Author: Lefeuvre, Caroline; Salmona, Maud; Bondeelle, Louise; Houdouin, Véronique; Feghoul, Linda; Jacquier, Hervé; Mercier-Delarue, Séverine; Bergeron, Anne; LeGoff, Jérôme
                    Title: Frequent lower respiratory tract disease in hematological patients with Parainfluenza virus type 3 infection.  Cord-id: phd562pa  Document date: 2021_7_29
                    ID: phd562pa
                    
                    Snippet: Human parainfluenza virus type 3 (HPIV-3) may cause lower respiratory tract infection disease (LRTI-D) after hematopoietic stem cell transplantation (HSCT). Most previous studies focused on recipients of hematopoietic stem cell transplantation (HSCT) whereas data on characteristics and outcomes in patients with hematological malignancies (HM) compared to non-hematological patients are limited. The prognostic value of viral load in respiratory specimens remains elusive. In a two-year retrospectiv
                    
                    
                    
                     
                    
                    
                    
                    
                        
                            
                                Document: Human parainfluenza virus type 3 (HPIV-3) may cause lower respiratory tract infection disease (LRTI-D) after hematopoietic stem cell transplantation (HSCT). Most previous studies focused on recipients of hematopoietic stem cell transplantation (HSCT) whereas data on characteristics and outcomes in patients with hematological malignancies (HM) compared to non-hematological patients are limited. The prognostic value of viral load in respiratory specimens remains elusive. In a two-year retrospective study, we determined frequencies of LRTI-D in HM, HSCT and in non-hematological patients, and HPIV-3 levels in respiratory tract secretions. Among 98 patients with HPIV-3 infection, including 31 HSCT and 40 HM, 36 had a diagnosis of LRTI-D. LRTI-D was significantly more frequent in patients with HM or HSCT (n=32, 45.1%) than in non-hematological patients (n=4, 14.8%) (p=0.006). The median HPIV-3 loads were high in upper respiratory tract secretions regardless of the presence or absence of LRTI-D (8.3 log10 vs 7.6 log10 TCID50 /106 cells). HPIV-3 loads in respiratory tract samples in HM were not significantly higher than those found in HSCT but significantly higher than in non-hematological patients (p=0.007). In conclusion, LRTI-D was frequent in HM patients who were diagnosed with HPIV-3 infection. This article is protected by copyright. All rights reserved.
 
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