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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorMartínez Martínez, Luis
dc.contributor.authorde Lossada, Alfonso
dc.contributor.authorMaroto-Diaz, Marta
dc.contributor.authorMoya-Alarcón, Carlota
dc.contributor.authorMoya-Alarcón, Carlota
dc.contributor.authorFerrer, Ricard
dc.contributor.authorLUQUE, SONIA
dc.date.accessioned2025-10-06T12:09:11Z
dc.date.available2025-10-06T12:09:11Z
dc.date.issued2025-09
dc.identifier.citationFerrer R, Luque S, Martínez-Martínez L, de Lossada A, Maroto-Diaz M, Moya-Alarcón C, et al. Estimating the Value of Aztreonam-Avibactam in Treating Metallo-beta-Lactamase-Producing Enterobacterales Infections in Spain Using the STEDI AMR Value Framework. Infect Dis Ther. 2025 Sep;14:2071–2092.
dc.identifier.issn2193-6382
dc.identifier.urihttp://hdl.handle.net/11351/13796
dc.descriptionAntimicrobial resistance; Carbapenem-resistance; Cost effectiveness
dc.description.abstractIntroduction Treatments for serious infections caused by multidrug-resistant gram-negative bacteria, including metallo-β-lactamase-producing Enterobacterales (MBL-EB), are limited and aztreonam with avibactam (ATM-AVI) is the first β-lactam/β-lactamase inhibitor combination active against MBL-EB approved in Europe and approved for reimbursement by the Spanish National Health System (NHS). This study aims to estimate the value of adding ATM-AVI as a new first-line treatment into the current strategy (ATM–AVI → cefiderocol → colistin + meropenem) in patients with hospital-acquired/ventilator-associated pneumonia (HAP/VAP) and complicated intra-abdominal infections (cIAI), caused by MBL-EB from the Spanish NHS perspective. Methods A dynamic disease transmission model was developed to assess the value of ATM-AVI considering the transmission, diversity and enablement components of the value framework for antibiotics, called STEDI (spectrum, transmission, enablement, diversity, insurance). Transmission and diversity value were described by estimating direct population-level impact on treatment outcomes and resistance development. Enablement value was estimated by linking population-level improvements in antimicrobial effectiveness into improved prophylactic effectiveness. Inputs for efficacy, resistance, adverse events, and costs were sourced from the REVISIT study, literature and expert opinion. A 10-year infection transmission horizon was used; quality-adjusted life years (QALYs) were estimated over a lifetime and valued using a willingness-to-pay (WTP) threshold of €25,000/QALY gained to calculate the net monetary benefit (NMB). Costs and benefits were discounted at a rate of 3%. Results Over 10 years, the intervention strategy introducing ATM-AVI was dominant, leading to a 2.96% proportional reduction in resistance, 19,533 fewer infections and 4662 lives saved (47,319 QALYs gained) and a cost saving of €40.5 million. The NMB was €1.22 billion. Conclusions In Spain, ATM-AVI is a highly cost-effective and urgently needed treatment option for patients with MBL-EB including HAP/VAP and cIAI infections. Using the novel STEDI framework unlocks the considerable value of a new antibiotic which is essential to support incentives for the development of new antimicrobials.
dc.language.isoeng
dc.publisherAdis
dc.relation.ispartofseriesInfectious Diseases and Therapy;14
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.sourceScientia
dc.subjectMedicaments antibacterians - Ús terapèutic
dc.subjectMicroorganismes - Resistència als medicaments
dc.subjectEnterobacteriàcies
dc.subjectMalalties bacterianes gramnegatives - Tractament
dc.subjectInhibidors enzimàtics - Ús terapèutic
dc.subjectBeta-lactamases
dc.subject.meshEnterobacteriaceae Infections
dc.subject.meshGram-Negative Bacterial Infections
dc.subject.mesh/drug therapy
dc.subject.meshAnti-Bacterial Agents
dc.subject.mesh/therapeutic use
dc.subject.meshDrug Resistance, Microbial
dc.subject.meshbeta-Lactamase Inhibitors
dc.subject.meshDrug Combinations
dc.titleEstimating the Value of Aztreonam-Avibactam in Treating Metallo-beta-Lactamase-Producing Enterobacterales Infections in Spain Using the STEDI AMR Value Framework
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1007/s40121-025-01202-6
dc.subject.decsinfecciones por Enterobacteriaceae
dc.subject.decsinfecciones por bacterias gramnegativas
dc.subject.decs/farmacoterapia
dc.subject.decsantibacterianos
dc.subject.decs/uso terapéutico
dc.subject.decsfarmacorresistencia microbiana
dc.subject.decsinhibidores de betalactamasas
dc.subject.decscombinaciones de fármacos
dc.relation.publishversionhttps://doi.org/10.1007/s40121-025-01202-6
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Ferrer R] Servei de Medicina Intensiva, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Grup de Recerca de Shock, Disfunció Orgànica i Ressuscitació, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. [Luque S] Servei de Farmàcia, Hospital del Mar, Parc de Salut Mar, Barcelona, Spain. Infectious Pathology and Antimicrobials Research Group (IPAR), Institut Hospital del Mar d’Investigacions Mèdiques (IMIM), Barcelona, Spain. CIBER of Infectious Diseases (CIBERINFEC CB21/13/0002), Instituto de Salud Carlos III , Madrid, Spain. [Martínez Martínez L] Unit of Microbiology, Univ. Hosp. Reina Sofía, Córdoba, Spain. Department of Agricultural Chemistry, Soil Sciences and Microbiology, University of Córdoba, Córdoba, Spain. Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, Spain. CIBERINFEC, Instituto de Salud Carlos III, Madrid, Spain. [de Lossada A, Maroto-Diaz M, Moya-Alarcón C] Pfizer SLU, Madrid, Spain
dc.identifier.pmid40719947
dc.identifier.wos001537781400001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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