@article {Godfrey412, author = {Rebecca Godfrey and Sally Curtis and William HK Schilling and P Rachael James}, title = {Blood culture negative endocarditis in the modern era of 16S rRNA sequencing}, volume = {20}, number = {4}, pages = {412--416}, year = {2020}, doi = {10.7861/clinmed.2019-0342}, publisher = {Royal College of Physicians}, abstract = {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 Coxiella and Bartonella 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.}, issn = {1470-2118}, URL = {https://www.rcpjournals.org/content/20/4/412}, eprint = {https://www.rcpjournals.org/content/20/4/412.full.pdf}, journal = {Clinical Medicine} }