Invasive Fungal Infections in Immunocompromised Children: Novel Insight Following a National Study

被引:13
作者
Olivier-Gougenheim, Laura [1 ]
Rama, Nicolas [2 ]
Dupont, Damien [3 ]
Saultier, Paul [4 ]
Leverger, Guy [5 ]
AbouChahla, Wadih [6 ]
Paillard, Catherine [7 ]
Gandemer, Virginie [8 ]
Theron, Alexandre [9 ]
Freycon, Claire [10 ]
Pluchart, Claire [11 ]
Blouin, Pascale [12 ]
Pellier, Isabelle [13 ]
Thouvenin-Doulet, Sandrine [14 ]
Desplantes, Claire [15 ]
Ducassou, Stephane [16 ]
Oudot, Caroline [17 ]
Rouger-Gaudichon, Jeremie [18 ]
Cheikh, Nathalie [19 ]
Poiree, Maryline [20 ]
Schneider, Pascale [21 ]
Plat, Genevieve [22 ]
Contet, Audrey [23 ]
Rialland, Fanny [24 ]
Gouache, Elodie [5 ]
Brethon, Benoit [25 ]
Bertrand, Yves [1 ]
Domenech, Carine [1 ,2 ]
机构
[1] Univ Lyon 1, Hosp Civils Lyon, Inst Pediat Hematol & Oncol, Pl Prof Joseph Renaut, F-69008 Lyon, France
[2] CRCL, Apoptosis, INSERM, U1052,CNRS,UMR5286, Lyon, France
[3] Inst Agents Infectieux, Parasitol Mycol Unit, Lyon, France
[4] CHU Marseille, Pediat Hematol Oncol Unit, Marseille, France
[5] AP HP Trousseau, Pediat Hematol Oncol Unit, Paris, France
[6] CHU Lille, Pediat Hematol Unit, Lille, France
[7] CHU Strasbourg, Pediat Hematol Oncol Unit, Strasbourg, France
[8] CHU Rennes, Pediat Hematol Oncol Unit, Rennes, France
[9] CHU Montpellier, Pediat Hematol Oncol Unit, Montpellier, France
[10] CHU Grenoble, Pediat Hematol Oncol Unit, Grenoble, France
[11] CHU Reims, Pediat Hematol Oncol Unit, Inst Jean Godinot, Reims, France
[12] CHU Tours, Pediat Hematol Oncol Unit, Tours, France
[13] CHU Angers, Pediat Hematol Oncol Unit, Angers, France
[14] CHU St Etienne, Pediat Hematol Oncol Unit, St Etienne, France
[15] CHU Dijon, Pediat Hematol Oncol Unit, Dijon, France
[16] CHU Bordeaux, Pediat Hematol Oncol Unit, Bordeaux, France
[17] CHU Limoges, Pediat Hematol Oncol Unit, Limoges, France
[18] CHU Caen, Pediat Hematol Oncol Unit, Caen, France
[19] CHU Besancon, Pediat Hematol Oncol Unit, Besancon, France
[20] CHU Lenval Nice, Pediat Hematol Oncol Unit, Nice, France
[21] CHU Rouen, Pediat Hematol Oncol Unit, Rouen, France
[22] CHU Toulouse, Pediat Hematol Oncol Unit, Toulouse, France
[23] CHU Nancy, Pediat Hematol Oncol Unit, Nancy, France
[24] CHU Nantes, Pediat Hematol Oncol Unit, Nantes, France
[25] AP HP Robert Debre, Pediat Hematol Unit, Paris, France
关键词
ACUTE LYMPHOBLASTIC-LEUKEMIA; STEM-CELL TRANSPLANTATION; ACUTE MYELOID-LEUKEMIA; PEDIATRIC-PATIENTS; RISK-FACTORS; DISEASE; CANCER; EPIDEMIOLOGY; DIAGNOSIS; EXPERIENCE;
D O I
10.1016/j.jpeds.2021.05.016
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective To obtain a national overview of the epidemiology and management of invasive fungal infections (IFIs) in France for severely immunocompromised children who were treated for acute leukemia or had undergone allogeneic hematopoietic stem cell transplantation (a-HSCT). Study design We performed a national multicenter retrospective study to collect epidemiologic data for proven and probable IFIs in children with acute leukemia under first- line or relapse treatment or who had undergone a-HSCT. We also conducted a prospective practice survey to provide a national overview of IFI management in pediatric hematology units. Results From January 2014 to December 2017, 144 cases of IFI were diagnosed (5.3%) in 2721 patients, including 61 cases of candidiasis, 60 cases of aspergillosis, and 23 cases of infection with "emergent" fungi, including 10 cases of mucormycosis and 6 cases of fusariosis. The IFI rate was higher in patients with acute myelogenous leukemia (12.9%) (OR, 3.24; 95% CI, 2.15-4.81; P <.0001) compared with the rest of the cohort. Patients undergoing aHSCT had an IFI rate of only 4.3%. In these patients, the use of primary antifungal prophylaxis (principally fluconazole) was associated with a lower IFI rate (OR, 0.28; 95% CI, 0.14-0.60; P = 4.90 x10(-4)) compared with a-HSCT recipients who did not receive antifungal prophylaxis. The main cause of IFI in children receiving prophylaxis was emergent pathogens (41%), such as mucormycosis and fusariosis, which were resistant to the prophylactic agents. Conclusions The emerging fungi and new antifungal resistance profiles uncovered in this study should be considered in IFI management in immunocompromised children.
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页码:204 / 210
页数:7
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