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Functional hyposplenism after hematopoietic stem cell transplantation

机译:造血干细胞移植后功能不全

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Functional hyposplenism is associated with chronic GvHD (cGvHD) following hematopoietic stem cell transplantation (HSCT). We hypothesized that hyposplenism measured by pitted red cell counts in cGvHD was transient and related to the severity of disease. We performed a serial, retrospective review of 36 pediatric post-HSCT patients' pit counts at BC Children's Hospital from 2005 to 2013 and compared those counts with the clinical course of patients with late acute GvHD (aGvHD)/cGvHD. Of the 36 patients, 22 had late aGvHD/cGvHD based on National Institutes of Health consensus criteria. Fourteen of 22 GvHD patients had an abnormal pitted red cell count. Ten of 14 abnormal patients had late acute or overlap GvHD syndrome, primarily gastrointestinal disease. A second cohort was prospectively evaluated in a multicenter adult HSCT biomarker trial. We identified 3 out of 10 control patients who had an abnormal pitted red cell count, 3 out of 10 with classic cGvHD and 5 out of 9 patients with overlap syndrome were abnormal. In both the retrospective and prospective studies, hyposplenism was present in patients without late aGvHD/cGvHD suggesting current guidelines regarding antibiotic prophylaxis against encapsulated bacteria after HSCT need to be re-addressed and abnormal pit counts could be used to guide prophylaxis in all HSCT patients.
机译:功能性脾功能不全与造血干细胞移植(HSCT)后的慢性GvHD(cGvHD)相关。我们假设通过cGvHD的红细胞计数测量的脾功能低下是短暂的,并且与疾病的严重程度有关。我们对2005年至2013年在BC儿童医院进行的36例小儿HSCT术后小儿计数进行了系列回顾性回顾,并将这些计数与晚期急性GvHD(aGvHD)/ cGvHD患者的临床病程进行了比较。根据美国国立卫生研究院的共识标准,在36例患者中,有22例晚期aGvHD / cGvHD。 22名GvHD患者中有14名的红细胞计数异常。 14名异常患者中有10名患有晚期急性或重叠GvHD综合征,主要是胃肠道疾病。在多中心成人HSCT生物标志物试验中前瞻性评估了第二个队列。我们确定了每10名对照患者中有3名出现空洞红细胞计数异常,10名经典cGvHD患者中有3名以及9名重叠综合征患者中有5名异常。在回顾性研究和前瞻性研究中,无晚期aGvHD / cGvHD的患者均存在脾功能低下,提示目前需要重新处理HSCT后针对包膜细菌的抗生素预防的现行指南,并且异常窝数可用于指导所有HSCT患者的预防。

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