Association Between Corticosteroids and Infection, Sepsis, and Infectious Death in Pediatric Acute Myeloid Leukemia (AML): Results From the Canadian Infections in AML Research Group

被引:66
作者
Dix, David [2 ]
Cellot, Sonia [3 ]
Price, Victoria [4 ]
Gillmeister, Biljana
Ethier, Marie-Chantal
Johnston, Donna L. [5 ]
Lewis, Victor [6 ]
Michon, Bruno [7 ]
Mitchell, David [8 ]
Stobart, Kent [9 ]
Yanofsky, Rochelle [10 ]
Portwine, Carol [11 ]
Silva, Mariana [12 ]
Bowes, Lynette [13 ]
Zelcer, Shayna [14 ]
Brossard, Josee [15 ]
Traubici, Jeffrey [16 ]
Allen, Upton [17 ]
Beyene, Joseph [18 ]
Sung, Lillian [1 ]
机构
[1] Hosp Sick Children, Div Haematol Oncol, Toronto, ON M5G 1X8, Canada
[2] British Columbia Childrens Hosp, Vancouver, BC V6H 3V4, Canada
[3] Hosp St Justine, Montreal, PQ, Canada
[4] IWK Hlth Ctr, Halifax, NS, Canada
[5] Childrens Hosp Eastern Ontario, Ottawa, ON K1H 8L1, Canada
[6] Alberta Childrens Prov Gen Hosp, Hematol Oncol Transplant Program, Calgary, AB T2T 5C7, Canada
[7] Hosp Univ Quebec, Pediat Hematol Oncol Ctr, Quebec City, PQ, Canada
[8] Montreal Childrens Hosp, Montreal, PQ, Canada
[9] Univ Alberta Hosp, Stollery Childrens Hosp, Toronto, ON, Canada
[10] CancerCare Manitoba, Hematol Oncol, Winnipeg, MB, Canada
[11] Chedoke McMaster Hosp, Hamilton, ON, Canada
[12] Canc Ctr SE Ontario, Kingston, ON, Canada
[13] Janeway Child Hlth Ctr, St John, NF, Canada
[14] London Hlth Sci, Hematol Oncol, London, ON, Canada
[15] CHU Sherbrooke, Quebec City, PQ, Canada
[16] Hosp Sick Children, Dept Diagnost Imaging, Toronto, ON M5G 1X8, Canada
[17] Hosp Sick Children, Div Infect Dis, Toronto, ON M5G 1X8, Canada
[18] McMaster Univ, Dept Clin Epidemiol & Biostat, Populat Genom Program, Hamilton, ON, Canada
基金
加拿大健康研究院;
关键词
VERSUS-HOST-DISEASE; FUNGAL-INFECTIONS; HIGH-RISK; CHILDREN; METHYLPREDNISOLONE; PREVENTION; MYCOSES; GROWTH; CANCER;
D O I
10.1093/cid/cis774
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. Infection continues to be a major problem for children with acute myeloid leukemia (AML). Objectives were to identify factors associated with infection, sepsis, and infectious deaths in children with newly diagnosed AML. Methods. We conducted a retrospective, population-based cohort study that included children <= 18 years of age with de novo, non-M3 AML diagnosed between January 1995 and December 2004, treated at 15 Canadian centers. Patients were monitored for infection from initiation of AML treatment until recovery from the last cycle of chemotherapy, conditioning for hematopoietic stem cell transplantation, relapse, persistent disease, or death (whichever occurred first). Consistent trained research associates abstracted all information from each site. Results. 341 patients were included. Median age was 7.1 years (interquartile range [IQR], 2.0-13.5) and 29 (8.5%) had Down syndrome. In sum, 26 (7.6%) experienced death as a first event. There were 1277 courses of chemotherapy administered in which sterile site microbiologically documented infection occurred in 313 courses (24.5%). Sepsis and infectious death occurred in 97 (7.6%) and 16 (1.3%) courses, respectively. The median days of corticosteroid administration was 2 per course (IQR, 0-6). In multiple regression analysis, duration of corticosteroid exposure was significantly associated with more microbiologically documented sterile site infection, bacteremia, fungal infection, and sepsis. The only factor significantly associated with infectious death was days of corticosteroid exposure (odds ratio, 1.05; 95% confidence interval, 1.02-1.08; P = .001). Conclusions. In pediatric AML, infection, sepsis, and infectious death were associated with duration of corticosteroid exposure. Corticosteroids should be avoided when possible for this population.
引用
收藏
页码:1608 / 1614
页数:7
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