TIGRIS and EUPHRATES eventually join and provide new evidence

Septic shock driven by endotoxemia is associated with high mortality despite advances in supportive care. Polymyxin B hemoperfusion (PMX-HP) selectively removes circulating endotoxin and has shown variable efficacy in randomized trials. While earlier studies, such as EUPHAS, suggested benefit, subse...

Descripción completa

Detalles Bibliográficos
Autores: Iba, Toshiaki|||0000-0002-0255-4088, Helms, Julie|||0000-0003-0895-6800, Nagaoka, Isao|||0000-0003-0824-7406, Mineshima, Michio, Ferrer, Ricard|||0000-0002-4859-4747
Tipo de recurso: artículo
Fecha de publicación:2025
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:326367
Acceso en línea:https://ddd.uab.cat/record/326367
https://dx.doi.org/urn:doi:10.1186/s40560-025-00835-6
Access Level:acceso abierto
Palabra clave:Endotoxin
Extracorporeal circulation
Sepsis
Shock
Biomarker
Descripción
Sumario:Septic shock driven by endotoxemia is associated with high mortality despite advances in supportive care. Polymyxin B hemoperfusion (PMX-HP) selectively removes circulating endotoxin and has shown variable efficacy in randomized trials. While earlier studies, such as EUPHAS, suggested benefit, subsequent trials, including ABDO-MIX and EUPHRATES, yielded neutral results, partly due to heterogeneous patient selection. The recently completed TIGRIS trial addressed these limitations by enrolling septic shock patients with intermediate endotoxin activity (EAA: 0.60-0.89) and high multiple organ dysfunction syndrome (MODS>9) using a Bayesian design. In 151 evaluable patients, PMXHP achieved the primary endpoint, with a 95.3% posterior probability of 28-day survival benefit (adjusted odds ratio [OR]: 0.67; absolute risk reduction [ARR] 6.4%). At 90 days, mortality reduction was greater (ARR: 17.4%; adjusted OR: 0.54;>99% posterior probability of benefit), corresponding to a number needed to treat of 8.1. These results support the targeted use of PMX-HP in a biomarker-defined subgroup and may facilitate broader regulatory approval.