Rodríguez-Fernández, Miguel
Herrero, Rocio
González-De-La-Aleja, Pilar
Valverde-Fredet, María Dolores
Ventero, María-Paz
Trigo-Rodríguez, Marta
Giner, Livia
Aller-García, Ana Isabel
Pinargote-Celorio, Héctor
Espíndola-Gómez, Reinaldo
Parra, Mónica
Martínez Pérez-Crespo, Pedro
Ramos-Rincón, José-Manuel
Fernández-Pevida, Antonio
Lanz-García, Joaquín
León, Eva
Valiente-De-Santis, Lucía
Corzo, Juan E.
Rodríguez, Juan-Carlos
Merino, Esperanza
Merchante, Nicolás https://orcid.org/0000-0003-1120-8942
Funding for this research was provided by:
Instituto de Salud Carlos III (PI20/P1450)
Article History
Received: 13 September 2025
Accepted: 24 October 2025
First Online: 7 November 2025
Declarations
:
: Marta Trigo-Rodríguez has received payment or honoraria from Tillots for lectures or speakers bureaus. Esperanza Merino has received payment or honoraria from MSD and Tillots for lectures or speakers bureaus. Nicolás Merchante has received payment or honoraria from Tillots, Merck, Sharp, and Dome for lectures or speakers bureaus. All other authors (Miguel Rodríguez-Fernández, Rocio Herrero, Pilar González-De-La-Aleja, María Dolores Valverde-Fredet, María-Paz Ventero, Livia Giner, Ana Isabel Aller-García, Héctor Pinargote-Celorio, Reinaldo Espíndola-Gómez, Mónica Parra, Pedro Martínez Pérez-Crespo, José-Manuel Ramos-Rincón, Antonio Fernández-Pevida, Joaquín Lanz-García, Eva León, Lucía Valiente-De-Santis, Juan E. Corzo, and Juan-Carlos Rodríguez) have nothing to declare.
: This study was designed and performed according to the Declaration of Helsinki and was approved by HUV Ethics Committee (ref. no. 1254-N-20). Following this approval, all participating centers were formally notified and adhered to the study protocol on the basis of the favorable evaluation from the coordinating center’s ethics committee. With respect to informed consent, a waiver was granted. This was based on the consideration that the intervention implemented—namely, the introduction of a specific clinical pathway for CDI management—was intended to become part of the standard clinical practice routinely conducted by our institutional ASP team dedicated to CDI. Therefore, it was not deemed necessary to obtain individual patient consent.