Schuster Mindy G, Cleveland Angela A, Dubberke Erik R, Kauffman Carol A, Avery Robin K, Husain Shahid, Paterson David L, Silveira Fernanda P, Chiller Tom M, Benedict Kaitlin, Murphy Kathleen, Pappas Peter G
University of Pennsylvania, Philadelphia.
Centers for Disease Control and Prevention, Atlanta, Georgia.
Open Forum Infect Dis. 2017 Mar 22;4(2):ofx050. doi: 10.1093/ofid/ofx050. eCollection 2017 Spring.
Infection is a major cause of morbidity and mortality after allogeneic hematopoietic cell transplantation (HCT). Our object was to better define the epidemiology and outcomes of infections after HCT.
This was a prospective, multicenter cohort study of HCT recipients and conducted from 2006 to 2011. The study included 4 US transplant centers and 444 HCT recipients. Data were prospectively collected for up to 30 months after HCT using a standardized data collection tool.
The median age was 53 years, and median follow up was 413 (range, 5-980) days. The most common reason for HCT was hematologic malignancy (87%). The overall crude mortality was 52%. Death was due to underlying disease in 44% cases and infection in 21%. Bacteremia occurred in 231 (52%) cases and occurred early posttransplant (median day 48). Gram-negative bloodstream infections were less frequent than Gram-positive, but it was associated with higher mortality (45% vs 13%, = .02). infection developed in 148 patients (33%) at a median of 27 days post-HCT. There were 53 invasive fungal infections (IFIs) among 48 patients (11%). The median time to IFI was 142 days. Of 155 patients with cytomegalovirus (CMV) infection, 4% had CMV organ involvement. Varicella zoster infection (VZV) occurred in 13 (4%) cases and was disseminated in 2. Infection with respiratory viruses was seen in 49 patients. pneumonia was rare (1%), and there were no documented cases of nocardiosis, toxoplasmosis, endemic mycoses, or mycobacterial infection. This study lacked standardized antifungal and antiviral prophylactic strategies.
Infection remains a significant cause of morbidity and mortality after HCT. Bacteremias and infection are frequent, particularly in the early posttransplant period. The rate of IFI is approximately 10%. Organ involvement with CMV is infrequent, as are serious infections with VZV and herpes simplex virus, likely reflecting improved prevention strategies.
感染是异基因造血细胞移植(HCT)后发病和死亡的主要原因。我们的目的是更好地明确HCT后感染的流行病学情况及转归。
这是一项针对HCT受者的前瞻性多中心队列研究,于2006年至2011年开展。该研究纳入了美国的4个移植中心及444例HCT受者。使用标准化数据收集工具前瞻性收集HCT后长达30个月的数据。
中位年龄为53岁,中位随访时间为413天(范围5 - 980天)。进行HCT最常见的原因是血液系统恶性肿瘤(87%)。总体粗死亡率为52%。44%的死亡病例归因于基础疾病,21%归因于感染。231例(52%)发生了菌血症,且多发生在移植后早期(中位时间为第48天)。革兰阴性血流感染比革兰阳性血流感染少见,但与之相关的死亡率更高(45%对13%,P = 0.02)。148例患者(33%)在HCT后中位27天发生了侵袭性真菌感染。48例患者(11%)发生了53例侵袭性真菌感染(IFI)。发生IFI的中位时间为142天。155例巨细胞病毒(CMV)感染患者中,4%有CMV累及器官。水痘带状疱疹感染(VZV)发生了13例(4%),其中2例为播散性感染。49例患者出现呼吸道病毒感染。曲霉菌肺炎罕见(1%),且没有诺卡菌病、弓形虫病、地方性真菌病或分枝杆菌感染的记录病例。本研究缺乏标准化的抗真菌和抗病毒预防策略。
感染仍然是HCT后发病和死亡的重要原因。菌血症和侵袭性真菌感染很常见,尤其是在移植后早期。IFI的发生率约为10%。CMV累及器官的情况不常见,VZV和单纯疱疹病毒的严重感染也不常见,这可能反映了预防策略的改进。