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单中心接受造血干细胞移植儿童的巨细胞病毒感染:危险因素的回顾性研究

Cytomegalovirus infection in children who underwent hematopoietic stem cell transplantation at a single center: a retrospective study of the risk factors.

作者信息

Yoon Hoi Soo, Lee Jae Hee, Choi Eun Soek, Seo Jong Jin, Moon Hyung Nam, Kim Mi-Na, Im Ho Joon

机构信息

Department of Pediatrics, Kyung-Hee University Medical Center, Seoul, Korea.

出版信息

Pediatr Transplant. 2009 Nov;13(7):898-905. doi: 10.1111/j.1399-3046.2008.01084.x. Epub 2008 Nov 18.

Abstract

CMV infection is one of the major causes of morbidity and mortality after HSCT. The aim of this single center retrospective study was to analyze risk factors for CMV infection in pediatric patients who underwent HSCT. We retrospectively reviewed the medical records of 117 pediatric patients who underwent allogeneic HSCT at Asan Medical Center between December 2000 and January 2007. After HSCT, CMV antigenemia was detected by identifying CMV pp65 early antigen in white blood cells. The incidence of CMV antigenemia was 24% (28/117) at a median of 38 days (range: 19-123 days) after HSCT. In multivariate analysis, CMV antigenemia occurred significantly more often in CMV seropositive recipients, patients who received grafts from alternative donors, T-cell depleted grafts, patients on ATG-containing conditioning regimens, or patients who received steroid for acute GVHD (p < 0.05). CMV antigenemia tend to develop earlier in patients who received ATG-containing conditioning regimens (p = 0.09). A second episode of CMV antigenemia was observed in three out of 28 patients (11%). The incidence of CMV disease was 5.9% (7/117) at a median of 97 days (range: 34-120 days). Manifestation of CMV disease included retinitis in two, pneumonitis in two, hepatitis in one, hepatitis with colitis in one, and gastritis in one. Six of the 12 patients (50%) with HG antigenemia (CMV pp65 antigen positivity > or =40 cells) developed clinical CMV disease, a rate that was significantly higher than seen in patients with LG antigenemia (6.25%; p < 0.01). We recommend that patients with these risk factors should carefully undergo regular evaluations for CMV infection. We also suggest that earlier and more aggressive preemptive treatment and serial follow-up of CMV disease is necessary in patients with HG-antigenemia.

摘要

巨细胞病毒(CMV)感染是异基因造血干细胞移植(HSCT)后发病和死亡的主要原因之一。本单中心回顾性研究的目的是分析接受HSCT的儿科患者发生CMV感染的危险因素。我们回顾性分析了2000年12月至2007年1月在峨山医院接受异基因HSCT的117例儿科患者的病历。HSCT后,通过在白细胞中鉴定CMV pp65早期抗原检测CMV抗原血症。HSCT后中位38天(范围:19 - 123天)时,CMV抗原血症的发生率为24%(28/117)。多因素分析显示,CMV血清学阳性受者、接受替代供者移植物的患者、T细胞去除的移植物、接受含抗胸腺细胞球蛋白(ATG)预处理方案的患者或因急性移植物抗宿主病(GVHD)接受类固醇治疗的患者发生CMV抗原血症的频率显著更高(p < 0.05)。接受含ATG预处理方案的患者中CMV抗原血症往往发病更早(p = 0.09)。28例患者中有3例(11%)出现了第二次CMV抗原血症。CMV疾病的发生率为5.9%(7/117),中位发病时间为97天(范围:34 - 120天)。CMV疾病的表现包括2例视网膜炎、2例肺炎、1例肝炎、1例肝炎合并结肠炎和1例胃炎。12例高负荷(HG)抗原血症(CMV pp65抗原阳性≥40个细胞)患者中有6例(50%)发生临床CMV疾病,这一发生率显著高于低负荷(LG)抗原血症患者(6.25%;p < 0.01)。我们建议具有这些危险因素的患者应仔细接受CMV感染的定期评估。我们还建议,对于HG抗原血症患者,有必要更早、更积极地进行抢先治疗并对CMV疾病进行系列随访。

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