DALBACEN cohort: dalbavancin as consolidation therapy in patients with endocarditis and/or bloodstream infection produced by gram-positive cocci

Identifier:  imarina:9267386

Handle: https://hdl.handle.net/20.500.11797/imarina9267386

Authors:  Hidalgo-Tenorio, Carmen; Vinuesa, David; Plata, Antonio; Davila, Pilar Martin; Iftimie, Simona; Sequera, Sergio; Loeches, Belen; Eduardo Lopez-Cortes, Luis; Carmen Farinas, Mari; Fernandez-Roldan, Concepcion; Javier-Martinez, Rosario; Munoz, Patricia; del Mar Arenas-Miras, Maria; Javier Martinez-Marcos, Francisco; Maria Miro, Jose; Herrero, Carmen; Bereciartua, Elena; De Jesus, Samantha E; Pasquau, Juan

Abstract:
Objectives To analyse the effectiveness of dalbavancin (DBV) in clinical practice as consolidation therapy in patients with bloodstream infection (BSI) and/or infective endocarditis (IE) produced by gram-positive cocci (GPC), as well as its safety and pharmacoeconomic impact. Methods A multicentre, observational and retrospective study was conducted of hospitalised patients with IE and/or BSI produced by GPC who received at least one dose of DBV. Clinical response was assessed during hospitalization, at 3 months and at 1 year. Results Eighty-three patients with median age of 73 years were enrolled; 73.5% were male; 59.04% had BSI and 49.04% IE (44.04% prosthetic valve IE, 32.4% native IE, 23.5% pacemaker lead). The most frequently isolated microorganism was Staphylococcus aureus in BSI (49%) and coagulase-negative staphylococci in IE (44.1%). All patients with IE were clinically cured in hospital; at 12 months, there was 2.9% loss to follow-up, 8.8% mortality unrelated to IE, and 2.9% therapeutic failure rate. The percentage effectiveness of DBV to treat IE was 96.7%. The clinical cure rate for BSI was 100% during hospital stay and at 3 months; there were no recurrences or deaths during the follow-up. No patient discontinued treatment for adverse events. The saving in hospital stay was 636 days for BSI (315,424.20euro) and 557 days for IE (283,187.45euro). Conclusions DBV is an effective consolidation antibiotic therapy in clinically stabilized patients with IE and/or BSI. It proved to be a cost-effective treatment, reducing the hospital stay, thanks to the pharmacokinetic/pharmacodynamic profile of this drug.