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

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  • معلومة اضافية
    • Contributors:
      Service d'Oncologie Médicale Centre hospitalier Lyon Sud - HCL; Centre Hospitalier Lyon Sud CHU - HCL (CHLS); Hospices Civils de Lyon (HCL)-Hospices Civils de Lyon (HCL); Centre de Recherche en Cancérologie de Lyon (UNICANCER/CRCL); Centre Léon Bérard Lyon -Université Claude Bernard Lyon 1 (UCBL); Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS); Institut des Agents Infectieux Lyon (IAI); Hospices Civils de Lyon (HCL); Assistance Publique - Hôpitaux de Marseille (APHM); CHU Trousseau APHP; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU); Service d'Hématologie Cellulaire Lille; Centre Hospitalier Régional Universitaire CHU Lille (CHRU Lille); Université de Lille-Université de Lille; Département d'Oncologie et Hématologie Strasbourg; Les Hôpitaux Universitaires de Strasbourg (HUS); Département d'oncologie médicale Rennes; CRLCC Eugène Marquis (CRLCC); UNICANCER-UNICANCER; Centre Hospitalier Régional Universitaire Montpellier (CHRU Montpellier); CHU Grenoble; Institut Jean Godinot Reims; UNICANCER; Clinique d'Oncologie et de Radiothérapie Tours (CORAD); Centre Hospitalier Régional Universitaire de Tours (CHRU Tours)-Hôpital Bretonneau; Centre Hospitalier Universitaire d'Angers (CHU Angers); PRES Université Nantes Angers Le Mans (UNAM); Centre Hospitalier Universitaire de Saint-Etienne CHU Saint-Etienne (CHU ST-E); Service de Pédiatrie Enfants - Hématologie Oncologie CHU de Dijon; Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon); CHU de Bordeaux Pellegrin Bordeaux; Service d'Oncologie médicale CHU Limoges; CHU Limoges; Unité d'hémato-immuno-oncologie pédiatrique CHU Caen; Université de Caen Normandie (UNICAEN); Normandie Université (NU)-Normandie Université (NU)-CHU Caen; Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Tumorothèque de Caen Basse-Normandie (TCBN); Service d'Hématologie et Oncologie pédiatrique CHRU Besançon; Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon); Hôpitaux Pédiatriques de Nice Lenval (CHU-Lenval); Centre Hospitalier Universitaire de Nice (CHU Nice); Service d'hémato-immuno-oncologie pédiatrique Rouen; CHU Rouen; Normandie Université (NU)-Normandie Université (NU)-Université de Rouen Normandie (UNIROUEN); Normandie Université (NU); Centre Hospitalier Universitaire de Toulouse (CHU Toulouse); Service d'Oncologie Pédiatrique CHRU Nancy; Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy); Département de pédiatrie CHU Nantes; Centre hospitalier universitaire de Nantes (CHU Nantes); Service d'Hématologie Biologique Hôpital Robert Debré, Paris; AP-HP Hôpital universitaire Robert-Debré Paris; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
    • بيانات النشر:
      HAL CCSD
      Elsevier
    • الموضوع:
      2021
    • Collection:
      Archive ouverte HAL (Hyper Article en Ligne, CCSD - Centre pour la Communication Scientifique Directe)
    • نبذة مختصرة :
      International audience ; 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 a-HSCT 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 ×10-4) 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.
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/33991540; hal-03666730; https://hal.umontpellier.fr/hal-03666730; https://hal.umontpellier.fr/hal-03666730/document; https://hal.umontpellier.fr/hal-03666730/file/S002234762100439X.pdf; PII: S0022-3476(21)00439-X; PUBMED: 33991540
    • الرقم المعرف:
      10.1016/j.jpeds.2021.05.016
    • Rights:
      http://creativecommons.org/licenses/by-nc/ ; info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.C7D2934A