Infections With Stenotrophomonas maltophilia in Children Undergoing Anticancer Therapy or Hematopoietic Cell Transplantation: A Multicenter Nationwide Study

被引:6
作者
Richert-Przygonska, Monika [1 ]
Czyzewski, Krzysztof [1 ]
Dziedzic, Magdalena [1 ]
Zalas-Wiecek, Patrycja [2 ]
Gryniewicz-Kwiatkowska, Olga [3 ]
Gietka, Agnieszka [3 ]
Malas, Zofia [3 ]
Semczuk, Katarzyna [4 ]
Chelmecka, Liliana [5 ]
Zak, Iwona [6 ]
Salamonowicz-Bodzioch, Malgorzata [7 ]
Fraczkiewicz, Jowita [7 ]
Zajac-Spychala, Olga [8 ]
Bien, Ewa [9 ]
Irga-Jaworska, Ninela [9 ]
Plonowski, Marcin [10 ]
Wawrykow, Pawel [11 ]
Bartnik, Magdalena [12 ]
Pierlejewski, Filip [13 ]
Gamrot, Zuzanna [14 ]
Badowska, Wanda [15 ]
Stolpa, Weronika [16 ]
Musial, Jakub [17 ]
Szmydki-Baran, Anna [18 ]
Hutnik, Lukasz [18 ]
Tomaszewska, Renata [19 ]
Urbanek-Dadela, Agnieszka [20 ]
Zaucha-Prazmo, Agnieszka [21 ]
Gozdzik, Jolanta [22 ]
Styczynski, Jan [1 ]
机构
[1] Nicolaus Copernicus Univ Forun, Coll Med, Dept Pediat Hematol & Oncol, Bydgoszcz, Poland
[2] Nicolaus Copernicus Univ Torun, Coll Med, Dept Microbiol, Bydgoszcz, Poland
[3] Childrens Mem Hlth Inst, Dept Oncol, Warsaw, Poland
[4] Childrens Mem Hlth Inst, Dept Microbiol, Warsaw, Poland
[5] Jagiellonian Univ, Univ Childrens Hosp, Coll Med, Dept Pediat Oncol & Hematol, Krakow, Poland
[6] Univ Childrens Hosp, Dept Microbiol, Krakow, Poland
[7] Med Univ, Dept Pediat Stem Cell Transplantat Hematol & Onco, Wroclaw, Poland
[8] Univ Med Sci, Dept Pediat Oncol Hematol & Transplantol, Poznan, Poland
[9] Med Univ, Dept Pediat Hematol & Oncol, Gdansk, Poland
[10] Med Univ, Dept Pediat Oncol & Hematol, Bialystok, Poland
[11] Pomeranian Med Univ, Dept Pediat Pediat Oncol & Immunol, Szczecin, Poland
[12] Pomeranian Med Univ, Dept Pediat Pediat Hematooncol & Gastroenterol, Szczecin, Poland
[13] Med Univ, Dept Pediat Hematol & Oncol, Lodz, Poland
[14] Chorzow City Hosp, Div Pediat Hematol & Oncol, Chorzow, Poland
[15] Children Hosp, Div Pediat Hematol & Oncol, Olsztyn, Poland
[16] Silesian Med Univ, Dept Pediat, Div Pediat Oncol Hematol & Chemotherapy, Katowice, Poland
[17] Univ Rzeszow, Clin Prov Hosp 2, Med Fac, Dept Pediat Oncohematol, Rzeszow, Poland
[18] Med Univ, Dept Pediat Hematol & Oncol, Warsaw, Poland
[19] Silesian Med Univ, Dept Pediat Hematol & Oncol, Zabrze, Poland
[20] Children Hosp, Div Pediat Hematol & Oncol, Kielce, Poland
[21] Med Univ, Dept Pediat Hematol Oncol & Transplantol, Lublin, Poland
[22] Jagiellonian Univ Coll Med, Univ Childrens Hosp, Stem Cell Transplant Ctr, Dept Clin Immunol & Transplantol, Krakow, Poland
关键词
acute leukemia; children; hematopoietic cell transplantation; Stenotrophomonas maltophilia; CENTRAL VENOUS CATHETER; RISK-FACTORS; BACTEREMIA; MORTALITY; HEMATOLOGY;
D O I
10.1097/INF.0000000000003633
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: Infections caused by Stenotrophomonas maltophilia (SM) have documented high mortality rate in immunocompromised patients. Aim: This nationwide multicenter study was performed to analyze the epidemiology of SM infections in children undergoing anticancer therapy (pediatric hematology and oncology [PHO]) or hematopoietic cell transplantation (HCT) over 2012-2019, including incidence and outcome of SM infections, as well as treatment regimens and multidrug resistance. Methods: Cumulative incidence of SM infections was calculated using the competing risk analysis from the day of diagnosis (PHO setting) or from the day of transplantation (HCT setting). The Kaplan-Meier method was used to determine survival from infection. Results: During the study period of 8 years, a total number of 1356 HCTs and 7337 children newly diagnosed for malignancy were analyzed. Diagnosis of acute leukemia was a predisposing factor for SM infection. The cumulative incidence of SM infections was comparable in HCT patients in comparison to PHO (0.81% vs. 0.76%). High rate of trimethoprim/ sulfamethoxazole susceptibility among SM isolates was observed in both groups of patients (80.8%). Although this was the drug of choice, survival rates from SM infections were significantly lower in HCT than in PHO (45% vs. 85%, P = 0.001, log-rank test). We found the transplant procedure and lack of clinical resolution after 18 days of antibiotic therapy to be independent mortality risk factors. Conclusions: The risk of SM infections and the occurrence of resistant bacterial strains in allo-HCT patients were comparable to PHO patients. Irrespective of target antibiotic therapy, the outcome of SM infections was better in the PHO setting.
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页码:846 / 850
页数:5
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