropenic infectious episodes are limited. We therefore prospectively collected over a period of 4 years of data on all infectious complications in children treated for acute lymphoblastic or myeloid leukemia (ALL or AML) and non-Hodgkin lymphoma (NHL) at two major pediatric cancer centers. Infections were categorized as fever of unknown origin (FUO), and microbiologically or clinically documented infections. A total of 210 patients (median age 6 years; 142 ALL, 23 AML, 38 NHL, 7 leukemia relapse) experienced a total of 776 infectious episodes (571 during neutropenia, 205 without neutropenia). The distribution of FUO, microbiologically and clinically documented infections, did not significantly differ between neutropenic and non-neutropenic episodes. In contrast to neutropenic patients, corticosteroids did not have an impact on the infectious risk in non-neutropenic children. All but one bloodstream infection in non-neutropenic patients were due to -positive pathogens. Three patients died in the context of non-neutropenic infectious episodes (mortality 1.4%). Our results well help to inform clinical practice guidelines in pediatric non-neutropenic cancer patients presenting with fever, in their attempt to safely restrict broad-spectrum antibiotics and improve the quality of life by decreasing hospitalization.
虽然小儿癌症发热性中性粒细胞减少症患者的临床治疗方法已得到充分确立,但关于非中性粒细胞减少性感染发作的数据却很有限。因此,我们前瞻性地收集了4年期间在两家主要儿科癌症中心接受急性淋巴细胞白血病或髓细胞白血病(ALL或AML)以及非霍奇金淋巴瘤(NHL)治疗的儿童所有感染并发症的数据。感染被分类为不明原因发热(FUO)以及微生物学或临床确诊的感染。共有210名患者(中位年龄6岁;142例ALL、23例AML、38例NHL、7例白血病复发)共经历了776次感染发作(中性粒细胞减少期间571次,非中性粒细胞减少期间205次)。FUO、微生物学确诊和临床确诊感染在中性粒细胞减少和非中性粒细胞减少发作之间的分布没有显著差异。与中性粒细胞减少患者不同,皮质类固醇对非中性粒细胞减少儿童的感染风险没有影响。非中性粒细胞减少患者中除1例血流感染外,均由革兰氏阳性病原体引起。3例患者在非中性粒细胞减少性感染发作期间死亡(死亡率1.4%)。我们的结果将有助于为出现发热的小儿非中性粒细胞减少性癌症患者的临床实践指南提供参考,以安全地限制使用广谱抗生素,并通过减少住院时间来提高生活质量。