Community-acquired West Nile virus infection in solid-organ transplant recipients

被引:93
作者
Kumar, D
Prasad, GVR
Zaltzman, J
Levy, GA
Humar, A
机构
[1] Univ Toronto, Immunocompromised Host Infect Serv, Toronto, ON, Canada
[2] St Michaels Hosp, Div Nephrol, Toronto, ON M5B 1W8, Canada
关键词
D O I
10.1097/01.TP.0000101435.91619.31
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. West Nile virus (WNV) is rapidly spreading through North America. In the general population, the majority of WNV infections are asymptomatic. During 2002, an outbreak of WNV occurred in Toronto, Canada. We observed four cases of severe symptomatic community-acquired WNV infection in our organ-transplant population. Methods. Patient data were obtained from chart review. WNV was diagnosed by acute and convalescent serology. Incidence was compared with data obtained from a population-based surveillance program. Results. Four transplant patients had WNV encephalitis (n=3) or meningitis (n=1). Mean age was 44.5 (range 26-58) years and transplant type included kidney (n=2), liver (n=1), and heart (n=1). The mean time posttransplant was 3.8 years (range 2 months-8 years). The presenting symptoms were fever (4/4), confusion (3/4), headache (4/4), and weakness (2/4). Cerebrospinal fluid showed a pleocytosis in all patients and elevated protein in three of four. All patients had identifiable occupational or recreational risk factors. There was no evidence that the infection was acquired by transfusion or the transplanted organ. Outcomes were full recovery (2/4), lower limb paralysis (1/4), and death (1/4). On the basis of active population surveillance data, the rate of WNV meningoencephalitis in the general population in the Toronto area was approximately 5 per 100,000. This compares to four cases in a transplant population of 2,000 patients (rate 200 per 100,000) (P<0.001). Conclusions. Transplant patients are likely at greater risk of severe neurologic disease caused by community-acquired WNV compared with the general population. Prevention of transmission and patient education may be more important in this population.
引用
收藏
页码:399 / 402
页数:4
相关论文
共 18 条
[1]   Efficacy of interferon alpha-2b and ribavirin against West Nile virus in vitro [J].
Anderson, JF ;
Rahal, JJ .
EMERGING INFECTIOUS DISEASES, 2002, 8 (01) :107-108
[2]   West Nile virus [J].
Campbell, GL ;
Marfin, AA ;
Lanciotti, RS ;
Gubler, DJ .
LANCET INFECTIOUS DISEASES, 2002, 2 (09) :519-529
[3]  
Centers for Disease Control and Prevention (CDC), 2002, MMWR Morb Mortal Wkly Rep, V51, P1129
[4]  
Chowers MY, 2001, EMERG INFECT DIS, V7, P675
[5]   Poliomyelitis due to West Nile virus [J].
Glass, JD ;
Samuels, O ;
Rich, MM .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (16) :1280-1281
[6]  
Hamdan A, 2002, Transpl Infect Dis, V4, P160, DOI 10.1034/j.1399-3062.2002.01014.x
[7]   A poliomyelitis-like syndrome from West Nile virus infection [J].
Leis, AA ;
Stokic, DS ;
Polk, JL ;
Dostrow, V ;
Winkelmann, M .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (16) :1279-1280
[8]   West Nile Virus in New York City [J].
Lopez, W .
AMERICAN JOURNAL OF PUBLIC HEALTH, 2002, 92 (08) :1218-1221
[9]   Epidemic West Nile encephalitis, New York, 1999: results of a household-based seroepidemiological survey [J].
Mostashari, F ;
Bunning, ML ;
Kitsutani, PT ;
Singer, DA ;
Nash, D ;
Cooper, MJ ;
Katz, N ;
Liljebjelke, KA ;
Biggerstaff, BJ ;
Fine, AD ;
Layton, MC ;
Mullin, SM ;
Johnson, AJ ;
Martin, DA ;
Hayes, EB ;
Campbell, GL .
LANCET, 2001, 358 (9278) :261-264
[10]   The outbreak of West Nile virus infection in the New York City area in 1999. [J].
Nash, D ;
Mostashari, F ;
Fine, A ;
Miller, J ;
O'Leary, D ;
Murray, K ;
Huang, A ;
Rosenberg, A ;
Greenberg, A ;
Sherman, M ;
Wong, S ;
Layton, M ;
Campbell, GL ;
Roehrig, JT ;
Gubler, DJ ;
Shieh, WJ ;
Zaki, S ;
Smith, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (24) :1807-1814