<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Brenner T</submitter><funding>Universitätsklinikum Essen</funding><funding>Innovation Fund of the Federal Joint Committee</funding><pagination>714</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8522064</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Sepsis is triggered by an infection and represents one of the greatest challenges of modern intensive care medicine. With regard to a targeted antimicrobial treatment strategy, the earliest possible pathogen detection is of crucial importance. Until now, culture-based detection methods represent the diagnostic gold standard, although they are characterized by numerous limitations. Culture-independent molecular diagnostic procedures represent a promising alternative. In particular, the plasmatic detection of circulating, cell-free DNA by next-generation sequencing (NGS) has shown to be suitable for identifying disease-causing pathogens in patients with bloodstream infections.&lt;h4>Methods&lt;/h4>The DigiSep-Trial is a randomized, controlled, interventional, open-label, multice</pubmed_abstract><journal>Trials</journal><pubmed_title>Optimization of sepsis therapy based on patient-specific digital precision diagnostics using next generation sequencing (DigiSep-Trial)-study protocol for a randomized, controlled, interventional, open-label, multicenter trial.</pubmed_title><pmcid>PMC8522064</pmcid><funding_grant_id>NVF1_2020-060</funding_grant_id><pubmed_authors>Grumaz S</pubmed_authors><pubmed_authors>Greiner W</pubmed_authors><pubmed_authors>Brenner T</pubmed_authors><pubmed_authors>Stevens P</pubmed_authors><pubmed_authors>Axnick J</pubmed_authors><pubmed_authors>Pletz MW</pubmed_authors><pubmed_authors>Skarabis A</pubmed_authors><pubmed_authors>Bruckner T</pubmed_authors><pubmed_authors>Haug P</pubmed_authors><pubmed_authors>Witzke O</pubmed_authors><pubmed_authors>Berger MM</pubmed_authors><pubmed_authors>Marschall U</pubmed_authors><pubmed_authors>Altin S</pubmed_authors><pubmed_authors>Ruprecht TM</pubmed_authors><pubmed_authors>TIFOnet Critical Care Trials Group</pubmed_authors><pubmed_authors>Luntz S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Optimization of sepsis therapy based on patient-specific digital precision diagnostics using next generation sequencing (DigiSep-Trial)-study protocol for a randomized, controlled, interventional, open-label, multicenter trial.</name><description>&lt;h4>Background&lt;/h4>Sepsis is triggered by an infection and represents one of the greatest challenges of modern intensive care medicine. With regard to a targeted antimicrobial treatment strategy, the earliest possible pathogen detection is of crucial importance. Until now, culture-based detection methods represent the diagnostic gold standard, although they are characterized by numerous limitations. Culture-independent molecular diagnostic procedures represent a promising alternative. In particular, the plasmatic detection of circulating, cell-free DNA by next-generation sequencing (NGS) has shown to be suitable for identifying disease-causing pathogens in patients with bloodstream infections.&lt;h4>Methods&lt;/h4>The DigiSep-Trial is a randomized, controlled, interventional, open-label, multice</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2026-05-27T23:25:43.95Z</modification><creation>2024-12-04T13:03:41.864Z</creation></dates><accession>S-EPMC8522064</accession><cross_references><pubmed>34663439</pubmed><doi>10.1186/s13063-021-05667-x</doi></cross_references></HashMap>