血培养
实时聚合酶链反应
发热性中性粒细胞减少症
中性粒细胞减少症
微生物学
细菌
生物
聚合酶链反应
16S核糖体RNA
效价
抗生素
医学
免疫学
内科学
化疗
基因
抗体
生物化学
遗传学
作者
Hideto Teranishi,Nanae Ohzono,Norikazu Inamura,Atsushi Kato,Tokio Wakabayashi,Hiroto Akaike,Kihei Terada,Kazunobu Ouchi
标识
DOI:10.1016/j.jiac.2014.11.008
摘要
Febrile neutropenia is the main treatment-related cause of mortality in cancer patients. During June 2012 to April 2014, 97 blood culture samples were collected from patients receiving chemotherapy for hematological malignancy and cancer with febrile neutropenia episodes (FNEs). The samples were examined for the presence of bacteria and fungi using real-time PCR amplification and sequencing of 16S and 18S rRNA genes. Bacteria were identified in 20 of 97 samples (20.6%) by the real-time PCR assay and in 10 of 97 (10.3%) samples by blood culture. In 6 blood culture-positive samples, the real-time PCR assay detected the same type of bacteria. No fungi were detected by the real-time PCR assay or blood culture. During antibiotic therapy, all samples were negative by blood culture, but the real-time PCR assay yielded a positive result in 2 cases of 2 (100%). The bacterial DNA copy number was not well correlated with the serum C-reactive protein titer of patients with FNEs. We conclude that a real-time PCR assay could provide better detection of causative microbes' in a shorter time, and with a smaller blood sample than blood culture. Using a real-time PCR assay in combination with blood culture could improve microbiological documentation of FNEs.
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