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Blood culture negative endocarditis in the modern era of 16S rRNA sequencing

机译:血液培养阴性心内膜炎在16S rRNA测序的现代时代

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摘要

Blood culture negative endocarditis (BCNE) accounts for up to 20% of infective endocarditis. While the most common cause of BCNE remains the initiation of antibiotics prior to culture, intracellular organisms such as and spp account for a significant proportion of cases. Identifying the infecting organism remains important to ensure optimal antimicrobial treatment. However, these organisms can be difficult to diagnose. We outline a systematic approach to BCNE. Over half of patients with infective endocarditis now undergo early surgery and 16S ribosomal ribonucleic acid (rRNA) polymerase chain reaction (PCR) of excised tissue can be vitally important to secure a diagnosis. Molecular testing is likely to become a key tool in improving outcomes from BCNE and contribute to an improved understanding of the aetiology. We advocate modifying the Duke criteria to incorporate organisms identified on molecular testing, including 16S rRNA PCR, in particular from explanted tissue.
机译:血液培养阴性心内膜炎(BCNE)占感染心内膜炎的20%。虽然BCNE最常见的原因仍然是在培养之前的抗生素的启动,但细胞内生物如和SPP占案例的显着比例。鉴定感染有机体仍然是确保最佳抗微生物治疗的重要性。然而,这些生物可能难以诊断。我们概述了BCNE的系统方法。超过一半的感染性心内膜炎现在经过早期手术和16s核糖体核糖核酸(RRNA)聚合酶链反应(PCR)的切除组织可能对确诊诊断至关重要。分子测试可能成为改善BCNE的结果的关键工具,并有助于改善对疾病的理解。我们主张修改公爵标准,以纳入分子检测上鉴定的生物,包括16S rRNA PCR,特别是来自脱盐的组织。

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