Fang Guo1, Lei Kang2, Lin Zhang3. 1. Department of Infections, Hebei Children's Hospital, affiliated to Hebei Medical University, Shijiazhuang, Hebei, China. Electronic address: 18231101770@163.com. 2. Department of Pediatric Intensive Care Unit, Hebei Children's Hospital, affiliated to Hebei Medical University, Shijiazhuang, Hebei, China. Electronic address: rxkanglei@126.com. 3. Department of Pediatrics, Hebei Medical University Third Hospital, Shijiazhuang, Hebei, China. Electronic address: lzhang79@126.com.
Abstract
OBJECTIVE: To investigate the application value of metagenomic next-generation sequencing (mNGS) in children with hematological diseases presenting with Febrile Neutropenia (FN). METHODS: We retrospectively analyzed the clinical data of 49 hematological children with FN, and compared the results of mNGS with those of traditional pathogen detection (TPD) and the prognoses of mNGS positive group and negative group. RESULTS: A total of 77 pathogenic strains were identified, of which 70 strains were detected by mNGS, 19 strains by TPD, and Aspergillus and G- bacterias were the predominant strains in FN children who developed bloodstream infections. 42 cases were in the mNGS-positive group, of which 17 were simple infections, 25 were mixed infections, and 7 were in the negative group; the TPD-positive group contained 19 cases, all of which were simple infections. The detection rate of total and mixed pathogens was higher than that of TPD, and the difference was statistically significant (P<0.05). The mNGS positive group was detected earlier than the negative group, and with lower mortality and drug-related adverse events (DRAE), and the difference was statistically significant (P<0.05). CONCLUSION: For FN children with hematological diseases, early mNGS can effectively improve the efficacy of pathogen detection, and precise treatment after clarifying the pathogens can reduce mortality and avoid antibiotic abuse.
OBJECTIVE: To investigate the application value of metagenomic next-generation sequencing (mNGS) in children with hematological diseases presenting with Febrile Neutropenia (FN). METHODS: We retrospectively analyzed the clinical data of 49 hematological children with FN, and compared the results of mNGS with those of traditional pathogen detection (TPD) and the prognoses of mNGS positive group and negative group. RESULTS: A total of 77 pathogenic strains were identified, of which 70 strains were detected by mNGS, 19 strains by TPD, and Aspergillus and G- bacterias were the predominant strains in FN children who developed bloodstream infections. 42 cases were in the mNGS-positive group, of which 17 were simple infections, 25 were mixed infections, and 7 were in the negative group; the TPD-positive group contained 19 cases, all of which were simple infections. The detection rate of total and mixed pathogens was higher than that of TPD, and the difference was statistically significant (P<0.05). The mNGS positive group was detected earlier than the negative group, and with lower mortality and drug-related adverse events (DRAE), and the difference was statistically significant (P<0.05). CONCLUSION: For FN children with hematological diseases, early mNGS can effectively improve the efficacy of pathogen detection, and precise treatment after clarifying the pathogens can reduce mortality and avoid antibiotic abuse.