Risks and outcomes of invasive fungal infections in pediatric patients undergoing allogeneic hematopoietic cell transplantation

被引:98
作者
Dvorak, CC
Steinbach, WJ
Brown, JMY
Agarwal, R
机构
[1] Stanford Univ, Sch Med, Div Pediat Hematol Oncol & Bone Marrow Transplant, Palo Alto, CA 94304 USA
[2] Duke Univ, Sch Med, Div Pediat Infect Dis, Durham, NC USA
[3] Stanford Univ, Sch Med, Div Bone Marrow Transplantat, Palo Alto, CA 94304 USA
[4] Stanford Univ, Sch Med, Div Infect Dis, Palo Alto, CA 94304 USA
关键词
invasive fungal infection; hematopoietic cell transplantation; children;
D O I
10.1038/sj.bmt.1705113
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Invasive fungal infections (IFI) are the leading cause of infectious mortality in adult patients undergoing hematopoietic cell transplantation (HCT) after myeloablative conditioning, but the extent of this problem in the pediatric population is unclear. We retrospectively examined risk factors for IFI among 120 consecutive pediatric patients undergoing allogeneic HCT at a single center. The incidence of proven or probable IFI in pediatric patients during the first year after allogeneic HCT was 13%, comparable to the rate reported in adult patients; however, unlike IFI in adult patients, the majority of IFI in children occurred within the first month after transplantation. The primary risk factors for IFI were duration of neutropenia, age greater than 10 years, transplant for severe aplastic anemia or Fanconi anemia, and high-dose corticosteroid administration for 10 days or longer. IFI were more likely to be successfully treated (42%, 5/12 patients) in pediatric HCT recipients when compared to previous reports of adult recipients. Non-relapse mortality was estimated at 17% (20/120 patients) after allogeneic HCT, of which 35% ( seven patients) were directly attributed to IFI. Thus, IFI is a significant cause of nonrelapse mortality in children undergoing allogeneic HCT and more effective strategies are needed to prevent and treat IFI.
引用
收藏
页码:621 / 629
页数:9
相关论文
共 38 条
[1]   Defining opportunistic invasive fungal infections in immunocompromised patients with cancer and hematopoietic stem cell transplants: An international consensus [J].
Ascioglu, S ;
Rex, JH ;
de Pauw, B ;
Bennett, JE ;
Bille, J ;
Crokaert, F ;
Denning, DW ;
Donnelly, JP ;
Edwards, JE ;
Erjavec, Z ;
Fiere, D ;
Lortholary, O ;
Maertens, J ;
Meis, JF ;
Patterson, TF ;
Ritter, J ;
Selleslag, D ;
Shah, PM ;
Stevens, DA ;
Walsh, TJ .
CLINICAL INFECTIOUS DISEASES, 2002, 34 (01) :7-14
[2]   Stem cell transplantation post invasive fungal infection is a feasible task [J].
Avivi, I ;
Oren, I ;
Haddad, N ;
Rowe, JM ;
Dann, EJ .
AMERICAN JOURNAL OF HEMATOLOGY, 2004, 75 (01) :6-11
[3]   Bone marrow transplantation from matched siblings in patients with Fanconi anemia utilizing low-dose cyclophosphamide, thoracoabdominal radiation and antithymocyte globulin [J].
Ayas, M ;
Solh, H ;
Mustafa, MM ;
Al-Mahr, M ;
Al-Fawaz, I ;
Al-Jefri, A ;
Shalaby, L ;
Al-Nasser, A ;
Al-Sedairy, R .
BONE MARROW TRANSPLANTATION, 2001, 27 (02) :139-143
[4]   Invasive mold infections in allogeneic bone marrow transplant recipients [J].
Baddley, JW ;
Stroud, TP ;
Salzman, D ;
Pappas, PG .
CLINICAL INFECTIOUS DISEASES, 2001, 32 (09) :1319-1324
[5]  
BENHAMOU E, 1991, BONE MARROW TRANSPL, V7, P127
[6]   Infections diagnosed in the first year after pediatric stem cell transplantation [J].
Benjamin, DK ;
Miller, WC ;
Bayliff, S ;
Martel, L ;
Alexander, KA ;
Martin, PL .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2002, 21 (03) :227-234
[7]   Successful treatment of invasive aspergillosis in chronic granulomatous disease by granulocyte transfusions followed by peripheral blood stem cell transplantation [J].
Bielorai, B ;
Toren, A ;
Wolach, B ;
Mandel, M ;
Golan, H ;
Neumann, Y ;
Kaplinisky, C ;
Weintraub, M ;
Keller, N ;
Amariglio, N ;
Paswell, J ;
Rechavi, G .
BONE MARROW TRANSPLANTATION, 2000, 26 (09) :1025-1028
[8]   Fungal infections in bone marrow transplant patients [J].
Brown, JMY .
CURRENT OPINION IN INFECTIOUS DISEASES, 2004, 17 (04) :347-352
[9]   Analysis of early infectious complications in pediatric patients undergoing bone marrow transplantation [J].
Busca, A ;
Saroglia, EM ;
Giacchino, M ;
Vai, S ;
Vassallo, E ;
Fagioli, F ;
Linari, A ;
Dotti, G ;
Miniero, R ;
Madon, E .
SUPPORTIVE CARE IN CANCER, 1999, 7 (04) :253-259
[10]  
BUSCA A, 2004, TRANSPL INFECT DIS, V5, P132